| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:210225268-210225291 | Rare:7 | ||||
| chr2:213284147-213284507 | Rare:112 | ||||
| chr2:215311910-215312139 | Common:8; Rare:94 | ||||
| chr2:215409562-215409900 | Rare:92 | ||||
| chr2:215435643-215435824 | Common:2; Rare:51 | ||||
| chr2:215435839-215435972 | Rare:23 | ||||
| chr2:215436000-215436307 | Common:2; Rare:98 | ||||
| chr2:216081724-216081932 | Common:1; Rare:70 | ||||
| chr2:216498736-216498909 | Common:6; Rare:79 | ||||
| chr2:217978855-217979019 | Common:1; Rare:48 | ||||
| chr2:218125929-218126046 | Rare:20 | ||||
| chr2:218217057-218217248 | Common:1; Rare:68 | ||||
| chr2:218270099-218270573 | Common:5; Rare:150; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:218322982-218323355 | Common:6; Rare:124 | ||||
| chr2:218382185-218382308 | Rare:28 |