| Tag | Content |
|---|
EnhancerAtlas ID | HS105-30520 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr16:30633820-30634990 | 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 | TGAAGCTCAG TTCCCACATT TTGACAGGCT TTGAGAAAAT TTCCTAAGTT TTTTGTACAT 60
CTTACAGAAG CCAGTGCACG TTTACAATCC TCATTTGCAT TCTCAAAAGC TAAAGTTAAA 120
GTTAGCATCT CTGCAGCCGC GGTATGAGGA ATCTGACACC TCACTGCCTC TAGTAATCAT 180
GCAAGAAAAT GTGCAGAGGG CTCCTGCAAC CCTTGCATGG CACGTAAAAA AGATTGTATT 240
GGGACCCCCT TCCTCTGGAA TTGTGGCCAA CGTGTGTTTA GCGGCCAGTG CACACTGCTG 300
ATAAGCAGCT TCTGGGAGTG CCATTTGATG TTGCAGGTCT GAATAAGGGC CATTACCCAA 360
CAGCATATCC TCTGTAATGT CCCTGTGTCC AGCAGCACGA TTCTGTCTAG CCTGGTCTGC 420
ACACAGTTCT TGCCAATTTA AATTCCATGT CAGGTATGAA CTAGCAGACA AACAAGTGCA 480
GGCCAAATGC TTTACATCAA AGGGTGGAAG GCGCATAGCA CCAAATACAG ATTCTAGCAA 540
TCCTAAAGTA AATGGGCTCT GTACTCCATT ATTCAGTACA TGAGCTTTTA ATTCCTTCAA 600
CAACTTAAAC TCTAGTGGGG TGTGTTCATG AATAAACTGC TGTGGATTAT TTGGATCCAG 660
CCTTATAGAA ATAGGAAAAG CACAAGGTTC GAAGGGCTCT CCAGCTATGG CAGCAGAGCG 720
TAGAATTCTT TGTTTTGGGG TCTCTATTTC TGTTACTGAA GGAGACAGTA CACGTGTGTC 780
CACTACTGGA GGGGGCGGTA CAGGCCAATT TTCATCCTCC CTCTCCTGTT TATTATTTCA 840
ATGGGCGCTG TTGGAGGGAC AAAAGATTCT TTTGAAATTT GAGATTCAGA ACATGGCTCC 900
TGCTGTCCGG CAGAATAAGA AGGAGACAAT GGCAGGAGGA CAGTATGGAA TAAAGTCAAA 960
ACAGAAGGAT CAACTTTAAG ACCTTTTTGA TAAGCCTGTT TTAATCCTTC CCCTACACTG 1020
TCCCAATTTT CCGCATCGAG ATGCCTGTCT GTGGAAACCA TGGGTTATGC ATAACAACCT 1080
CCTGCAGCAG CTTAGTGTTT GAGAACTAAC CTGAGCACCA GATTGTTTAA GTAAAACTTT 1140
AAGCAACTGC ACATAATGTT GCTCCTCAGT 1170
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