Tag | Content |
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EnhancerAtlas ID | HS040-21783 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr20:2235880-2237320 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr20:2236999-2237010 | ACAGGGTGTGG | - | 6.14 | SOX10 | MA0442.2 | chr20:2236502-2236513 | GTCTTTGTTTT | - | 6.14 |
| | 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 |
GH20I002255 | chr20 | 2236464 | 2237332 |
| Enhancer Sequence | ATTGTGTTTC TACCTCTAAT GAGAACAAAA TAGAGAAGGA GGAGCCAGGC ATACAGCCGA 60 ATTTGATCTC ACATACCAAG AAGAGGAAAC TGAGGCCTGG AGAGATAAGG CCACCCACCC 120 TTACCAGACC CTTTTACCAA GGTATCCAAA AACAGCAGCA GAGACTAAAA ACACACTTTA 180 CTGGAACCCA AAGAGGTTTT CTCTAAGTCA AGCTAACCCA GCCTCAATCA ATAGAGCCAG 240 TGAGAAAACA TTGATTGTCA AAACTCTGCT CTTCCTTCAG GGTCCATCTC AGATGCGGTC 300 TCTTTCATGA AACATTTCTG ATCTTTCCAG CCAGCGTCAA TCTTTTCCTA TTATTTCTGT 360 CCTGGATTGG GTTGTAGCAT TTACCTCATT CTCTCTTGGA CTATTTGTAC ACATGTCTTG 420 TCTCCTGAGA TATGTGGTAA ACTCCTGGGA AGACAGGCTT GGCTTGTTTC TTTTTGTTGG 480 CGATGGTGGG AGGGAGGCTT ATATAAATTA GTTGCTCAGT AAAAGACCAA ATTGAGTTGT 540 GTTGCTTCTA AGGAGAAAAG GCCTGAGGAA CTCCGTGTTT CCTGAAGCAA CTGACAGGCA 600 TATTCATATT GAATTTACAA ATGTCTTTGT TTTACGGTAG TATACATTTG ACAATGAGAT 660 CATGGGCCCC AGAGTCTCTG TAGATAAAGA GACCCTGGGT TGTACTTTCT TGGTAGGATG 720 CCCAAGGATG TGACGGCTGC TCTCCCTGCC ACACCCAGAG TTGGTGGCTA ACCCTTTTCC 780 TGCTTCTGTG TCACTTCGTG GTTCCATGGT AGACTCAAGA GCTACTCTGG GGCAGTCTTG 840 GAACTCTTAA GTTAAGCTAG GGTAGAGGAA TGAAGAGGAA CGGAAAGAGG AAGAGTGCCA 900 TGGCATGGGA AGGCTAAGGT CTCCTGTCTC CTTCTTCCTT CCTGCTTCTT GCCCAGGGGG 960 CCCAGGCCCC CAGCTGGCAG CCACAGCAGC ATGACAGTAC CAGCAAGGGC GTGTGCACGC 1020 ATCTTTCCTC AGCTTCCCTT GCAGTTGGTC TGTCCTGTCC TGCCCTCTCC TCCACCACTC 1080 ACCCTCCCTG CACGCAAGGT GACTGCAGAG TGGCAAGGCA CAGGGTGTGG GCAAAACGTG 1140 TCCTGTCACC ACTTGGGCAG GGCTCAGCCT TGGAAAACAC AGAGGTACTT GAAGTCCCCG 1200 GGGCTGTCAT ACACCAAGAT CCGGTAGTTG TACATTATAT GCCCTTTAAG GGAGCAGTCC 1260 TGACCTCAGG AAGAATTTCT TTGGACTTGG GAATATGAAT AAAATAAAAT CTTTTCTGGC 1320 CAAGCGCGGT GGCTCACACC TGTAATCCCA GCACTTTGGG AGGCCAAGGC GGGCGGATCA 1380 CCTGAGGTCA GGAGATCGAG ACCATCCTGG CTAACATGGT GAAACCCTGT CTCTACTAAA 1440
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