| Tag | Content |
|---|
EnhancerAtlas ID | HS197-21738 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr9:93922950-93929140 |
Target genes | |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EGR1 | MA0162.3 | chr9:93922993-93923007 | CCCGCCCCCGCACT | + | 6.21 | | EGR3 | MA0732.1 | chr9:93922992-93923007 | CCCCGCCCCCGCACT | + | 6.83 | | EGR4 | MA0733.1 | chr9:93922992-93923008 | CCCCGCCCCCGCACTG | + | 6.06 | | ESR1 | MA0112.3 | chr9:93925777-93925794 | AAGCTCACCATGACCCT | + | 6.2 | | EWSR1-FLI1 | MA0149.1 | chr9:93925033-93925051 | GCTCCCTTCCCTCCTGCC | - | 6.02 | | EWSR1-FLI1 | MA0149.1 | chr9:93923028-93923046 | CCATCCTTCCTCCCCTTC | - | 6.14 | | EWSR1-FLI1 | MA0149.1 | chr9:93923024-93923042 | GCTTCCATCCTTCCTCCC | - | 6.96 | | EWSR1-FLI1 | MA0149.1 | chr9:93925037-93925055 | CCTTCCCTCCTGCCTTCC | - | 7.71 | | IRF1 | MA0050.2 | chr9:93927978-93927999 | TCTTTCTTTCTTTTTTCCTTT | + | 6.19 | | Myod1 | MA0499.1 | chr9:93923899-93923912 | TGCAGCTGTCACC | + | 6.5 | | RARA | MA0729.1 | chr9:93924774-93924792 | AAATGACCATTTGACATC | - | 6.34 | | RREB1 | MA0073.1 | chr9:93923046-93923066 | CCCCCCACCACCCAAACTGC | + | 6.2 | | ZNF263 | MA0528.1 | chr9:93923037-93923058 | CTCCCCTTCCCCCCCACCACC | - | 6.17 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_20662 | chr9:93922920-93928116 | CD56 | | SE_25080 | chr9:93921861-93923935 | Colon_Crypt_3 | | SE_25080 | chr9:93926928-93927857 | Colon_Crypt_3 | | SE_27567 | chr9:93923550-93925696 | Esophagus | | SE_27567 | chr9:93925703-93927801 | Esophagus | | SE_39461 | chr9:93922903-93927981 | Jurkat | | SE_43889 | chr9:93923304-93928115 | MM1S | | SE_44347 | chr9:93924124-93928055 | NHDF-Ad | | SE_44911 | chr9:93923869-93928048 | NHLF | | SE_56573 | chr9:93923534-93928107 | u87 | | SE_66540 | chr9:93922903-93927981 | Jurkat |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 93924725 | 93924800 | | chr9 | 93924982 | 93925425 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I091160 | chr9 | 93923114 | 93929552 |
|
Enhancer Sequence | AAGACGCCTG AGCAGAGGCG CCTCGGCTCT ACCCAGCTCA GCCCCCGCCC CCGCACTGCA 60
CATCCCCTCT GTGGGCTTCC ATCCTTCCTC CCCTTCCCCC CCACCACCCA AACTGCCCCC 120
AGGGCTCTGC TGAGGCTTCC CTGCTGTCTG GGCAGGGGCT GTTGGTTCCT CAGGAGCACG 180
CCGTGAGATG AGCACCCAGG GAGTGACGAA GGGGGCTCCA GGGGATACTG GGGAGGGCGA 240
GTCAGAGCAG GGCCCAGAGG GGAGCAGCAG GCAGGGCACA ATTTCGGGCC AGTTCCGGGG 300
