| Tag | Content |
|---|
EnhancerAtlas ID | HS184-07623 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:52540440-52545030 |
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 | | HSF1 | MA0486.2 | chr12:52544866-52544879 | GAAGGTTCTAGAA | - | 7.12 | | JUNB | MA0490.1 | chr12:52541278-52541289 | CTGAGTCACCC | - | 6.02 | | KLF4 | MA0039.3 | chr12:52544905-52544916 | AGAGGGTGTGG | - | 6.02 | | Klf1 | MA0493.1 | chr12:52544907-52544918 | AGGGTGTGGCT | - | 6.02 |
|
| | Number of super-enhancer constituents: 22 | 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_32153 | chr12:52544564-52547299 | 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: 3 | Chromosome | Start | End |
| chr12 | 52540525 | 52544089 | | chr12 | 52542210 | 52542726 | | chr12 | 52540964 | 52541526 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I052143 | chr12 | 52536922 | 52551852 |
|
Enhancer Sequence | GAGTATCAGC TGAAGCAGGG GCCCCCATTT CACACTGGAA AGGGCCTGGG GTTTGGGGTT 60
CCCCCCTGCC GGGGAATCCA GGGTCCCCAC CCCTGCCTGC TGCCTGCCCT CCTGCCTCGG 120
CCTCACTCTG GGTCCTTGTC TGGGAACCTT AGCACCTTCT TTGAGCCGCT GGTGGTGTTG 180
GCGCACTTAG CAGAGCAAGC CCTGGCCCCT TTCCTCACAA ACCTCACTCC CAGGTCTAGG 240
CGGGGAGGCT GGGCTGCTCC TCATTGTCTT AAGCAGAGCG GTCACCTGAA GGCCTGGCCG 300
TCTCACCTTG TCATGATTCC TCCACATTTG AGAGTGACGG AGGGGCAGGG AGTCAGGGCT 360
GTGTCCACAG TGTGTCCTCA ACCCAGACTG AGCCAGGCCC ATGGCTCTCA CTGAGGTCCT 420
CTCCTTCTGC CTTGGTTTCC CTCTGAGTCC AGCCCCATGG GGAAGCTGGG CTCCTGGGCC 480
TCAGGCCTGA TGCTCCCTGT GCCAGGGCCT GTCCCCTGCT ACTGCACTGA GCTGGAGTCG 540
GGGGCCTGGT TGTGGGCTTC TGCTCCTGGT CTCAGCGAGA CCTCCAGGCT TCCTTGGGCC 600
CAGCTCCTCA TCTCAGCCGG TCGCACCTGG GCAAGTCCAG TCAGTGTGAG GGGCTACTTC 660
GGTTTCCTCA CTGTGGCAGG GATTGGGGGA GCTCCTGAGC CCTGGGCTGG GGTGGGTCCG 720
GAGGGGTGGG GGCTCCTGGC TGGGCTGGGT GTGCCTGTAT GTGACTCAGG CTGGATGCCC 780
AGGCCCTGAG CTGGCGGCTT TGTTCTCCCA CTGGCCGGGT AGGGTGCGTG CTGCAGCCCT 840
GAGTCACCCG GGTGTGGCCG AGCTGCTGGC GGGACACCAG AGCCATACAC CGCCACACTC 900
ACAGAGATCC ACACACTGGA GCTCAGGACA CGGCGCCCTG AGAGCGGAGG GCCCCCCTGG 960
TGTGGGTGCC GTCACTGGTG CCTTTCCCTC GGTGGTGCTG TGAGACATTC CCAAGAAGCT 1020
