| Tag | Content |
|---|
EnhancerAtlas ID | HS053-37707 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr7:139519090-139520570 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr7:139519747-139519762 | GGGTCACAGTGCCCC | + | 6.41 | | Foxd3 | MA0041.1 | chr7:139519300-139519312 | GTTTGTTTGTTT | + | 6.32 | | PPARG | MA0066.1 | chr7:139519745-139519765 | CTGGGTCACAGTGCCCCCTT | + | 7.2 |
|
| | 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 |
| GH07I139820 | chr7 | 139519941 | 139520263 |
|
Enhancer Sequence | GGCATCTGAG GTTCCAGTGG ACGACAGGGT TACAAGATGG AAAAAGCCTG AATTCCTGAG 60
TCACTGCATG GAAGGCTGCC TACTGAACAC ACACATTTGG GCTGTTACAT GAGTGACAGA 120
CACACTTCTG TAGTGTGAAG CTCTTGAGAT TTGGGGGCCC CTCATTACAA CACTTATGCT 180
ATTCATTCTT TCCCCCAACT CTCTTCTTTT GTTTGTTTGT TTTTTGTTTG AGATGCAGTC 240
TCACTCTGTC GCCCAGGCTG GAGTGCAGTG GCACTATCTT GGCTCACTGC AACCTCCGCC 300
TCCCAGGTTC AAGCGATTCT CCTGCCTCAG CCTCCCTAGT AACTGGGATT ACAGGTGCAC 360
GCCACCATGC CCGGCTAATT TTTGTATTTT TAGTAGAGAT GGGTTTTCAC CATGTTGGCC 420
AGGCTGGTCT GAAACTCCTG ACCTCAAGTG ATCCACCTGC CTTGGCCTCC TAAAGTGCTG 480
GAATTGCAGG TATGAGCCAC CACTCTCAGC CTCCCCAACT CAGCTCTTAT TTCTATATTG 540
CCATACTAGG TGGAGATTGG GGCCCTACCA CCTGCTGACA TATTTCCTTG GAGGCATCTG 600
CTGCCAGAAC TTCGAATTAT CTTCTGCTTG AGAGTTTCTA TTATTGGGCC TGTGCCTGGG 660
TCACAGTGCC CCCTTTGCTC TGTAGTGGGA CTTCCTGGTC CTGACAACTT GCCTGAAATG 720
CCATTTGTGA TCTTGCTGTC AAACTCTGGA TTCTAACTTT TGCTTTCTGA GCATGCTGTC 780
TGTCTCCTTA TGCCTGCTCC CACTCTCACT CCCAGTGACT AGGAGGTGAA AAATGACTGT 840
TCCAGGCACC AACTTGCCTG AAAGCTCTAA GACTTGCCTT AAGGCAGTCA AGCCGTCTGC 900
TGACTCTCCA CTTTTGCAAG GAGAACTACG TCTAGTCATC AACATGTAGC CGCATCCAGC 960
CATGAGGAGG GGCGGGAGAG ATTTGACAAC ATCTCAGGAA GTGCTAACAT CTGACAAGCT 1020
GAGATCATGG GTGTCATAAA TTGATAGAGA GGCTGAAATG AGAAGGAGAT AGGATGGGCC 1080
ATGTGTGGTT AGCAACATCA AGAGCAACTT GTAGTTGACA ACCTCATTGC TCATCTTCTG 1140
CTGACACATA CAGCCAAAGT CTGAATGGTG GCATTGCTTC AACTCCCCTG CTGTGTGATG 1200
GGGGCACCTG ATTGATGTTG ACACGCCAAT GTTGGGCTAT CATCGGAGGA GGTCTGTATT 1260
AATTTTAACA ATGAAAATAG ACGGGTTACA GTTACCCTAA ATAGCATCAA GTCACCCCAC 1320
TTCATAAAGC CCTTCAATGG CTTTCCTTTC CTTTTGGAAG GAAGTAGTGC ATTTTTCACA 1380
TGGTCCACTG GGTCTTAGAT GTCCTGACCC TACCTTATCT CTCCTGTGTA GGCCAGTCCT 1440
ACCCTTTCTT CTGCTTAATG CCTCCCAGCC ATGCTGGTGT 1480
|
