Tag | Content |
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EnhancerAtlas ID | HS147-03057 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:146763660-146765290 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUND(var.2) | MA0492.1 | chr1:146764771-146764786 | TGTGGTGATGTCATC | + | 6.03 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 146763756 | 146764051 | chr1 | 146764275 | 146764979 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I147291 | chr1 | 146762954 | 146765694 |
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Enhancer Sequence | TCAATATATG AATTTGGGGG GACACAGTTC AGCCTATAAC AAGCAGATTG GGCCATAGTC 60 TCCACTGTAC TTCCCCTGTC CCCAGGCTTC CATCCATCTG TCCCCGGAGC ACCGTCCAGA 120 TAGCAGATCC CATCTTAAGT ACGAGGATTT CTATTTGTCT TTTTATCCTC AGTACCCTAC 180 ATAGTACTAG CTCATAAGAA ATGCTCCATA AACATTTACT GCATGAGTAA GAAAGCATGA 240 CTCAGAACTC TGACGGTTTC ATTTCTTACC ATGTGAAAAT TTCTATGAAA GATTGTGTTT 300 TCTAGTCAGC CATAATAAAG CAGGAGAGAG GAACTAACAC ATATGTCCTC TGCCCACATC 360 AGAATCCTTT TGCATCTTAG GCATCTTGGG ATGCCTGCAG TGAGTTTGAT TAACCCCACC 420 TACCTGGCTT TCTCCAAGGC CTGGGTTCAT GTTCAGATTT TAAGCCAGAA TTAAGAAATT 480 TCAAAATCAG GCCAAAAGAG AGGTTCATCC TTTTGAGGTT GCTGTCTATG TGACTGTGTT 540 AGGCTGTTTT TGCACTGTGA TAAAAGAATT CCCTGAGACT GGGTAATTTA CAAAGAAAAG 600 AGATTTATTT GCTCATGGTT CTGCATGCTG TACAGGAAGC CTGATACTGA CATCTGCTCC 660 TGCTGGGGGC TTCAGGAAGC TCACAGTCAT GGTGGAAGGC AAAGGGGAAG CTAGTTTATC 720 ACACATGGCA AGAGCAGGAA CAAGAGAGAG TGGGGGAAGG TGCCACACTG CTTTAAATAA 780 CGAGATGTCA TGTGAACTAC CAGAGCAAGA ACTCATCACC AAGGGTATGG CATTAAGCCA 840 TCCATGAGGG ATCCACCCCA TGATCCAATA CCTCCCACTA GGCCCCACCT CCAACACTGG 900 GGATTACATC CTAACATGAG ATTTGGAGGG GGACACACAT CCAAACTACA CAGTGACTAA 960 CAGCAAAGTG GTTTCTGTTG AGTCATTCCT TCAGTAATTT CTAAAATGCT AAAAAAGGAG 1020 AAAAGTAAAG TGTCTGTGCA TGAGAAACTC AGAATCCAGT GATTCAGGAA AACTGTTTAC 1080 AGGGAGTAGA GCACCATGTC TATGATATGA CTGTGGTGAT GTCATCCCGG AAGCTCCCTT 1140 GACACTCTCC AGCTCTGCCC ACTTAGGTTA GGATGGTTGA GAGATACTTG GCATTTTGTC 1200 CTCATGGGAA TTGTTCGAAC AGAGATGGAA TGACTGCTTG TCCTGGGGGT TGTGGAGCTG 1260 ACTCAGGCAT CAAAGGGCTG GGATACAGGA GCCTCTAAGA TCTTTTCCAT GCCTACAATT 1320 CAGAAAAATT CTCTTTTTTT TTTTTAACCC TTGAGAGCTT TTGGAAAGTA TATGTTTTGG 1380 ACTCATTCTC TGGTTTTAAA GTATTTTAAA AAGAAGAAGA AAACCCTGTA TAAAGTGACC 1440 ACAAAGTAAG AATTATGACG GGATGTGAAG TCATACATAT AGTAGGACAT TGCTGTTCAG 1500 GCATAGCATC CGAAAGAGAC AGAGCCAAGC CCAAGTGACC CATCAAGGGC TGTGCCGCCT 1560 CCATGGGCGG TCACTTGGTT GAGTGTGGCT GTTTCATGTT GGGTTGGTCA TCTAATGGTG 1620 GTTCTTTCCA 1630
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