| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202634784-202635015 | Common:5; Rare:87 | ||||
| chr2:202871408-202871617 | Common:3; Rare:65 | ||||
| chr2:202871623-202871732 | Rare:40 | ||||
| chr2:202911886-202912300 | Common:2; Rare:113 | ||||
| chr2:203014665-203014925 | Common:1; Rare:76 | ||||
| chr2:203238856-203239050 | Common:1; Rare:76 | ||||
| chr2:203239201-203239358 | Rare:53 | ||||
| chr2:203328112-203328553 | Common:2; Rare:151 | ||||
| chr2:205682351-205682603 | Rare:44 | ||||
| chr2:206085772-206085975 | Common:1; Rare:58 | ||||
| chr2:206086281-206086303 | Rare:3 | ||||
| chr2:206159178-206159982 | Common:6; Rare:224; Clinvar (benign):2 | ||||
| chr2:206274517-206274770 | Common:1; Rare:73 | ||||
| chr2:206274918-206275067 | Common:1; Rare:52 | ||||
| chr2:206765270-206765668 | Common:3; Rare:112; Clinvar:4; Clinvar (benign):5 |