| Tag | Content |
|---|
EnhancerAtlas ID | HS052-39254 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr9:116980450-116982070 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr9:116981224-116981235 | TGCTTTGTTTT | - | 6.02 |
| | | 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 |
| GH09I114218 | chr9 | 116980798 | 116983611 |
| Enhancer Sequence | GACGATCTAC CTTCAGCATG ACCAAGAAGA GCTGGTTTAG GTGAGACTGG AATTTACCAG 60
GGGAGACCCT AAAGATGTGG GGGAGGAAGC TTGGGTAAGG TCAGATATGC CCCCACAAAG 120
ACATGATCTG GAAACACACA CACACCCTCC CCTGCCACAC TCCTCTGCCA CCCTCTGCAA 180
CCAGTTGGAC ACGCGTTTGA GCAGCTTCTA CATACCAGGC TTTGCCCGTG CATAGCTCAT 240
ATGAACATGC CAAACTCCAG AGGTGGACCT GGGCTCTGCT TGCTTTATGA CCTTGGCCAT 300
GTGATGTTGC CTAACCGAGT CTCAATTTTC CCATCTGTGA AATGGGACTG ATAACTTTTC 360
CCTCAAAGAT AGATATCAAA TGCAAAATGA AGTCTTGCAT GCAAAGTGAC TACCTTGGTC 420
TGAATTTCAT TATCGTCTTC TCGTTTCCTC CTTTTGGTGT CTGAATGAAG CCACACCTTC 480
TATGGGGTGA ATGTCAATCC AAGAGGACTT CCTGGCAGGG GAGAGATTTA AAGGGAGTAG 540
GGCTGCGGGG CAGGGCCAGG CTAAACACCT GGTTACATAC ACACATTTCA AGGTGTCTTT 600
GCCTAACCAG TAGAGACTTT GGTTTGGGTT TTGTTTGTAG GTTTGGTCTT TTGGGTTTAG 660
TGTACTCACT GGACTCCTCC AGTAGTATTA GAAACCGAAA ACAGGATCAT CCTCCATGAG 720
GAATGTTTAC CATTTGAATC ATAGCCCCAG CATTCACTTG GTCAGGAAAA CATGTGCTTT 780
GTTTTTTTTT TTTTTTAATT ACATTTCCCT GGAAAAACAA TGATTTGAAT TCAAGGAGGG 840
GAGGAGAACA GGTTTCCCCC AACTCCAAGC TTGAGGACTT TCTTTTCCTT TTGAAGTAGG 900
AATGGAGTTC TGTCCCCGGC CCCCGAAGGC GTCCTTACAG CTGATATTTT TCCAGCTGCC 960
TATCTCCCCA GAGCGTGGAG CGGCCTCCAG AGTGGGGTCA GGGATGGGGC GAGAGGGCCA 1020
GACCTGCCTG GGCCGGGCAG CTCAGCATCT CTCTGAGCTG CTGAACACCT ATGGAGGCTG 1080
TGCTCATGTT CACTGGTGGT GTGACTTTGT GTGACCTTGC CACTTCACTC TTTCACAGCC 1140
TCGTTTCCTT TATCTGTCAA ATGGGGATCA TGAGTTCACT GGGTGGCTTT TGAAGAACGT 1200
GCCACAATCA GAGAAGGTCT GAGCTGGGAA ATGCAACAGA GGCCTTCTCC TCCTTGACCA 1260
GTGGGGAAAC AGAGGCTCTT AAAACTGGCA TAGATCCAGC TTCCTGCCCC TAGTCTCTGT 1320
CTTTCCCATT CCATCAGGAC CAGATCTCAG AATAGGGGAT TGGCATTTTC ATGCTGGGGA 1380
GCTGGGTATC ATTTTCTTTT CAGAGACTTA GTAGAAAATA AAAGGATCCC TGAGAAATTC 1440
TTTATGTTCA GGTGCTTGTC GATGGTAGGG GTGACCTCAG GACCGCACTG TCTGCCCATG 1500
ACCAAGGAGT GAGACTGCTT GGACATTGTC CTTGTGTCCC CCCTGGGGGT CTGGATCAAA 1560
GCCCACCCTG AAGGTGACAA CACTAACCTA CAGATGTTTG TTCTCTCTCA TGCCCTCCAG 1620
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