Tag | Content |
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EnhancerAtlas ID | HS180-08791 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr11:61808860-61810590 |
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) |
ZNF263 | MA0528.1 | chr11:61810163-61810184 | GGAGGAGGGGGCAGAGGAGTG | + | 6.84 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34671 | chr11:61808749-61817734 | HeLa |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I062041 | chr11 | 61808858 | 61816941 |
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Enhancer Sequence | CAAAAGGATC ACTTTGGCTT CTGATAATGG ATCTTAGGGG GACAAGAGGG GAGGTAGAAA 60 GGCAGGCAGA AAGCTCCTGA AGGAGTCTCA TGATGGGGAC ATCCACAGCT ACAGCCACCC 120 TGCACCTGAG CAAGTCTCTG AGCCATCCCC GCCCTTATCC CCTTGCACAT CCTGCAGTCC 180 TATCCCATTT CTGCAGTCCT CTCTCCCCTT ACACAGTGAA CATAGTTCAA ATATCCTGCC 240 CTGGCTGACC CCACTCCTAA GCCCCCAGAC ACTTTCTCTG TAGACAATTA GGTGACCCTG 300 CTTCACATGT CTTGAGGATA AAATATGACA CATGCCTCAA ATCTGGGTTT TTTTTAAAAG 360 GGAAATATCT TTTATTTTAT TTTAGACAAG TCTTGCTCTG TTGCCCAGGC TGGAGTACAG 420 TGGTGTGATC TTGGCTCACT GCAACCTCTG CCTCCTGGGT TCAAGAAATT CTTGTGCCTC 480 AGCCTCCCAG GTAGCTGAGA TTACAGGCAC CCACCACCAC GCCTGGCTAA TTTTTGTATT 540 TTTAGTAGAG ACGGGGTTTC CCCATGTTGG CCAGGCTGGT CTCGAGCTCC TGACCTCAGG 600 TGATCCACCC ACCTCAGCCT CCCAAAAGTG CTGGGATTAC AGGCGTGAGC CACTGTGCCC 660 AGCCATGACT GTTTTCCCAC TGAACTTTAG ACAACTGTAT CTTTGAGTCT TATCTTTGCA 720 GTTCAGCTGA CCACAGGCAA TTGAGTGGGC CTTGAAGGAA AGAATGTGGA ACTGAATCTG 780 TTATCTGGCA GCCACCTGGG AGACTGGCAG GGCAGAGACG GTTCTGACTG TGGTGATTAG 840 GAAACAGGGC CGCGTGGATG CACCTGCAGA CTGGGTCACC AGAAAAGATA CAGATCACTG 900 GAGTGTGTGA GACCAAACTG GAATCCATGG GGCACGTGAC ATCCTCGAAA GAGTAAAGGC 960 AGGTGGGGTG AGTTAGAGTG GTTGCAGTAA TAGTGGCACA CACGCTGTGC CACGGGGAGT 1020 GAGCTGGAGG TGCCCAGGGC TGGGGCCGCC CTATAATGCC AGCTGGAACA CACCTTGCTG 1080 TTGCTTAACT AAGAGTGAGC CTCTCTTATC GCTCCTCCTG CAACGTTAAC TACCATAAAC 1140 TGTTAGCAGT TGTTACAACC GCCTCTGCCC CAAGATACCT TGGCTCCACT CCCACCTGTT 1200 CTCTGAGAAG CTGCAATACA AATTAACTCA TCAAAAAAGG TCAAGACATC CAGTTAGTTT 1260 GGAATAAAGG GAGAAGAAGA GGAGGGAAGT AGAACTGACT GTTGGAGGAG GGGGCAGAGG 1320 AGTGGATTGG AAAAGGATAA ATACTGTTTT TTACAATTGT AAACAAGTTA TTTATAATAT 1380 TATAATAAAG GATATGTTTT ATTAAAAATA CAGCAGATTA TTTCAAGGTA GGCTAAACTA 1440 GTACTACACA CACTGTGTCC CTGGGACAGG ACCTGGTCCA TGAACTGTTG GTTACCAGTC 1500 TGAGAAGAAG TAAGTAGAGA AGTTAAGAGA AATTCTTTAG AAAGTTTTGT AGCAATTGGA 1560 CAGCACAATT TTCTGTCTGT TGTGAAAGGA AAATAAATCT TGGGACTCCA AAATCACCAA 1620 GCTAAAGGGA AAAATCAAGC TGGGAACTGC TTAGGCCAAA CCTGCTTCCT GTTCTATTCA 1680 AAGTTATCCC CCTGAGGCTC ACCTAAGACA AATGCATATC TGATTGCTTC 1730
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