Tag | Content |
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EnhancerAtlas ID | HS012-15479 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr19:18421020-18422300 |
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) |
HNF4G | MA0484.1 | chr19:18421495-18421510 | TGGCCTTTGCCCCCG | - | 6.29 | KLF5 | MA0599.1 | chr19:18421444-18421454 | GCCCCGCCCC | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_24690 | chr19:18418803-18423834 | Colon_Crypt_3 | SE_52990 | chr19:18413901-18423828 | Small_Intestine |
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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 |
GH19I018309 | chr19 | 18420357 | 18423714 |
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Enhancer Sequence | TCACCTGCAG CCCAAAGCCC AGAGCGGGTG GGGGCCTCCC TGTGCACCAG ACACAGCCGA 60 AGCCCAGCTA CTCCTCCTCC TGCCCCAGCC CCACCTCACT TCTGGAAGCC TCTCTACATG 120 CCCTGACTCA TTCATTCATC TAAGTATCTC CTGACAGGGC CTGCGCTGGG TGCAGGGACA 180 TGCGAGCAAG CTACAGGCCT AGTGTGGTGG GTGAAGAGGG GCGGGAAATG GGGGGACTTG 240 GGTCCTGCCA GGGTGGCTCA AGGGCGGCTC CCAGCGATGC CAGTTTTAGG AGAGCTAACC 300 AAGACTGGAG AAATGGGGGC CTTGCAAAGA CACAGACTCA TGCTGCAATG CCTCCGAGGC 360 CCCCACTGGG ACAGATCGAG GGATTAGCAG GGGCCAGGGC CATTCCTACC ATATCAGTTT 420 CCCAGCCCCG CCCCACCGCC CAGGTTCCTG GACAGACCCA CGCACGACGC CTGGATGGCC 480 TTTGCCCCCG ATGCCCTTTA AAGTCAGATC ACAGTATGTT CCAGCTTGGA ACCCACCCAG 540 GGCCCCCTCC AGCCTGGGGG CAAGGTCTAA GAACCTCAGC AGGGCTCTCT AGGGCCCGAG 600 ATCCTGCCCC GCCCTGGCGG TCCTCTCCCA GCCCGACGAC ACTCCCTCCA GATGGAACTT 660 TCTGTTTCCG GAACACACGC CATGGGCTTG CCCCCAGAAC TTTGCACGTG GTTTTCCCAC 720 TTCTCATCTG GCTAACTTTG ACCCCAAAAG GCCTTACCTG CCCGAATCCC CAAGTCCTCC 780 TGTCAGACAC TCTCCTCCAC ACCTGGGTAG GTGTGGCCTG GCCTAGCGCT GGGCGGGGAG 840 GAACAGCCCC TTTGGGTGCT CACTCTCCCA GGAACCCCTC GAGGGCTCGT GGGGCGGACA 900 CACCATGGTT CTGTGGGGAC TCAGGGCCTG GGCAGGTGAC TTGGCGCCCA GCTCTCCCAG 960 GCAGGGCCCA GAGGCTTCCT CGTGCAGGAA CCTGGGCAGG GCCTGAGCTC ACTGCAGGGA 1020 GGCCCCTGCC TCCTGCCCAC AGCGCTCCAG AGGTCTCTCA GCCCGGGGTC TCTGCATCCT 1080 GCGGCCTGCC TCTGAGGGAG GGAGGGCCCC ACTTAGATGG GGACGATGTG AGTTCCCATC 1140 GCCTCTCCTC CCAGCCACAT GTGACGGCAG CATCACCGCC TGGCCACAGA GGCAGGCTGC 1200 TCAGGGAAAG CCATCCGTCC ACTCGAAGCT GGAGGCAGAG GCCAAACCAA CCCCTGGAGA 1260 CCACGCAGCC TCTGAATCAA 1280
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