Tag | Content |
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EnhancerAtlas ID | HS040-05291 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr10:116172370-116173620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr10:116173378-116173389 | CTGAGTCATCC | - | 6.32 | JUNB | MA0490.1 | chr10:116173378-116173389 | CTGAGTCATCC | - | 6.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_47410 | chr10:116170934-116173935 | Panc1 | SE_53388 | chr10:116172227-116173825 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I114412 | chr10 | 116172474 | 116173653 |
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Enhancer Sequence | GTCTGGAGGA AGCAAAAGGA CCAATTCTGC AGTTATCGTC CCATCAAAAT CAGAGGTTCT 60 GTCACTCAGT GAACAGACAC ATCCTCAATT GGTCTTTGTC TCCTACCATT TCCCTCTTGT 120 CTTTATCTCA TACTCCCTGG CTCACCTGCA GGCCCTTTGC CTCCCATTTC CTACCATGAT 180 TTCTAGCCCA TGGGTGTAGA CTATTTCAGA GCTGTTTGGA AACTTAGAGT CAATACTGAA 240 CCCAACCCTG TGGCCTCACA TTCAAGATGC GGGAACCCAG GGAGATGCCA GCCCCAGAGC 300 CCAGACACAG TATCCCAGCA AGGGCTCCTT GTCCCTCTGC TTCTCTTCAG GGCTCTGCTG 360 ACCTATCTCA CTGGGCAGTC CTAACCCCAC ATCATCCTGA GTAAGTCTCA CAGCTTCGCT 420 GAAATTTGCC TGAGTTGTTC TGGTTCCTGG ACATTTGCCA AGGTCTTGAT CTTGGATTCA 480 CTTCCTTGAT GATTTTTTTT TCCTCTTTTT TTTGCTGACT CTTCCTGTGA TTGCTAAGAT 540 CTTCATTTCT CAGATGAGGC TCAAGCAGAA ATGCAGCTGG ACCAGAATTG GCAGCTCCAC 600 GGATTCCTCA GAGTCCCCAG ACCAGGGTAG CTCGGAGAGG AATCATTGCT TCACGCCTGG 660 AAGCACTTCC TTATCAGCAG AGCAATGCCT TCCCCTTCTG GAATGCCCTC CCAGACCCAG 720 CCAAGACTTC CTCTTCCATC AAGGCGCCAA GAACTTCTTG AAAGGATTGA AAAGTTGAAA 780 GGATTCTTGC AATCCTGTGA TACTTTTAGT CAAGATTCAT TTCTTGCTTG ATAACAGAAA 840 ATAAAGACCA TTTTTCTAGG TCTTCTCTCT CCAAATAGAC TACAACTGCA TGTGAACAGG 900 AACTCAACAG AGGTGCCTTG GAAGCCAGTC AGGGCTGGCA GACCTCGGGT GGTTGGGTTT 960 ATAGATTTGT TGGTTGGCAG ACCTGCTGCA TGCCTACGGC CGCTCACACT GAGTCATCCA 1020 CTTCTCTGCA GTGGGTGCTT CCTCCAGCAC CTCGCTGCCA GCAAGCTCAG CTCCCCAAGG 1080 CCTCTTGAGG CTGCCTGGGC ACCTCATCAG ACCAGAAAAG CTCAGCTTCT GCATCCTTCT 1140 TCATTTAGCA TGGCTGAGCT TCTTCCACCT CTCTCACTCC TGGGTTTCAG AACACCACTC 1200 TCTCCTGGTT TACATGCCTG GCTGCAACCT CTTCCAGCTC CTCAGATCCT 1250
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