Tag | Content |
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EnhancerAtlas ID | HS118-04586 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr12:69447390-69450140 |
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 | chr12:69448987-69449008 | TTCTCATCCCTGTCCTGCTTC | - | 6 |
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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: 2 | ID | Chromosome | Start | End |
GH12I069052 | chr12 | 69445805 | 69447919 | GH12I069055 | chr12 | 69449484 | 69449868 |
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Enhancer Sequence | TAGACATTGA ACTGTATTTT AATCAGTATT ATTCCTCTTT CTTGCTGTGG AGATATCCAG 60 TTACCTTGCA CTGACAGATC TTTGTCTTAG GAAGATCCAT CTGCTTAGCC CCTTTTAGCA 120 AAGGGCCCAG ATGTTGCTGC AAATAAATTG CAAACTGGCA CAAAAGCCAA GGAGATTCAA 180 AGGAGAAGGT TAGGAATGCC AAGCCCCTTC CTTCTTTGAG ATGTTAATAA AACATCTATA 240 CTGGATTAAA CTGGCCACAG TACAAGGCCA CGAGGCAGAC AGCACTATGA CCCCATGGAG 300 AAGCTCACCT CTGGAGAGAA CAATGTGGCA CAAGATTTCA GTTTCTTCCC ATGGCCTGGG 360 TAGTCATGGC AGATGGTTCG ACACGGGCTG ATGTGGGAGA CCCTCCTCTC TGACCCTCCT 420 AGACACTCCA CCACTGTGCG TGGCCTTGAG GAAATGACCA AGAGTGAGTT TAAACCATAT 480 AGTTCTCTTT CTCAAAAACT TTTAGTTTTT GACTTAACAT CTTAAATATA AACATCCCAA 540 CTGGATATTC AAGGCCCCAA AATCTGACCC TGAAGTTCTT TTCCCAGGTT GTTTTTCCAA 600 ATGACCCCTA CAAGGTTGCT CTGGTCGGTC GACTTGAATA GCCTGATATG CTCCTTTCTC 660 ACCTCCTTGC CTTTGCTCGG TTGGGAACAT TCTCCCTCTT TCTACGTATC AACACCCCGC 720 TCACCCTCTG AGACCCAGCT CATATGTAAC TTCCTCCAAA ACTCCTCTCC TAAATCCCTC 780 CCACCAAGAT TTCCTTCTCT GGTTTACTTT TCTCTTGCAC GTTTCCACTG CTCTTCATGC 840 ACTTATGTAC TGGAGCCTCA TCTGTTTTTA GCCTGTACAC TGAAAGACAC CATTGTAGGT 900 ACTGTGAGTT GCAGCCCAGA AACACAGGAG ATCTGTAAAC GGTTACTGAA TTGCAACAAA 960 TTGTGTTGTC AAAGGTCACA CAGCTGGTTA GCGATAGCAA CAGAGGTAGC AATCACCTTT 1020 CCTGACACCT AATCTGATAG TGTCAGTAAA ATAAACTGGA ATCCTCTTTT CTTCTAAAAC 1080 TTACATGTAT CGCTTAAAAA GTATGACATG TATGGTATAT ATCATAAAAA ATCTTTTAAT 1140 ATGTCTTTAT CACTTCTTTC TGGCTATAAG TAACCCTCCC AGTTGTCAAT GAGAAGCGTG 1200 TTTACCAGGC AGAGAGAGCA TGCAGCATGC TGGTGGGTGC AGCAACGCTG TGTTCTGCCC 1260 AGATCTCCTT GGATCCCCTG TAGGAGTCTG TGCTCCTGTT GGACTTCTGT GTGCCTGTAC 1320 TTCTAAATGG CCTGCAACGG CAACTCACCT TGAGCCCTGC CCTAGGGTAC CAGAGCCATT 1380 TTTCCCACAC ACAGAAAACT GTCTGCATAC CTAGGAATGT ATGTTTCCTT GGGGTGGCCC 1440 TTAGTCAATG AGTGATTGGT GTGGATGTAT GAAAGACCAA CTGCCTGGCC TCCAGTTGGG 1500 ACAAGCTCTA AGGCATAATT CATTCTCCTG AGCTGCTCTC CTGCAGGAGC AGGCGGGAGC 1560 TGGGACTTTG CCTGATATCG TGCCTTCGCT CAGATCCTTC TCATCCCTGT CCTGCTTCTC 1620 AAACTCCCCC CTGCCCCACC CCGGCCTCCT CACAGGCCAC TTTCTCTATA CATCCCTTGC 1680 CCATGAATCC ACATCTCAAG GTCTGCTTTG GAAGAACTTA AACTAAGGCT GTGTTGTATG 1740 GAAGACAATG GAAGATGGAG CAAGACTTAA TCATTGCTCA CAAAGACCAA AATCAAATGG 1800 AAAGTCCCCT CTATGGACAG TTGACGTTCC TAAGTGGCTC TTTTTGGCTC ACAATCAGAA 1860 GCATCCAGAG TTCAAAATGC ACAGTCCAGA TGATGACACA CATGAGGACT GAGGCTTTGT 1920 AAGTCTCACA TTAACACAAT ATTACATTTG GCCACATCCC CTGGCCTTTT GACTGTTTAC 1980 ATCCTCAGAA TTGAGGGGTG TTTGAGAAGG CCTGCCACCA GGAAGAGTGC CGGTCACTGG 2040 ATTATTGAGT GACATTGGAC TCTGCCTACT TTCCCAAAGT GAAAAAGTCT GTTACTGCAG 2100 CAAAGGCAGT GCTGAGGAGC GAAATGTATG TGGATGACAT TGAATATAAT TGACCATCAT 2160 TTCCTATTTG CCGTCTTCCT ATGTCCACAG GCTGGAATAC CAATATTGCC CAATCAAAGG 2220 GCAACTTCTC TGAAAGAAAT AGAGAAAAGA GTAGGATGCA GCTCTATTCC TGGGTGCTCC 2280 CTCTCACGTG GTCCTGAGGC ACTTAGCACT TTCATAATCA CTGTTGTAAG AACCTGCTTC 2340 CTTTTCTTAG ACTGTGAGAT CTCTGAGGAC AAAAACCCAT CTTGCACGTG ACTGTGTTTC 2400 CAGAGCCTGG CACAATGCCT GGCACTAAGT AGGTGCTCAA TAAATATGTT CTGACTCTAC 2460 ATGGGAGCCC TTTGAACATG AGGCTGGGTC CCTGGAGTCT GATCACATTA GGTTTACCTT 2520 CTTAGAACGG ATATAGATTA AAGGATTCTG GAGTTGAGGC TGTCCCTGCT ATGGGCCACA 2580 GTCGTCACAT ACCAGAGAAA TGGCTGCTCC AGTTGCCTCT TGAACCATTT CCAATGTTTC 2640 TGCCTGCTAA GTTTTAGTAA GAAGTGCTCC TCCTGGAGAC CCTGAAGGAG GCACAGTTTC 2700 CTCAGACCTA GGAAATCTTG GAGGAAGGCT CATTAGAGTT CCCTAGCTTA 2750
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