| Tag | Content |
|---|
EnhancerAtlas ID | HS105-18688 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:52538610-52543240 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr12:52542755-52542770 | GGGGCTGTGTGACCT | - | 6.23 | | FOSL2 | MA0478.1 | chr12:52541278-52541289 | CTGAGTCACCC | - | 6.02 | | JUNB | MA0490.1 | chr12:52541278-52541289 | CTGAGTCACCC | - | 6.02 | | KLF16 | MA0741.1 | chr12:52539330-52539341 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr12:52539331-52539341 | GGGGCGGGGC | - | 6.02 | | Zfx | MA0146.2 | chr12:52538774-52538788 | CTGGCCGAGGCCTG | + | 6.55 |
|
| | Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
| SE_02848 | chr12:52539469-52544270 | Astrocytes | | SE_03090 | chr12:52537464-52541166 | Bladder | | SE_03090 | chr12:52541180-52544017 | Bladder | | SE_23126 | chr12:52536930-52548073 | Colon_Crypt_1 | | SE_23778 | chr12:52537491-52544411 | Colon_Crypt_2 | | SE_24790 | chr12:52537298-52547328 | Colon_Crypt_3 | | SE_26568 | chr12:52536245-52551492 | Esophagus | | SE_32153 | chr12:52536995-52544558 | Gastric | | SE_33678 | chr12:52540418-52544073 | H2171 | | SE_34302 | chr12:52536323-52548139 | HCT-116 | | SE_34629 | chr12:52536709-52551617 | HeLa | | SE_35885 | chr12:52537041-52552074 | HMEC | | SE_43322 | chr12:52536940-52547179 | Lung | | SE_43468 | chr12:52535274-52548206 | MCF-7 | | SE_45270 | chr12:52539380-52543199 | NHLF | | SE_57381 | chr12:52537540-52541212 | VACO_503 | | SE_57381 | chr12:52541277-52544554 | VACO_503 | | SE_57927 | chr12:52540569-52542459 | VACO_9m | | SE_64182 | chr12:52539345-52543937 | HSMM | | SE_64292 | chr12:52537455-52551439 | NHEK | | SE_68885 | chr12:52536855-52544359 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr12 | 52539319 | 52539712 | | chr12 | 52542210 | 52542726 | | chr12 | 52539375 | 52540098 | | chr12 | 52540120 | 52542400 | | chr12 | 52540964 | 52541526 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I052143 | chr12 | 52536922 | 52551852 |
|
Enhancer Sequence | GAATCGAGGT TAGATGACTA GAAGAACTTC CTGGCGCAGA TCTGGGGAAG CCCTGGCCCA 60
GAGGCCTGGC CTTTACCCAT CCCTGGATCC TCTGCCTCTC CCCAGCTCCC ACTGTCCTCA 120
GACACCCCTT GCCCCTGTCT GGGATTCTGG GGGTGAGCCC CGGCCTGGCC GAGGCCTGCT 180
GCAGGGTGAG AGTTATGTTC CAGCTCCATT GAGTGATAAG TGCCACACTG CGACCTCTCT 240
GGGTCTTCCC TGCCCACTAC GGTGGGGGCG TGGGGCCCCT GCTCCATGGG CTGGGCTTCT 300
GACAGGACAG TGGCAGGCCA AGGAAAGGAC CTACCAAGCC CACCTTGGCT TGAAGGCTGA 360
GGGGGTGAGA GAGGGCTGGG CGGGCCTGGT GAGTCTGGGG CACCTGGGCC TGCCTGCGAG 420
