Tag | Content |
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EnhancerAtlas ID | HS012-15324 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr19:2241880-2243380 |
Target genes | Number: 28 | Name | Ensembl ID |
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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) |
Hnf4a | MA0114.3 | chr19:2242290-2242306 | GGGGTCAGAGTCCAAA | + | 6.81 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr19 | 2242184 | 2242549 | chr19 | 2242790 | 2242840 | chr19 | 2242908 | 2243073 | chr19 | 2242200 | 2242600 |
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Enhancer Sequence | ACATCTGAAC TTCTGATGGG GCAGCCGTGA TACTGCAGTG AGCTGGGAGG TCCACCTCAC 60 CAGTTACCAT GCTTGATCAT TTTCATAAAC TTGCCCAGGG AATAAAAACT GGTTGGGGAG 120 GGCTCCTGGG CCCCCATAGA GTAAGGGGTG ACTTCAGGCC CCACCACAAG TCAGCAGTAC 180 AGCTGGCCTG TCCCTCAGCA TGCCCCTGCA CACCTGCGGC CACTGTGGCC TGTCCCTCAG 240 CGTGCCCCTG CACACCTGCC GCCACTGTGG CCTGTCCCTC AGCGTGCCCC TGCACACCTG 300 CGGCCACTGT GCCCTGTCCC TCAGCGTGCC CCTGCACACC TGCAGACACT GTGACACATC 360 ACTGCAGACG CAGTAGTTCA GATGACACGG CTGTATCAGC TTCTGGTTCT GGGGTCAGAG 420 TCCAAACAGT CCACAGGGCT CCATTCCTTC TGGAGGCTCT GGGGGACAAC TCGTTTCCTG 480 CCTTTCCCAG TGTCCAGAGG CACCTGTGTG CCTTGCCTCG GGGCCCCTTC CTCCCCATTC 540 ACAGCCACAG CGCAGCCTCT CTGACTCTCA GCCTCCCGCC TCCTCTCATG AGGTCACCCA 600 GGATCACCTG CCATTTTAAG ATCCTCAAGC CCACCTGCAC ATCCCTTTTC TGCCATGAGG 660 GGACATGTTC ACAGGTCCCA GGGATTAGGA TGTGGACATC TTTTGGGGGC AGTGATTCAC 720 TCAGTCTCAT GGGCCCCATC TCTCTGAGCT CACCCAAGAC CCTTAAACCA GGGCCCGGGG 780 CCAACATTGA GCAGGCAAGG GAAAGACTAC CAGGAGATGA GAGGAGGCTG CCTGGAACTC 840 AGATTTGCAC AGAGCCTGAA AGGGCGTGGG AGACCTTGGC AGAGGCCTGC ATCAGGAAGA 900 GGATGTTGGG GACTCAGCAG AGCCCCCTGC GCCACAAGCA GATGTGGCAG ATCTCCCAGG 960 TGTTACTCAG TGAGGATGCG AAGATCAGTG TCCTCACTGA TCTCCGCCTA ACAAATTTAC 1020 ATCGAGCCCA AGAGATTAGG TTGGGACAAG TAAGCGTAGC CAACCAGAGA GGGAATTCAG 1080 AGGAAGGCGT GAACACTAGG GGCTTGGGCA GTCCGGGATG GCTTCCTGGA GGTGGTGACT 1140 CGTTTGTGAG ATCTTGGTCT TGTCTTCCCT TTATGCCTTC TCTGGGCTCC CTATTACAAT 1200 TTCAGGTCTC CAGGCCTTGG CACCCTGGGC TGGAGCGGCT TCCTCTCCAT CCCTCATGCC 1260 TGGTCACTTG GAGACAGGCT CCAGCTTCCT TGTGTCTGTG CCTGTCCACA GTGGGCCTCA 1320 GCCTCCTGGA AGAGACTGGG TGCGCTATGG GGTGGCCCCC TCAGGGCTGG TTAGACCCTG 1380 GCGCTGGGAG TGCAGGGTGA GGGGCAGTCT CGAGGGCTCC AGCCCAGCCC GCCCAGGGAG 1440 GTCCCAGCAG CAGCCCCGAG TTCTGAGCCA TCTTCCTCAC TCTCCTCTTG GCCTCCACAG 1500
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