| Tag | Content |
|---|
EnhancerAtlas ID | HS184-13747 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:47957630-47959020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr17:47958584-47958602 | GGAGGGAATGGAGGAGGG | + | 6.15 | | RREB1 | MA0073.1 | chr17:47958919-47958939 | ACCCACAACACACACTCCCC | + | 6.35 | | ZNF263 | MA0528.1 | chr17:47958650-47958671 | GCTTCTTCCTCCCCCTCCCTT | - | 6.15 | | ZNF263 | MA0528.1 | chr17:47958657-47958678 | CCTCCCCCTCCCTTCTCCCCT | - | 6.38 | | ZNF263 | MA0528.1 | chr17:47958541-47958562 | GAGGAAGAAAGGGGAGGAGGA | + | 6.48 | | ZNF263 | MA0528.1 | chr17:47958666-47958687 | CCCTTCTCCCCTCCCTCATCA | - | 6.59 | | ZNF263 | MA0528.1 | chr17:47958654-47958675 | CTTCCTCCCCCTCCCTTCTCC | - | 6.7 | | ZNF263 | MA0528.1 | chr17:47958662-47958683 | CCCTCCCTTCTCCCCTCCCTC | - | 7.05 |
|
| | 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 |
| GH17I049880 | chr17 | 47957570 | 47958610 |
|
Enhancer Sequence | GTGTTGGAAT TACAGGCGTG AGCCATCGCG CCCGGCTCTT TTCTCCCTTT GAACCGCCGT 60
CCTGTCTCCA GCCCTCAGCC TGTCTCCTCT ACGGAGACCG CTGCCCTTGC CCCTTAACCT 120
TCTCCCTGCC ACCCCTCAGC CGGGACCTAG CCCTCTCCTG GCACCTCCCC CCATCCTGCC 180
CCCGTCCTGG GGTCCCCGGC TATGGCAGCC CAGGCCTAGA CACCACTTTG AGACGGGAGC 240
TCCCTGCCGA TGGAAGACCC AGTCTCCGCC TCTCTTGGCC TCTCCTTTGC CCACCCCGCC 300
CCCGGAATGC TGCCGAGGAC CCAGCCCGGT AGGACAGGGC AGCGGGACTT GTCTCCGATT 360
CTACGGCCTC CTCTCCGCGG AGGGACCCGG ACGGGGCAGC TGCAGTTCCC GCGCAGGCCT 420
CTGGGTGCTG CTCGGCAGCT GCGGTCGCTC ACCGCCCCAG GCGGCCCTAT ACCTGACAGG 480
TCCTCACCCG GGCCTTACGG CTCCCTCCCG CTCCCCGCAA AGGGGCCACC TTCATTTACT 540
AAAAGGGAAA CAGCCACTCA AAGGGCCGAA GTGATCCTAC TTGGCGTTAG TATTGCTGAA 600
TCCCATTTAC ACACGGGGAC ACTGGAGCTC CGAGGCCAAG CGGATTGTCT AGGTCTCACA 660
GAAACGGGGG GTGGTGGGGA TCCTGGCAAA AACCTTAGAA AGACCCCTCT AAGCCCCTCC 720
CTTCTATATC AGTTAGATTT CCAGAAGAAC TTCCCATTCA TAGGTGTGCC AGGAAAATCT 780
TCAGCAGGTG AGAAAAGAAA AAGCAATTCA GGGACATTTG GGGCAGTTCA GGGCAAGGTG 840
GGTGAGCGCC CCTCATTCCC CTTCCATGCC CAGTGTCATG GACTCTGCCC CTCCCTGTCC 900
TGGGCCTCTT CGAGGAAGAA AGGGGAGGAG GAGCCTCTGT CTTGGCAGCC CTTGGGAGGG 960
AATGGAGGAG GGGAGCCCGA CAGAGGGGCT CCTCTGCAGG GGGCCACATC ATGAAGGAGG 1020
GCTTCTTCCT CCCCCTCCCT TCTCCCCTCC CTCATCATCT GCCCCGCCTT GCCCCATGCC 1080
CAGCATTCTC CCAGCAGGGT CTGGGGGGAC AGCAGCAATT TTGACGGTGG GCCTAAGAGT 1140
ATACAATATG GTATCAGCAT CAGCATGTGA GAGAGGCTGT GTGTGTGTGT GTGTGTGTGT 1200
GTGTGTGTGT GTGTGTGTGT GTCCTGTCCT AGCTGGAGTC CTTTCCAGGC TTCTTTACTG 1260
TAGATTCCCA AAACTCTGTG AAGCCCCCTA CCCACAACAC ACACTCCCCA GAGACAGACA 1320
GCTGGTCTCC AGTCACCCCT CCTCAGCCCC TGTATGTGCG CGTGCGCATG TGTGTGTGAA 1380
CGTGTGCACA 1390
|
