| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:72887130-72887544 | Common:4; Rare:243; Clinvar (benign):4 | ||||
| chr2:72917173-72917573 | Common:16; Rare:259 | ||||
| chr2:73070360-73070810 | Common:6; Rare:173 | ||||
| chr2:73071197-73071545 | Common:6; Rare:300 | ||||
| chr2:73071631-73071864 | Common:6; Rare:175 | ||||
| chr2:73112770-73113270 | Common:12; Rare:336 | ||||
| chr2:73213930-73214365 | Common:3; Rare:252 | ||||
| chr2:73214422-73214656 | Common:5; Rare:129 | ||||
| chr2:73233122-73233606 | Common:5; Rare:317 | ||||
| chr2:73234148-73234416 | Common:5; Rare:178 | ||||
| chr2:73234537-73234768 | Rare:88 | ||||
| chr2:73284240-73284590 | Common:2; Rare:183 | ||||
| chr2:73293500-73293920 | Common:2; Rare:287 | ||||
| chr2:73385560-73386414 | Common:11; Rare:812; Clinvar:44; Clinvar (benign):31; Clinvar (pathogenic):5 | ||||
| chr2:73737184-73737647 | Common:9; Rare:374 |