Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151254955-151255090 | Rare:24 | ||||
chr1:151281222-151281396 | Common:1; Rare:50 | ||||
chr1:151281419-151281706 | Common:4; Rare:88 | ||||
chr1:151281829-151282252 | Rare:107 | ||||
chr1:151282256-151282560 | Common:1; Rare:96 | ||||
chr1:151282659-151282782 | Rare:22 | ||||
chr1:151327349-151327463 | Common:2; Rare:36 | ||||
chr1:151327576-151327873 | Common:3; Rare:61 | ||||
chr1:151328131-151328338 | Common:1; Rare:47 | ||||
chr1:151346807-151347075 | Rare:72 | ||||
chr1:151347206-151347568 | Rare:82 | ||||
chr1:151372652-151372817 | Common:2; Rare:37 | ||||
chr1:151399233-151399292 | Common:6; Rare:14 | ||||
chr1:151399339-151399615 | Common:3; Rare:75; Clinvar (pathogenic):1 | ||||
chr1:151399686-151400018 | Rare:96 |