| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200889045-200889445 | Common:3; Rare:128 | ||||
| chr2:200963630-200963871 | Common:1; Rare:59 | ||||
| chr2:201071633-201072047 | Rare:85 | ||||
| chr2:201642629-201642764 | Rare:67 | ||||
| chr2:202238472-202238610 | Rare:48; Clinvar:1 | ||||
| chr2:202911886-202912291 | Common:2; Rare:111 | ||||
| chr2:203238691-203239026 | Common:1; Rare:98 | ||||
| chr2:203239240-203239322 | Rare:30 | ||||
| chr2:203328045-203328453 | Common:2; Rare:146 | ||||
| chr2:205682351-205682502 | Rare:26 | ||||
| chr2:206085824-206085961 | Common:1; Rare:38 | ||||
| chr2:206159371-206159695 | Common:3; Rare:104; Clinvar (benign):1 | ||||
| chr2:206274921-206275034 | Rare:42 | ||||
| chr2:206765278-206765668 | Common:3; Rare:106; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207529754-207529988 | Common:3; Rare:76 |