Tag | Content |
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EnhancerAtlas ID | HS101-29829 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr3:53539230-53541680 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1B | MA0153.2 | chr3:53540675-53540688 | GCTAATGATTAAT | + | 6.22 | Zfx | MA0146.2 | chr3:53539379-53539393 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29518 | chr3:53539642-53541279 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I053505 | chr3 | 53539797 | 53541150 |
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Enhancer Sequence | GTTCATACCT CTCTCCTGCC TCAGCCTCCT GAGTAGCTGG GACTACAGAC GAGCGCCAAC 60 ATGCCTGGCT AATATTTTTG TATTTTTAGT AGAGATGGGG TTTCACCGTG TTAGCCAGGA 120 TGGTCTCAAT CTCCTGACCT TGTGATCTGC CCGCCTCGGC CTCCCAAAGT GCTGGAATTA 180 CAGGCTTGAG CCACCGCGCC TGGCCTATAT GCACATCTTT ATCCTCTGGA GCGTCTTCAA 240 AATACAGTTA ATAGTGAAGC ATTCTGAATC CCCAGCCATG CCTGATGCAG TGGTAGGGGT 300 ATACAGTAGA TGTTCAGTAA ATAAGTATTG CTGATGTGCA CCAAGCGAAT GACTTTCCCA 360 GGAGAAGCGC CACCATCATT CCTTCCTCTG AGCCATGTTT CAGATTTTCT TGGGTGGCAG 420 GTCCCTTTGT GGATTTCTTG CAGGTCCTTA GCTGGGAATG AGTGGGAAGG TGTACGTGTT 480 ATTCCTGAAA AGCTTAGGGT CTGCGGCCCT TCTTGTGCAC CTCTGCTTAA AAGAGCCCAC 540 AGTGTTGGCT TTCATAGCAG AGCAGTCTAG GAAATTTTGT ACTCTGGTTC CAGGGCTCAG 600 AGTAGCAAGA GTGCTGGGAC CTGTCTGAGA AGCAGTGCTG GGCTGTGGAT GCTTGCCTGT 660 GGCACCAGAT GCCTTACAGT GGCCAGGAAT GCTGCGGGAC AGTCTACTTT GATTGCTTTC 720 TTTCCTCCAT GGCTGAGATC TGAGTGTAGT GTTAACTGGG CTTAAAAATC AAGTCCGTTG 780 TATCTGCATG GTCACGTAGT TCGGCATCTC ATGGCTTTTG CACCTAGAGG TGTGAACCAT 840 AATACCTGAA ACACAATTTC ATAACCTGGC TCCTTGGGCT TAGCCTATAT GGTGGAGGTT 900 AGGTCTGTAT ATCATCAAGA CTGTGTCTTT GCATGGTTGT CATTCTGTTG GAATTGAACT 960 TTCTTATTTC TGTAGGCCTA GGTTCTGTCT ATTCTTCTCA GACAGCTCAT ATGCTGCTTC 1020 TTCCCTTCAG CCTTCTCTGA TACTTGTCCA CTCCCCGCCT GCCTACATCT GAGTACTTGC 1080 TTTCCCTCTG GACACCCCTG TGCCCAGTCC AACTCTCCTG TACAGACACC AGCCCCTTTC 1140 CCCTGGTTTA TAACTGTTGT GGGAAGTGGC GTGGAGTGTG ATGGTCTGCT CATGGGCTGT 1200 GGGGTCTGAC AGCCTGACTC TTTGGCTGAT TAGCTGAGTG ACTTTGGATG GAACTAGAAT 1260 ATGAGTTCCT AGAGGCTGAG ACTGCAGTCT GATTTGGGTG TATAGCCTTG TGAACTTAAT 1320 CCTGTGCCTG GCACACAGGA AGCACATCAG GAAATGCACG TCAAATGAGT GAATAAATAA 1380 ATGAATGACC ATACAAGGAC TCCATGGTAT ATTCTTGTAG ATCATTAGTT AATTATCAAC 1440 AATTGGCTAA TGATTAATGT TTGCCTGAGA GGCTGACTTT TTGTCCATTA GTAATGACAT 1500 CCCAGGAAAC ACCTGGCAGA GTTCGTCTTT AATTTCAGGA GTATATCTTT CTTTCTTGGC 1560 AAATTTAACT ATTAAAGAGA GAAGAAAGAC AAGTACTTGA TACTTTTTGA ATCTGTAAGT 1620 TATAAACCTG TCTTCTGTAT TCAATGTTGT ATATTAGCCA CATTGCAGAT GATTCTATTT 1680 GGATGGATGT GTGACTGTCA CCTTTCACAT AAAAATTGAT TGAGCCAGTC ATAGTGGTAT 1740 GTGCCTGTAG TCCCAGCTAT GTGGGAGGCT GAGGCAGGAG TCTTGGTTGA GCCCAGGAGT 1800 TTGAGACTGT AGGGGACTAT GAGTGAGCCA CTGCACTCTA GCCTGGGTGA CAGAGCAAGA 1860 CTCTATCTCA AAAAAAAAAA AAAAAAAAAA CAAAAAAATG TGGTAGAAGG GGAGAGAGCC 1920 TCAAAATGAC CAGAGTAGAT GGACTCGTGT AGTAAAACTT TACCCAAAGT TGGTTTCCTA 1980 ATGATATAAT GTGAAACAGT CTATGTGCTA TACAAATAAT TATATCTCTT TTGTTAAGCC 2040 TTACGTCATT TTGACAAAGG CTTTACTTGA TTGAGTATTG ACGGCTTTTC CAAAATAAAA 2100 TCCAGCTCTT AATTGAGATT TGTGGCTGGG CATAGTAGCT CATGCTTGTA ATCCCAGCAC 2160 TTTGGGACAC TTAGCAGGGA GGATTGCTGG AGGCCAGGAG TTCAAAACCA GAATGGGCAA 2220 CATAGTGAGA TTCCATGTCT CCCCCCGCCA AAAAAAAAAA AAAAATTAGC TGGGTGTGGT 2280 GGCGTGCACC TGTGGTCCCA GCTACTCAGG AGGCTGAGGT GGGGGGATTG CTTGTGCCTG 2340 GGAGGTCAAG ACTATAGTGA GCTGTGATTA TGTTACTGTA CTCTAGCCTG GGTGACAGAA 2400 TGAGACCCTG TCTCAAAAAT AAAGGAAAAA AAGAAGAATT TAGGTTTTTT 2450
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