Tag | Content |
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EnhancerAtlas ID | HS095-29189 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr8:24799120-24800260 |
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 | GCTTAAGCGA CCTTCCCTCC TTCGCCTCCC AACGCTCTGG GATTACACGT GTTAACCACC 60 GCGCCAGCCC TGCCCTTAGC TTATAAGGGA AAGGGAGAAG CTGCTCCTCT TCTCGCCTCT 120 CTTCTGTTAC AAAAAGCAAC CTGCTGCCTC CTCTGCCTCC CTTCTCCACT CCCCAGTGTA 180 AGAGTGAGCT GCAGATAAGC GTTATGTTTA CCAGGTCGTC TCACACTTAA TGTGCACAGG 240 AATCGCCTGG GTGTCCGGTT AAAATGCAGA TTCCGGTTGG GTGGGAGCCC TGGCGGGGGA 300 GGAGGGGGTC CAAAACTGCA TTTCCAACCA GCGGCGAAGG ATGCAAAGGC CGCTTGTCCA 360 CACTCCACCC AGGAATCCGT AGGAGGCCCC GCCCCGCCTC CCGGTGGCCT GGTGCTGGGC 420 CGCCCTCCCC CTCTTCCTTC CTCCCCAGCC TCCTAGCCCC TCCTCCTTCC TCCCCAACCT 480 CCTACCCCCT CCTTCTTCCT CCTTACCCCT CCTCCCTCCT CCTCCTCCCT CCTTTCTGCC 540 CACCTCCCTC CCCTTCTCCT TCCCCTGTCT TCCCCATCCC CACCGCAGCC TCGCCGCACC 600 CTCGGAGTCC AGCTTCTTCA CGTTAAACTC AGACTCCAGA GCGGCTGGGG CGTGGCTCTC 660 GGGGCCAGGC CTCGATGAGG AGGGGCACCG TCCAGAATGA CTGCGGATGC CCCCTTCCCA 720 GCCCCATGTT GGAGTCTGGG GTCCCAGAAC GGGCCGGCTC TGGAGGAGAC ACCTCTAGGC 780 TCCCCGAGTA GGGCAGGCGG CAGAAGTTCC CTAAGAGGAC ACCCCCACAC CACGATGCCC 840 ACCTCCCGAC CCCCGCGCTG CCCACTCAGT CCTCTGGCCA CTGGGTTTCT GGCCGCAGAT 900 CTCGCTGCCG CCTCCTCCTC CGGGCGCGGC CACCTGGAGA AAGATCCAGC AAAACCCTGA 960 TTCCCGGCGC CTCCTCCCTC CCCCGCCCCT GTCCATCTCC AATGGCGGAG CTTTCTGCAA 1020 AGCCGCGTGG CTCTACCAGC TCTAAAGTAT TTCAAAAGTC TTGGAACTTG TTCGTTTGCG 1080 GGATGGGGGT CTCAATAGTT AAGGAATTGG AAGCTGCAGC ATTTTGCACC TTAGGGGGAG 1140
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