Tag | Content |
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EnhancerAtlas ID | HS095-24414 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr5:106849370-106850800 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr5:106849539-106849560 | GGATGAGCAGAGGGGAGAGGA | + | 6.35 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCTGCAAAAC TGCTTGTGAT TCATAAGATG TTTCTGAACA GAAAGAGGCT GGTGGTATCC 60 GTCCATTAAA AACAGGCTCT TCACTGAGAT ACTGGGCTCT ATGTTGTTTT TTCTTTAATT 120 CCAAGAACTC AGAGGGAGGG ACAGAAATGC TCAGTGGATA GCTATGGATG GATGAGCAGA 180 GGGGAGAGGA AATAAGTGTG ACATGTAAGC TGATCTGTGT GATACAGTAA GAGAGGAGGA 240 TGTTGCGAGG TAGGCCTGGG TCAGCGTCGC ACAGGTGTTG GTGCTGGAAT CTGTTTCCTG 300 AACGTCTGTG CTGAACACAA AAACAACCAG GACCACGGGG GTAGAAATAA CAAGTCTCAC 360 ATTGCTTTAA CAAAAACAAC AAAATAAAGC ACTATTCCTG TTTTCTGCTG TTTCTGTCAT 420 GCTAAATGAC ATCCCTGTCC CCAGGTTTAG CTATGTATTT TGCCACCTCA TAAAACCCCA 480 ATCAATCTTC CCTTCTCTTC TGGCACCAAG TTATGAAGCA TCCCTGATCT TCCAGACCTA 540 AAGAAAACAG CAGAGAGACG GGGCTCCTCA TCAGGTAGAG GTTTTCTTTT TTGTCAGAAT 600 TTGAGACTAA ATACAGATTG GAGTATTCAC TTGGGAATTC AACAGAGATC CATCTTAAGG 660 AACATTCCAA ATACACAATC AGAAAGAAAG CATTTGTGTG CTTTTCTGCT CCTAGGAAAA 720 TGCAGAGAGA AAGAAAAGGT TACTGTTTCA TGTGAACTGA TTTCTCCCTT CTCTGTGGTA 780 GGCAGAGAAC ACATCATCCC ACCTGGAACG TGAGTCATTT GTGAAATGCT TGTTTTAAAT 840 TCAAACTTCT CCACAACCTG ACGAGTGTGT GGGAGACCCA AGGAAGCTGA CATACAAGGG 900 CAGATTTATT TTTCTGCCAG AAGGAACCAT CAACACAAAG GCCAATGGTA ACCCTAAAAA 960 TGGAAATGTG CTAACCCTTT TTATTGTCAA GCAAATAAAA AAATTATTCT TCAAAGGAGG 1020 AGAAACAAAT GCTCAGACCC TCCAATGGCT TCCTGTCTCA TTCAGAGTAA AAGCCCAAGT 1080 CTCTACAAGG ATTCTATGAG GTCCTACGTG ACCTGCCTCC CGTCTCCTCT TTCCTTACTT 1140 CACTGACTTA ATCTCCTACC TCTCCTTATG ATATAGGAGT TAAGAAGAAA TTAGGCAGAT 1200 AGCAAGGGCA TGGGAGTCCT TGATAAGGCT TTTCTTTTTA ATGAAAAACA GAAAAACAGC 1260 CCCAAATCAT TTTCTAACAA AGAGCTGCCT GCAAGCTAGG AGCTTGCATG GGTGAATGCC 1320 GGCAGGAACT AAGGACTAGA CATGTGCAGG ATGGCAGCTC CATCTTCCTT TCTCTGCCAG 1380 CCACGTGTAC TGTCAAGGAG CAGACAAGAT GGTCCCAATC AACTAGAAAG 1430
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