| Tag | Content |
|---|
EnhancerAtlas ID | HS184-00399 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:25987550-25988980 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:25988135-25988153 | GGAAGACAGGCAGGAAGC | + | 6.37 | | IRF1 | MA0050.2 | chr1:25987581-25987602 | TTTTAATTTCAGTTTTATTTG | + | 6.22 | | PBX1 | MA0070.1 | chr1:25988626-25988638 | TTTGATTGATGT | - | 6.74 | | ZNF263 | MA0528.1 | chr1:25988766-25988787 | GGAGGAGGGAGATGGTGTGAG | + | 6.1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 25987800 | 25988135 | | chr1 | 25988655 | 25988755 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I025661 | chr1 | 25987892 | 25988091 |
|
Enhancer Sequence | CATTGATAAA CACATGAAAT TCTGTTTTTT TTTTTAATTT CAGTTTTATT TGTTAAGGTA 60
CATGAAAATA TCAACCATCG CCCATGTTGG AGCTACATGC AGAGGGTTAG TTGTTAAACC 120
GCACACTGCT GGATGCAGCT GTGCTGCGTG GCCCATGTAT TTCATCACCT CTATGCCTTT 180
GCTCCTGGCT ATTTCCTTTT ACTGTCTTGC CCGAGTCCCA TTTCATTCAC TGACTCATTT 240
ATTTAACAAA TAAGTATCCA GTGTGGACTA TGTGCCAGGC ACCAGGGACA CAGCAATGAA 300
CAAGACAGAC CCAAAATACA AATTCTGTTC TAGTGGAGTT AGAGGAACAA TAAGCAAAAT 360
AAATATGTTA ACGGCATGGT ATGCAGTTTC AAACTCTTCC CTCTTTTCCC CAGAGCACAA 420
ATGTCCCCCT CTGTGTCTTG CTCTCCCCCA CCGAGGGTGA GTTCTGCCTC CATTGTGGCA 480
GGATCTTTCA ACCTCACACC AAAGGAGACA AGGCTTAGCT TGAGCACAGG GTCTGAGCAG 540
AGATGTGTGC ATAGCTGGGA ACTCGAGACT GAGGCCTGGC TTTGTGGAAG ACAGGCAGGA 600
AGCAGGAAGC AGAGCCACAG TTTTATTAGA GTTCGTGAAA ATGGGATGTC TCCTCCCAAT 660
GTAATGATTT GCTAATTGTT CTCAGTGCTG TGTGTGGGGT TGAAGGGAGA TCTAAGATGA 720
AACCTTTGCA CCTGCAAGGA GTTAAAAATA TGTAATGAAA GAAATATCAC AGGATAGCCT 780
GCTCATTCCC TCATCTATTT GTTTTGCAAA TACAAGTCCT ACCCCACATC AGGTGCTATA 840
AGCTCTATAA ACTGTAAAGC CAAATGATCT ACGGTCTCTC CCCTTGAGGA ATTTTTTTAA 900
CTTGGGGGCA ATTTATAATC CAGATTGCTG GCCAGCGAAC AGTGGTCAGA ATGCTCTGGA 960
AACCTTCCCC ATCTCTCTGG AGTCATCAGG CCCTTGCAGG TAGTCAGCCT CCTCTCTCTC 1020
TGTTGTCCCC TCACTTATAA TTGACCTCAG TTTATAATTC TGCATCTGTT TTTGTGTTTG 1080
ATTGATGTCT ATCTCTCTCA CAAGAATGTC AGCTCCAGGA GGCAGGGACC CATGTCTGTC 1140
CTGTTCACTG AGCCTGGCAT GAGGAAATGC TCAGGAAAAC CTTGTTGAAT AAGCAAATGC 1200
AGGGAGGACT GAGAGTGGAG GAGGGAGATG GTGTGAGAAG CCTCAGGGGT GTTCTGGAGA 1260
ACGAGCCTTC ATTCTTTGAC ATCAGGCAAG TGAATCCAGA CTCCTCAGCA TTTGTCAAGG 1320
TGCGGCTAGA CAACACCTCC ATTGTGTAGT CATATTCCTC TGTGGAGAGA CCTCTAGAAC 1380
AGAGCACAGC AGTTTGTATT ACAGCTTATA CATGATTCTT AACATTTTCT 1430
|
