Tag | Content |
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EnhancerAtlas ID | HS092-16425 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr14:71757610-71758630 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr14:71758124-71758139 | CTTGCTGAGTCATAT | - | 6.79 | Nfe2l2 | MA0150.2 | chr14:71758126-71758141 | TGCTGAGTCATATTT | - | 6.9 |
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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 |
GH14I071290 | chr14 | 71757125 | 71758706 |
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Enhancer Sequence | GAGACGGAGT TTCACCATGT TGGCCAGGCT GCTATCGAAC TCCTGACCTC AAGTGATCTG 60 CACCCCCCCT CAGCCTCCCA AAGTGCTGAG ATTACAGGTG TGAGCCACAG CGTCCGGCCT 120 GTGACTTGTA TCTTGTGACC TCCTATCTCA TCCTGTGACT AAGAATGCCT AACCTCCTGG 180 GATTGCAGTC CAGCAGGTCT CAGCCTTATT TTACCCAGCC CCTATTCAAG ATGGAGTCAT 240 TCTGGTTTAA ATGCCTCTGA CAATGGCTCT CCAGCCACAA AGGAGGAAGT GATTAAAGCA 300 TGGAGTCAGA GTTTTTCTGC ACTGTTCCAC ACAGGAGGGC TCTCTTCAAA CACAGTTTCC 360 ACGTTGAGCT GACTCACTGG CTTCCTCCTC CTACAGTGTC ATAGTTACCT CTTTTCCAAC 420 TGCACTGCTG AGCAAGTGCA GAGATTGCTT GTTTCAAGGT AGATTGTTGA AAACTTCTTT 480 CGTTTCTCAT TTCTATTTCT AGGCATGTCA CTGACTTGCT GAGTCATATT TGGCAAGCTC 540 AGGATCTCTT TTTTCCTTGT TTTTCCATCT GGATAATATG ATTTATAAAA AGCTCTAAGG 600 CATTTTATTT GGAAAAAGGC ATAAACATAT AAAAATGATA GTGTTGTTTA CCAAAAGACT 660 TTTATCCATA CATAGTTCAA TTAAAACATC TGGCCAGGGA TGGTGGCTCC CGCCTGTAAT 720 CCCAACACTG TGGGAGGCCA GGGCAGGAAG ATTGCTTGAA TCTAGGAGTT TGAGACCATC 780 CTGGGCAAAA TGGCAAACCC CTGTCTCCAC AAAAAAATTA CAAAATTAGC TGGGCATGGT 840 GGTGCACAGC TATACTCTCA GCTACTCAGG AGGCTGAGGT GGGAGGCTCA CCTGAGCTGG 900 GGAGGTCAAG GCTGCAGTGA GTGTGATTGC ACCACTGCAC TCCAGCCTGG GCTACAGAAC 960 AAGACCTTGT CTGAAAAAAA AAAAATTGTC TCATCATAAT AAAATATTTT TGTCTAATTT 1020
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