| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202634692-202635026 | Common:11; Rare:196 | ||||
| chr2:202635790-202636130 | Common:10; Rare:178 | ||||
| chr2:202911607-202912299 | Common:5; Rare:262 | ||||
| chr2:203014627-203014958 | Common:2; Rare:184 | ||||
| chr2:203238890-203239035 | Rare:109 | ||||
| chr2:203239196-203239358 | Rare:98 | ||||
| chr2:203328047-203328558 | Common:4; Rare:284 | ||||
| chr2:203535065-203535511 | Common:6; Rare:257 | ||||
| chr2:205682353-205682502 | Rare:26 | ||||
| chr2:205685291-205685514 | Common:2; Rare:41 | ||||
| chr2:206085813-206085984 | Common:2; Rare:73 | ||||
| chr2:206085996-206086580 | Common:1; Rare:140 | ||||
| chr2:206159341-206159970 | Common:8; Rare:339; Clinvar (benign):2 | ||||
| chr2:206274770-206275100 | Common:2; Rare:153 | ||||
| chr2:206765284-206765676 | Common:5; Rare:181; Clinvar:9; Clinvar (benign):7 |