Tag | Content |
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EnhancerAtlas ID | HS028-00291 |
Organism | Homo sapiens |
Tissue/cell | Colo829 |
Coordinate | chr1:206654130-206655000 |
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) |
ZNF263 | MA0528.1 | chr1:206654792-206654813 | GGAGCAGGGAGGAGGAAGAGG | + | 6.39 | ZNF263 | MA0528.1 | chr1:206654786-206654807 | GGTGGAGGAGCAGGGAGGAGG | + | 6.59 | ZNF263 | MA0528.1 | chr1:206654789-206654810 | GGAGGAGCAGGGAGGAGGAAG | + | 6.91 | ZNF263 | MA0528.1 | chr1:206654783-206654804 | GGAGGTGGAGGAGCAGGGAGG | + | 7.17 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 206654677 | 206654826 | chr1 | 206654444 | 206654508 | chr1 | 206654628 | 206654823 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I206480 | chr1 | 206654141 | 206655107 |
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Enhancer Sequence | TGGCCTCCCT ATCCCAAGAA GGGGCTTGTG TCCTGCCAAG TCCTTCTCTG AATGATTTAG 60 AGTGCTCACC CTATGCCAAG TGCCAGCAGA ACTCTAGGGG GAGGACACAC ACCCACGCAC 120 AGTTCCTGGA TGTGACCAGG GATGGAGATC CAGGTGGTCT CGTTCTCCAT GCCTCATCTC 180 CTGCTTTCTC TGAGTCTTCA ACTTATCCTT GCCTTCCTTG GGTTCCCTGC CCCAATCTTT 240 GGAACCCCAC TCCCTCCACT CCCTTGTCTT GGGCTAATAA GGGGGGATGG GTTGGAAAAA 300 GAGAGAGACC GGGCAGGAGG AAGCCAAGTG GAAGGGTCTG GAGATGGGGA ATGTGGGAAG 360 ACTTCATTGG CCAGAGCACG ATTGAGAAGT AGGCACAGCA CCCCAAATCC TGGAAGGCAC 420 GAGGCCATGG TACGGGTGAG GGTGGGAGCT CTGCAGCCTA GGGATGCCAC TGGTGACAGG 480 AGTCTTTGGG AACAGAAGAT CAGAGACTGC CCATATGCCT GAAGGCCCCC TCCTCCCGCC 540 ACCCCCAGCC CTTGTCCTCA GGGAGCTCCA GGGAGTTTCC CAGCTGTGGG CTGACTCATG 600 CAGCCCCGCG TGCCTCCTGC TTCGCAGCAG CAACTCAGTT GATGGGGCAG CTGGGAGGTG 660 GAGGAGCAGG GAGGAGGAAG AGGAGCATCT CCAGATAACA GGGATGGAGT CTCCATCCAG 720 ACTGAGCCCC TCTCAAATGG TGACAGAGAG TAGGGTTCAG TCAGCAGAAC TGCAAGTGAA 780 TCTCCTTTGA GCAGAGCTCT GTCCAGGGCA CAGAGGGGGC TCCAGGGGTA GATGTGGCAT 840 CCTGTCATTC AGAGAGGCCC ATGCTTCCTC 870
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