Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150282303-150282602 | Common:3; Rare:62 | ||||
chr1:150321418-150321590 | Rare:55; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150487188-150487461 | Common:6; Rare:69; Clinvar (benign):3 | ||||
chr1:150579057-150579271 | Rare:95 | ||||
chr1:150579582-150579820 | Common:9; Rare:78 | ||||
chr1:150629112-150629388 | Common:1; Rare:81 | ||||
chr1:150629415-150629825 | Rare:93 | ||||
chr1:150926339-150926452 | Rare:35 | ||||
chr1:151070440-151070598 | Common:2; Rare:56 | ||||
chr1:151146561-151146826 | Common:1; Rare:66 | ||||
chr1:151156635-151156691 | Rare:11 | ||||
chr1:151165830-151166201 | Common:3; Rare:104 | ||||
chr1:151254627-151254811 | Rare:48 | ||||
chr1:151281933-151282318 | Rare:114 | ||||
chr1:151327639-151327787 | Rare:27 |