Tag | Content |
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EnhancerAtlas ID | HS147-43137 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr9:114636240-114637610 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HEY2 | MA0649.1 | chr9:114637423-114637433 | GACACGTGCC | + | 6.02 | Npas2 | MA0626.1 | chr9:114637423-114637433 | GACACGTGCC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGTTTAATTG GCTCATGGTT CTGCAGGCTA TACAGGAAGC ATGACTGGGG AGGCTTGGAC 60 AGCTTCCCTC CCACATCTGG CACCCTGGCA GTGATGGCTG GAAAGCTGGG TTTATCTGGG 120 ACAATTGACT GAAATACCTA TGGATCCTCT CCAGCCTGGT GATCTCAGAG AGGTAAGATT 180 TCTTTTTTTT TTTTCTGAGA CGGAGTCTCG CACTGTCACT CGGGCTTGAG AGTAATGATG 240 CAATCTCGGC TCACTGCAAC CTCCTGAATA GCTGGGATTA CAGGTGCCTG CCACCATGCC 300 CGGCTAATTT TTTGTATTTT TACTAGAGAC AGGGTTTCAC TATGTTGGCC AGGTTGATCT 360 CGAACTCCTG ACCTCGTGAT CTGCCCGCCT TGGCCTCCCA AAGTGCTAGG ATTATAGATG 420 TGAGCCACCA CGCCCAGCTG AGAGGTAAGA TTTCTTATGT GGGAGCTCAG GGCACCCAGA 480 GTGTTCCAAG AGGCCTGGGT AGAAACAGCA AGGCTTCTCA TGGCCTAACC CTAGGTGTCC 540 CAGATTGTCA TTTTTACCCG TTTGTAGGTC AAGCAAGTCA TTAAATCAAC CCAGATTCAA 600 GAGGAGGGAA ATTAGACACC ACCTCTCAAA GGGAAGGGAA ACAAAGCTCT ATGGCCATCT 660 TTAATCTACC ACAGATGCCT AATAGGTGTC TCATTTGTAA CATGTCCAAA CAAAACTCTC 720 AATTTCCTCT CTATACCTGC TCCTTTCTGG TGATCACCCT CCCAGTAAAT TGGACCGATT 780 GCTCAGGCCC CAATTCTTGG AGTCATCCAT GACTGTCCTC TTAGTTCCAT ACTCTACATT 840 CTATTCATTA GCAAATCCTG TTGGCACCAC CTTGAAAATA CATCCTCAGT CTGACTGCTC 900 ACTCTCTCTA CCTCTATTGC TATCACTCTA GTATGACCCA CTATCGTTTT TTTCCTGGAC 960 TACTTTCATA GTTTCCCAAC CGGATTATCA GCTACCACTC TTGACCTCAT GACTCCTCCA 1020 CACAACAGCC TCAGAGATCC ATTTATTTAT TTATTTTTGA GACAGGGTCT TGCTTTGTTG 1080 CCCAGGCTGG AGTACAGTGG TGTGATCACA GCTCACTGCA GCCTCAATCT CCCCAGGCTC 1140 AGGCAATCCT CCCACATCAG CCTCCTGAGT AGCTGGGACT ACAGACACGT GCCACCAAAC 1200 CCAGCTTATT TTTGTATTTT TTGTAGAGAC AGGGTTTGTA GGTCTCTGGC CTAGAGCAGT 1260 GGTAATGAGG ATTGAAGAGC CAAAGTGAAT TCCAAAGCTA TCCCAGTGAT AGGGCAAATT 1320 ATTTAAATAA GACCCTCTTT TCTGTGGGGA AAAGAGAGAT CAGACTGTTA 1370
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