| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203238899-203239058 | Common:2; Rare:66 | ||||
| chr2:203239210-203239352 | Rare:47 | ||||
| chr2:203328187-203328511 | Common:2; Rare:118 | ||||
| chr2:203867728-203867972 | Rare:42; Clinvar:2 | ||||
| chr2:205682356-205682603 | Rare:43 | ||||
| chr2:205721900-205722244 | Common:16; Rare:58 | ||||
| chr2:206085765-206085975 | Common:1; Rare:60 | ||||
| chr2:206086258-206086303 | Rare:4 | ||||
| chr2:206159345-206160058 | Common:4; Rare:214; Clinvar (benign):1 | ||||
| chr2:206274906-206275058 | Common:1; Rare:53 | ||||
| chr2:206765276-206765668 | Common:3; Rare:107; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165928-207166142 | Rare:42 | ||||
| chr2:207529768-207530119 | Common:3; Rare:95 | ||||
| chr2:207624566-207624728 | Rare:37 | ||||
| chr2:207625176-207625598 | Common:1; Rare:117 |