CCTTGGTGAC TAAGGGCCCT GTGCTCCTGG AGCAAACTCA GCTGTTTGCT GAGAAGGCCT 1080
TCCTTCTCTT CGTGGTTACT CCCTGGTTAG GGCCTGGAGG GGGACCTGCA GGCACAGCTG 1140
GAGACCCTGA GGGGCACACA GAGCCTTCCC CCGCTGCCTG ATAAAGGGCA TATGCAGGTG 1200
ACCATGTGCC ATCTGTCCAA ACTGTGCACC CACTGGATCC TTGAAACAGT TCTGAGAGGA 1260
AGGTGCATTG TTCCCACTTT ACAGATGCGG ACACCGGGGT TGCTAATAGT TGTCCAGAGT 1320
CACCCGACTA GCATGTGTCC CACTGGGACG CTCCTCCTCA GGTGCTCTGT GTGGCCTGGT 1380
CCCGGCCCTT CCTCCACTTC AGTCCAGCTC ACCACTAGGA CCCCCTCGAC ACCACCCCTC 1440
GCTCAGTCAG GCAGGGGCCC ACAGGGCCTG GGGCCAGATC TTCCCATGGG GAGTTGTGTC 1500
ACTGTCCCTC CCAGGCATGG GGCCTGGCGC CCAGGCCCCT CCACTGCCTC TGAGGATGAA 1560
GACACAGGGC TCTGCTGGAC TCCCTGGAGC GGCCCTGACC TGCTTTCTCT GGGCTAACAG 1620
TGGGAGGTCC TGGGGGACCT CCCTACTTGG GGGATCCAGG CCTCACTGCC CCCAGGGACA 1680
GCGCAGGAAG TGTGTGCATA TCTGTGTGTG TGGGATGGGG CAGGAGAGGC AGCTTGGCTT 1740
ATACCGGGTG TTGGGGGAAA GCAGTGCAGG TTCGGGGAAC CTGGGCCCTG AACTGCATGT 1800
GGACAGCCCC CTCCCACAAG GGTGAGGATG GGCACACAGG GGCCCTGCAT CCTAGGCCAG 1860
GCTTGGGTTC TCGGAGGCCA GCTGGAGCTC GCCTGCTTTT CTCAGGTAGA CCAGGGTCTG 1920
CTACAGACCC TGCTGCCCCC AGAAAGGCCT AGCCTGGTGC AGTGGGGTGA GCGGGCGGGG 1980
TGTGGCCCCA GGAGCTGGCC CCACCCCCTG CACCACCCTG CTTTGTCAGA AGCTGTTTGA 2040
GGCAGAGAAT AAAGCACCTT ATTAGGTAAG AAATGCCTTC TGCCAGGTGG GGAGAGGCCA 2100
GGCCCGCCTC TGCCCCCAGG CCTGCCTGCC CCGCCCTGGC AGAACACCAG CTTCTGTGGC 2160
ATCTCAGTCC TGGCCCGAGC CCAGCAACCC CACACCCCCT CACCCCATGG AGCTCCGGCC 2220
GTCCTGCCCC AGACTTGGGT GGGGGCACCT GGCATGGGGA AGCCTGGCCC TCCCACCTGG 2280
GAGGCAGAAG AGGCAGCCTC ACGAGTGTCA GCTTGGGGGC TGTGTGACCT TGGCCAGGTG 2340
ACCCCTCCTT CCTAAGCCTG AACTTTCTCT TCTATACAAT CAGCGGGTGT GCAAGGGGCC 2400
TTGAATTCTC CTGAGGCTTC TTAACCCCAT TGGGTGTCCC TCCACTTACA AACACGGGCC 2460
CAGGGTGCAC CCGTCTCCAA GGGCGTAGTC TCAGCCCCCT TGCTCCAAAC CCAGAGCTTG 2520
CCTATGGGGC TCCCCATCTC TGTTCCAGGG AAGCAGGGGT CCAGGGCAGG TCAGTCAGTT 2580
TTCCAGGCAG GGCAGCCTGC TTGGCTTGGC TAGTTACAGC AATGGGGCCT TGTAGAGACA 2640
GGACCTGAGG AAGCTGGCGC TGCCTCCTTA GACCTGTTTC TCTGCCAGAA ATGCCTCCAT 2700
TTCCAGCTGT CAACTAGAAG CCGACCGTCC CCAAAGCCCC CAGGCCAGGC CTTAGGTACA 2760
ATGTGTTTTG CATCTTCTGT TGCCCGTTGG AACTTGGCTT TGGAGATAAA AGTCCTGACT 2820
