| Tag | Content |
|---|
EnhancerAtlas ID | HS098-54297 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr8:23583890-23584880 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr8:23584857-23584873 | TATTATTTACTTAATA | - | 6.23 | | ZIC1 | MA0696.1 | chr8:23584455-23584469 | CGCCGCAGGGGGTG | - | 6.02 | | ZIC3 | MA0697.1 | chr8:23584454-23584469 | GCGCCGCAGGGGGTG | - | 6.62 |
|
| | 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 |
| GH08I023726 | chr8 | 23583914 | 23584113 |
|
Enhancer Sequence | TGTTTACGTG GTGCCAGGAC CTGTTCTAGT CCTTTATGGA TATGAACTCC TTTAATCCTC 60
ACCCAGATGG TTTGAGCTGA GTACCTCTTA TTGCAGCGGG GATACTAAGG CCGGGACAAC 120
AAAAGTACGT CGCTGACTCG AAGCTGGGCG GCGGGTTTCA GAGGCTGAGT TCTTAACACC 180
AGGGCACTTC CTTGTAGCCA CCACGCCCGG CTGCATCCTC CACCCGGCCG GTTTCTAGAA 240
ATAGGAGATA CCGAGAAGTT AGGGTGGCCC AGGTCTGGCC TTAGATCTGC AGAGGGGCGA 300
GTGCAGATTG CGCGATGGCG AGGCTCCTGC GACAAGGCGA ACACCAAGGA CGCGAGCTAT 360
CTGGAACCAC AAATAAAACA AATTCAGGGA CGGCGTTGAC ACCGCGGCCA CCTCCTAGGC 420
GCTTCTTGGA AGGGCGCGGC TGTGGTGCCC GCTCTGCCCG TGGTCCCGCT TACTTTTGGA 480
CTCTGTCCCC CATGGGGCTG GGGTCCGGGT CCGCGCCCTG ACCCCCGCCT CCGCCGTCAG 540
TCTCTCTCCG CTCCCAGCCG GGTGGCGCCG CAGGGGGTGG GGTTGTTTTC GTTTGGCCCC 600
GGGGACGTCC TTGTCATTCC AACAGCCTCC CGGTGCGGCC CAAACACCCT GGGCCACCCG 660
ACACCTCGCG CTGTTGACGA CGCGGGGCCG CCGGCGCCAG GGCGGGTGGT GGAGCTCCGC 720
GCAGGCCGGG GGGAACCGCA AGAGGAGCCG GGGCGGGCGG CGGCCCCGGG CGGGTCAGGG 780
GCGGCGCGAG CCCACACAGA GCGGTGAAAC TACCAGGGGC CCTCCCACTC TTCCCGGACT 840
CCGGAGGAGC TAAGCCGGCA GGGATCGCTC GCCCACCCTG AGCACTTTAC CTGCATGGTG 900
GCCAAGACCC TTCGTCCGGA CCCTACTCCT GTTTTCCTCT AGCACTCACT TCCCTCCGTA 960
CTGTTAATAT TATTTACTTA ATAGTTTATG 990
|
