Tag | Content |
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EnhancerAtlas ID | HS110-03656 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr3:197247230-197248510 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr3:197247725-197247740 | TGTTAATTATTAAAC | - | 6.15 | HNF1B | MA0153.2 | chr3:197247726-197247739 | GTTAATTATTAAA | + | 6.14 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_23371 | chr3:197246499-197251007 | Colon_Crypt_1 | SE_23997 | chr3:197246552-197250392 | Colon_Crypt_2 | SE_26695 | chr3:197247245-197251171 | Esophagus | SE_28312 | chr3:197245750-197250196 | Fetal_Intestine | SE_29351 | chr3:197245736-197250317 | Fetal_Intestine_Large | SE_46517 | chr3:197246905-197247617 | Osteoblasts | SE_52905 | chr3:197245723-197250278 | Small_Intestine | SE_56113 | chr3:197247002-197248452 | u87 | SE_57970 | chr3:197246718-197249417 | VACO_9m | SE_65692 | chr3:197245559-197250293 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I197515 | chr3 | 197242748 | 197250290 |
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Enhancer Sequence | GCGTGGGAAA AGCAGCAGGG AAAGGTCTGC GCGTCAGGCT GGTGCTGGGG TTGGAGCCCA 60 GATCCCCGGG CAGGGGGTGA GTGCCTCCCC TCTGTGTGGG CCGGGGCCCA CCCTGCCTTG 120 TAGGTTAGGC TGCCTGGCCA GTCCAGTACA GACAATGGAA GTGATTCTGC CCCAGAGTCA 180 GGGGGGCAGG GGACGAGGAC CGCCAGCCTG AGCAAGCCGG CCTGGTGCGT TCTCTGCTTG 240 GGTCTCCGGT GATGACGCCT TTCCACGGGC ATTTTAGATC ACCACAAAAC CCACGCTATA 300 ATCAAGTGGC TTTATGGTGC CGATGCAGCT GTTTTCCTGC CCAGTAGTTT ATGAAGGAAA 360 ATATAGCAGC TGCCCAGGGA AGGTGGGAGG GAGGAGAATT TACCGCCAGG GAAGGGCGAA 420 GCAGGCTGCA GGTTCTGAGC CGGTAATCAC CCCAGCGGGA CCCATCCTGC CTTTTCTTAA 480 TGGGCTGGCT CTGCCTGTTA ATTATTAAAC AGATGTTCAG CGAGAACAGA GAACAGAGAG 540 GCCTGTGAAT GGCCTGTTGG GAGGATGGGA GCGACAGTGG GCTGATGAGG TGGCACATCA 600 GAGACAGGCA GAGGAGCGGC ATCACCGACA GCCACACACG CAGCCTCTGA GGCAGCTGCT 660 GTGACAGACA GCACATCCAT CTGGCTGATA CAGGCTCAGC AGAGCTCCCC GCATGGGATC 720 TGGTCACTCC TGCCTTTTCC GCCTCCTTCC CCAGCCACTG AAGTAGCTGC TCCTGAGAGC 780 TGCCCCACCC CATTCTGAGG GAAAGCAGAG GCCTGAATGA CGCACACCCT TTCTGCCTGG 840 GCTGTCAGGG AGCTCAAAGG TAAACTTCAT AGATTCGCTT CTCCAGATGC TGCTGGGCGG 900 CCCGGCTCCA GGGAGCTCCA TCCCCCACTG CTGTATTCTA CATGAATGGC ACCCCGAGGT 960 TGCAGACAGA GCTCCTCCCA CAAGGCCCTC CACTGGCTGA ACTGGAAGGA TATTTTAGTC 1020 CTTATGCTAC TGGAACTTTC TGTAGCTTTT GACCCTGTTG GCTACTGGTA CTGCCCTCTC 1080 CTCCAAACTT TCTGTTGTTT AGCCTCTGGG GAACTGTATC CAACCTCTCT GACAGCTGCC 1140 TCTCCCCCTC CTCTGATCCC CGAACACTCA CATTCCCAGG GGTCCCTCTG TGCATCTCCC 1200 CGACTCCCAG TGTCACCTGC CGTGGGCACC TGCTCTTCTA GCCTGGACAT TCCCTCAGGG 1260 TGGGCGCTTC AGTGTCTCCC 1280
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