GGTCCCTGAA GCATTGTGAC AGTGACTGCA GCAGGAGGAC TTCAGGCTGA GGCTGAGGGA 480
AGAGTCCCAG CAGCTTCCTG GGAAGCAGAG GAGGGTGCTG AGCTCAGCTT GTGTGTCCCT 540
GAGTGGCAGG CCTGGGCTTT CTGGGAATGC AGCCTGGGCC TGAGGGCAGG CGAGGGAGGC 600
CAGCCAGGGG TCCTGCACCA CCGCCCCCAC CCACTGCCGG CCCCAGTCTG GCTAGGAGAG 660
TGGGGGGTCT CCATTTCAGC CTGCTGGGCC TTTAGAGTAG GGCAGGGACT GGGGTGCTCT 720
GGGGGCGGGG CAGGATCGAG GGGTGTGGGG TGAGGGGGAA GATGAGTCCC CTGGGCGTAT 780
TGGAACCCAT GCCAGGGGCC TGGGTTTGAC TCCCTCCCCT AAGGTGCGCA TTCCCAGGGC 840
CTGGGGGAGA GGAGTGGGCT TGGGGCTGTG TGCAGTGGGG CCCTGAGCTG GGAAGGCACG 900
GAAGTGCCTG CTCTGACCCA TCCCCCACCT CCGCAGGGCA GGCAGGCTGA GGCCTGAGTC 960
TGAATGACCC CCTACAAGTC TTGCCATAAA GCCACTGGTG CTGGGAGGGC GTCTGCTGTT 1020
CTTAGTGGGG AACACGTCAT GTCCCCAGCC CCTGTCCCTC TGTGTCAGCT CCCAGCCTGG 1080
GCGTGCACAG TCGGGTGCAG CAGAGGCTCC TGATGGCTGG ACAGGGGGCC AGTGTGGGCG 1140
CAGTGTGGGC AGTCTGAGCA CAAGTGGGGT TTGTGGGCAG TGTGGATGCT GGGGGGCTTA 1200
GCGGAGGGTT ACTGGAGACG ATAGAGGTGT GCGGTGCTCC TGGGCTATAG AATAGGGAGG 1260
AGGATTAGAA AGGGCCTGGG AAGGCAAGGC TTGGAGGGCT GGTTAGGTTT TGGAGCAGTG 1320
GTTGGGCTGA CAATGGAATT TTGGGCACAC AGATGATCTG AGAGGGGTGA GGGTCAGAGC 1380
TGGGGTTTAG GATGGGATTG GTTTAGGGCT GGGTTGTGAG GATGGAGTAG GGCTTGAGCA 1440
CAGAGAAGCA AGTAGAGTTT GGGGCACAGT TCAAATTTGG GGTTAGGGTT GGGATTAGTA 1500
CCATGTCAGA TGAAGGGATG GATTCAGGGC TGAGGGTGAG GGCCATTTGC AGTTAGCACC 1560
GGGCACAGCT CGGGGTTGGG TGAGGCTGGG TCAGGGCGAG GGCTTCTGGG GTAGGATCAG 1620
GTGCGTGGGG CCTGCTGAGA GTGTCCGAGG ATCTGCTCGT TCTGCCCTGT GGTGTCCCTG 1680
ATGGGCTTTT TCTCCCTTTT TGCAGGGTTG CTCTCAGCTA TGGCCTTGGT TGGAGACCCA 1740
GCTGGTGGCC AGACCCCACC ACCCTTTGGG TTTGGACCAG GGCTCCAGGA GGTGGCATCC 1800
TGCAGTGGAG CCCCAGACTC TCCAGGGATG GAGTATCAGC TGAAGCAGGG GCCCCCATTT 1860
CACACTGGAA AGGGCCTGGG GTTTGGGGTT CCCCCCTGCC GGGGAATCCA GGGTCCCCAC 1920
CCCTGCCTGC TGCCTGCCCT CCTGCCTCGG CCTCACTCTG GGTCCTTGTC TGGGAACCTT 1980
AGCACCTTCT TTGAGCCGCT GGTGGTGTTG GCGCACTTAG CAGAGCAAGC CCTGGCCCCT 2040
TTCCTCACAA ACCTCACTCC CAGGTCTAGG CGGGGAGGCT GGGCTGCTCC TCATTGTCTT 2100
AAGCAGAGCG GTCACCTGAA GGCCTGGCCG TCTCACCTTG TCATGATTCC TCCACATTTG 2160
AGAGTGACGG AGGGGCAGGG AGTCAGGGCT GTGTCCACAG TGTGTCCTCA ACCCAGACTG 2220
AGCCAGGCCC ATGGCTCTCA CTGAGGTCCT CTCCTTCTGC CTTGGTTTCC CTCTGAGTCC 2280
AGCCCCATGG GGAAGCTGGG CTCCTGGGCC TCAGGCCTGA TGCTCCCTGT GCCAGGGCCT 2340
GTCCCCTGCT ACTGCACTGA GCTGGAGTCG GGGGCCTGGT TGTGGGCTTC TGCTCCTGGT 2400
CTCAGCGAGA CCTCCAGGCT TCCTTGGGCC CAGCTCCTCA TCTCAGCCGG TCGCACCTGG 2460
GCAAGTCCAG TCAGTGTGAG GGGCTACTTC GGTTTCCTCA CTGTGGCAGG GATTGGGGGA 2520
GCTCCTGAGC CCTGGGCTGG GGTGGGTCCG GAGGGGTGGG GGCTCCTGGC TGGGCTGGGT 2580
