Tag | Content |
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EnhancerAtlas ID | HS051-15915 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr2:113896000-113897010 |
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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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I113138 | chr2 | 113895561 | 113897437 |
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Enhancer Sequence | TCCATAAAAG TTTCTGGAGA CAATGAAACT CATCTATTGG GTTCTTAGCT TTAAACCTGA 60 GAAAGCTTAA AAACAGGGAA GATTAGCTTT GACGTCTTGC CTCTGGGTCT CCTTCATGTG 120 GAGCTAAAAG AGTAGTTCAG GAAATATCCA CCAGGGGTCA GCATTTTGTA CACACCTGAC 180 TGCTCTGGAA AGTGTTTTTG TTTTTTTTTT TTTAAATAGA AACGGGGTTT CACCATTTTG 240 CCCAGGCTGG TGTCCAACTC CCAGACTCAA GCAATCCGCC CGCCTCAGCC TCCCAAAGTT 300 CTAGCATTAC CGTGTGAGCC ACCACACCCG GCCTGGAAAG AATCTTGACA AGGCAAATAA 360 TCAGTTTGGT TCATGCTCTC AAATTAGTGA AGGTCTGGTT TTTCAAGACT CTCTAGGTGT 420 TTCACTCTAA GGAAAAATTT ATTTTCATTC ACCTATCAAT CAAGCTGAGG TGGGGCCTGA 480 CTCCTGACAA GTATCCAAAT GTTGCCTATT GCCAATGTCT AGTCTCCAAG GGGTGACACC 540 CGAGAAATTC TAAGTCTTCT GTGCCTGCTT TAAAGTCCAC TTCCTGTCAT CCTGTTATCT 600 GTTGCAGACC TTTTACCTGT ATGATTGACT GGTGTGTGGA ATTAACACTT CCCTCCTCGG 660 CCGGGGGAAC ACACCCACAT GTTGGAACTC AGCACAGGAA TCCCAACGGC GTGCCTACAA 720 GGGAAATGCG TACTTTTGTG TGTTGGTGGG TAGTGGACAG AACTCGTAAA AGAGATAGAT 780 AAAATACCCA GGCACTCACT ACAGTGGGGA ATGGATCTGT TCAGGGGCCA GCTATGCCTG 840 CATTCTTTCC CAGGGACAGT TGACACAGTC AGATGACTCA GGAAACTTGA TTTGCTTGGA 900 GTCAGAGCAG AGGAAAGATC TTAGTGACCA GGGACCTCAA GCTGCCCCAC CTGAGCGCTC 960 CACCTCCACT CCAAGGGGCT TCCTGCCAAG AGATCAGTAT GTCTGTGTGT 1010
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