Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42924326-42924487 | Common:1; Rare:52 | ||||
chr1:42936683-42936771 | Rare:17 | ||||
chr1:42941088-42941255 | Rare:36 | ||||
chr1:42957401-42957433 | Rare:6 | ||||
chr1:42957909-42958014 | Common:2; Rare:26 | ||||
chr1:42958016-42958332 | Common:5; Rare:106 | ||||
chr1:42959677-42959745 | Rare:10 | ||||
chr1:42963908-42964234 | Common:2; Rare:58 | ||||
chr1:42967136-42967410 | Common:6; Rare:38 | ||||
chr1:43021719-43021801 | Common:1; Rare:11 | ||||
chr1:43206823-43207160 | Common:1; Rare:88 | ||||
chr1:43207694-43207850 | Common:1; Rare:29 | ||||
chr1:43348508-43348776 | Common:1; Rare:45 | ||||
chr1:43348800-43349280 | Common:2; Rare:153; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:43349335-43349550 | Common:1; Rare:64; Clinvar:1; Clinvar (pathogenic):1 |