Tag | Content |
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EnhancerAtlas ID | HS007-04375 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr13:27542120-27543700 |
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 | CGGAATCAAC TCAGATCCAA ATAAATGTAG CCACCGCAGG GCTGCCCCCA GCTCTGAGCC 60 CGTGGGCATG TGTGCTGAGG GTGCAGGAGA GAGGAGAGAG GGGATCCCTG CAGCGGGGCC 120 CGAAGCACGC AACACTCCTT TGTCACCCAG CTTTGCGGAA GGGAAGGCCA GTCTAGATCA 180 GGAGAATGGT CACAAGGGCA GGGTCTAGGA GGTGGTCAGT TAGTGAGGAG GAGGGAAAGC 240 AACAGTGGCG TGGGACAGGC AGGGTCCCTG TGGGAACGGG CGTGATGTGA GACACAGCAC 300 AGAGGGCTGG AACAGCAAGG GGACAAAGCA CATTCAGGAC GCAGGGACTT TGTGGGGGCC 360 AGGGCTTTCC CGTGAAACCT GGGAAGTTGA GGGGGTGTCA TCAAGGATCA CCAGGACCCT 420 TCTCCAACTT TAATTACTGA GGACTTTCCC ATGGTTAGCA AGAAAGCTAG GTGATGCTGC 480 TGGGGACAGC CATCTTGCTT CTCCAACAGA TGCAGCGAAC AGCTCGGGCT TATCTCCGCT 540 CCCGAGCAGA CACATAGTGG GAGAAAGGGG GAGAACACAT GGCAAAGGGA GAACTTCAGA 600 GCAGGATGCA TCCCTAAGCC CCAGCTGCCA GGACTGGGAC CAGGAGTCCC CAAGGACTGC 660 AGCCGTGACT CATCCAGGCC TCGGTACCCT CCCATCTCTG AGGTTTTCTG CTGTGGCTCT 720 GGGGCTCTTG TGCCCAGTGT CGCTTTGGGG CTTTCTCCTG GTGGAGACTT GGGACACTCA 780 GTGTCGGAGC CTCCCAGCAG CATGAGGAAC GGGGTGCAAA CAACGCAGAC GACCCAGCTC 840 CCCAAGAGGG GTCTGACTCC TGCATCCAGT GAGGGCTGAG TCAGAGCCAA GCGGAGCCTA 900 TCAGTGCACA ATCCAAACAC CAGCCAAGGC CCCGTGGCCA GGCCAGTCAT AAACCCACGG 960 CCACAAAAAC AGGCCAGAGA GCCCAGGAAT ACAGCCCTGC CCGGGTAATG ATTAACTGGC 1020 ATCCAGGGGT CCTGGAGGTC AGAGCGATAA TGAGAAAGTT TCCCTGAACT CTCTCAAGTG 1080 CAGAGGGCCT GGGGAGGGGC CCTGCTGGCG CCGATTCCTG GGCAAACACT TCCTGCCCCT 1140 CTCTTTTCAA CGACCAAACA GCCTCAGCCC CTCTCACCTC CTTCCTGAGA ACTGGGGAAC 1200 TGACATCACA AACGCAGGGC CTCAGGGCCC TGGTAAAATC CACTGGGAAT AGCCAACGAG 1260 GGCATCTTCC CAGGAGGCTG AATTTCCTCA AACACGAGGC TGATAAGCCC TTTCAAGAAG 1320 ACAGGGCTTC ATGCTTATCT TTATTGTCTG GCATGTCCTG AGACATGGGA GCCACTCTGT 1380 TTGAGTGAAA CTAGAATATT ATGTTCAGCG AGACTTTCTG CTTTCTGATT TTTCTAGTGC 1440 TTTTGTATCT TGCAGTGGAA TTCTCCAGCA ACTTTCTTCT GAAATTCCCA AACAACTTCC 1500 AGTGCAGAAC TCCTGCCTCG GTTTAAGTTA AGGAGGTTTG CTAAGGCCCC GCTATGTGTC 1560 TAGTTGGGGT GCTTTGCACA 1580
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