Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150487209-150487491 | Common:8; Rare:140; Clinvar (benign):6 | ||||
chr1:150549248-150549446 | Rare:97 | ||||
chr1:150578380-150578790 | Common:4; Rare:166 | ||||
chr1:150579055-150579931 | Common:23; Rare:503 | ||||
chr1:150629072-150629407 | Common:1; Rare:168 | ||||
chr1:150629417-150629833 | Rare:189 | ||||
chr1:150697065-150697471 | Common:2; Rare:139 | ||||
chr1:150876415-150877150 | Common:11; Rare:335 | ||||
chr1:150926138-150926464 | Rare:197 | ||||
chr1:150926500-150926710 | Common:1; Rare:52 | ||||
chr1:150974614-150974942 | Common:4; Rare:176 | ||||
chr1:151006750-151007130 | Rare:108 | ||||
chr1:151008200-151008608 | Common:4; Rare:192 | ||||
chr1:151047656-151047857 | Common:2; Rare:104 | ||||
chr1:151048514-151048619 | Rare:39 |