Tag | Content |
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EnhancerAtlas ID | HS187-01877 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:172861680-172863180 |
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) |
FOXP1 | MA0481.2 | chr1:172863017-172863029 | AAGTAAACAGAA | + | 7.22 | FOXP2 | MA0593.1 | chr1:172863017-172863028 | AAGTAAACAGA | + | 6.32 | IRF1 | MA0050.2 | chr1:172861706-172861727 | CTCCTCTTTCTCTTTTTCTTC | + | 6.24 | RREB1 | MA0073.1 | chr1:172862898-172862918 | GGGTTGGGGCTGAGTGGGGG | - | 6.36 | ZNF263 | MA0528.1 | chr1:172861710-172861731 | TCTTTCTCTTTTTCTTCCTCT | - | 6.22 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_34373 | chr1:172860985-172869043 | HCT-116 | SE_37971 | chr1:172861577-172870576 | HUVEC |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I172892 | chr1 | 172861752 | 172869066 |
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Enhancer Sequence | GGGTAAGCTT TCCATTCTTT CCATTCCTCC TCTTTCTCTT TTTCTTCCTC TATCAAATGG 60 AAAGGTGAGG AAAGGCAGAC ATTGGCCCAT TCCACCCCCA CCTGCAGTGT GCTCCTCCTG 120 TCCAGGATCT GCATTTCTTG GCCTGAAGGT TTCTAAGCCT TTGGGAGGAT GCTTTACCTA 180 GGTTTGTGTC AGGACAGAAG TCCCAGAATG TCTATTCACC CCCTAGAAGA GCCCTCAAAC 240 AATGACGGAA GAAATTTGGT GTATACATTC CTCCCTGGAC ACACAGTAAG ATTCCTCTGT 300 GGCAGCTCCC AGGCTGGTTC CTGGGGCTTT CCACAGGATT ACTCTTTGGT CTGCTCCATT 360 GTAGTAACCC TTGGTTGCTC CCCTTTCCTG TCTCACTTCT CCACTCCCCT GATGACTTTC 420 CAAATAAACT ATCAGTATGT GAATCTTTGT CTCAGTGTCT TCTTTTAGGG GATCCCATGC 480 TAAGAAGGAA TGGGTTCATA AATGATGGAA CCAGGCTCTA GAAAATCAGG GAGGAATGAA 540 AATAGAAGCA TATATTGAGG GACTACTCCA GGGGAAGAGG AAGGATGTTT CACAGAGTTG 600 GAAAGAGCAG TCTATTGATG GCCAAGCTAG CTGCCTTGCC TATGTCATCC TGCCCTCTCT 660 GAGTTTTTCT TTTTTCATTC CAGGCCTAAC CAACATAATC TCAGAATTCT CATTATCAGG 720 TCTACTGGAA AATCCTGTAT GGCAAGGCTG TTGGGCTGTC CTTTCCTTTC CAAGGCTGAT 780 GATATCTCTG GCTTTCTTGA TAGCTGACTG AGGAGGAGGA AGCCACCAGT GCTAACATGC 840 ACTGTGATTC TGGGAAGAAG GGTATTCCCA AAGCACAGAG ACACCAATAA CTGTCATTTT 900 CAGAATTACT GTGATGGTGC TGGTGGTGAA GGTAACCCAG AATAGTTGCC TGCATATTTA 960 AAGGACAATG AGGTTTCTGG AACCATGGAG ATGGGCCTGG GCAGGAATAG TCTTTTTCCT 1020 GAAACGACAT GAGCTTTGCC AACAAAAACA CAGAACTCTG GTAGCTTAGC CTTATTCTTG 1080 CACCAAGGAG AGTAAGGCTG GTCTTTGGCT CTTTGCCTGC TGGTGTTTGG CTCCTTGCCT 1140 GTTGATGTAT CCTTATCCTA ATTAGACCTT CTTTATGCTA CAAGGCAGAA TCCCAGAGAG 1200 GAGGCTGTGC ATGAGGTGGG GTTGGGGCTG AGTGGGGGGA AGGTGTCTTT AGTAGACTCC 1260 TGTGAAAATA TCTTTAAAAG TCTAGAGAAC AAGGAGAGTA AAGCTGACTA ACATTCAAAA 1320 GGACCTCCTA GCATTCCAAG TAAACAGAAA CATCCAGATT TCAGTAAAGA TTAAGACGAG 1380 ACTTTCTGAT AAGATTTGAT ACGTCGAGAT CACCTTTGTG GCCAGATAAC AATAAAACTC 1440 TTTTCCTGCA GTAAACTAAC TACCTAGGCT ACACAAATAA TGTGAGAAAT AGTTTCCAAA 1500
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