| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40505945-40506145 | Rare:43 | ||||
| chr3:40524815-40525023 | Common:1; Rare:60 | ||||
| chr3:41962045-41962365 | Common:4; Rare:79 | ||||
| chr3:42159937-42160216 | Common:1; Rare:55 | ||||
| chr3:42581877-42582081 | Common:2; Rare:71 | ||||
| chr3:42582284-42582354 | Rare:22 | ||||
| chr3:42600366-42600749 | Common:2; Rare:152 | ||||
| chr3:42600875-42601000 | Rare:44 | ||||
| chr3:42773206-42773334 | Common:1; Rare:41 | ||||
| chr3:42804272-42804671 | Common:2; Rare:112 | ||||
| chr3:43621907-43622322 | Common:2; Rare:121; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690811-43690993 | Common:3; Rare:97; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44338095-44338199 | Common:2; Rare:38 | ||||
| chr3:44338378-44338518 | Common:1; Rare:50 | ||||
| chr3:44338675-44338807 | Common:3; Rare:48 |