| Tag | Content |
|---|
EnhancerAtlas ID | HS184-07725 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:56422580-56423900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:56423214-56423232 | GGAAGAAAGGAAGGGGGA | + | 6.24 | | EWSR1-FLI1 | MA0149.1 | chr12:56423210-56423228 | GGCAGGAAGAAAGGAAGG | + | 7.74 | | Stat6 | MA0520.1 | chr12:56423641-56423656 | CTTTTCCTCAGAAAA | + | 6.23 | | ZNF263 | MA0528.1 | chr12:56422782-56422803 | TCATCATCTTCACCCTCCTTC | - | 6.22 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_28988 | chr12:56422562-56423667 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I056028 | chr12 | 56422359 | 56424036 |
|
Enhancer Sequence | AACTCTTGAT CTCAAGCAAT CGGCCCACCT CAGCCTCCTG AAGTACTGGG ATTACAGGCG 60
TGGTGTCAGC CACTGTGCCT GGGCTTTCCT GACTTTTATA TTTTAGATTG TTGATGCCAC 120
AATCCATGCC CTATTACCCC CAACATCTAA GCCCCTGGGA AATCCCTCCT CTCACTCCCA 180
TCTGCCTCAG GCCCCACACC TGTCATCATC TTCACCCTCC TTCCTCCCAC ACCACCAGAG 240
GTCTTGAGCA ACCAGTCTGT CCTCTCCTTT ACTTCCTTCT GGCTCCTGGA AATATCCATA 300
GCCCTCTCAA ATTGCAAAAA AGGGAGCCTA GGACTTCCAA ATAGGAAAAG AGTATCCTAT 360
TTCTGTTCCC TATCCCAAGA GGTTGTCACC TTCCCAGAGG CAAGAGAAAG TCCAGAGGGT 420
ACCTAGAGAT CAATGTTTGG AACAGTGCTG GGAAACTGGA TTAACAAGGT TTTCTAGCCC 480
AGTCAAGACT GTTTGAATCA GTATCTGTCT GAATCAGCTG GACAGATAGC ACTTTTTAGG 540
CATTTTACTA AGCTTTAGGC TTTTGGCTTG GACTTGGGAA GAGGCCAGGA GCTGAGCTGG 600
CAGGAAGGAG GGAGCTCAAG ATTGGGAAAA GGCAGGAAGA AAGGAAGGGG GAAAGAATTA 660
GTAGGGTCTG TCCTTGGAAA CTTTCCTGGC TATTTTTCTC TTCTTAAACT CTCCTGAGCC 720
AGGATTTAAA GGGACAGAGC AATCATTTCA TCACCCTCTA CTTTCTCCAT CCACTTACCT 780
TGTTCCAGGT TCTCCCACCT TGTAATTGGG ACCTCTTTAT CTCTATGTAT GTGGAGAAAC 840
AGGGAGAAAG ATCATCGTTG ATACATGCTT TATATCTACA GAGCATTTCA CTTGTGTTTC 900
TCCATGTGAT CCTCATAACA ATTCCAAGGT AGATGTGATT ATCCCCATTT TGTTGACAAG 960
GAAAATGAAG CTGTTGGGGG GAAAAATGAG TTGCGGGTCA CATAGCTATT CTTCAGCCTA 1020
GCTGGAACCC CATCAAGGTC CAGTGCCAGA AATACATACT CCTTTTCCTC AGAAAAGGGG 1080
CTGCTCCCCC TGCTGGTTTG GAACAAGGAT GGCTTGGCCC CTAGAATTCT TACCAACTAC 1140
ACAGTGAGGT GAACTGGGTA GATTTTGGAT GTTGATCTGT AGATTATTAA CAACAGAAGC 1200
AGACACAGAT ATACTGTCAG GTCCCATCTC TGTGAAGTGC TTTCTGTTGC AACCCCTATT 1260
ATAAGAAAAA AGAGACTGGA TGCATGTTCT CACTCATGTG GGAGCTAAAA AAGTTGATCT 1320
|
