| Tag | Content |
|---|
EnhancerAtlas ID | HS092-38636 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr9:116980400-116982070 |
Target genes | |
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 | AGGATCCCCT GGACACAGCC CACCTGGCTG ATTCTTGTCC CAGGAGGTGA GACGATCTAC 60
CTTCAGCATG ACCAAGAAGA GCTGGTTTAG GTGAGACTGG AATTTACCAG GGGAGACCCT 120
AAAGATGTGG GGGAGGAAGC TTGGGTAAGG TCAGATATGC CCCCACAAAG ACATGATCTG 180
GAAACACACA CACACCCTCC CCTGCCACAC TCCTCTGCCA CCCTCTGCAA CCAGTTGGAC 240
ACGCGTTTGA GCAGCTTCTA CATACCAGGC TTTGCCCGTG CATAGCTCAT ATGAACATGC 300
CAAACTCCAG AGGTGGACCT GGGCTCTGCT TGCTTTATGA CCTTGGCCAT GTGATGTTGC 360
CTAACCGAGT CTCAATTTTC CCATCTGTGA AATGGGACTG ATAACTTTTC CCTCAAAGAT 420
AGATATCAAA TGCAAAATGA AGTCTTGCAT GCAAAGTGAC TACCTTGGTC TGAATTTCAT 480
TATCGTCTTC TCGTTTCCTC CTTTTGGTGT CTGAATGAAG CCACACCTTC TATGGGGTGA 540
ATGTCAATCC AAGAGGACTT CCTGGCAGGG GAGAGATTTA AAGGGAGTAG GGCTGCGGGG 600
CAGGGCCAGG CTAAACACCT GGTTACATAC ACACATTTCA AGGTGTCTTT GCCTAACCAG 660
TAGAGACTTT GGTTTGGGTT TTGTTTGTAG GTTTGGTCTT TTGGGTTTAG TGTACTCACT 720
GGACTCCTCC AGTAGTATTA GAAACCGAAA ACAGGATCAT CCTCCATGAG GAATGTTTAC 780
CATTTGAATC ATAGCCCCAG CATTCACTTG GTCAGGAAAA CATGTGCTTT GTTTTTTTTT 840
TTTTTTAATT ACATTTCCCT GGAAAAACAA TGATTTGAAT TCAAGGAGGG GAGGAGAACA 900
GGTTTCCCCC AACTCCAAGC TTGAGGACTT TCTTTTCCTT TTGAAGTAGG AATGGAGTTC 960
TGTCCCCGGC CCCCGAAGGC GTCCTTACAG CTGATATTTT TCCAGCTGCC TATCTCCCCA 1020
GAGCGTGGAG CGGCCTCCAG AGTGGGGTCA GGGATGGGGC GAGAGGGCCA GACCTGCCTG 1080
GGCCGGGCAG CTCAGCATCT CTCTGAGCTG CTGAACACCT ATGGAGGCTG TGCTCATGTT 1140
CACTGGTGGT GTGACTTTGT GTGACCTTGC CACTTCACTC TTTCACAGCC TCGTTTCCTT 1200
TATCTGTCAA ATGGGGATCA TGAGTTCACT GGGTGGCTTT TGAAGAACGT GCCACAATCA 1260
GAGAAGGTCT GAGCTGGGAA ATGCAACAGA GGCCTTCTCC TCCTTGACCA GTGGGGAAAC 1320
AGAGGCTCTT AAAACTGGCA TAGATCCAGC TTCCTGCCCC TAGTCTCTGT CTTTCCCATT 1380
CCATCAGGAC CAGATCTCAG AATAGGGGAT TGGCATTTTC ATGCTGGGGA GCTGGGTATC 1440
ATTTTCTTTT CAGAGACTTA GTAGAAAATA AAAGGATCCC TGAGAAATTC TTTATGTTCA 1500
GGTGCTTGTC GATGGTAGGG GTGACCTCAG GACCGCACTG TCTGCCCATG ACCAAGGAGT 1560
GAGACTGCTT GGACATTGTC CTTGTGTCCC CCCTGGGGGT CTGGATCAAA GCCCACCCTG 1620
AAGGTGACAA CACTAACCTA CAGATGTTTG TTCTCTCTCA TGCCCTCCAG 1670
|
