| Tag | Content |
|---|
EnhancerAtlas ID | HS098-25449 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:80028700-80030180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr17:80029882-80029903 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | | SOX10 | MA0442.2 | chr17:80029643-80029654 | AAAACAAAGGA | + | 6.32 | | Sox3 | MA0514.1 | chr17:80029643-80029653 | AAAACAAAGG | - | 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 |
| GH17I082072 | chr17 | 80029941 | 80030069 |
|
Enhancer Sequence | TTATGGAACA CTTCACCCAT GGCTACACCA TATACTAGGC CATTAAAGAA GACACAATAA 60
AACATTTTCC CTCCAGCCTG GGCAACAGAG TGAGACTTCA TCTCAAAAAA AAATTAAAAT 120
TAAAATAATT GGAAAGCTAT TCTCTAGCCA CAGTGGAATT AAATTAGAAA TCAGGCCACA 180
CACACTGGCT CATGCCTATA ATCCCAGCAG TTTGGGAGAC TGAGGTGGGA GGATTGCTTG 240
AGTCCAGGAG TTTGAGATCA GCCTGGGCAA TAGAGTGAGA CCTCAGCTCT ACAAAAAAAA 300
AGTTAAAAAT TAGTTGAGTG TGTTGGCATG TGCTTGAATC ACAGCTACTT GGGAGGCTGA 360
GATGGGAGGA TGTTTTGAGC CCAGGAGGCA GGGGTTGCAG TGAGCTGAGA TTGCACCACT 420
GCACTCCAGC CTGGGCAACA GAATGAGACC ATGTCTAAAT AAATAAATAA GAAACAAACA 480
AAAATAGAAA TTTGAGGTAT GCACAAATAC TTGAAAATTA ATAACACACT TCTGAGTAAC 540
CCATGGGTCA AAGAAGAAAC CAAAAGGAAA ATTTAAAAAT ATTTTGAAGT TAATGCAAAT 600
GAAAACACAT TTCAAAATAT GTGGGATGCA ATAAAGCAGT TCCTAAAAGG AAAATTTTGG 660
CTGGGTGCAG TGGCTCATGT CTGTAATCCC AGCACTTTGG GAGGCTGAGG CAGGTGAATC 720
ACCTGAGGTC AGGAATTTGA GACCAGCCTG GCCAACATGG TGAAACCCCG TCTCTACTAA 780
AAATACAAAA ATTAGCCGGG TGTGGTGGCG GGTGCCTGTA ATCCCAGCTA CTAGGGAGGC 840
CGAGGCAGGA GAATCACTTG AACCCAGGAG ATGGAGGCTG CAGTGAGCTG AGATCATGCC 900
ACTGCTTTCC AGACTGGGCG ACAGAGCGAG ACTCCATCTC GAAAAAACAA AGGAAAGTTT 960
TAACTATCAA CACCCATGTT AGAAAAGAAA AAAGATCTCA AATCAATAAT TTATGCTTTT 1020
TTTTTTTTTT TTTTTTTCCT GAGATGGAGT TTTGCTCTTA CGCTCTTACT GCCCAAGCTG 1080
GAGTGCAATG GCAGGAGGAG GAGGTTGCAG TGAGCCGACG TCGCACCACT GCACTCCAGC 1140
CTGGGCGACA GAGTGAGACT CTGTCTCAAA AAAAAAAAAA AAAAAAAAAA AAAGAAAGAA 1200
AGAAAGGGCA GAAATGTCCC TATTTGCACA AACTATGGAT ACATAAAAAA ACATGGATGG 1260
TTCTCAAAGT TATGCTGAGT GAAACAGAAA GGCCAATCTC AAGAGGTATA TATGATTCAA 1320
TTTATATAAT GCTCTCGGAA TAATAGAATT ACAAAGATGG GAAACGTCAC CAGGCCCCTG 1380
GCTTGGGGTG CCTTCCTTCC CCATGATGGG ACACCTGCCT TTGGATTTTG CCTTCTCACC 1440
CCTCCAGGCG ATGGAGGTGA TGGGCTGGGG GGCCACAGCC 1480
|
