Tag | Content |
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EnhancerAtlas ID | HS111-01061 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr11:119991950-119993660 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PLAG1 | MA0163.1 | chr11:119993155-119993169 | GAGGGCCAAGGGGG | + | 6.73 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_26582 | chr11:119985447-119997137 | Esophagus | SE_36164 | chr11:119990825-119996181 | HMEC | SE_57595 | chr11:119991279-119993904 | VACO_503 | SE_64461 | chr11:119991394-119996028 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I120119 | chr11 | 119990523 | 119996803 |
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Enhancer Sequence | CTTTGTGCCT GTGTTCCCTG ATGCCCTCTG CCCTTCGCAG TCATGCTCCC TCTACTGAGC 60 ACAGGTTCCT GGAAATTCAC CCCTCCAGGG AAGGAGTCAC AGCCACTGTC AATCCCACTG 120 ACCTCAAAGC TCCCAGACTC AGGACCCAGT CCCTTTAGGG GCCTTGTTTC TTTCATCTCC 180 TTGGTGATTG CTTCCTGTTC TCCCCCCAAC TCCACCCTGA GCCTGGGAGC TCCCAGAGGG 240 CAGATTTCCT GTCCCTCCTG TCCTCGGCAC AGGCTACCCA CAGTGCTTGG GCAGGGATGC 300 CGGGGGAACC TGTTTCTTCC ATCACAGACA TCATAGACTG ACTCACAGTG CAGAGCTGGG 360 AAGTCTCCCA GCATGTGAGC ACAACCTCCC CTCTCTTCAG ATACAGGTAC TGAGGCCTGC 420 CCAAGATGCC CCAGGCCCTA GGCCCTCGGG GTGGCATCAT AGTGGGTGCT GCTGTTCCCT 480 CCACCCCCTC CCACAACCTG CAGGAGGCTC ACACTGGGCC CTCAGTCTCC TACAGAGCAG 540 GAGAGACCCG CAGGAGCCTG TCAGGGCACT CGATGGCACC CCAGGGCCTG GTCCATGGAT 600 GGAAGGGAGA GACAGGAGGG ACAGGGCCAG GGCGAGGCCA GGTAGGGGTT CTGAGGAGAG 660 GGGTGCTGGG GCCGGCACTC CCAGAACTTG CCCAAAGGCA CAGCACCCCA GGCAGGGAGG 720 AGGCAGGCTG GCCGGCTGGG GCCTGGCCCA CACCAGGAAT GTCAGAGGAG GGAAAGCCCA 780 ACAACCAAGA AGCCCAGGGG TTGTTTTCAA ACTGGGTGGG GCGGCACAGG TGCTTTTCTG 840 TTGAGCTCAT CTCTCCAAAT CCCCCAAGCC TCTCCCATTG TGTGTGTGAG TGTGTGTGTG 900 TGTGTGTGTG TGTGTGTGTG TGAAAGACGT GTGTGAATTA CTGATTAGCT CCCGGAGGCT 960 TCCCCCTCCC CAGCCCCTGT GCCTTACCCA GGCCTCCCTC CTCCCCCAGC CTCCCTCTCC 1020 CACATGCACA GGCACACACC CTCATGGTCC GAGGGCTGGC ACACCCACCC TTATGTAACG 1080 GGTATTGCTG TGGTTTGTTG CTGGCGCCCA AGAATGTGAG AGGCCACCAC AGGGCAAGGA 1140 CAGGCAGGCA CTGGTCTGTG CTAGGCCGGC ACCTTGCAGG CTGGGACTGT CCAGGGCCTG 1200 AGAGGGAGGG CCAAGGGGGC CAGGGTGCAG AGCCAGGAAA CTCAGAAGAG GAGGGACCAC 1260 TCTCCCTGCC TAGGGGAGCA GAATGGTCCT GGGGTCGGCA GCCATCTCAC AGGGCTCAGC 1320 CCCTACAAAA CCTGAGCCAA AGCAAAACAC AGCACCGGCC TGGCAGAAGG GAGCCCAGGA 1380 GACCTCCGGA AGGAAAGAGA AGCAGAGGTG TGGGCTGGAA GTGAGAAGGC AAGGAGGGCA 1440 AAGAGGTGCT GCCTGTGTGG CCCGGGAGGA ATGCCTCTGA GGAGCTGGCA CCAGGTAACT 1500 TCTCATTCGA ACCAGGACAC TTCTGAGAGC TAACACAGAC CTGTTCATCA TCACATCAGG 1560 ACAACACGTA GATGCCAGGA CTTTCCCAGG CAAACTGGAC ATGCCATCAC CCCCACTCAG 1620 AAGGAACCTG GCTGAGAGTC ACTGCACGGA CTTTGGGGGC CCCTGGGCAG CAGGAGAGAC 1680 ACTAGGTCTG GGGTGAGGGG CTCCCTCTTA 1710
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