Tag | Content |
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EnhancerAtlas ID | HS040-14293 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr16:88973950-88974560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-5 | MA0063.2 | chr16:88974526-88974536 | ACCACTTGAG | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr16:88974533-88974548 | GAGGTCAGGAGTTCA | + | 6.22 |
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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 |
GH16I088907 | chr16 | 88974381 | 88974450 |
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Enhancer Sequence | GCTTCTCTAT CTTACGAGTG GGGAAACAGA GGCACAGAGA GGCTGAGGAG GGGGAGAGCC 60 AGGTGTGGAT CCAGGTGACC TGGCCCAGCT ACCCCTTCCC CACTGGCCAC AGAGGGCACC 120 TGCAGCCTGG GAACCCCGAG GGGAGGCACC TGCCCTCCTG GCCTCCCTCT GTGGCTTGGG 180 CCTCTGCCAA GTGTCCTTCT CACTCCCCCT GCCCATGACT GACGGTGGCA TCTTCTAATT 240 GTCCCCTCAC CCCAGAGCAG GGGCTTTGCC TGTCCTTCCC ACCCTCGATG GCTCAGGCAC 300 TGGCTCTGGA CACAGTGCGC CCCTCTCTGG GCATGCCTGA GTCTGCCCTG ATGTTGGGTT 360 TCCCTCTATG CGGTTTTCCC CAAAGGGTCT GGGCATGCAG GAACTGGTCA GATGTCTAAA 420 GGAAGAGGAC AGGGAGAGAG TGCCAGTTCC TCCCCCAGCC CTGGCTGCAG CCTCATCTGC 480 CTCCCAAGCT CCCACTCATC AAGAAAGTTC CCAGACCTGC CAGACGTGGT GACTCACACC 540 TGTCATCCCA GCACTTTGGG AGGCCAAGGT AGGCAAACCA CTTGAGGTCA GGAGTTCAGG 600 ATCAGCCTGG 610
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