CAGGGTGGGT GGAGCCCAAC CCCTAGGGGA ACTCGGATCC TAATGACACC CTCAAGTCTG 360
CCCGTCTGCC CGGGCTTCTT ACTCCCACTC TGGTCCTCTT GGCCAAAGGC ATGAGGCCGG 420
GAGGACGGCG ATGAGGATCA AAACCCCTGG GTCCTTCCTG CCTCTGCGCC TGCCAGCAAA 480
ACAGCTCCAT GAGTCCAAGG GCAGCTCAAG GGCAGCTCAA GGGCAGGCCA CGGGAGCCAC 540
AGGTCCTGGC CATACAGCAA AAACATACGG AAGCCAGGGC AGTGCAGACA CAGCAACAGG 600
ACAGAGGGGC CTGGCTGGAG CGCCAATGCC AGGGGTCTCT CAAGGCCCGC AACACGGTGT 660
CCTTCTTGGA CTAGAGTCTC AGTTAAATAA CAAAGAGGGG ATCTGATGAC GTCCACGTGG 720
GCTTCTCCCT GCCTTTGGTG GCGCCCCGGC CCTCCTGTGC GTCCTCCTGG CCCTGCTCAG 780
ATCCTAGGAG CCATCACACA CTCAACATCC CCAGGCAGCA CCAGCACCAA AGCCCCTCAT 840
TCCATAGCCC TCTAACACCT GGCTCAGAGT GAGCTCAGCT TCTTTTCTTC ACACATGTCT 900
TCATGGCAGC AAGGGAATCA AAAACTCTCC TCCTGGCCAC CCACGGAAAT GCAGCTGTCA 960
CCAGATGGAA AAGGAGGAGA AGATGCAGTG GGCTTGGGTG GTCCCAGGTG GCCCCTGGCC 1020
GGACTCTTTC CCTCAGTTGG GGGACAGAGG CTGATTGGAA GAGCACCTCC TTCCCAACGC 1080
TTGAGGACAG GGCCTTCCCT GACACCTGTG CCTGGGCTGG TCTTCTGCAC CCTTAGCCTC 1140
AAGTAGCCTC AGACCACTGC AGTGCTGTTG AGGGTTATCC ATAGCGTTTT TTTCCTGTGC 1200
TTTGGGTCTC CTTTGCCATC TGCAGCTGGA CTAGGGGTCT TGGATTGCCA GGGAGGCTTC 1260
TGTGAAGTGG GCTGAAGAGA GCCCTTCCTC ACTCGGAAGG CACAGCACAG CCCCGCCGCA 1320
TTTATAAGTG AAAAGGGAGA CCCCACTGTG ATGGGGATCC TTCTGCCATT CCCCCAAGAC 1380
CCCGGGATTG ATGAGAGGCA TTCAGAACTG CAAGGGGCAT GAGGGGGCTG TCATGTCCTT 1440
GTCTGGGCGG CCTCCCAGGC TCAAATTGCT GCCTGAGAAC AGGTGGCAGA ACATTCCTGA 1500
ATATTTAACC CTTGGCTCGC AAGAGTGCAG GAATGACAGT TCTGTGCCTG AGGAAAAGAT 1560
TCGTGTCACT CGCACCTCAC TTAGGACAAC TCGTGCTTTA CAGAAATTTA CTAATGTTAA 1620
AGAATGATTT GTGGTTTCTT TGCTCAAATA CAGGAAACTG ACTTTTCTCA AAAATGAACT 1680
CTCCCTACCA ATCTGCACCA TGAAATTATT TCAGCAAACA AAAAATAATG GTTGCCCATC 1740
ACCGCACACT GCGTGTGACT CAGCCATCAC TCACAGGCAA AGAAGGGTGT TCTCTCCTCT 1800
CCCTGTCAGT TACTAATTCT CTGTAAATGA CCATTTGACA TCCTGGCCGG GGAGGATTCA 1860
GATCAGAGAT GACTTCCCCA CTGCCACAAA GTATGGTTCT GGGAAGGACA ACCAGCCCCA 1920
AGGCCACGAA GATTCTGAAA AAGTTTCTTC TCATTTGAAG TCCAGTATTT CCTCGGCCCC 1980
ATTTTTCTGT TAAACAATCC TTTTCCCTTG GAGATTGCTA AAGCTTAGCT CCAGGGCCAG 2040
CCTAAGCTCC AGCAGAACTG GGAGCGTCTC CTGTGTCTAC ATAGCTCCCT TCCCTCCTGC 2100
CTTCCTACTA TCAAAGGAGA AACAGCGTGT AATTTGATTT TTTCCCCTTC TCCTCACTTG 2160
CCATACTGTG TTCTTTGCCT GGGCCTGTGC CTCTCCTTGC AGAGGCTGTG GACAGGAGCA 2220
CCGAGAGCCA CTTCCTGGAG CATGCTCCCC ACCCCCGCAG CCTGTGGCTT CAGCCTCTGC 2280
