Tag | Content |
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EnhancerAtlas ID | HS147-41372 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr8:130688600-130689740 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr8:130689308-130689319 | AACCAATCAGA | + | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH08I129676 | chr8 | 130688846 | 130689247 |
| Enhancer Sequence | TTGAGCAAAG CTTGAAAGAG GTAAAAGGAT TAGCCGAGCA GCTATCTGAA AGAAGAGAAC 60 TCAAAAGATG GGAAATGACC ATTGCAAAAG CCTGAAGGTG GAAACAAGTC CAAATTGCTT 120 GAAGAATAGC AACAAAGCAA GTGTGGCAGG AGAAGCAAGC CTGAGGAATG TAAAAGGGTG 180 GGTGAGGTCA TAGAGGAAAA GAGGGGCTGG ATCACAGAGG ACCTTGTATA TCATTATCAT 240 GTCACCAACT TTTTTTCTGT ATAACATAGG AAGTCATTGG AAGGTTTTGA TCTAGTTTGT 300 GCTATAAAAG ATCCACCCTG GCTGTCATTT GAGAATACAT GACAGATTGT AAGGGAGAGG 360 CAGGGAGACC ATGGCAGTCT TCCAGGTGAG CAATCAGGGT GACTTTGAAC AGGTGTTAAT 420 GTGGAGGGCT GAGAAATGGC CAAATACTGG ATGTGTCATA GTTCACTGAA GCCAACATGC 480 CTCTGCCTGT GGGCCACATC CCTAATTTGG ATATATTATT ATAAAAGGTG ACATAATCTC 540 TATCTTGGTA TTGAGGAACT ATGGTATTTC AAAGTTGAAC TAAAGGGTTT GCTGGCAGAA 600 CAGAAGTGAG GGTGAGAGAT AGGATGACTC AAGGACGCCT ACAGAGTTTG ACATCTGAGC 660 AACCAAGGAT GGAGCTGCCC TCAGCTGGGA TGGGGAAGTG CTGGGAGGAA CCAATCAGAA 720 AGAGTGGGTG AGGCTTAGGC CAGAGTACAG TTTAAGACAT GTTAAGTTTC CATGTCTATT 780 AAAAATATAA GCGAACAGGC CGGGCACGGT GGCTCACGCC TGTAATCTCA ACGCTTTGGA 840 AGGCCGAGGC AGGAGGATCA CGAGGTCAGG AGATCGAGAC CATCCTGGCT AACACGGTGA 900 AACCCCATCT CTACTAAAAA CACAAAACAT TAGCTGGGTG TGGTGGCGAG TGCCTGTAGT 960 CCCAGCTACT CAGGAGACTG AGGCAGGAGA ATGGTGTGAA CCAGGAGGCG GAGCTTGCAG 1020 TGAGCCGAGA TCGTACCACT GCCCTCCAGC CTGGGCGACA GAGTGAGACT CCATCTCAAA 1080 AAATATATAT ATATATATAA TATATATATA ATAAAATATA TATATAATGT ATATAATATA 1140
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