Tag | Content |
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EnhancerAtlas ID | HS175-13260 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr19:33764170-33766010 |
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 | chr19:33765463-33765484 | TTTTCCTGCTCCACCTCCCTC | - | 6.06 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_09601 | chr19:33763698-33766425 | CD14 | SE_23205 | chr19:33764413-33767578 | Colon_Crypt_1 | SE_23808 | chr19:33764326-33767580 | Colon_Crypt_2 | SE_24807 | chr19:33763936-33767669 | Colon_Crypt_3 | SE_27406 | chr19:33764404-33766196 | Esophagus | SE_27669 | chr19:33764408-33767743 | Fetal_Intestine | SE_28569 | chr19:33764450-33767650 | Fetal_Intestine_Large | SE_31890 | chr19:33764433-33767612 | Gastric | SE_35421 | chr19:33764588-33771627 | HepG2 | SE_43051 | chr19:33764035-33767549 | Lung | SE_50571 | chr19:33764237-33766629 | Sigmoid_Colon |
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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 |
GH19I033273 | chr19 | 33764308 | 33767610 |
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Enhancer Sequence | GTGCAGAGTA CGGAGGTCTG TGGCAGGTGG GTGGCCAGGA GGGCCTCACA GAATTCATGG 60 GGTGGCTGCA AGCAGAAGAG GCTGGAAAGG CTTTGGGGGC TGGGCCAGGA ACACGATCTG 120 ATTGACTTTT GCAAGGATCC CTGGCTGCTG TTGAGAGGTG GAGGGCAGGA CCTGCAGGGC 180 GGGAGGCCGG TGCTCCTGGG AGGCTGCCGT GTGGATAAGA GTCGGGGGCC AAGTCTCCCG 240 CTGGAGCAGC ATGGAAGGCT GGGCCGGACG TGGGCGGTGG GCAGGCCCCA GGACTGCTGC 300 TCTTGGCCTG GCTCTGGCGT TGGCTTAGCG TGCAGCCGCG GGGGAGCCGT GTGTGGGCAC 360 GTCCCTGTGC TGCCGCCCCC GCTGCCCCAG AGACACAGCC ATAGGCAGGC TGGCTCCCCT 420 GGGCCTGGCT CACACGTGGT GGAGGTGATC AGGGATGACG AGGCGGGTCG CAGGGTGGCA 480 GGGACCTACA GGGCCCCAAG GCCAGCCCGG GGGACAGAGG ACTCCCTTGC CAGGTCCTTG 540 TTCATTCATC CCCCCCCTTT GTATGGTGAG ACCACTGGGA GCCAGACACA GCCCTGCCCC 600 AGGGGCCATG GGGAAACGAG TGTCTGTCTC TGGTCCGGGG CCAACCTCAA GGTGGGTGTC 660 CTCTCCTGCA GCAGGGCCAC GGGCACCTTC CGGCTCCAGC CCCAGCCCAG CCAGGCTCTG 720 AGGGAGCCTG AGGCTGCCTC TCCTCCTCCA GGTTCCTGTT TCCCGGGTGG CCCCAAAGAC 780 AGAAGATGGT GTGAGGTTCA AGGGCTCAGT CCCAGGCTCG GATTTCCTGG GCGTGTCAGA 840 TTTCCTGGGC GCTGTGTGGC TGGTGTCTGC CAGGGAGGCC ACTGAATAAC GTGAAGACCA 900 CTGGGAAAGC ATAGCAGAGT GTGCAGTGGC TGAGTCTGTG TGTGTGTGTG TGTGTGTGTG 960 CGTGCGTGTG TCTGTGTGGG TGTGGGGTGT GACTCACACA GGCCTGGGCT TCATGATGTC 1020 TCTTGGGAGC AGGAAGGTCT GTGTGAGTCT GTGTCTGTCT GTGTGTGCAT GTGTGTGTGT 1080 ACCCGTGTGA CTACAAGCAT GTGTATGAGT GCACACAGTT GGTGCAGGTG TACCTATGTG 1140 TCTGTGCACA TGTGTGTGCA TGTCTGTGAG CGTGTGTGCA TGTGGTTATG AGTGTGTCTG 1200 TGGGTACGCA TGTGACTGTA GTGTGTGTGA CTGTGTGTGT GCACGTGTGT GTGTGTGGAC 1260 ACAGCCCTCT CTGGCCTGCA CTCCTGGAGC CTGTTTTCCT GCTCCACCTC CCTCCTCGGC 1320 AAGTGTTGAC TCAGGGAGGG ATAGGCAGCC TTGGTTCAGG ATTTCCTGGT CAGGCAGAAG 1380 TGGTGCCTTG AAAAGGGAAC AATCTCGTGC TAAAGTGGAC GCTGAGGGTC CACACAGTGC 1440 AGTGCTCTAG GGTGCCCAAG GCCGAGAGAC CTTGTGCCTT CCTTGCCTGG GTTTACAGTG 1500 GGGGTCCCAG AAAGCTTTGC CCCTAGGGTG GCCCATAGGA TGTGCCCTCA GGCTTTTTCT 1560 AAATGCTTCC TGATCTGGGC TGCCCGGGGT GGGGGCTCTG GAGCTGGACA CTCCTCTGAC 1620 TGCTGTGGAG GCAGGGACAG CACCCCCACA AGAGGTACCC CAAGAGAAAT GGGGGCCCCC 1680 AATGTCCCCA GGCACTAGCT GTCCCAGGTT CCCTTCCACA GTGGGCAGCT TTACCCCTGC 1740 ACCGCCCCAT CCCCCAAAGC CTTAACAAAT AAAAATGAAG CTCTTTGAGG CTAAGAGTCT 1800 ATTCAAGCTC CAAGAGCTCT CTGCCATGTT GGGAGGAGCC 1840
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