Tag | Content |
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EnhancerAtlas ID | HS114-00116 |
Organism | Homo sapiens |
Tissue/cell | Kidney |
Coordinate | chr12:3206110-3208300 |
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 | chr12:3206371-3206392 | TCCCCCTCCCATGCCTGCTTC | - | 6.32 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_40860 | chr12:3205261-3208083 | Left_Ventricle | SE_42349 | chr12:3205341-3208092 | Lung | SE_54275 | chr12:3205895-3208054 | Spleen | SE_65939 | chr12:3205830-3207742 | Pancreatic_islets |
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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: 1 | ID | Chromosome | Start | End |
GH12I003096 | chr12 | 3205478 | 3208137 |
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Enhancer Sequence | GCCTTGGCCT CCCAAAGTGC TGGGATTACA GAGGATCTTT CTTAAGTCAG GAGCTCCTTG 60 TTAAAGTGTC TATGGCTCTG GGAGGGGAGT TATGCTGCCT TTCCCAAAAG AGGTGGCGAG 120 GACGTTGAGG GAAGAGGAGG CCATTGCTCA GAATTTCATG CTGAGGATAC TGAGGCTGGC 180 TTTCCTTGGG TGTCTGGGCA GTTGAGCAGA GGAGGCTGGA GCCAGGCTTT CTGGATTGTG 240 ACCCAGATTC TGTCGTTTCT CTCCCCCTCC CATGCCTGCT TCCGTCTTCG TCAGCTCGAC 300 CCAGGGTCAC CTCAGAGCTC CCAGCAGAGT CTGTGGGCAG CTTTGGAGGA AAACATGCGC 360 CCAAAATGGC CAAATCCATG AGGACTTGAG AGAGGCACGT GTGTGGCTAT TTTGGGTTTG 420 GTGGGCTGAG CTCAGATCTC TCTGGCATTC CCAGCCACTG GCTTCTGAGA ATTGAGCAGA 480 ATGGAAGGAT GTTAAAAAGC GAGGCTCCAG GAGCAGCCCA AGAATTTGCT CATTCTTTAC 540 CTCTGGGAGG AGGTGCTCAC CCCGGAACCC ACAAGGAGGA ATGGGGCTGA GGGAAGGGAC 600 TATGGCAGGG AGGGGGCAGG GGAAGAGAGG GAAAGTTCAA GACGATTTCC TCTTCCTCTT 660 CTGTGACTTC CTGGAGGAGG GGTGGCAAGT ACAGTGCTGG CCCAGGGCCA ATCTGATAAG 720 GTAGCAGGAC TTAGAGCCCA GAGGAATGGC TCCCCCCGCA ATCCATGCCT CTGGGGGAGT 780 TGCCTGGTAA CAGCCATTGG CTGGGGTGGT GCATCAGCCT CTCTGCCTCT CTGAATGTCT 840 CTTTCAATTT CTCTATCCTT CTCCCACATC AGGCTAGGGA CAGCTCTGAT CTCAAATGAC 900 TGGGGAGTCT TCATCTCTTT CTCCCTTCCC CAGAGTCAGG CAGAGAAGCC CCTTTCACTC 960 AGTGCACATG AGGGAGACAT GTGAGCACCT CCTCCGTGGA AGTTCAGGAG CTCAGTGATG 1020 CCGGGGTCTG TCTTTGCCCC TGAGGAGCTA GTGTGGACGT GTGGAGACAC GCATGTGTAG 1080 ATGTGCACCG ATGCAGGACG TCGGCCAGAG TGCAGAGTGC AGAGTGCAGC CGGATGTGAC 1140 AGGCAGAGCG GGTCAGTGGG AAGAGCTGCC CAGTAGGAGT CAGGGCCCCC AGCTGGCCTG 1200 GGGCAAGTCA TGTCATTTCT TGGTGCCTCA GATTTTTCCA TCTGTCAAGT GAGGGGTTTA 1260 TGATGCCTGA AGTCCTTTCT GGCTTAAGAG TTACCTGATT CCAGGAGTTG CAGGGAGAAG 1320 AGCCTTAAAG ATGGGTAGAA TGTTTTCATT GCCTCTGTCT TTGTTCCAAA TTGGGTCTAC 1380 CCTTGGACCC ATCTCAGCTG GGTTGTTCCC ATGAAGAGGG GGCAGGCTGA GGGCTCAGGT 1440 GTTACACTCG GATCCCAGAC CTCGCTTCTG TTCTCTGGAC CCTCCTGTTA GGAAAACTGC 1500 CAAATTTGCC TTTAGGTTCA GAAAATCAGT TGCACCTGTC TAGAACAAGG TGGTTCATCC 1560 TTGGCCTGCA AGGGAGGGCT GAGTGACTGC CTGAGACCCA CAGAGCCTGC TGGGGACTGA 1620 CATCTGCTCC CATCCAGCCT CGTTCTTTGC TTAGAGTCAC TTTGTCCGTA TTGTTTCTGT 1680 AATGCCAAAT TACTTGTAGC TCTTTCTTCC TTTCCCAGTC ATGAGGTTTC ATTTTTCATT 1740 GTTCTCAGTG TGATCTACCT TGCTTGAAAT GCTTCCCGGA TATGGCATTG TTTTTTTTTT 1800 TCTCTCTCTC TCTTTTTTTT TTTTGGGATG GAGTCTCACT CTGTTGCCCA GCCTGGAGTG 1860 CAGTGGAGTG ATCCCGCCTC TCTGCAACCG CAGCCTCCTG GGTTCAAGTG ATTCTTGCTC 1920 CTCAACCTCC TGAGTAGCCA TGTGACTATG GGTGTGCATC ACCACGCCCG GCTAATTTTT 1980 GTGTTTTTAG TAAAGATGGG GTTTCACCAT GTTGGCCAGG CTGGTCTCGA ACTCCTGACC 2040 TCAGGTGATC CACCTGCCTT GGCTCTCCAA AGTGCTGGGT TTACAGGTGT GAGCCATGGT 2100 GCCTGGCCTA TTTTATCTCT TAACTGCATT GTTTTAGCAA ATTTGAAAAT TTGCTCAGCT 2160 GTTGTTTAAG TATTTTTCCA TCTCCACTTC 2190
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