Tag | Content |
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EnhancerAtlas ID | HS053-17136 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr17:53315380-53316800 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NRF1 | MA0506.1 | chr17:53315795-53315806 | TGCGCATGCGC | - | 6.32 |
| | 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 |
GH17I055237 | chr17 | 53314453 | 53316761 |
| Enhancer Sequence | GACTGTTTCT GGCCGTTTGT GATGTCCAAC AATGATGTAA TGATTATCCT TGCAGGGACT 60 TCACTTCGCA GGAGCAGAAG CCCATTTGCA GGATAAATTC TGAGTTGCGG AACTAGTGAT 120 TTACAGGGCA GAGGTGCAGT CTTTGTCTTA ATTTCTGAAT TCACGAATGT TGAATGTGAT 180 GAATTCGTGG GAAGCCCCGC AGGGAGCCTA AGCAGCTCTC CAGAGGCTGT GGTTGTCACG 240 GATGATGATT GCGGGACCCG CAGACTGAGT CTCCAAGCGC TCCGCCCCGC CGCGCCCCTC 300 TCCGCGGGTC CCACCGCGGA CCCGCCCCTG CGCGCCCCGG GCCAGGAGCC CCTAGCTGCA 360 GGACCAGGCA CGTGCGATTC CACGTGAGCC TCCCGGCCGG AGCGCAGATG GGAAGTGCGC 420 ATGCGCCTAC CGCCTGGAAA GTAGGTCAGA CTCCTCCTCT CACGTGACCT GCTCCCCTTA 480 GCTACCCTCG GCGCCTCCCC GCCGGGGCGC AGCCGGGATG CGCTCGGCAG CCAACGTGAC 540 GGGGCTGGGC GCGGGCGGCT CCGCGAGCGC CCAGCGCCCG CGAGGATTTG CCGGTTCTCC 600 TCACACCCGA GCGCTCCGCT CAGAAGTCGG GCGGGCAAAA GGGAGCGCCT CGGGAAGTAT 660 CTGGGAGCCG GGCTGGAAAT GAATGGGGCC CGGAAGCGAG CTCAAATCGC TGACACCTGG 720 CACCGGGCTG CGTCCACTTT CATGCTTCCT AAGGCAGTTC TGCCTGCAAG AAGGGAACGC 780 GCATCGCCTT TCAGTAGATC ACACCGATCG TTTGCACGTT TGCATTCTCA ATTTCTGCAC 840 TATATAGGGC AACTCAGACA TGAAAACAAT CTTTGTAAGA AGAAGTGGAA TGCTAATGGT 900 TCCTGGAGTT TTGCAGGAAT ATTCCACCGG CCCCATTTCT AATCTCCCAC TCACTCCCTC 960 CCCAAAGACA CTCCTACTAG AAAGCTTATC GGTAGATTTC TCACCTTCCA CAAGAGACTT 1020 CAGGGGCGCT GCTGCTGCTG CTGCTGCTGC TGCTGCTGCT GGAGGCTGGA GGGGGTTGGG 1080 AGCAGGGAAC GAAGGCAGGT CTGAATTAGC TGAAGCTAAA TTCTATATAT CAGAAATAAT 1140 TTTATTTATT GCCCCATTGC TTTCTGATTT TTAACTTGTT GCACAAATGA CAGACTCTGC 1200 CTCAGTGAGT TGCAATCCAG TGGAGGGCAC TAACAGGCAA AATCATGGGT TACAATGCAG 1260 TGGGCTATAC ATGTTTTAAT AGAGGTGTGC CCAGGTGTTA TATAAGCACA GTGGTGGGTA 1320 CCCTGAGTCT TGAAGACTAA GTGGGAGTTA GCTGGCAGAG AAATAAGGCA GAGGGGGTGG 1380 AAAGTGTTCC AAACAAAGGG AATAACTAAT AGTTACATAA 1420
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