Tag | Content |
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EnhancerAtlas ID | HS062-08927 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr2:43836070-43837330 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr2:43836631-43836650 | CTCTGCCATCTGGTGGTCA | - | 7.22 | POU2F2 | MA0507.1 | chr2:43836465-43836478 | ATATGCAAATGAG | - | 7.52 | Pou2f3 | MA0627.1 | chr2:43836463-43836479 | TTATATGCAAATGAGC | + | 7.28 | Znf423 | MA0116.1 | chr2:43837309-43837324 | GGCACCCAGGGGTGC | + | 9.03 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 43836787 | 43836930 | chr2 | 43836422 | 43836775 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I043609 | chr2 | 43836581 | 43836710 |
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Enhancer Sequence | CCCACCTTGC CTACAAGATA ATGGAGTATT CTTTTTCTAA AATCTGCATT GCAGCATTCC 60 AGGAGCTGCT ATCCTATCTT TCCTTTACCT CGAGGTCTGA GCCTCAAGAA AGCCTAGGAA 120 CCCAGACAGT GCCTCTCCAC CCACACAGAA TTGATCCCGC TTCCCATACT CGGAGCTCTC 180 CTGGACTAGG GAGAACTTCA ATCAGGCCCC TTCCTGCAAC CCTGGTAATT TTCATTTATT 240 CCTCACAAAA GGCCTGTGAA GCACGCAGGG CTGGAATTCT CTCTCTTTTT TTTAACTGAT 300 GAAGAAACAT GTTCAAATGG AGCAAGTGGT TGGTGTGCAG TGATTCTGAT GCTCAGTCCG 360 GGGCTCTTTC CATTATATTC CAAACCCTCC TTTTTATATG CAAATGAGCC AATTGTGGCA 420 GTGACACTTT CCTACAAAAT GAAACAATGC CGTAATTACA AGGGCTTGGG AATTAATGGC 480 ACTAAATGGG TAATTTGGGT TTAATGTTAA ATCCTGGGAT AGGCGACCCA GGGCCAGAAA 540 GAGAGGCTTT CCAAGTGTCA CCTCTGCCAT CTGGTGGTCA AATGACAATA TAACTGCAAC 600 AACTCAGTGT GGATACCATC ATCATGTGAA AGTCACCCAT GACCCCAGGG TTGGGTGAAC 660 TATTTGAGGC TGGGCTCTGA CTTTTACGGC CTGAGATGAG AAAATAAAAT GTTGAATACA 720 CAAATAAAGG TCAGAGGTTT TCCCCTATAT CTCTGCTCAG GGTGAGGAAC TGTGTAGTTT 780 ACAATGGAAG AGCCCATTCA TCCATTTATT CAACAAATAT TTATTAAGCA CTGTCTTAGG 840 TTGGCTTCCT AGGAAACAGA TTCTAGGCAG AGATTTGCTT AAGGAGGGTT ACTGGGGAGC 900 ATTCTTGAGG ATCACCCTTG TAAGGGGTTG AGGGAAACAG AACTCGTCAG AAAGAGTTGA 960 ACTGGAATGA ATTTGCAACA GTGGCGTCAG CCAATCTTAC TGGGAGCTCT GGTGTTGGCT 1020 TGGCAAGGGG ACTGAGCCTC TGCACTTCTT TTTCCACCAG TTATTGGATT CGCTGAGAGC 1080 TGTAACAGAG CTGCACCTAG GGGGATGAGT GCCTTGGTCC TAAAAGGGGG TATCTGGGCA 1140 GTGCCCTACA GCATCCACTA CAGACACCTA CTATGTTCTG GGCACTGTGC CAAGCTCAGG 1200 AGATGTAAAG TTGAACAAGA TAACATCTCT GCCTTCAAAG GCACCCAGGG GTGCAGAGGT 1260
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