GTGCCTGTAT GTGACTCAGG CTGGATGCCC AGGCCCTGAG CTGGCGGCTT TGTTCTCCCA 2640
CTGGCCGGGT AGGGTGCGTG CTGCAGCCCT GAGTCACCCG GGTGTGGCCG AGCTGCTGGC 2700
GGGACACCAG AGCCATACAC CGCCACACTC ACAGAGATCC ACACACTGGA GCTCAGGACA 2760
CGGCGCCCTG AGAGCGGAGG GCCCCCCTGG TGTGGGTGCC GTCACTGGTG CCTTTCCCTC 2820
GGTGGTGCTG TGAGACATTC CCAAGAAGCT CCTTGGTGAC TAAGGGCCCT GTGCTCCTGG 2880
AGCAAACTCA GCTGTTTGCT GAGAAGGCCT TCCTTCTCTT CGTGGTTACT CCCTGGTTAG 2940
GGCCTGGAGG GGGACCTGCA GGCACAGCTG GAGACCCTGA GGGGCACACA GAGCCTTCCC 3000
CCGCTGCCTG ATAAAGGGCA TATGCAGGTG ACCATGTGCC ATCTGTCCAA ACTGTGCACC 3060
CACTGGATCC TTGAAACAGT TCTGAGAGGA AGGTGCATTG TTCCCACTTT ACAGATGCGG 3120
ACACCGGGGT TGCTAATAGT TGTCCAGAGT CACCCGACTA GCATGTGTCC CACTGGGACG 3180
CTCCTCCTCA GGTGCTCTGT GTGGCCTGGT CCCGGCCCTT CCTCCACTTC AGTCCAGCTC 3240
ACCACTAGGA CCCCCTCGAC ACCACCCCTC GCTCAGTCAG GCAGGGGCCC ACAGGGCCTG 3300
GGGCCAGATC TTCCCATGGG GAGTTGTGTC ACTGTCCCTC CCAGGCATGG GGCCTGGCGC 3360
CCAGGCCCCT CCACTGCCTC TGAGGATGAA GACACAGGGC TCTGCTGGAC TCCCTGGAGC 3420
GGCCCTGACC TGCTTTCTCT GGGCTAACAG TGGGAGGTCC TGGGGGACCT CCCTACTTGG 3480
GGGATCCAGG CCTCACTGCC CCCAGGGACA GCGCAGGAAG TGTGTGCATA TCTGTGTGTG 3540
TGGGATGGGG CAGGAGAGGC AGCTTGGCTT ATACCGGGTG TTGGGGGAAA GCAGTGCAGG 3600
TTCGGGGAAC CTGGGCCCTG AACTGCATGT GGACAGCCCC CTCCCACAAG GGTGAGGATG 3660
GGCACACAGG GGCCCTGCAT CCTAGGCCAG GCTTGGGTTC TCGGAGGCCA GCTGGAGCTC 3720
GCCTGCTTTT CTCAGGTAGA CCAGGGTCTG CTACAGACCC TGCTGCCCCC AGAAAGGCCT 3780
AGCCTGGTGC AGTGGGGTGA GCGGGCGGGG TGTGGCCCCA GGAGCTGGCC CCACCCCCTG 3840
CACCACCCTG CTTTGTCAGA AGCTGTTTGA GGCAGAGAAT AAAGCACCTT ATTAGGTAAG 3900
AAATGCCTTC TGCCAGGTGG GGAGAGGCCA GGCCCGCCTC TGCCCCCAGG CCTGCCTGCC 3960
CCGCCCTGGC AGAACACCAG CTTCTGTGGC ATCTCAGTCC TGGCCCGAGC CCAGCAACCC 4020
CACACCCCCT CACCCCATGG AGCTCCGGCC GTCCTGCCCC AGACTTGGGT GGGGGCACCT 4080
GGCATGGGGA AGCCTGGCCC TCCCACCTGG GAGGCAGAAG AGGCAGCCTC ACGAGTGTCA 4140
GCTTGGGGGC TGTGTGACCT TGGCCAGGTG ACCCCTCCTT CCTAAGCCTG AACTTTCTCT 4200
TCTATACAAT CAGCGGGTGT GCAAGGGGCC TTGAATTCTC CTGAGGCTTC TTAACCCCAT 4260
TGGGTGTCCC TCCACTTACA AACACGGGCC CAGGGTGCAC CCGTCTCCAA GGGCGTAGTC 4320
TCAGCCCCCT TGCTCCAAAC CCAGAGCTTG CCTATGGGGC TCCCCATCTC TGTTCCAGGG 4380
AAGCAGGGGT CCAGGGCAGG TCAGTCAGTT TTCCAGGCAG GGCAGCCTGC TTGGCTTGGC 4440
TAGTTACAGC AATGGGGCCT TGTAGAGACA GGACCTGAGG AAGCTGGCGC TGCCTCCTTA 4500
GACCTGTTTC TCTGCCAGAA ATGCCTCCAT TTCCAGCTGT CAACTAGAAG CCGACCGTCC 4560
CCAAAGCCCC CAGGCCAGGC CTTAGGTACA ATGTGTTTTG CATCTTCTGT TGCCCGTTGG 4620
AACTTGGCTT 4630
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