Tag | Content |
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EnhancerAtlas ID | HS118-17320 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr7:73036400-73038520 |
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) |
ZNF263 | MA0528.1 | chr7:73037320-73037341 | TGGGGAGGGAGGGAGAAGGGA | + | 6.03 | ZNF263 | MA0528.1 | chr7:73038280-73038301 | GGAAGAGGGAATGGGGGAGGA | + | 6.32 | Zfx | MA0146.2 | chr7:73037767-73037781 | CGGGGCGCGGCCTG | + | 6.43 |
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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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Enhancer Sequence | GGTGGAGTGC AGTGGCACCA TCATGTCTTA CTGGAGCCTC AACCTCCTGG GCTGAAGTGA 60 TCCTCCCACC TCAGACTCCC CAGTAGCTGG TACTAGGAAT GTGCCATCAC ACCTGGCTGA 120 TTAAAGAAAA TTTTTTTTGG CCAGGCATGT TGGCTCATGC CTGTAATCCC AGCACTTGGG 180 GAGGCCAAGG CAGGTGGATC ACCTGAGGTC AGGAGTTTGA GACCAGCCTG GCCAACATGG 240 TGAAATCTCG TCTCTACTAA AAATACAAAA AATTAGCTGG AGGTGGTGGG CGCCTGTAAT 300 CCCAGCTACT CAGGAGGCTG AGGCAGGAGA TTCTCTTGAA CCCGGAAGGC AGAGGTTGCA 360 GTGAGCTGAG ATGGCACCAC TGCACTCCAG CCTGGGCAAC AAGAGCAAAA CTCTGTCTCA 420 AAAAAAAAAA AAAATTTTTT TTTTTTTGGT AGAGACAGGT TCTCAGTATG TTGCCCAGGC 480 TGGTCTCCAA CTCCTGGGCT CAAGCAATCC TTGGATGAGA ACCTTGGCCT CCTAAAGTGC 540 TGGGCTTACA GGCAGGAGCC ACTGTGCCCA GCCAGAGATT TACTATTAAT ATTTGGGTAT 600 TTGGGAAGAA AACACAGTCC TCTCTACCCC AGCTATCTCT GACTGGGGTT ACATCAGCCT 660 TGAGTCAGCC TCTGGGTGGG GGGGCAATTT TGGGGGTGCG CTCTGTCCCT TACCTTGCCA 720 GCTCCCCAGA ACCTCTCCTC TTTGGTCACC CATCGTCAGG GTTGGAAGTG AGGCCCCCTC 780 CCAAATAGAG TGATGTGTAG TATATAATGA GCAGCCAAAG TTGGGGTTGG GTGGGAAATG 840 GGAGACCCTT AGGAGGAGGA GTGCCGGCAT CCGGTGTACC AGGACCTTAG ATGCCCTGTC 900 CCAGGCAGTC GCGTGACATT TGGGGAGGGA GGGAGAAGGG ACGGGAATTT GAACTTTCCA 960 CACGGGTCCG ACGCCCTGGC CGATCGGGTT GCAACATGAC CTGGGCCAGG GGCCAGAGCT 1020 TGTGGGCCAA GGTTACTCCG CCTCCAGCCA ATGGGGTCGC AGCTGGGCGG CTGCGGTTGG 1080 GGGCAGGCAA CACTCCCCTC ACAGTCCCCA CCCCAGCTCC TGCTCCCCCG CAGGGCGGCA 1140 GGTGCCGATC TGTAGCCAGC GGTTCTCAGA AGGGGAGGAG GCGCCGCGGA GGAAGAGGAA 1200 TATTTGCACA GAGAAAAGAT CAAGGCCGGC CGATCCCCCT TTCTCCCCTA CGGGTTTTCG 1260 GTTGATAATT TATACTGGCC CCTCAACTCC GGGGAACTTT GCTCCAGGGC ACTGGGCCAG 1320 GCCTCGGGTT CGCGCCCTCC TCTGGGACGC GGGGCGTGGA GCGGCAGCGG GGCGCGGCCT 1380 GTGCGCTCTC GGTGGCACTA AGCGGGGGTC CCAGGCAGCG ACGGGCGCTC AGCCTAGTGT 1440 GGCGACGTGG GTAGGCGAAC CCAGGCCTCC CGGGCACCGG CGTAACCTCT GCGAGCTGCG 1500 CCTCTTGGAC ATTTCTGGGA CATCCTCCTC CCGCCACCCT TAATGTAGCA GATCAAGAAG 1560 AGGTGTCTCA GCAATTGCGG GGAGGTGGAC GTGAGAGTGG GCCAGTTCCA GTCCACTTTG 1620 GTTATGAACT GGGACAATCA GGGGCGCTGG GAGTATCTCA GGGTCCAGGA ATAGGGCGGG 1680 CTTGGGCCGG GGCTGCTGGG GAGAAGGCCG AGGCCTGCAG GGGGTCGGGT GGAGTGGCTC 1740 CAGAGTGGAG AGTGGGGATG GGCGCGGGTG GCCTAGGGAC CAGGGGCGCC TGGCATTTTT 1800 GTAGGGACGG AGGGGCTGGG ACCAGAGAGA GGGGACCAGA GGTCCAGGTA GAGGTGGGGC 1860 GCAGGCGGTC TGCGCTTCGG GGAAGAGGGA ATGGGGGAGG AATGGGAATC AGAAATGCGT 1920 GGGTCCGTCA GGGGCCAGCG GGCTGGGCCG CTGTAGGAGG ACCTCGGGGC TGGGAGAAAG 1980 GGGGTGTCCA GGGCGTGATC GGAGCCTCCG GGAGCCGCAG GACCGGGCTC GGGTGGGGTG 2040 TTGAGGGCCC CAGCGCGCAG TCCTGCCCCG GACCCCCCCC CCATCCCCAC CTGGAAGCCA 2100 AGGCCGTCAG GGCCCGGAAC 2120
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