Tag | Content |
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EnhancerAtlas ID | HS095-09250 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr14:71757440-71758540 |
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 | TTTTGAGATG GAGTTTCGTT CTGTTGCCCA GGCTGGAGAG CAATGGTGCA ATCTCGGCTC 60 ACTGCAACCT CCACCTCCAG AGTTTAAGTG ATTCTCCTGC CTCAGCCTCC CGAGTAGCTG 120 GGATTACAGG TGTGTGCCAC CACACCCGGC CAATTTTTGT ATTTTTAGTA GAGACGGAGT 180 TTCACCATGT TGGCCAGGCT GCTATCGAAC TCCTGACCTC AAGTGATCTG CACCCCCCCT 240 CAGCCTCCCA AAGTGCTGAG ATTACAGGTG TGAGCCACAG CGTCCGGCCT GTGACTTGTA 300 TCTTGTGACC TCCTATCTCA TCCTGTGACT AAGAATGCCT AACCTCCTGG GATTGCAGTC 360 CAGCAGGTCT CAGCCTTATT TTACCCAGCC CCTATTCAAG ATGGAGTCAT TCTGGTTTAA 420 ATGCCTCTGA CAATGGCTCT CCAGCCACAA AGGAGGAAGT GATTAAAGCA TGGAGTCAGA 480 GTTTTTCTGC ACTGTTCCAC ACAGGAGGGC TCTCTTCAAA CACAGTTTCC ACGTTGAGCT 540 GACTCACTGG CTTCCTCCTC CTACAGTGTC ATAGTTACCT CTTTTCCAAC TGCACTGCTG 600 AGCAAGTGCA GAGATTGCTT GTTTCAAGGT AGATTGTTGA AAACTTCTTT CGTTTCTCAT 660 TTCTATTTCT AGGCATGTCA CTGACTTGCT GAGTCATATT TGGCAAGCTC AGGATCTCTT 720 TTTTCCTTGT TTTTCCATCT GGATAATATG ATTTATAAAA AGCTCTAAGG CATTTTATTT 780 GGAAAAAGGC ATAAACATAT AAAAATGATA GTGTTGTTTA CCAAAAGACT TTTATCCATA 840 CATAGTTCAA TTAAAACATC TGGCCAGGGA TGGTGGCTCC CGCCTGTAAT CCCAACACTG 900 TGGGAGGCCA GGGCAGGAAG ATTGCTTGAA TCTAGGAGTT TGAGACCATC CTGGGCAAAA 960 TGGCAAACCC CTGTCTCCAC AAAAAAATTA CAAAATTAGC TGGGCATGGT GGTGCACAGC 1020 TATACTCTCA GCTACTCAGG AGGCTGAGGT GGGAGGCTCA CCTGAGCTGG GGAGGTCAAG 1080 GCTGCAGTGA GTGTGATTGC 1100
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