| Tag | Content |
|---|
EnhancerAtlas ID | HS066-02106 | Organism | Homo sapiens | Tissue/cell | GM18516 | Coordinate | chr16:30633830-30634960 | 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 | TTCCCACATT TTGACAGGCT TTGAGAAAAT TTCCTAAGTT TTTTGTACAT CTTACAGAAG 60
CCAGTGCACG TTTACAATCC TCATTTGCAT TCTCAAAAGC TAAAGTTAAA GTTAGCATCT 120
CTGCAGCCGC GGTATGAGGA ATCTGACACC TCACTGCCTC TAGTAATCAT GCAAGAAAAT 180
GTGCAGAGGG CTCCTGCAAC CCTTGCATGG CACGTAAAAA AGATTGTATT GGGACCCCCT 240
TCCTCTGGAA TTGTGGCCAA CGTGTGTTTA GCGGCCAGTG CACACTGCTG ATAAGCAGCT 300
TCTGGGAGTG CCATTTGATG TTGCAGGTCT GAATAAGGGC CATTACCCAA CAGCATATCC 360
TCTGTAATGT CCCTGTGTCC AGCAGCACGA TTCTGTCTAG CCTGGTCTGC ACACAGTTCT 420
TGCCAATTTA AATTCCATGT CAGGTATGAA CTAGCAGACA AACAAGTGCA GGCCAAATGC 480
TTTACATCAA AGGGTGGAAG GCGCATAGCA CCAAATACAG ATTCTAGCAA TCCTAAAGTA 540
AATGGGCTCT GTACTCCATT ATTCAGTACA TGAGCTTTTA ATTCCTTCAA CAACTTAAAC 600
TCTAGTGGGG TGTGTTCATG AATAAACTGC TGTGGATTAT TTGGATCCAG CCTTATAGAA 660
ATAGGAAAAG CACAAGGTTC GAAGGGCTCT CCAGCTATGG CAGCAGAGCG TAGAATTCTT 720
TGTTTTGGGG TCTCTATTTC TGTTACTGAA GGAGACAGTA CACGTGTGTC CACTACTGGA 780
GGGGGCGGTA CAGGCCAATT TTCATCCTCC CTCTCCTGTT TATTATTTCA ATGGGCGCTG 840
TTGGAGGGAC AAAAGATTCT TTTGAAATTT GAGATTCAGA ACATGGCTCC TGCTGTCCGG 900
CAGAATAAGA AGGAGACAAT GGCAGGAGGA CAGTATGGAA TAAAGTCAAA ACAGAAGGAT 960
CAACTTTAAG ACCTTTTTGA TAAGCCTGTT TTAATCCTTC CCCTACACTG TCCCAATTTT 1020
CCGCATCGAG ATGCCTGTCT GTGGAAACCA TGGGTTATGC ATAACAACCT CCTGCAGCAG 1080
CTTAGTGTTT GAGAACTAAC CTGAGCACCA GATTGTTTAA GTAAAACTTT 1130
|
| |
|
|
|
