| Tag | Content |
|---|
EnhancerAtlas ID | HS065-01946 | Organism | Homo sapiens | Tissue/cell | GM18508 | Coordinate | chr16:30633870-30635030 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr16:30634545-30634556 | TTCTTTGTTTT | - | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTTGTACAT CTTACAGAAG CCAGTGCACG TTTACAATCC TCATTTGCAT TCTCAAAAGC 60
TAAAGTTAAA GTTAGCATCT CTGCAGCCGC GGTATGAGGA ATCTGACACC TCACTGCCTC 120
TAGTAATCAT GCAAGAAAAT GTGCAGAGGG CTCCTGCAAC CCTTGCATGG CACGTAAAAA 180
AGATTGTATT GGGACCCCCT TCCTCTGGAA TTGTGGCCAA CGTGTGTTTA GCGGCCAGTG 240
CACACTGCTG ATAAGCAGCT TCTGGGAGTG CCATTTGATG TTGCAGGTCT GAATAAGGGC 300
CATTACCCAA CAGCATATCC TCTGTAATGT CCCTGTGTCC AGCAGCACGA TTCTGTCTAG 360
CCTGGTCTGC ACACAGTTCT TGCCAATTTA AATTCCATGT CAGGTATGAA CTAGCAGACA 420
AACAAGTGCA GGCCAAATGC TTTACATCAA AGGGTGGAAG GCGCATAGCA CCAAATACAG 480
ATTCTAGCAA TCCTAAAGTA AATGGGCTCT GTACTCCATT ATTCAGTACA TGAGCTTTTA 540
ATTCCTTCAA CAACTTAAAC TCTAGTGGGG TGTGTTCATG AATAAACTGC TGTGGATTAT 600
TTGGATCCAG CCTTATAGAA ATAGGAAAAG CACAAGGTTC GAAGGGCTCT CCAGCTATGG 660
CAGCAGAGCG TAGAATTCTT TGTTTTGGGG TCTCTATTTC TGTTACTGAA GGAGACAGTA 720
CACGTGTGTC CACTACTGGA GGGGGCGGTA CAGGCCAATT TTCATCCTCC CTCTCCTGTT 780
TATTATTTCA ATGGGCGCTG TTGGAGGGAC AAAAGATTCT TTTGAAATTT GAGATTCAGA 840
ACATGGCTCC TGCTGTCCGG CAGAATAAGA AGGAGACAAT GGCAGGAGGA CAGTATGGAA 900
TAAAGTCAAA ACAGAAGGAT CAACTTTAAG ACCTTTTTGA TAAGCCTGTT TTAATCCTTC 960
CCCTACACTG TCCCAATTTT CCGCATCGAG ATGCCTGTCT GTGGAAACCA TGGGTTATGC 1020
ATAACAACCT CCTGCAGCAG CTTAGTGTTT GAGAACTAAC CTGAGCACCA GATTGTTTAA 1080
GTAAAACTTT AAGCAACTGC ACATAATGTT GCTCCTCAGT TGACAAATTC TGCCCCACGT 1140
TACCCTGATT CACAAACTTC 1160
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