Tag | Content |
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EnhancerAtlas ID | HS040-09240 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr12:133047500-133048370 |
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) |
MEOX1 | MA0661.1 | chr12:133048257-133048267 | GTTAATTAGC | - | 6.02 | SPI1 | MA0080.4 | chr12:133047843-133047857 | AAAAAGCGGAACTC | + | 6.25 | ZNF263 | MA0528.1 | chr12:133047634-133047655 | GGAGGAAAAGGGAAGGGGGGG | + | 6.73 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_10775 | chr12:133047106-133048987 | CD19_Primary |
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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 |
GH12I132470 | chr12 | 133047235 | 133049786 |
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Enhancer Sequence | GGAAGAAATA CACACACATG CGTACACACA CACGTATACA CACACATGCG TACACACACG 60 TATACACACA CATGCGTACA CACACGCGTA TACACACACA TGCGTACACA CACATACAGG 120 AGTGTTATTC CACAGGAGGA AAAGGGAAGG GGGGGAGAGA GAGAGAGACA GAGAGAGAGA 180 AAGGAGAGAG AGAGAAGGGA AGGGAAGGGA GGGCAGGGCA GGGCAGGGCA GGGCAAGCCC 240 GCCATTTGTG AGGACACGAT GAACCTGAAG GGCATTTGTG GTAAGTGAGA TAAGCCAGGC 300 ACAGAAAGAC AAACAGCACA TGGCCTCACT CGAGTGACGT GTGAAAAAGC GGAACTCACA 360 GAAGCAGAGT GAACAGTGGC TGTCAGGGCT GGAGGGGACC GGGAGTTGAG GGTCACAGGG 420 AACAAAGGTG CAGTTATGAG ATTAGCGGGT TCTAAGATGT AATGAACGTG GTGACTACAG 480 CTGATAAGAA TGTGTCCTTT ATTTATTTAT TTTGAGATAG GGCCTCCCTC TGTCGCCCAG 540 GCTGGAGTGC ACCGCAACCT CCGCCTCCCA GGCTCAAGTG ATTCTCCAGC CTCAGCTTCC 600 CAAGTAGCTG GGACCACAGG TGTGCACCAC CACGTCCAGA TAATTTTTTT ATATTTGTAG 660 AGACAGGGTC TCACTATGTT GCCCAGGCTG TGTGTCCTCT ATTTAAAATT TAGTGTTCTC 720 ACCACAGAAA GAAGTAACCA TGTAAGGTGA TGGGTGTGTT AATTAGCCCA ATTGTGGGAC 780 TCATTTCACA ATGCCTACGT GTGTCAGGTT GTGATGCTGC ATACCTTGAG TGCACACCGT 840 CCTGAATTGT CAACTATACC TCAATAAAGC 870
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