Tag | Content |
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EnhancerAtlas ID | HS113-24312 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr3:13495810-13498180 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PBX1 | MA0070.1 | chr3:13497247-13497259 | ACATCAATCAAA | + | 6.74 | RREB1 | MA0073.1 | chr3:13496160-13496180 | GGTTGGGGGGTGATGGGGGT | - | 6.9 | ZNF263 | MA0528.1 | chr3:13496145-13496166 | TAAGGAGGAAGGGGAGGTTGG | + | 6.14 | ZNF263 | MA0528.1 | chr3:13496148-13496169 | GGAGGAAGGGGAGGTTGGGGG | + | 6.91 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 13497200 | 13497600 | chr3 | 13496801 | 13497100 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I013455 | chr3 | 13496650 | 13497518 |
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Enhancer Sequence | CTGGGCATGA TGGTGGGCGC CTGTAGTCCC AGCTAGTCGG GAGGTTGAGG CAGGAGAATG 60 GCGTGAACCT GGGAGGCGGA GCTTGCAGTG AGCTGAGATC GTGCCACTGC ACTCCAGCCT 120 GGGTGACAGA GAGAGACTCC ATCTCAAAAA AAAAAAAAAA GAAAAAAGTA AAGATTCCCA 180 GATCCCCGTG TGGAGAGTCT CAAAAATGGA AAGCAGAGGC TTCTGAGGGG AATGTGTCAG 240 CCTTTTCTCC TTCCTCACTT TCATTCATCT TCTGGAAAGG GGCACACATG AACTGCATGG 300 ACTTTAGTCA CCTTGGTTAA TTTCTACCTG CCTCCTAAGG AGGAAGGGGA GGTTGGGGGG 360 TGATGGGGGT TGGAGGGTCT ACAGGCCCAC AGGAGGATTG GACTAAAGGT GTCCCATGAA 420 GAGCAGTATT TAAGATTAGA TTCAGGCTGG GTGTGGTGGC CCACACCTGT AATCCCAGCA 480 TTTTGGGAGG CCAAGGAGGG CGGATCACGA GGTCAGGAGA TCGAGACCAT CCCGGCTAAC 540 ATAGTGAAAC CCCGTTTCTA CTAAAAATTC AAAAAAAATT AGCTGGGCAT GGTGGCGGGT 600 GCCTGTAGTC CCAGCTACTC AGGAGGCTGA GGCAGCAGAA TGGCTTGAAT CTGGGAGGTG 660 GAGCTTGCAG TGAGCCAAGA TTGCGCCACT GCACTCCAGC CTGGGTGATA GAGCAAGACT 720 CCGTCTCAAA AAAAAAAAAA AAAAAAAAAA AAAGATTAGA TTCTGAGAGA GTCATTCCAC 780 CTGTGTCCCA CACACCAGGT AAGGGGTTGC TCTGATGTCT TCCTGGAGTT AGGTGAGAGC 840 TTTGCCTGCT TTGTCTCAGT TCAGGAGAGT CTGTCCATGG GATGTGGAAA AAAAAACCTT 900 GAGCAGGAGC TGGACACTGA TGTATCATTT AGCAACTGTT GCATAACAAG GCACCAAACT 960 TTGTTGCTTT AAGAAAACAG TGACTTAGTA TTGTTTAGGA CTCTACCGGT CCGCTGAGCG 1020 GTTCTGCCCT GGGCCAGGTT TGGCTGACCC TGGCTGGGCT CCCCACTGCA GTCATCCAGA 1080 AGCTCAGCTG GACTGGCAGG TCTAGCACAG CCTCACACAC CTCTGCCAGT TGGTTAGCTG 1140 ATGTTTGGGG TGGTGCCGTG TCTCCCTCCC TCCAGCAGGC TAGCCTGGGC TTGATCCTAG 1200 GGCAGTGGAT GACACTCTAT TTCCCGTGAG AGTAGAGCAT GCAGGGCCTC CCAAAGCCTA 1260 GGTTTGTAAT GGGTACCATA AACCAAAATG TATCTGTGAC AGGTCTCAAC CAATTTAGAA 1320 AGTTTATTTT GCCAAGGTTA AGGACATGCC TGCGACACAG CCTCAGGAGG TCCTGACGAC 1380 ATGTGTCTAA GGTAGTCAGG GTACAGCTTG GTTTCATACA GTTTAGGGAG ACACGAGACA 1440 TCAATCAAAA CATGTAACAT GTACATTGGT TTGGCCCAGA AAGGTGGGAC AACTTGAAAC 1500 ATTCTTTTGA GTTTCTGATT AGCCTTTCAC TGAATGCACA ATTTACAGGA ATAGTCACGT 1560 GCCTTAGTCT GGCTTAGTGA ACCAATAGGG CAGAGGAAGC AATCAGATAT GCATTTGTCT 1620 CACATGAGCA GAGGGATGAC TTTGAGTATT GCCTGTTCTT TGTCCTCAAG GAATTTCTTT 1680 GTGGGTAAAT TGCAAGCGTG GTATGTAGCT TTTTAAAATC TTGACCGGGT GCAGTAGCTC 1740 ATGCCTGTAA TCCCAGCACT TTGGGAGGCT GAGGCAAGTG GATCACTTGG GGACAAGAGT 1800 TTGAGACCAG CCTCACCAAC ATGGTGAAAG CCCGTCTCTA CTAAAAATAC AAAAACTAGC 1860 TGGGTGTGGT GGCGGGCACC TGTAATCCCA GCTACCTCGG AGGCTGAGGC AGGAGACTTG 1920 CATGAACCCA GGAGGCGGAG GTTGCAGTGA GCTGAGATCA CGCCACTGCA CTCCAGCCTG 1980 GGTGACAGAG CGAGACTCTG TCTCAAAATA AATAAATAAA TAAAATAAAA TAAAATAAAA 2040 CATCTGTAGC TGTGTTATTT AGGAATAGAA TGGGAGGCAG GTTTGCCCTA TGCAGTTCCC 2100 AGCTTGACTT TTCCCTCTGG CTTAGTGATT TTCGGGAGAC TTATTTTCCT TTCACAGTAC 2160 AACCTCACTC CATCACATTC TAAAGACCAA AACAAGGCAT GAAGCCACCA CAGATGTCAC 2220 TGCTTGATGG GAGGAGCTGC CATGTCACAC TGGGAAAGGC ATGGACATTA GGCAAAGGCA 2280 AATTAAAACC ACAATGAGAT GCCATCTCAC ACTCACTAGC CTGGATATTA TCAAAAACAC 2340 AGAACCCAAC CAGTCTGTTG GCGAAGATGT 2370
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