| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203328070-203328426 | Common:2; Rare:130 | ||||
| chr2:203535208-203535546 | Common:3; Rare:138 | ||||
| chr2:205682356-205682603 | Rare:43 | ||||
| chr2:205682804-205683180 | Common:2; Rare:55 | ||||
| chr2:205763616-205763680 | Rare:15 | ||||
| chr2:206085824-206085981 | Common:1; Rare:43 | ||||
| chr2:206086281-206086384 | Rare:18 | ||||
| chr2:206159366-206160057 | Common:4; Rare:210; Clinvar (benign):1 | ||||
| chr2:206274909-206275057 | Common:1; Rare:52 | ||||
| chr2:206765276-206765658 | Common:3; Rare:105; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165928-207166099 | Rare:31 | ||||
| chr2:207166184-207166380 | Common:3; Rare:84 | ||||
| chr2:207167223-207167557 | Common:2; Rare:67 | ||||
| chr2:207529774-207530126 | Common:3; Rare:96 | ||||
| chr2:207625182-207625565 | Common:1; Rare:107 |