| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48918760-48918989 | Common:2; Rare:133 | ||||
| chr3:48989738-48989946 | Rare:51 | ||||
| chr3:48990147-48990250 | Rare:24 | ||||
| chr3:49021503-49021746 | Rare:57; Clinvar:1 | ||||
| chr3:49022011-49022174 | Rare:55; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49029252-49029328 | Rare:24 | ||||
| chr3:49029352-49029577 | Common:2; Rare:164 | ||||
| chr3:49104679-49104910 | Common:1; Rare:97; Clinvar:1; Clinvar (benign):6 | ||||
| chr3:49120894-49121172 | Rare:62; Clinvar:1 | ||||
| chr3:49132836-49133103 | Rare:61; Clinvar:2 | ||||
| chr3:49166284-49166434 | Common:1; Rare:40 | ||||
| chr3:49358142-49358174 | Rare:14 | ||||
| chr3:49411844-49412432 | Common:2; Rare:212 | ||||
| chr3:49429272-49429408 | Rare:28 | ||||
| chr3:49674222-49674402 | Common:1; Rare:70 |