Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:231241135-231241238 | Rare:49; Clinvar:2 | ||||
chr1:231528546-231528694 | Common:2; Rare:50 | ||||
chr1:234373363-234373578 | Common:1; Rare:108; Clinvar (benign):4 | ||||
chr1:241848107-241848233 | Common:1; Rare:23 | ||||
chr1:243255815-243256067 | Rare:74; Clinvar:3 | ||||
chr1:244864386-244864686 | Rare:115 | ||||
chr1:246566209-246566507 | Common:1; Rare:100 | ||||
chr10:988206-988470 | Common:3; Rare:95 | ||||
chr10:1048874-1049086 | Common:2; Rare:112 | ||||
chr10:7787964-7788232 | Common:1; Rare:107 | ||||
chr10:7818364-7818520 | Common:1; Rare:35 | ||||
chr10:12195800-12196241 | Rare:119 | ||||
chr10:13300049-13300164 | Rare:42; Clinvar:1 | ||||
chr10:14878676-14878884 | Common:2; Rare:53 | ||||
chr10:14954062-14954363 | Common:1; Rare:74 |