| Tag | Content |
|---|
EnhancerAtlas ID | HS176-39018 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr7:155457950-155459340 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr7:155458753-155458764 | AGTGACTCATG | + | 6.14 | | IRF2 | MA0051.1 | chr7:155458345-155458363 | TTTTAACTTTCATTTTCC | - | 6.69 | | SOX10 | MA0442.2 | chr7:155458184-155458195 | TTCTTTGTTTT | - | 6.62 | | STAT1 | MA0137.3 | chr7:155459250-155459261 | TTTCCTAGAAA | - | 6.14 |
|
| | 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 |
| GH07I155665 | chr7 | 155457836 | 155459443 |
|
Enhancer Sequence | CGTGCACCCT GTGCTTCACC TAACTGCCTG TGCCGATCTC TCTCATTCTG ACACTTGGCT 60
CCTGAGGGAT CTTTACTGAA CGCAGCACCT TGACTACCTG GCGCTCTCTC TTGAGTGGGG 120
CTGTCCCTCC TGAGCTAAAG TGAAGCTTCT CCATGCAGAA GGCTGAGGTG TGCTCCTGTT 180
CCAGGCCTGT GTTGTGTGGA GGGCTGCCAA TAGATCATAG GTCTTCTGTC CTTTTTCTTT 240
GTTTTTGTAC AGTAATGATA CTGACTTTGT GGACACCCAG AACCATTACT GGAGTGGCCT 300
TGTGCCAGAG TTCTTTAAGC TCTACTTTGT ACTGAATATC TGGCTACACT TTAACGTTTT 360
TTCCATTCTA ATATGTGTAG ATGGTATTTC ACTAATTTTA ACTTTCATTT TCCTGGTTAC 420
CAGTGAAGAT GAAAATACCT GTTTAGGAAT GGATGAAAAT GACCTGTTTA GGAATACACA 480
CAAACACAAT TTAAAAATCC ACAGTGATGA TAGATGGTAG TTTGATATAG TGGTTACCTC 540
TGGCAAGGAG TTAATAATAG AGGTTAGAGA TGTGTTCTGG GAGAAATACA CAGTGGGGCT 600
TAATCTGGGT GGTGGGGCTG AGAAATGATG GTTATTCTTT ATAACTTTTT TAACACCTTA 660
AATACTGTGT TGAGAAAATG TAACAATTAC TTTGAAGCTG CAGTCAATTT GAAAACGGCA 720
GTGTCACATC TGGAAGTTTT ATAGAATAAT CTAACTTGAG AACTATGAGG CCCTTACAGT 780
TCACATAAAG CTGATTGCTC TTTAGTGACT CATGCAGTGT ATTAGTCAGG ATTCTCCAGA 840
GGAGCAGAAC CAAAAGAATA TATGTAGAAA GATTCATTAT GAAGGACTGG CTCACGTGAT 900
TATGGAGACT GAGAAGTTAC ACGGTCTGTA GAATGGTGTA GTTCCAGTCT GAGCCCAGTG 960
TTCTGTGAAC CAGGGGAGCC AGTCATGGAA GTCCCTATCT GAGCCTGGAG GCCTGAGAAC 1020
CAGGAGCACC CATGTCTGAG GGCAGAAGAT AGCTCAGCTC AAGAAGAGGG TGAATTTGCC 1080
CAACTCCAAC TTTTTGGGTA ATGTCTGCCC ACATTGGTGA GGATGGATTT CTTTACTCAG 1140
TCTGTGGACT CATTGCTAAT CAGCTCTGGA AGCACCCTCA TGGACTTTCA CAGAAATAAT 1200
ATTTTGTTAG GTAGCTGGGC ATCTCTTATC CCAGTCAAGC TGTCGCACAA AATCAGCCAG 1260
TATGCATTCT AAAAGTTAGA TAGTGCTTAA AAACGATGTC TTTCCTAGAA AAGAAATGGT 1320
CTTACTAGTA AGTACTAAAG CTAGTTTTGA TTAAAAGACT GTGATGGTGA GCTGAATAAA 1380
ATATTAAGTG 1390
|
