Tag | Content |
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EnhancerAtlas ID | HS187-13858 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:113895810-113896990 |
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) |
CTCF | MA0139.1 | chr2:113896144-113896163 | TATCCACCAGGGGTCAGCA | + | 6.35 | RREB1 | MA0073.1 | chr2:113896736-113896756 | TGTGTGTTGGTGGGTAGTGG | - | 6.12 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26693 | chr2:113896004-113896910 | Esophagus |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I113138 | chr2 | 113895561 | 113897437 |
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Enhancer Sequence | GGCTAAAACA CATTTCAAGC TTCATTCTGG GGGGAACATA AATTGGCCTT CAACAGGGGG 60 TGTCAAATTG GGGTAAAATT CTTGCAAATC TTGGGGAAAC CAAATAAGTT TTTGTTTTCT 120 CTTCACATAA CTATGAAATC CCTAGCCACA ACAGCAAATC TCAACATGCT TGATATTCAG 180 CCCAGTTCTC TCCATAAAAG TTTCTGGAGA CAATGAAACT CATCTATTGG GTTCTTAGCT 240 TTAAACCTGA GAAAGCTTAA AAACAGGGAA GATTAGCTTT GACGTCTTGC CTCTGGGTCT 300 CCTTCATGTG GAGCTAAAAG AGTAGTTCAG GAAATATCCA CCAGGGGTCA GCATTTTGTA 360 CACACCTGAC TGCTCTGGAA AGTGTTTTTG TTTTTTTTTT TTTAAATAGA AACGGGGTTT 420 CACCATTTTG CCCAGGCTGG TGTCCAACTC CCAGACTCAA GCAATCCGCC CGCCTCAGCC 480 TCCCAAAGTT CTAGCATTAC CGTGTGAGCC ACCACACCCG GCCTGGAAAG AATCTTGACA 540 AGGCAAATAA TCAGTTTGGT TCATGCTCTC AAATTAGTGA AGGTCTGGTT TTTCAAGACT 600 CTCTAGGTGT TTCACTCTAA GGAAAAATTT ATTTTCATTC ACCTATCAAT CAAGCTGAGG 660 TGGGGCCTGA CTCCTGACAA GTATCCAAAT GTTGCCTATT GCCAATGTCT AGTCTCCAAG 720 GGGTGACACC CGAGAAATTC TAAGTCTTCT GTGCCTGCTT TAAAGTCCAC TTCCTGTCAT 780 CCTGTTATCT GTTGCAGACC TTTTACCTGT ATGATTGACT GGTGTGTGGA ATTAACACTT 840 CCCTCCTCGG CCGGGGGAAC ACACCCACAT GTTGGAACTC AGCACAGGAA TCCCAACGGC 900 GTGCCTACAA GGGAAATGCG TACTTTTGTG TGTTGGTGGG TAGTGGACAG AACTCGTAAA 960 AGAGATAGAT AAAATACCCA GGCACTCACT ACAGTGGGGA ATGGATCTGT TCAGGGGCCA 1020 GCTATGCCTG CATTCTTTCC CAGGGACAGT TGACACAGTC AGATGACTCA GGAAACTTGA 1080 TTTGCTTGGA GTCAGAGCAG AGGAAAGATC TTAGTGACCA GGGACCTCAA GCTGCCCCAC 1140 CTGAGCGCTC CACCTCCACT CCAAGGGGCT TCCTGCCAAG 1180
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