Tag | Content |
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EnhancerAtlas ID | HS134-09068 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr11:2933380-2935040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIA | MA0670.1 | chr11:2933841-2933851 | ACTTGGCACC | - | 6.02 | ZNF263 | MA0528.1 | chr11:2934215-2934236 | GAGGGAGGAGGGGATGGGAGG | + | 7.2 | ZNF263 | MA0528.1 | chr11:2934218-2934239 | GGAGGAGGGGATGGGAGGGGA | + | 7.65 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23133 | chr11:2931364-2935694 | Colon_Crypt_1 | SE_41783 | chr11:2931568-2936483 | LNCaP | SE_52971 | chr11:2932014-2935450 | Small_Intestine | SE_57518 | chr11:2932144-2933908 | VACO_503 | SE_57518 | chr11:2934013-2935147 | VACO_503 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I002910 | chr11 | 2931972 | 2935380 |
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Enhancer Sequence | CTTGGGCACT GTGGCAAAAG CTGGCTGCCC AGAGTGGTGG TGGCACAGGA GGGCTGCGGG 60 GTTGACCTTG TGGCTGGTAA TCTGCCTTTG TCCAACCCAG ACAGGGTGAG GGAGGCCCAC 120 ACCTCCCCCT CGGGGGCTCA CCGAAGGCAG TGGGGCCAGG TGCCAGCCAG GCTCCAAAGC 180 CTGGTGCCCC ATGGCAAGGG CCAGCCCCCT GGCCCTCTTG GTCCAGCTGC CCCAACGCCT 240 GCAGCCTGTT CTGGCTCCTG GCCTGGTGCG GGGCAGGAGT CTGGTGCAGC TGTGAACATC 300 CCCCGCCTTG CAGCCTTCCT GCCCTTCCTT GATGGAAACC GAGGCACAAC ATGTGTGGGC 360 TTTCCCTCCC TGCCCACCCA CCTGTGTATC CCATTCCTCT GGAAGGCCCC AGTCCTGCCT 420 CATCCGCACC CACCTGGGCA GCAGGTGGGA GGAGGAAGTG GACTTGGCAC CCACAGGCTG 480 CGGGGGCGGG CACTGGTATA ACTGGTTTGG GCCCAGCCTC CAGAGCCCAG GGCTGAGAGG 540 CCAGGCTGGC CTGAGGAGGG ACCCGGGACC TGAGTCACTG CACACACGCT GGGTGGGGGG 600 TGGCTCTGTG ACTCATGTTC TGAGCCCAGC CCCTCACAGA CTGGGGAGGG ATGGGGAGGG 660 GCCATAGAGT CCTATCCTGA GCCAGACAGC AGGGAGCCCT GCAGGGTTTG CCTTCCCCAG 720 GTGGACAGGC AGCCACCAGG GCCATGCCGG TGCCATGGGG GTGCCAGGGC CCTGTGGGCA 780 GGACACCCCT GCCCAGCCAA GAAAAAACAA GGAGCCAGGG GCACTGGAGC TCAGAGAGGG 840 AGGAGGGGAT GGGAGGGGAG GTGAGCAGTG TCCCATACGA CCCAGGGCAC CCCAAGCGCT 900 GAGCGGAGGC TGAGGAGTGC AGGGGTGTTT GTAACAGGGC ACCTGCTGTA CAGGGAAGAG 960 GCTCTCGGGG GCAGATAGAT GCAGGGCAGG GGCTGGCAGG CAGCTGAGGG AGCAGCAGGA 1020 TATGGGCGAC CCAGGCCCGC CGCCCCCCCA GCCAGGTGAC TCAGCTACTG CCTTAGTTCG 1080 TGTACCTCGC AGTGCCCAGG ACACTCCGGT TCTTTCTGTT CTTCCCACAG TGGGCAGGCA 1140 GCAGGCCCCG CTGAGATGGT TCTGGCCCCG CTGTCCCTCA GGACAGCCCT GTTGAGCAGC 1200 AGGCTGGACA GGCCTCCTGC TGGGCCCGTG AGTCACTCCA GTCTCAGAGC CCATTTGGGG 1260 CAGGAGGGAG CTTGTGGTTT GGTTGGAGGG CTATGTGTTT GGGGAATGGG GGGACCAGGT 1320 ACGAGGAGAC ACGAGGACTG GGAAGGGTCA GGCCAGAGGG GCCTTTAGGA CCTTCTGGGG 1380 CACGCTGGAA GCCAGACGGC AGCTGCGTTA GGAGTGGCAT GGCAAGATGT TCATTTTCAA 1440 ACATGGTTCT AACTGCAGCA TCCTGGAGCA CGGATGACTT CTCTCAGCCC TGGGCTGGAC 1500 ATCCAGGGAC GCTCTGGACA GCCCCCTGCC CCATCGTCTT GTGAGCTAGG TGTCCCACAA 1560 AGCCAGGTCC CAGCTGACCT AGCCTCAGCC CCACCTGTGG GTTCGCTCCT GGCAGCAGGA 1620 TGACCTGGGC ACATGCTGTC ACCTTGTGCG TCCCCTTTCA 1660
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