| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46916313-46916391 | Common:2; Rare:20 | ||||
| chr2:46941086-46941244 | Common:1; Rare:62 | ||||
| chr2:47175864-47176268 | Common:6; Rare:144 | ||||
| chr2:47176307-47177044 | Common:8; Rare:339; Clinvar (benign):5 | ||||
| chr2:47344976-47345315 | Common:2; Rare:91 | ||||
| chr2:47345337-47345491 | Rare:35 | ||||
| chr2:47402721-47403230 | Common:3; Rare:218; Clinvar:59; Clinvar (benign):35; Clinvar (pathogenic):1 | ||||
| chr2:47403434-47403705 | Common:3; Rare:97; Clinvar (benign):1 | ||||
| chr2:47782658-47783243 | Common:5; Rare:233; Clinvar:8; Clinvar (benign):23; Clinvar (pathogenic):1 | ||||
| chr2:47783339-47783464 | Common:2; Rare:45; Clinvar:22; Clinvar (benign):17 | ||||
| chr2:47783697-47784068 | Common:7; Rare:88; Clinvar (benign):2 | ||||
| chr2:47811178-47811194 | Common:1; Rare:4 | ||||
| chr2:47904976-47905003 | Rare:4 | ||||
| chr2:47905174-47905285 | Rare:38 | ||||
| chr2:47905328-47905551 | Common:2; Rare:90 |