| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49021502-49021673 | Rare:47; Clinvar:1 | ||||
| chr3:49029365-49029564 | Common:2; Rare:144 | ||||
| chr3:49104738-49104932 | Rare:76; Clinvar (benign):3 | ||||
| chr3:49120767-49121027 | Rare:75 | ||||
| chr3:49132953-49133161 | Rare:40; Clinvar:2 | ||||
| chr3:49166289-49166426 | Common:1; Rare:36 | ||||
| chr3:49340020-49340134 | Common:2; Rare:48 | ||||
| chr3:49358232-49358458 | Common:4; Rare:119 | ||||
| chr3:49411909-49412427 | Common:2; Rare:194 | ||||
| chr3:49429223-49429453 | Common:1; Rare:56 | ||||
| chr3:49469964-49470325 | Common:1; Rare:115 | ||||
| chr3:49674225-49674404 | Common:1; Rare:72 | ||||
| chr3:49689460-49689613 | Rare:47 | ||||
| chr3:49723922-49724214 | Common:9; Rare:101 | ||||
| chr3:49786491-49786756 | Rare:86 |