Tag | Content |
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EnhancerAtlas ID | HS129-04029 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:236164930-236166350 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:236165803-236165815 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr1:236165807-236165819 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr1:236165811-236165823 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr1:236165815-236165827 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr1:236165819-236165831 | AAACAAACAAAC | - | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_38812 | chr1:236161622-236166053 | HUVEC |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I235997 | chr1 | 236161015 | 236165602 |
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Enhancer Sequence | TTATGAACTC TCTTCATGTC CCTTCCCAAC ATTTACCCCC ATTCTCACAG GGCTAGAGAG 60 GAAGACGAAT GGCCAGGGAG GGGCACTGAA CTCGCAGTTA GGAAAAGGCA AACAAAGAAG 120 GGAAAACAGA AAGGTCGTAA ACCAGCATGG AAGAGAGCTT GCACTCCTCC TCTGTGTGCA 180 GTCTCTTCTG TCACAGTGTG AAACTGCATT GTTGAGTTTC ATCACACCTG TTTCCTGGAG 240 CAGCTCTTGG CTCCCAGCTG CCTTCCTCTC CCAAAATTCT ACCACAGCAG GGCTTTTAAA 300 ATCACTGTAG TCATCATACG CTTCAGGTCA AGAGCCCCAT GGACACGTGA AGCACTTACT 360 CACTAGTGTT ATAAGCATTT AGTGAAAGCT GCCATCAGCC AGGCGCCCTG CAAGGGCTAA 420 ATAGGAGAGT CCTTGATTGT ACAGGCTAGT GCAAAAGATG AGGGCCCTGG TCAGTGGCAC 480 AGTGGGAGAA GCGGCTGGCT GTGGTCTGGA CAGGCTGCTA TGGGACAGAG AGGAAGAGCA 540 CCACACCTGC CTTGGTCAAG GGCTTGGCTG ACATTAAAGA CAATAAATCA GGCTGGGCGC 600 GGTGGCTCAC GCCTGTAATC CCAGCACTCT GGAAAGATGA GGCAGGCAGA TCACCTGAGG 660 CAAGGAGTTT GAGACCAGCC TGGCTAACAT GGTGAAACCC CGTATCTACT AAAAACACAA 720 AAATTAGCCA GGCGCAGTGG CACATGCCTG TAATCCCAGC TACTCGGGAG ATTGAGGCAG 780 GAGAATCGCT TGAACCCGGG AGGCGGAGGT TGCAGTGAGC CGAGATGGCA CCACTGCACT 840 CCAGTCTGAG CAACAGAGCG AGACTCTGTC TAAAAACAAA CAAACAAACA AACAAACAAA 900 CAAAAAATGA CGATAAATCT GCGGTGTGTC CAATACACCC AGCCACAGCA GCCTAGGCGC 960 AGTGGCTGAA CGGACTTAAG ACAAGAGCTT TGCAGGCTGA GAGTGCAGAC GGATAGGAAG 1020 TCAAGAAATT CCAAGCATTG GTGAGGACGG TTGCCTTTGT GCTTCCTGGG GTTAGGTTAG 1080 AGAGGACTTC AAGAAAAAGA AGGGATGGAG GAACCACAGG CTCAGCGATC ACTCCGCGGA 1140 TTTGGAAACG AGGCCATGTG AGAGTCACAA GGGAAGGAGG TGGCGGTCAG ACGTGGCCAC 1200 AGACATCAAG ACCGGGAGCT TGTCAAGCCT TTGGGTGGCC TGGTTTGGAC CCTCCTCAAC 1260 ATCAACTCCC CCATTTGCCT GACTGCCCCT CCTCCTCATT ATTCCTCCCT GTCTCCTATT 1320 CAAATCTCAC CTGTCCTTCA AGGCTGAGTG CAAATCCTCC CTCTCTCACT CTCCCCAGCT 1380 TTTTTAGCCC ACCTGCATCT CTGCTTCCTG CTGCTAGTTA 1420
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