| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203328031-203328509 | Common:2; Rare:171 | ||||
| chr2:203535179-203535557 | Common:3; Rare:148 | ||||
| chr2:205682356-205682466 | Rare:20 | ||||
| chr2:206085764-206085987 | Common:1; Rare:64 | ||||
| chr2:206086272-206086417 | Rare:24 | ||||
| chr2:206159339-206160090 | Common:4; Rare:224; Clinvar (benign):1 | ||||
| chr2:206213338-206213567 | Rare:31 | ||||
| chr2:206274549-206274728 | Rare:49 | ||||
| chr2:206274909-206275065 | Common:1; Rare:55 | ||||
| chr2:206443318-206443590 | Common:1; Rare:99 | ||||
| chr2:206765276-206765668 | Common:3; Rare:107; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165937-207166106 | Rare:28 | ||||
| chr2:207166184-207166409 | Common:3; Rare:101 | ||||
| chr2:207529547-207530131 | Common:3; Rare:148 | ||||
| chr2:207624548-207624637 | Rare:19 |