Tag | Content |
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EnhancerAtlas ID | HS012-13330 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr14:101539330-101540120 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN | MA0488.1 | chr14:101539709-101539722 | ATGACATCATTAC | - | 6.48 | JUND(var.2) | MA0492.1 | chr14:101539708-101539723 | AATGACATCATTACC | - | 6.2 | NR2C2 | MA0504.1 | chr14:101539588-101539603 | AGGGGGCAGAGGCCA | + | 6.05 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I101070 | chr14 | 101537262 | 101542129 |
|
Enhancer Sequence | ACGGAGGCCA TCTGCCTTCA GCAGGGATTC GCACAGAATG TCACTGGCCT TCGCCCAACA 60 AGCACTTTGC AGGGAGCAAC CTCCTGAAGT CGGGGCTCAC TCCTGGGTCC CCCTCCACTG 120 CATGCGAGCC CCCCGTTCCA AGGCAGGAGC CAGGGTCACG AAAATGCATG CTTCTTCATC 180 AATCCGAGGT CTCAAACGGC TCCCCCAGCC CCACTGCCTG CCCGTTCCAG GCCTGGGGCT 240 GGCAGCCTGG GCCCCACGAG GGGGCAGAGG CCAGAGCCCG GCGGCAGAGC CCGTGCCCAC 300 GCCTCGCTGC TGCCAGCCTC CGCTTGGTCA CGACACAGCC AGGCTGACTC AGACACAGCC 360 CCAAGCGGGA GCCTCATAAA TGACATCATT ACCTATGAAA CCTGCCGTGT AGTGCGCTAG 420 CAGGGAAGGA CACACTCTGG CCGCCCGGTG ACTCACACTG TTTTCCCCAG AGCCTTCCTG 480 CTCCACCGCC TGGGTCTGAG CTGGCTGGGC AGGGGGAGGG GGCACTCAGC TTGGCCTCAC 540 TCCCCCGCTC TGCTGCAAAT GCAAAAGCAA TCGGCCAGGC AGCCACCATC CTGCTGAGGG 600 CTGTGTGTGG GGGTGGCGGG GAGGAGGGGG GGCACCATCT CTCCGGCCTC CCTCTGCAGC 660 CCCAGTGGCG CTCCAGAGGG ACTGTCAGTT GCCTATGACA GGGGAGGAAA CTGAGGCCTA 720 AAGAGGCCCA ATGCCTGGCC TCACAGATCC CACAGGGGAG GGTGGCTTCG GCTCATGCTG 780 GGAACCCCCA 790
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