Tag | Content |
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EnhancerAtlas ID | HS050-65287 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr8:24799260-24800370 |
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) |
KLF5 | MA0599.1 | chr8:24799505-24799515 | GCCCCGCCCC | + | 6.02 | ZNF263 | MA0528.1 | chr8:24799646-24799667 | CCCTCCTTTCTGCCCACCTCC | - | 6.16 | ZNF263 | MA0528.1 | chr8:24799581-24799602 | CCTCCTTCCTCCCCAACCTCC | - | 6.34 | ZNF263 | MA0528.1 | chr8:24799601-24799622 | CTACCCCCTCCTTCTTCCTCC | - | 6.36 | ZNF263 | MA0528.1 | chr8:24799664-24799685 | TCCCTCCCCTTCTCCTTCCCC | - | 6.42 | ZNF263 | MA0528.1 | chr8:24799617-24799638 | CCTCCTTACCCCTCCTCCCTC | - | 6.43 | ZNF263 | MA0528.1 | chr8:24799665-24799686 | CCCTCCCCTTCTCCTTCCCCT | - | 6.47 | ZNF263 | MA0528.1 | chr8:24799546-24799567 | CCCCCTCTTCCTTCCTCCCCA | - | 6.4 | ZNF263 | MA0528.1 | chr8:24799597-24799618 | CCTCCTACCCCCTCCTTCTTC | - | 6.52 | ZNF263 | MA0528.1 | chr8:24799539-24799560 | CCGCCCTCCCCCTCTTCCTTC | - | 6.53 | ZNF263 | MA0528.1 | chr8:24799634-24799655 | CCTCCTCCTCCTCCCTCCTTT | - | 6.83 | ZNF263 | MA0528.1 | chr8:24799614-24799635 | CTTCCTCCTTACCCCTCCTCC | - | 6.85 | ZNF263 | MA0528.1 | chr8:24799658-24799679 | CCCACCTCCCTCCCCTTCTCC | - | 6.89 | ZNF263 | MA0528.1 | chr8:24799661-24799682 | ACCTCCCTCCCCTTCTCCTTC | - | 6.92 | ZNF263 | MA0528.1 | chr8:24799568-24799589 | CCTCCTAGCCCCTCCTCCTTC | - | 6.93 | ZNF263 | MA0528.1 | chr8:24799543-24799564 | CCTCCCCCTCTTCCTTCCTCC | - | 6.96 | ZNF263 | MA0528.1 | chr8:24799604-24799625 | CCCCCTCCTTCTTCCTCCTTA | - | 7.08 | ZNF263 | MA0528.1 | chr8:24799542-24799563 | CCCTCCCCCTCTTCCTTCCTC | - | 7.17 | ZNF263 | MA0528.1 | chr8:24799621-24799642 | CTTACCCCTCCTCCCTCCTCC | - | 7.23 | ZNF263 | MA0528.1 | chr8:24799624-24799645 | ACCCCTCCTCCCTCCTCCTCC | - | 7.86 | ZNF263 | MA0528.1 | chr8:24799630-24799651 | CCTCCCTCCTCCTCCTCCCTC | - | 8.75 | ZNF263 | MA0528.1 | chr8:24799627-24799648 | CCTCCTCCCTCCTCCTCCTCC | - | 9.36 |
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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 |
GH08I024941 | chr8 | 24798943 | 24800313 |
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Enhancer Sequence | CTGCTGCCTC CTCTGCCTCC CTTCTCCACT CCCCAGTGTA AGAGTGAGCT GCAGATAAGC 60 GTTATGTTTA CCAGGTCGTC TCACACTTAA TGTGCACAGG AATCGCCTGG GTGTCCGGTT 120 AAAATGCAGA TTCCGGTTGG GTGGGAGCCC TGGCGGGGGA GGAGGGGGTC CAAAACTGCA 180 TTTCCAACCA GCGGCGAAGG ATGCAAAGGC CGCTTGTCCA CACTCCACCC AGGAATCCGT 240 AGGAGGCCCC GCCCCGCCTC CCGGTGGCCT GGTGCTGGGC CGCCCTCCCC CTCTTCCTTC 300 CTCCCCAGCC TCCTAGCCCC TCCTCCTTCC TCCCCAACCT CCTACCCCCT CCTTCTTCCT 360 CCTTACCCCT CCTCCCTCCT CCTCCTCCCT CCTTTCTGCC CACCTCCCTC CCCTTCTCCT 420 TCCCCTGTCT TCCCCATCCC CACCGCAGCC TCGCCGCACC CTCGGAGTCC AGCTTCTTCA 480 CGTTAAACTC AGACTCCAGA GCGGCTGGGG CGTGGCTCTC GGGGCCAGGC CTCGATGAGG 540 AGGGGCACCG TCCAGAATGA CTGCGGATGC CCCCTTCCCA GCCCCATGTT GGAGTCTGGG 600 GTCCCAGAAC GGGCCGGCTC TGGAGGAGAC ACCTCTAGGC TCCCCGAGTA GGGCAGGCGG 660 CAGAAGTTCC CTAAGAGGAC ACCCCCACAC CACGATGCCC ACCTCCCGAC CCCCGCGCTG 720 CCCACTCAGT CCTCTGGCCA CTGGGTTTCT GGCCGCAGAT CTCGCTGCCG CCTCCTCCTC 780 CGGGCGCGGC CACCTGGAGA AAGATCCAGC AAAACCCTGA TTCCCGGCGC CTCCTCCCTC 840 CCCCGCCCCT GTCCATCTCC AATGGCGGAG CTTTCTGCAA AGCCGCGTGG CTCTACCAGC 900 TCTAAAGTAT TTCAAAAGTC TTGGAACTTG TTCGTTTGCG GGATGGGGGT CTCAATAGTT 960 AAGGAATTGG AAGCTGCAGC ATTTTGCACC TTAGGGGGAG GGGCGGGATC TCTTACTGCA 1020 GGGGCTGTGG AGGCTGCACC CCGCACAGGT TTTGCCCCCG GGGGGCATCC TGGGGTCGTG 1080 CCCACCCACT AAGGAGACTG GAGCGGCTTT 1110
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