Tag | Content |
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EnhancerAtlas ID | HS145-11692 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr19:34310210-34312360 |
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) |
Klf12 | MA0742.1 | chr19:34310995-34311010 | GGCCACGCCCTCCTG | + | 6.46 | POU2F2 | MA0507.1 | chr19:34310384-34310397 | TTGATTTGCATGT | + | 6.12 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_26999 | chr19:34310151-34312404 | Esophagus | SE_32421 | chr19:34310338-34312371 | Gastric | SE_54276 | chr19:34310171-34312632 | Spleen |
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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 |
GH19I033819 | chr19 | 34310149 | 34312946 |
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Enhancer Sequence | CCTCCCACCT TGGCCTCCCA AAATGCTGGG ATTACAGGTG TGAGCCATTG CGCCCAGCCA 60 GGAATTGTTT ACTTTCAATT GTGTACTTGA AGCTCTGTAA ATTTAACAGG AAGAGAGACC 120 ACATTGCAGT TTTCCACTTC GTCATGACAC TGAACATGGA TTACCCCAAA TGCATTGATT 180 TGCATGTAGA GAGAACCACC TCTCAGGCCT CAAGACTAGC GTCTCCATAG CAAAGGAAGC 240 TTCTGTGAAA TTCTAATGAG AGACCCAGAG AAAGAGGCAG GCACACTCCC GGGGACACAC 300 AAAGGAGAGG GGTTAGGGGT CAGCTGCATT TGGGGTTTTG TCTTTATTTC CATTACACAG 360 AACAGCCAGT CCCGACAGCG CCCAGGCCCC ACAGGACAAT GCTGTTCCTG GACCCGGAGC 420 CATGGCCGTG GAATAAGAGC TAGGTCTTCA GGGCCTCCTC CTAGGATCCT TCTTAACACA 480 GAAATCACAA ACCAGGCCAA AGTCTTAAAA AGCAGAGCCT GGGAGGGGCA GGGACGCCCA 540 AGCCACGCTG GGGCCCGGGA GGCCTCCCGT CCTGCCCGCG GGAGAACCCA GGCCGCGCAT 600 CCCTGGCTGG ACGGCGTCAC CAGCCGTAGC TGGGCCAGGC CTGCTGCTCA AAGCCCGTGT 660 CTAGGATGTC ACCAGAGCTC CCTTTTCTGT GTCCTGGACC CGGTTCAGGG CCCCCGAGGA 720 AGCTGCGGTT TGGGGCGAGC CGATTGCACC AGCAGGGCCG GGCTGCTGCT CCCGGGGCTG 780 ACGCGGGCCA CGCCCTCCTG GACGCGGACA CACCCCCATT TCCCCGGGCC CACAGAGCCA 840 CGCCTGGCCC TGCAGCCAAA CAGCGGGAAG GCAGATTGGT ACGAGTAGGT ACAAGGCCCT 900 GGAATTCTCG CCCGGTTGCC ACACACTGCA CGGAGCATAA TTGGGGGAGG TTGTGCAACT 960 GCCCGGGAAG CCGGGGCTCG CAACGAGGGC TCTCTCCAAG TCCCCATCAC AGGCCTCCGG 1020 GGAGCCTCGG GACAGAGCCT GACGCCACCT TCGGGTGACA TCGATGGCCT CGCTCTGGCA 1080 GAGGAGTAGT GTGGCTCTGC CGAGAACTGG GGAGCCCGGG TCCCCGCAGG GCCAAGGGGA 1140 GGGAGGGCTG GCGGAAGGGG CCGCGCCCAC AGCCCCAGGT GGCAGCAGCG GCGGTGGCGG 1200 TCCCGACTGG CAGAGCCTAA CGAGAACAGG GCCTATCCCC AGGGGCCCCG GGCTGGACGC 1260 AGACCAGATC TCGCGGGGGT GGGCTGGGAG GCGCCCGCCA GAGGCCGGAG GCTGACAGTG 1320 CCTTTCCTAT CCTATGGGTC TATTGTGGGC CCGCGGAGCC CCCATGGGTG GGTCCATCCC 1380 CGGGCCCAGT GAGTCACTTC CCCAGGCCCC GGAGGCCTTC GTGGAAGGTG CCTCCCTTTC 1440 CGGCAAAGCA TCCTTTGTTC TCCTGCTGGC TTTGCTTCCC AATCCTCTCT GAGTTGCAAC 1500 CTTGAGGGTT TTAGGGGCAC CAAGCTCCCA GGAGCACAGA GGTGGGCTTG GGTGCCACCT 1560 GGAGAGCGGG CTGCAGAAGG CTGCAGCTGC TTTTTTGCTT CCTCAGTTCC CTGCCCTCTC 1620 AAGGCCCAGG CTCTCCCACC TCCCCAGACG TCTGGGGAAA CCCACACTGC CCTGCATAGG 1680 TTGTGGTGTG CAGCCTCCGG ACTGCAGATC CTGAACGCGC ATCAGGAGGG AGGGAGGGAG 1740 GTTTCGATGC TCTCGCCCTG GCCAGCACCG CTCTGAGTTG CTGAACTGGC CTCAAGGCTT 1800 CTCTTGCATC AGGGAGAGGC TTCCGGCACC ACCACTGGCA CTCCTCCTTC TCCCTCCCTT 1860 TAGCCTCCCC CAGTTCCCAT GCCCAGGTGG AGGAACCCGT GTAGAAGCCC AGCCCAGGGA 1920 GGGAATTCAT CAAAGCACCT TCCCACACAG CCTCTAGTTT GCCTCCTCTC CACTCCCACC 1980 TTCCAGCCCC AGCCTGGCTA GCCACGTGGG GGGCTCCTGT GCCAAGGAGT GCCCAGCTGC 2040 CGGGTGAGTG AGCAGCCCTG CACAGAAGGC AGCTGACTAC CATACACACT ACATGTGTGG 2100 AGAGCACCAG CCTTGCAGCC TGGCGAGGCT CTTGCTTTGA AGAAATAGAA 2150
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