Tag | Content |
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EnhancerAtlas ID | HS197-06193 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr13:99427760-99428910 |
Target genes | |
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 | TTGTCTGTTC GCGGCTGCTG GGCTGCAGGT CACCCCTTGA CCAACAAGAG CTTAGACGGA 60 GGCTTCTCCG CCGTGGCTGT ACTGCTGTCC TGGACGATCT CTGTCTGTTG TGGGGGCTGT 120 CCCGTGCACT GTGACATGTT CAGCAGCATC CCAGCCCTCC ACCCACAGGG TTACAGTAGC 180 ACCCCCACCC TCAACCATGA CAACCAAAAA TGTCCGCAGA CGTTTTCGTT TGCATCCCCT 240 GGTGGACTGG GGCATGGGGG CGGGGTGTTG AGAACCACCG ATTAGTAGAC TTTCAAAGAC 300 TCTCCCAAAT CCAGTTTTTT TGTGATCAAA AGTCCACATC AAATCCTCTT AGTTGGAAAA 360 CACGCATCAC TCTAAGGCTG AAAAAGATGA CTCCACAGCT GAGCTCTAAA TGTCCTCTTA 420 AAAATATAAA ATCCCAGATC AACCTGTCTT CACAATGGCC GCATGTAGCA GCCCCTCCAC 480 AAAGACTGGG TACAGTGGCA TTTGCACCTT CTAAGGGACC CTGGAGTGCG GCCTGACTGA 540 GAGAGTGGAT GGGGAGGGGA TGCCGGGTCT CTGGCTCAGG TGTTGCGTGT TGGGAGCCCA 600 CTAGGTAGAA CAAGTGTCCT CCACCCAGCT CAGCTCCGGA GCCTTCCTCG AAAGGCAAGA 660 GGTCAATTCA TCTTCTGCCT CAGCAGAATC GTCCCTTCCT TTACAAGGGG ACTTTGCTCC 720 ATGATCTGAC AGACCTGGGA AGTGTGTGGA GGTTTTACAC GATGACTCAG TGCACATCAG 780 AGTCAGAGAC AGGACGGCCG AACACTGATT CCAGAGATAG GCATGTGGGC CCCGCCCGGG 840 AAGGAGAGCT GCCTGGGAGA TGGGGAGCTG CAAGAGAGCA CCCAGAGGGG TAAATTTGCA 900 CAAGGCCACT GCGTACACTG GTACGTGCTT CCTTGAAAAT GTGACATTTT CAGGCAGGGC 960 GCGGTGGCTC AAGGCCGGGC ACGGTGGCTC ACGCCTATAA TCCCAGCACT TTGGGAGGCC 1020 AAGGCGGATG GATCACGAGG TCAGAAGTTC AAGACCAGCC TGGCCAACAT GGTGAAACCC 1080 CATCTCTACT AAAAATACAA AAATTAGCGG GGCGTGGTGG TGCATGCCTG TAATCCCAGC 1140 TACTTGGGAG 1150
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