Tag | Content |
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EnhancerAtlas ID | HS113-11401 | Organism | Homo sapiens | Tissue/cell | Keratinocyte | Coordinate | chr14:68130060-68131420 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr14:68130802-68130814 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr14:68130806-68130818 | GTTTGTTTGTTT | + | 6.32 | SPI1 | MA0080.4 | chr14:68130640-68130654 | AAAATGAGGAAGTA | + | 6.98 | SPIC | MA0687.1 | chr14:68130640-68130654 | AAAATGAGGAAGTA | + | 7.58 | Zfx | MA0146.2 | chr14:68130150-68130164 | GAGGCCGAGGCGGG | - | 6.01 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATGTATTTTA CATGAAATAA GTTGACATAA AGAAAATGTA AGTGACAAGG CTGGGCACGG 60 TGACTCACGC CTGTAATCCC AGCAATTTGG GAGGCCGAGG CGGGCGGATC ATGAGGTCAG 120 GAGATCGAGA CCATCCTGCC TAACACGGTG AAACCCCATC TCTACTAAAA AATACAAAAA 180 ATTAGCCTGG TGTGGTGGTG GGCGCCTGTA TTCCCAGCTA CTCAGGAGGC TGAGGCAGGA 240 GAATGGTGTG AACCCAGGAG GCGGAGCTTG CAGTGAGCCA AGATTGTGCC ACTGCACTCC 300 AGCCTGGGCG ACAGAGGGAG ACTCCATTTC AAAATAAATA AATAAATAAA TAAAATGTAA 360 GTGACAGTAA TAATGATACT TGCGGATGGC AAAAATTATG AAGGTGGTAC CAGAATGCTG 420 TCACCTGGTA AACATTTGTA TGGGGGAAAG GCATACAAGC ACCTTTTCTG GTTAGTCAGC 480 GGGGTGAGGT TCTGGTGCCA GGTTCGGGCC TGCCTCAGCA TGTAAACTTA GATAATTTCC 540 TTCATTTCTT TGGGACCTCA CATTCTCCTT CATTGACTAC AAAATGAGGA AGTAGGTCAT 600 TCCCTTATAT CTAACAAGCA AAAATTAGCT CCTTTTAAGA GGAGCTTGAT TTTTTAAAAA 660 AATTTATACA TCCAAATGAC TGTTCTCCCT GGAAATCTAC ACATAATCTA CTTATCACCA 720 TAAAGTTACC ATCATTTACA ATGTTTGTTT GTTTGTTTCA AGACAGAGTC TCACTGGTCA 780 CCTAGGCTGG CAAAATACAT GTAATATAAA ATTTACCATT TTGACCATTT GTGAGGGTAT 840 AGCTTAGTGG CTAGGTACAT TCACACCGTT GTGGAGCCAT CACCACTAAC TGTTCTCCAG 900 AACTTGTTTA TCCTCTCAAA CTGAAATTCC GTACCCATCA AATACCTCCC CATTCTATGA 960 ATTTCACTAC TCCAGGTACA CCATTAAGTG GAATCATACA ATATTTGTCC TTTGTGTTTA 1020 GCTTATTTCA CTTAGCACAA AGTCAAGGTT CATCTATGCT GTTGCACGTA TGGGGATATG 1080 GCCTTTTAAA GCTATGTATT TTTCAATGTG ACTCCTAAAC ACAAGCCAGC AGCACTTCCA 1140 CCAACTAAAG AGCAATTTTT TTTTTTTTCT TGAGACAGAG TCTTGCTCTG TCTCCCAGGC 1200 TGGAGTGCAG TGGCTCGGTC TCGGTTCACT GCAACCTCCA CCTCCCAGGT TCAAGCGATT 1260 CTCTTGCCTC AGCCTCCCGA GCAGCTGGGG TTACAGGCAC CCACCACCAT GCCCGGCTAA 1320 TTTTTTTACA TTTTTAATAA AGACAGGGTT TTGCCATGTT 1360
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