| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203328206-203328437 | Common:2; Rare:89 | ||||
| chr2:203535155-203535542 | Common:3; Rare:147 | ||||
| chr2:205682356-205682583 | Rare:40 | ||||
| chr2:206085765-206085975 | Common:1; Rare:60 | ||||
| chr2:206086098-206086262 | Rare:22 | ||||
| chr2:206086275-206086303 | Rare:3 | ||||
| chr2:206159345-206159989 | Common:4; Rare:188; Clinvar (benign):1 | ||||
| chr2:206274911-206275057 | Common:1; Rare:51 | ||||
| chr2:206765276-206765661 | Common:3; Rare:106; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165876-207166150 | Rare:55 | ||||
| chr2:207529579-207530119 | Common:3; Rare:138 | ||||
| chr2:207625183-207625421 | Common:1; Rare:71 | ||||
| chr2:207711585-207711886 | Rare:98 | ||||
| chr2:208253884-208254176 | Rare:52 | ||||
| chr2:208254942-208255234 | Common:2; Rare:71 |