Tag | Content |
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EnhancerAtlas ID | HS062-00191 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr1:20848670-20849520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:20848992-20849011 | TAGCCACAAGGAGGCACCA | + | 6.58 | FOXH1 | MA0479.1 | chr1:20849304-20849315 | TGTGGATTGGG | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I020522 | chr1 | 20848921 | 20849070 |
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Enhancer Sequence | TTCATGTTAT TGTCCCTAAA ATCAACTTGA TTGATCAAGC TGAGTCCACA GATTGATTGA 60 TTGATTGATC AGGTCATTTC CTTCCTTGAA TTACAGTCAC TCCTACTCAA ATACTTAGTA 120 AGTGACTGCC CATTTGGAGA ACTTGTCTAG AAACCAGGGT TCCTGGGTTC TAACCTGGGC 180 TCAGATCAGT ATCGCCACTG GGAAAAAAAT GCAAATACGA GTTATTTCTA AAATCACCTC 240 TAAGGGTCCT TCAATCTCGG CAGCCTAAAA TCTCTGGGAT TTTCCTGCGA ATTTAGTCAG 300 TCATTGCTGC AGTTGACATT TTTAGCCACA AGGAGGCACC AGGAGCACAG AATGGAGAAG 360 GCGAAGCAAA GCGCCCTGAA GGAGGATCTG AGACCTGGGA ATGGGAGGCG AAGGCGGAAG 420 GGTGAAGGAG GTCTGGAGAT TGAAGGGGAA ACTGAGGCTA ACTGTGGCCC ACGCCGAGTT 480 GTATCCAGGG ACCCAGTTCA GCCTCAGGCT TGCTATTTGC CAGCAGGCCC TGGGCCCGTC 540 ACCAGTAACT ACCTTCACCT CCAGCCTCCG TTCCTGAGAA CGACAGGAAC CCCGTCTTTA 600 TCAAGGAGCC TGCTGGTCAC CTGAAAGCTG CCGGTGTGGA TTGGGAAAGG GTGAACTAGG 660 ACAGGCTTGG GAGTCAGGCA CCGGAGTCTG GGATCCGCGC TGCCATTTAC TTACCCGCCA 720 TGTGATCTCT GGCAAATGTC CTGAGGTCCC TGAGTCTCTT TCTCATCTGC AAAATGGGGA 780 GATGGAAATA GATGATTCCT CGGGTGTCTT TCATCTGGGA TACTTTTTTT TTTTTTTTTT 840 TTTTTTTTTT 850
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