CCACATTTCC AAAGTGTCTT TTAAGCATTA TCCGGTTTGA CTCTTATCTA CAGGACACTT 2880
TGGCAAATGA GGCTTCACAG CATGGCTGGT GCTCTCTGCC CTGGAAAGGA CAGTAAAGGA 2940
AGGGAGCCTG TCTTGTCTCT GTCGGTCCTG GAAAGATTGG AGCTGGGGGC GTCCTTGGAT 3000
AATGTCTAGA CCAGCCTCCC ACTGTGGAGT CCAGATTGGC CTAGAGCCCA GGATCCTGCC 3060
CCCTCCTCCT GCCCCCTGTC CTGGCCAGAG GCTGCCTGCT CTCCCTATTC CATGTCTTTC 3120
TGGCCCAGCC AGGGGACACA GGGTTGGGGC AGGTTCCAAG CCTCCACCTC ATGGAGGATC 3180
CCTGCTGTGG GCCTTCCTTC CCTCTGCCTC TGTCCCGTGG AGCCTTCTGG CTTTCCCATT 3240
CCTAGCATAG CAATTGCACA GAGGTTTTGC AGGAGGACTG ACAAGGCAAC TTCTGCTGTG 3300
CGAAGAAAAC AAGGCAAGAC ACTTGACCAT GGCCGCCATG CACAGCTGCC CTCTCCCGTT 3360
CCCAGCCTCC CCTGCATGGA GTGGCCCTCA GAGGCTTTTT GCGCTCCCCT GGCCAAGTGC 3420
ACAAAGGGCC CTTCAATTCC AAGTTCCTGT GGCTGCACCC CCTCCTGAAA GCCCTGGGGC 3480
TCAGGGAATC CCCCAGTATC ATGCCAGTTT GGAATCCAGG AAGTCCTAGC AGGAAGTTCT 3540
CCCTGTTGCC TGGCTCCAGT CTCTCCTGCT GTGTTTCAAG CCCCTTCTCT TCTTGCCCTG 3600
TCCTCTGGAG GGAGCAGACT GCCCAGTGCT CAGGCCACAG TAAGTTGGAG GTCAGAGCCA 3660
CAGGGGCCCT AGTTCTCTCC TGTTTGTCCC TATCTGTGGG TTTTGGGCAA AGTGAGGCTC 3720
CTTGCTGAGC CCCCACTGGG GATGCCCTCT GTTCTCCTTC CACTGGCTTG TCCTGGCTTT 3780
CCACACCTCA CGCACGCTCT CCTCTCCAGG AAGCACTGCC TGCTGCTCCC CCCCGTCTAG 3840
CCTTGATTCT GCATCTTAGT CGGTCCCCGC ATCCTCTCTG TGTCCCCTGC CAGCCTGTGT 3900
CCCCAGTGCC TTCGACAGTG CCTGACACTA GTTGGTGCTC AATAAGTATT TAAGAGCTTG 3960
AACAGTTTCC ACAATGGGGA ACTCACTACC TCATTATGGC ACCAAACATT GTGGGAAGCT 4020
CTAATTCTTT GAAAGGTCTT TCTGGCACGG AACTGACACC TACCTCCCAT CAACCTCCAT 4080
TCTGGGGAAG GACACACAGG GTCTCCACCC TCTTCCCAGG CCAGCAGCCC TTCAAACACA 4140
TGCTGAGAAC CATGGTCAGC TGACTCTTCC TGACTTTCCA AATGGAAATT GCAGAGTAGA 4200
CCCTGTAGGT CCAACCCGCT AGGGCCTTTG CTTTGGTTCA CAATGCTTTA CCTGGGGGCA 4260
TCTGAACACC ACATGTAAAC TTAGACTATC TTTTTCTCCT GGGCTGTAGG CTGATACTAG 4320
GCCCTGGAGG GGGTTAGAGA GAAGAGGGGA CTGCAGGGTC TCTTCAGATC ACCACCCCCT 4380
CTGGGTCACT GATGTGCCTT CTTTGGGCCT GGACCAGGAT TCATGAGAAG GTTCTAGAAG 4440
CCAGGAGGGC CAGGGCATGG GAGGCAGAGG GTGTGGCTTC TCCCAGGGCC TGGGATCAGA 4500
GAAGGCCTGA GAGCAGAGTT ACAGTCTGTG AACAACTGTT AGTGAGCACT CACTGGATAC 4560
AAAGCCCCAT GACCCTGAGA GAGGAGAGCA 4590
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