TTCTGCAGAC AGCGGTGGAG GAAGTCAGGA CTGTCCCTTC TGACCTGAAC ACCTACCTCC 2340
AAGTCCTCCC TGTCGCCACA GAGACCCGGC AATGCAAGTG AGTCCTGTTT GACCTCGTCA 2400
ATCATCGCAG ACTGTAAAGG TGACTCGGAT GCTCAAGAAA CGAGCATACC CAGCAGTGGG 2460
CCCCAGACTT CTCGCAGGCC CAGGTCCTCC TGGGTGCACA GAGACCTACC AGACAACGGT 2520
CCGGCTGCAC TGGTGTTGTG AGATGCCTGT GTCAGAAGAC ACTGAGTTCC TCACTCGCCT 2580
CCTATCATGC CGATGATCAC AGGAGAAAGA GCAGGGCACA TGCATGCCAG CATGCTGAAG 2640
GGAGGCCAAA ACCCATGCTT GAAAACCACA GGTCCTGTTC TAGGAGCAGG AGATATATTT 2700
AGCCAAGCAG GATGTTTGTG GGTAAACCAA CATTTTGCTG TAAATAAAAT TCTGCAAACT 2760
CGGGACTTTG AGAATTGCAG AAGCTTACTT TGCCTGCGTA TTGGCAAGAG AGCTATTTTC 2820
CTAACACAAG CTCACCATGA CCCTCATTCA GAGATGCGCT TGACGCCGAG GGTGGTGCCT 2880
TTTCGCTAAG GGGTGCTGTC AGGGGATTGA GTAGGAGCCT GAAGAGCTAG GAGTATCTTC 2940
TCCCTGGGCA GACCAGCAGG CAGACCCTGT CCCTTCACAC TACAGTGGCA CGTGATGGGC 3000
CCCACTGCCC ACCTGGTTCT GGTGTCCAGG CTGAAGTCCT CGTGTGACAC TCCAAACTGT 3060
TCTGGCAAGG AAGGCTCACG GGTTCTGACC TACACTCTGA AACTGACCAG TAGTGATAAA 3120
CTCCGCATGG ACTTCAGCCA TCATTGCGTA CGTAAGAAAT ACGTGTTGCA CACAGAGTGC 3180
TTCTCTACAT TCCCAGGTTT GCCACTCCCC GACTTTTGCT GAAGCAGGTT TCTACTCCAT 3240
CAGTCCCACA GATGTGTTCA CAGGGCCAGC ACTGAGTGTG GTGCTGGGGA AGGCATGTGC 3300
TTGGAGGCAG CCCTGTGAGA TGGCACAGCC TAGGGGAGGA GTCGTGGTGG GGAAGACCCT 3360
GGCCACGCAT GATAGAGGAA GCGTGGCCAC ACAGTCTTTG CTGTCCCTGC CACAGCATGG 3420
TGCTGTAAGT CTCCTCCTTC CGAGTCTGTG CAGACTTATG TGACACATTT GACCCAACAG 3480
AAATGCAGCA TTTGTGGTGT GTGAAAGTTC CAGACCAGGC CACAGCGAGC TCCGTGGCTT 3540
CGGCTGTGTC TCCTGGAGCA CTTGCTCTCA GGACCCCCTC TCTCAGAGCC CAGGCACCAC 3600
GCCGTGAGAG AGCCCCAGCC ACAGAGACAG GCTACGTGTA GGTGCTTTCA TCAAAGTGCC 3660
ACCTGTGCCT CCCCGCAGCA GTGTCAGGCC ACCAGCTTGG ACAGGCAGCT CCAGCCTCCA 3720
GTGGAGGCTT CAGAGGACAG CATCAAACAG CATCCACAAA GGAGACCCAC CTTGTGAAAA 3780
GCGCCTAGCC AAGCCCTGCC CAAATCCCTG GCCTGTGCAA TTGTGAGCAA AGCAATTCAA 3840
TTTGGAGTGG TTTTATGCTG CAGTAGGTGA CCAAAGCACT ATGGAAGTGA ATATCAGGAG 3900
CCCCTCACTG GGATGTCAGA AGACATTCAA GGAAGGTTTC CTGGAAGATT TAGTACCTCA 3960
GGTGGTACAG GAGAAGGTGA GATGGAGAGA AAGCAACCCC AGTCTGAAGA CGCAGTGGTA 4020
AGAAAGGGTC ATTCCCCTGG GCATGTGTGG TCTGCTGGGG GATGACAGCC GAGGTGAACT 4080
TGAAGCAGAG GACACTCAGA CAAGCTGCAC TCTGAATCCC GCTACGCTGA CCGCAGCACT 4140
TGCTGAAGAA GCCGCCTCGC CACGCCCAAG CCCTGCAGAG GGAAGGACTG AGGAAGGCAG 4200
CTCAGAGGCC TCAGGCAGCC ACAGTGTGCA TGCTTGTCTA TGACTCACAG CTACGACGTG 4260
