Tag | Content |
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EnhancerAtlas ID | HS062-06953 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr17:34074960-34076120 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr17:34075821-34075842 | AGTGGAGGAGAGGGAGGGTGG | + | 6.19 | ZNF263 | MA0528.1 | chr17:34075824-34075845 | GGAGGAGAGGGAGGGTGGTGG | + | 6.27 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGATCTGAGG GGGCAAGGGT GAGGTTAAGG GCGGGGTGGA GGGCAGCCCC TCTTCCTGGA 60 CCAGCTCGCG GGCTTCCGGC ACTCACTCAG GGATGCTCTC ATCCATGTAC CCATCCACAC 120 GTAGATGTAT GTGTGTGCTG TAAAAAGGCA GCCCGAATCT CCTCCTCCAT GACTGGCATC 180 AGATAACACA TGCGGTCAAG GTGGGAGCCA GGCTGAAAGC TGTCCCACAA CTGGTCAAGG 240 GATCCCAAAG CCTGCCCCCA GAGCGCTCCT TTTGCTGTAA ACGGTTTTGC ATCTGTACAT 300 GCCTGTACCC AAAACAGGGC CCTAATGCCA CTGGCTTTGC CCCTGTGGCC TGTGTGGAGA 360 GCCCATGGGA GTCCTGGTCC CACTCCACCC TCAGGCAAGT CACATGTCTC TTCAAGCTTC 420 AGCTTCCTGT GTTGGGAAGT GGGGCCACAG GTTCTTGCCC CTATCTGCAT CACAGGGCTA 480 CTGCCTCAGG TCTAGGGGAG GGCCCAGAGA GCTGGCTCTG CTCCCAGGTT TGGCCTGTGC 540 CCAAGGAAAT GGCTGGGCCA TGCCCCGAGC TGCTGGCCGC TCATGTGGGT ACAGACCGTT 600 TCTGGTGAGG CACAGCCAGG TATTGGGGTA GGAGGCACAT TTTCAGACCT GTGCTGCTAC 660 TCACTCTGCT GAATGTACCC CCAGGCAAGT GGTAGGGGTG GAACTATGGG GTCCATGTGG 720 CTGGGGCCGT GCACTGAAAC CAAACTTGGG GTTCTCAAGC TGCTTCCTCT AATCAAGTCT 780 GTGGGTGGAG TGGAATGGAA AAGTGTGATC ACCCTTCTCC ATACCCCACT CTGCCTGAGA 840 ACATGCTCTA GATTAGGCTA CAGTGGAGGA GAGGGAGGGT GGTGGCTCTG GCTGCCCTGA 900 TGGGAGGAGG AGATAGGCTT GCCACCTTTG CCAGGAATCT CCTGGAATTC TCCCAGGGTG 960 AGAAGGAGAG CTCCAAGGCC TGATGGCTTG GGGTGAATGA TGACTTACTG TCATTGTCCT 1020 CAAGCCTGGA CAAAGTCCCA TATTCTGGGA GGTGTCATTG TTCCAAGCCT GGGCAAGGTC 1080 CCATATTCTG GGAGACTTAG TGTCATTGTC CCAAGCCTGG GCAAGAAACC CTATTCTGGG 1140 GGTCCCTTGA CCCCCAGCCT 1160
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