Tag | Content |
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EnhancerAtlas ID | HS184-30448 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr8:134332530-134335020 |
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) |
Arid5a | MA0602.1 | chr8:134333543-134333557 | TGTTGCAATATTAG | - | 6.67 | Nr2f6(var.2) | MA0728.1 | chr8:134334105-134334120 | TGAACTTGTGACCTC | - | 6.29 | RARA | MA0729.1 | chr8:134334102-134334120 | ACCTGAACTTGTGACCTC | - | 6.6 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_29358 | chr8:134332116-134333572 | Fetal_Intestine_Large | SE_36277 | chr8:134331645-134338386 | HMEC | SE_64645 | chr8:134331998-134338371 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I133319 | chr8 | 134332087 | 134338134 |
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Enhancer Sequence | CATCCCCACT GTATAAATGG AAATACCGAG GCAGAAAAAA AATAATTTGC CGAAGACGTC 60 CAGTAGAGCT GGGATTGGAA CCCAGGCAGT CAGTCAAGTG TGTCCCTAAC CACCATTATC 120 TGGATGACCC CAAACCTCCA TGGTTTCTTT TTCCTAAGCA ACCAAGTGTC TTCTGAATGC 180 AAAGGTTGGT GGGGAAATGC TTGAAGTCAA CATTCTTCCT GTGTAGTCTG AGGAACCTGA 240 CACCCAGAGA GAGTGTTCCT GGCTCTAGGT CCCAGGTCTT ATGACTGCAG ATCCAGTCTT 300 ACCACAATCC AGCCCACACT GCCTCTACTC AAAGGGAGAA AGGGCATTGC TGCTGATCTC 360 ACCTCCTCCC TGCCCCCTCG GTGGTGGTGG GCCAGGACTC TCTCTGAAAC AGTGATCATG 420 GTTTAATCAC TAGGTGAGTA ACCATGGGAG GCTTCCTGGC TGATTATTAA TAGAAGCTGG 480 AGAAGGTGTG CGTGTTTAGC AACAGGCCAG CAGTTTGGGA TGCCAGGCTG GCTTGGTCTC 540 TTGGTTTCTG GAGTCATCTG AATGATTTGA CTCATCTCCT GGCTGAGGGC TTGGCTTCTT 600 ACTTCTGAGA CACCCCATTC CCAAGGCAAA TTGCTGCCTT GCCTCTCTCC TTACACTCAT 660 TTACATCATC TGTTTCCAGG CTGCCTGCAG GAACTGAAGC TTCTAGACAA AGAGACCTGG 720 GTTTAATCCT TGCAGACCTT AGCTATATTG TCTAACCTCT TGGGACGTCA GTTTCCTCAT 780 CTTTGAAATG GGCATGCCAA CATCCAACTT CTCATGAGGA CTTATGGAGA TGATTGCACA 840 GCAGACATTC AGGAAGCTGC CACCATTGTG ACTAGTACCA TTCGGAGGCT GCCACGCTGG 900 AACCTGCGGG CCACAGGCCC TAACAAAACT GTTCCTTTGC TGCAAATGTC TTTTCCAGGT 960 CTTTCCCCCT TTTCTTCACA TTGGGAGTGA CGGTCCTATG GGGAAGAATA ATGTGTTGCA 1020 ATATTAGAGA GTGAGGTTCT TCTTTTTGTT TTTTTCAGCA GGGCTCTTGG GAAGAAACCT 1080 GGCCATTTGA GCCCACTTTA CCTGGGGGTC AGGGTGACTG GGCCTAAAGC AAGACACAGT 1140 CATTGCTGGC TTTTGTTTTG ATAAAACTTA AGGCATGAAA ATATTTGATC AAGAATTCCA 1200 GAAGGGAAGG AGAGAAACTT AAAGTTGGAG AAGGAAGAAC ACTTTGCCTG AGCTGGGGGC 1260 AGGGTCTGGG GTTCTGTTAG CAGCAGGGAC CCTTGCTCCT GCCCTAGGGA GGTAGACAGG 1320 CTGCTATGTC CTCAGCCCAC CCTCTCTGGA GAGCCTGGTG CCCAGGCAGC AACCCCTGCT 1380 CTGAAGAAAC CCTGAGTTCC CCAATGCCTG CCTGCTCTGT AACACAACCC GTGAAACTTT 1440 GCTTGACATT GGTGCAGGGG AACTGGGTGT CCGCTCATGA CAGAGACTGA ATTTCCCCAC 1500 TGAGCCAGCG GAATGAGGAC TGCAAGTCCC CACGGACTGA AAAAAAGTAA GAAAAATGGA 1560 TATTTCTTGC ACACCTGAAC TTGTGACCTC AGATTTTTGC CCACCACCCC TGTGTTGGGA 1620 CCTCTGCCTC ACTGCAAGGG CCAGAGCAAC AGTGCATGAA GCTCCCATGT AGAAAACAGG 1680 TCTTGAGAAG AAATGTCCAT GATAATACAG TGGCTGCAGT TCTGCGAAGG AGAAGGCTAG 1740 ACCTGTGCCG TTTAATACAA CAACCGGTAG CCACACAGGT CTGTGTTTAA ATTCATTCAA 1800 AGGAAATGAA ATTAAAAATT AGCCATGTTT CAAGTGCTCA ATAACCCTTG TGACCAGTGG 1860 CTACGGAGAC TGGCCAGCAC ACAGTTCTAT CACTGCAGAA TGTTCTATTG GTCTACCGGT 1920 TTATTTGTCT AGACAATTCC ATCTAGAGTA AGGAACACGG AACAATTCCC CAAAAAGCAC 1980 TGGAAAAAAA CTTTCTTTAC CCTCTGCACA ACAGGTGAAG ATTACCTCTG TTTTCAGGGA 2040 CAGTTTTAAT GATTCCTAAC AGTCAATGTG GAGGAGGAGG CCTACAATTA TGCATGGGGG 2100 TGGATACAAT TTGTGCGGAG GAAGGATGTG TGTGCAAATA ACTTCTACCT GGCAGGCACA 2160 GGAAGTTTGT GGACACTTTG TTCCTCGAAA CACATCTGTA GGGCCCTCCT TTGGAGACCT 2220 TCCAGGCTGG CCTCTCCAGC CAAGTCTCCA TTGCCCACGT GTCCCAGCCC CTCATGGTGA 2280 TGACTCTGAA AAAAGGTATT TTGGAAAAGC AATGTCACGT GTAAGCCCCA TTTTCTGTTT 2340 GCAGGCCTAT CTCTCCTCTG TGGGGGTTAG TTCTTTGAGA AACATCTCCA GTGTATCCCC 2400 AGCATCCAGA GCCTGGCTAC ACACAGTAGA GGCTTAATAA GTGTTGATGA GATGAATGGG 2460 CACGTTGGCA GATGGCAGGC TGACTTGGGG 2490
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