Tag | Content |
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EnhancerAtlas ID | HS034-08282 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr13:73633730-73634850 |
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) |
TCFL5 | MA0632.2 | chr13:73634000-73634010 | TCACGCGCAC | + | 6.02 | ZNF740 | MA0753.2 | chr13:73633910-73633923 | ATGGGGGGGGGGG | - | 6.07 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_23235 | chr13:73633053-73637700 | Colon_Crypt_1 | SE_24316 | chr13:73633076-73635399 | Colon_Crypt_2 | SE_24929 | chr13:73631683-73639879 | Colon_Crypt_3 | SE_26421 | chr13:73633805-73642018 | Duodenum_Smooth_Muscle | SE_27687 | chr13:73628614-73651570 | Fetal_Intestine | SE_28601 | chr13:73628476-73654730 | Fetal_Intestine_Large | SE_34966 | chr13:73627061-73637367 | HeLa | SE_36569 | chr13:73629841-73637236 | HMEC | SE_57068 | chr13:73633119-73635477 | VACO_400 | SE_57507 | chr13:73633139-73634965 | VACO_503 | SE_64296 | chr13:73628716-73641168 | NHEK |
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Enhancer Sequence | GAAGAGCCGC TCCCCTCCCA CCGCAGCACT CCCGGGCTCG GGCGTGTCCC GTTGCTGCGA 60 CTCGCGGGCG ACAGGGGCCG CTCCAGGCTG GGGCGTGCGT CGGGGCGCAC CGGAGCCGGT 120 GCTGGGTGGG CAGCCCCGCC CTGCACGCCT GGCCGGGGCC CCGCGTTTCG CTGAGAGTAA 180 ATGGGGGGGG GGGCCGGGGG TGGGAAGGAT GGAGGGGAAT CTGCCCCGGC GGGTCGGCCT 240 GGGAGAGGTA AGAGGGAGGG AACTGGGTGC TCACGCGCAC CTTAGTTGTT TTTCTTACAC 300 TTGAGGGACG AAACCTTGTA CCTTACGCTC AGTTTTACTT AAATTACGCC TTCGCCTGTA 360 CCGCTCTCCA ATGCCAAGGC ATTGGAGCCC TCCCCCCCAT CCCCATCGTC TCGGGTTAAG 420 TAGAAACGCA AATTGGGGTG CTGGGGAGAG GTTCCCCAAG GTTTCATACC CGGTGGCTCA 480 ACCTGCTTTA GAAGCGATTG CGGGCCGCGT TTGGAAAATG AGAGTTAGGA AAGCTAAGGT 540 TGTGTCGGAG CGCTTATTTT TCCTTAAAAA AAAAAAAAAA AAAAAAAGAC CGGGGGTGTT 600 GTTTTCTTCG TGTGCACGTA AATTTCCTCC CGGAGCCGCG TTGAAAGCTG GCAGTTGGCT 660 TTTACACTTG CCCAGCAGCC GAATTAGAGC AACCGCCTGT TTCTTTCGCC CACGCAGGGA 720 GTCATATAGC CCAGAAAAAA CTTCCCGGGA CTTTTAGCCT GTCCCAAGGA AAAAAAAATT 780 GGAAACATAC CCACATGCAA ACAGCTGGAA GAGCTAAAAT CAGAAACCAC TAACCGCCGC 840 GGGAGCGCAG TGCACGAAAG GGTTTAGTTC AGTTTATTTC AAGACACTTC ATTTAGTAGC 900 TCTTTGGCGT GTCGTATATT TGCTACCCAG CGCCTACTCC GTGGGGTCTG CCAGGGTCTT 960 GCTGTGAGAG GGCAGTGGCG TTTGTCAGAG ATGTGACTCA CATGATGAGA GCGTTAATTT 1020 TTATTTTTAA ATCATGTCTA TCCGGGAAAC CCCGTCCGCA TCCACACCAA GGTCCGAGAT 1080 GAAACGCATT TGAAATGAAG TAGTAGCAGA AAATGACTGT 1120
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