Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:243255045-243255398 | Common:1; Rare:83 | ||||
chr1:243255747-243256163 | Common:1; Rare:122; Clinvar:4; Clinvar (benign):1 | ||||
chr1:244048218-244048557 | Rare:107 | ||||
chr1:244451708-244452078 | Rare:125 | ||||
chr1:244835115-244835327 | Rare:85 | ||||
chr1:244835561-244835736 | Common:2; Rare:74; Clinvar (benign):4 | ||||
chr1:244862963-244863370 | Common:5; Rare:158 | ||||
chr1:244863934-244863977 | Rare:11; Clinvar (benign):1 | ||||
chr1:244863982-244864182 | Common:1; Rare:67; Clinvar:2; Clinvar (benign):3 | ||||
chr1:244864356-244864723 | Common:1; Rare:145 | ||||
chr1:244969734-244970204 | Common:1; Rare:151 | ||||
chr1:244970251-244970413 | Common:3; Rare:76 | ||||
chr1:244970568-244970846 | Common:7; Rare:79 | ||||
chr1:246507241-246507365 | Common:1; Rare:50 | ||||
chr1:246566142-246566596 | Common:3; Rare:152 |