| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203328179-203328511 | Common:2; Rare:121 | ||||
| chr2:203535114-203535546 | Common:3; Rare:158 | ||||
| chr2:205682356-205682567 | Rare:38 | ||||
| chr2:206085772-206085975 | Common:1; Rare:58 | ||||
| chr2:206086281-206086302 | Rare:1 | ||||
| chr2:206159389-206159982 | Common:3; Rare:179 | ||||
| chr2:206765273-206765645 | Common:3; Rare:101; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:207165937-207166142 | Rare:39 | ||||
| chr2:207166184-207166380 | Common:3; Rare:84 | ||||
| chr2:207529593-207530116 | Common:3; Rare:138 | ||||
| chr2:208255032-208255228 | Common:2; Rare:51 | ||||
| chr2:208266099-208266302 | Common:6; Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210477568-210477699 | Rare:41 | ||||
| chr2:213284210-213284494 | Rare:93 | ||||
| chr2:214809635-214809991 | Common:3; Rare:128; Clinvar:1; Clinvar (benign):2 |