Tag | Content |
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EnhancerAtlas ID | HS098-15278 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr13:27542160-27543540 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr13:27543122-27543137 | GGGTAATGATTAACT | + | 6.2 | HNF1A | MA0046.2 | chr13:27543122-27543137 | GGGTAATGATTAACT | - | 6 | HNF1B | MA0153.2 | chr13:27543123-27543136 | GGTAATGATTAAC | + | 6.01 | HNF1B | MA0153.2 | chr13:27543123-27543136 | GGTAATGATTAAC | - | 6 | Stat6 | MA0520.1 | chr13:27543298-27543313 | TCCTTCCTGAGAACT | + | 6.45 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_23155 | chr13:27534939-27544739 | Colon_Crypt_1 | SE_24001 | chr13:27541050-27544070 | Colon_Crypt_2 | SE_27831 | chr13:27540966-27545988 | Fetal_Intestine | SE_28781 | chr13:27540921-27547129 | Fetal_Intestine_Large | SE_47159 | chr13:27540566-27544254 | Panc1 | SE_50194 | chr13:27534824-27547226 | Sigmoid_Colon | SE_52911 | chr13:27540971-27544244 | Small_Intestine | SE_56765 | chr13:27538437-27543579 | VACO_400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I026961 | chr13 | 27535141 | 27546968 |
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Enhancer Sequence | GCTGCCCCCA GCTCTGAGCC CGTGGGCATG TGTGCTGAGG GTGCAGGAGA GAGGAGAGAG 60 GGGATCCCTG CAGCGGGGCC CGAAGCACGC AACACTCCTT TGTCACCCAG CTTTGCGGAA 120 GGGAAGGCCA GTCTAGATCA GGAGAATGGT CACAAGGGCA GGGTCTAGGA GGTGGTCAGT 180 TAGTGAGGAG GAGGGAAAGC AACAGTGGCG TGGGACAGGC AGGGTCCCTG TGGGAACGGG 240 CGTGATGTGA GACACAGCAC AGAGGGCTGG AACAGCAAGG GGACAAAGCA CATTCAGGAC 300 GCAGGGACTT TGTGGGGGCC AGGGCTTTCC CGTGAAACCT GGGAAGTTGA GGGGGTGTCA 360 TCAAGGATCA CCAGGACCCT TCTCCAACTT TAATTACTGA GGACTTTCCC ATGGTTAGCA 420 AGAAAGCTAG GTGATGCTGC TGGGGACAGC CATCTTGCTT CTCCAACAGA TGCAGCGAAC 480 AGCTCGGGCT TATCTCCGCT CCCGAGCAGA CACATAGTGG GAGAAAGGGG GAGAACACAT 540 GGCAAAGGGA GAACTTCAGA GCAGGATGCA TCCCTAAGCC CCAGCTGCCA GGACTGGGAC 600 CAGGAGTCCC CAAGGACTGC AGCCGTGACT CATCCAGGCC TCGGTACCCT CCCATCTCTG 660 AGGTTTTCTG CTGTGGCTCT GGGGCTCTTG TGCCCAGTGT CGCTTTGGGG CTTTCTCCTG 720 GTGGAGACTT GGGACACTCA GTGTCGGAGC CTCCCAGCAG CATGAGGAAC GGGGTGCAAA 780 CAACGCAGAC GACCCAGCTC CCCAAGAGGG GTCTGACTCC TGCATCCAGT GAGGGCTGAG 840 TCAGAGCCAA GCGGAGCCTA TCAGTGCACA ATCCAAACAC CAGCCAAGGC CCCGTGGCCA 900 GGCCAGTCAT AAACCCACGG CCACAAAAAC AGGCCAGAGA GCCCAGGAAT ACAGCCCTGC 960 CCGGGTAATG ATTAACTGGC ATCCAGGGGT CCTGGAGGTC AGAGCGATAA TGAGAAAGTT 1020 TCCCTGAACT CTCTCAAGTG CAGAGGGCCT GGGGAGGGGC CCTGCTGGCG CCGATTCCTG 1080 GGCAAACACT TCCTGCCCCT CTCTTTTCAA CGACCAAACA GCCTCAGCCC CTCTCACCTC 1140 CTTCCTGAGA ACTGGGGAAC TGACATCACA AACGCAGGGC CTCAGGGCCC TGGTAAAATC 1200 CACTGGGAAT AGCCAACGAG GGCATCTTCC CAGGAGGCTG AATTTCCTCA AACACGAGGC 1260 TGATAAGCCC TTTCAAGAAG ACAGGGCTTC ATGCTTATCT TTATTGTCTG GCATGTCCTG 1320 AGACATGGGA GCCACTCTGT TTGAGTGAAA CTAGAATATT ATGTTCAGCG AGACTTTCTG 1380
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