Tag | Content |
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EnhancerAtlas ID | HS146-01893 | Organism | Homo sapiens | Tissue/cell | NHDF | Coordinate | chr10:70884110-70884950 | 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 | chr10:70884122-70884143 | GGAGGAGGGGACGGGGGAGCA | + | 6.44 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCGGGCGTCG CCGGAGGAGG GGACGGGGGA GCAGGGCGGG GAGCGGGGTT AGGCCTGTCG 60 GGCCACCCCT GGGTCTGGGA AAAGCTGGCG GCGCCACCTC TTCCCGGTCT CGGCGAGGCC 120 CGAGCACCTA CGGGCGGCGG CGTGCTCTCC TGGCCATGTC GGAGCCTCTG CCCGCGTTCT 180 TCGACTGCTT GTTGGGGCTC TGGCTGGGGA CTCGGACCCC GCCTCTGCGG GGGCTGGTCG 240 CCGCCTCCCC TTCCTAGGTA GCCAGTCCCT GTTCTCCTCC CGGGCAGCCT CTCTTCCATC 300 CAGGTGGGGC GACCCGGGAG CCCCCCACCT CCGGACTCTT CGGGGGACTT GGGCACTCAG 360 TGTGTCACGA ACTTGATAAA CTCTGATATT TTAAAACCTG ACTATGGTGA CATTCTTTGA 420 TTTCATGACC CCAGTTCAGG CTTTCTGTTG ACACTTGTAA AATGGGAGAG AAAAATAAAA 480 GGACGTTGGA ATGGGGGATA TCTTTAACTC CAGAGACACC CGTTTGGTGC CCGCCGTTTT 540 AAGCATTGGC TCTCATTTCC GTCCGCAAGC TATTTCGCTG AACTTAACGC TCTGGGTTGT 600 TGAAACGGCC TATGAGGCAG AGGAGGGAGG GGAATCAGTG CTCTCACCAC AGTCCGCGGA 660 AGCACTAGCC TGGGCATTGT GGTATTTAGC TGGGTGTCGG CAGTCTCTAG GTTAGATCTC 720 ATTTTACCCA TTTTCTGGTA GTAGTCGTCA GTTCTCTTCA TTTAGCGCCT ACTGTATGCT 780 CTCCTAATAC TACCTGCTCT TCCCAAAGCT CACTGATTCA ATAGACTGCT TGAGACTTTT 840
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