GCCTGTGCTG CTGCAGCTGC TGATAAGCCT CAAACCTCAT ATACCACTCT CTTCCGAGGA 4320
TTTTTTAAAT ACACAAAACT GGGAGTGAGA GGGGTATTTA ATTCCCCTAC TAACACATGT 4380
TGGGCGCAGC TGGAGCAGCC AGGCCCACTG TAGCTGGGAA GATGCGGTGC CTTGAGGTGC 4440
AGGCACTGCT CACTGCCACA TGTGAGCACA GGTTCTGAGG GTGAAAGGTC CCTGGTATCT 4500
GGCCAGAGTG TTAGACTCTG GAACATAAGA AGCCCCCGAG GTGGTGGAGA AGGTCTAGCC 4560
AGGCTCCAGA CTGGCTTCAC AGAGGTAATG CTTTTTGGTT TGAAATCCGT AAGAGCGCAC 4620
TACAACTTCA GGGCAAGCTC CAACAGTGCT TCTCAAACTT TAATGAGCAC CCAAATCATC 4680
AGGGGGCGCG GGGGCAGTGG GTCGCTTACT AAAATGAAGA TTCTGCATCA GGAGGTCTGG 4740
GGCGGTGACA CGATTCTGTG TTTCTAACAC GTTCCTGGGT GAGGCTGAAG CCACTAGTCC 4800
ATGAAGCACA CTTTGAGTAG CAAGAATGTG GAGGAACTGT CCCAGGATGG GCCATGATTT 4860
ACCTGAATTC TCACAGTGGC TTAGACAATG GAGACCTTGT CCACAACTAA AAAATAAAAA 4920
TAAAATCGAA CCACACTCAT TGTTCCAGGA AACAGCAATA ACATTGGAAA TAAATCAAAT 4980
GGTTTATTAC TGAGATTGTA TTATCAGAGC TATATATTAA TTTTTTTTTC TTTCTTTCTT 5040
TTTTCCTTTT TTGAGACAGG GTCTCACTCT GTCACCCAGG CTGGAGTGCA GTGGCATGGT 5100
CACTGCTCAC TGCAGCCTCG AGTTTTCGGG CTCAGGTGAT CCTCCCACCT CAGCCTCCCG 5160
AGTAGCTGGG ACTACAGGCA TGCACCACCA CATCCAGCTA ATTTTTTGTA CTTTTAGTAG 5220
AGATGAGGTC TTGCCATGTT GCCCAGGCTG GTCTCAAACT CCTGGGCTCA AGTGATTCGC 5280
CCACCTCAGG CTTTCAAAGT GCTGGGATTA CAGGTGTGAG CTATACCCCC CCACCCCACC 5340
CACCTGTATA TTCATTTTCT ATAACTGTGT AACAAATAAT AAATTCCTAT TACTGTATAA 5400
CAGACTTAAT AGCTTAAAAC AACACCCATT TATGGTCTCA TAATTCTGCA GGTCAGAAGT 5460
CCAGGCGGGT TTAATGGGGT TTTCTGCTTG GAGTCTCACA AGGCCAATGT CAAGGTCTCC 5520
TATCTGGAGG TTTGGGGAAA AAAATCTACC TCCAAGTTTA ATCTGGTTGT TGGGCAAATT 5580
CACTTCCTTG CAGTCCCCTG AAATCCTCAT TTTCTTGCTG GCTGTCAGCC AGGGGTTGCT 5640
CTCGGTAACA GGGACCTCCC AGGGCCTCCT CCATCTCAAA GCCAGCAACA GAGACTCCAC 5700
CCTGGTGTCA AATCTAACTC CGGCTCTGTT ACCAGCCAGA GAAAACTCTG CTTTTAAAGA 5760
ACTTGGCCGG GTGCCGTGGC TCACACCTGT AATCCCAGCA CTTTGGGAGG CAGAGGCAGG 5820
CGGATCACCT GAGGTCAGCA CTTTGAGACC AGCCCGGCCA ACATGATGAA ACCCCGTCTC 5880
TACTAAAAAA TACAAAAATT AGCCAGGCAC AGTGGCAGGT GCCTGTAATC CCAACTACTC 5940
AGGAAGCTGA GGCAGGAGAA TAGCTTCAAC CTGGAGGCAG AGGTTGCAGT GAGCCGAGAT 6000
TGCCCCATTG CCCAGCCTGG GCGATAGAGC GAGACTCTGT CTCAAAAATA AATAAATAAA 6060
TAAATAAGAA CTCATATTAG GCCCCACCCC AGATAATCTT CCAATTTTTA GATCAGACAA 6120
TTAGTGACCT TAATTATATC TGAAAGAGTC TTTTGCCATA CAAGATAACA TAATCATGCG 6180
AATAACGCCA 6190
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