Tag | Content |
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EnhancerAtlas ID | HS012-12790 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr13:99427640-99428880 |
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) |
Nr2f6(var.2) | MA0728.1 | chr13:99428796-99428811 | GAGGTCAGAAGTTCA | + | 6.38 | RARA | MA0729.1 | chr13:99428796-99428814 | GAGGTCAGAAGTTCAAGA | + | 6.88 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27651 | chr13:99427477-99429705 | Fetal_Intestine | SE_28565 | chr13:99427274-99429851 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I098775 | chr13 | 99427743 | 99429621 |
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Enhancer Sequence | GAGCAGTGAT TCTCACACCC TACTGTGCAA AGGAATCCCC TGGGGCTTGT TGGAATGCAG 60 ACTTGCGCTC GGTGGCTCTG GGTGTGGACG AGGACCCTCT GCCCGCAAGC TCCCAAGTAC 120 TTGTCTGTTC GCGGCTGCTG GGCTGCAGGT CACCCCTTGA CCAACAAGAG CTTAGACGGA 180 GGCTTCTCCG CCGTGGCTGT ACTGCTGTCC TGGACGATCT CTGTCTGTTG TGGGGGCTGT 240 CCCGTGCACT GTGACATGTT CAGCAGCATC CCAGCCCTCC ACCCACAGGG TTACAGTAGC 300 ACCCCCACCC TCAACCATGA CAACCAAAAA TGTCCGCAGA CGTTTTCGTT TGCATCCCCT 360 GGTGGACTGG GGCATGGGGG CGGGGTGTTG AGAACCACCG ATTAGTAGAC TTTCAAAGAC 420 TCTCCCAAAT CCAGTTTTTT TGTGATCAAA AGTCCACATC AAATCCTCTT AGTTGGAAAA 480 CACGCATCAC TCTAAGGCTG AAAAAGATGA CTCCACAGCT GAGCTCTAAA TGTCCTCTTA 540 AAAATATAAA ATCCCAGATC AACCTGTCTT CACAATGGCC GCATGTAGCA GCCCCTCCAC 600 AAAGACTGGG TACAGTGGCA TTTGCACCTT CTAAGGGACC CTGGAGTGCG GCCTGACTGA 660 GAGAGTGGAT GGGGAGGGGA TGCCGGGTCT CTGGCTCAGG TGTTGCGTGT TGGGAGCCCA 720 CTAGGTAGAA CAAGTGTCCT CCACCCAGCT CAGCTCCGGA GCCTTCCTCG AAAGGCAAGA 780 GGTCAATTCA TCTTCTGCCT CAGCAGAATC GTCCCTTCCT TTACAAGGGG ACTTTGCTCC 840 ATGATCTGAC AGACCTGGGA AGTGTGTGGA GGTTTTACAC GATGACTCAG TGCACATCAG 900 AGTCAGAGAC AGGACGGCCG AACACTGATT CCAGAGATAG GCATGTGGGC CCCGCCCGGG 960 AAGGAGAGCT GCCTGGGAGA TGGGGAGCTG CAAGAGAGCA CCCAGAGGGG TAAATTTGCA 1020 CAAGGCCACT GCGTACACTG GTACGTGCTT CCTTGAAAAT GTGACATTTT CAGGCAGGGC 1080 GCGGTGGCTC AAGGCCGGGC ACGGTGGCTC ACGCCTATAA TCCCAGCACT TTGGGAGGCC 1140 AAGGCGGATG GATCACGAGG TCAGAAGTTC AAGACCAGCC TGGCCAACAT GGTGAAACCC 1200 CATCTCTACT AAAAATACAA AAATTAGCGG GGCGTGGTGG 1240
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