Tag | Content |
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EnhancerAtlas ID | HS147-29392 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr3:137762170-137763060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFK | MA0496.2 | chr3:137762682-137762701 | AAATGCTTACTCATCAACT | + | 6.25 | MAFK | MA0496.2 | chr3:137762682-137762701 | AAATGCTTACTCATCAACT | - | 6.49 |
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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 |
GH03I138042 | chr3 | 137761659 | 137763507 |
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Enhancer Sequence | AGGAAAACAA CTGTCAAGCT AGAATTTTAC ACCAAGCTAA ATCATCATTC CAAAGTAAGG 60 GCAAGATAAA GAGTAGCAAC AGCAACTATG ATCAAAGCCT TCATGGGACC AGCATAGAAA 120 ATACTGGAAA TTCCAGCTGT CATCATGCTC CAAATGTGTA AGCCACTCAG GATTCTCCTA 180 GCAAAAAGGG GTCAGACCTA AGGAACTGGA TATCCTGTTG ACCTTATTAG GTGGGGAATC 240 CCATACAAAT GTCACTGAGG ATTCTATCCA GACACTCAAG AGCAGGTGGG CCTTGAATAG 300 CAGTCATCAT CTTAGTTTTA GTGTTATTTA CCCATCTGAA ATGGCTTCAT TAGTTTGAGA 360 ACTGCAAAGA TACATACACT GGGTGGGAAG AGGGCCCAGA TTAAATGTAA GCTGTGCTCA 420 CCCTAAGATG CATACATCTA TGAATACCCT GGTCAAGTAT TTTCATATGC AAGGAACAGA 480 AAACCCACTC CAAGATTCTG GCTGTCCCTG CCAAATGCTT ACTCATCAAC TAACAATGGT 540 TGCCCCACCC AGATCCAATT CTGTGTGAAC TTCTAATTCA AGCTTCTACT ACTGCCTAAG 600 CAGAGTCTAT GTTTCTCTTA GTTTAAATTC TCTCGAGAGA AAATCTGATT GACCACTAGC 660 CAATGAAATG TCTGCCGCCC CTCTCTGAAG AGAGATCCCC TCTCTCAAGA GTCCACCTCT 720 GATCCAATCA GCTCTTTCCC TGTGGAGCAA GAACTGTTGG CTTGCCTACT CAACATCCAT 780 TCCACCATCA CTATCACTTT TTTCTTATTA ATATTGTAAA TCAACCCCTC CCTCCTATGG 840 CACTATCCTC GGCTCAAGGG GTATATTCTG ATTTGCCTAA GTCATGGTGT 890
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