| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49021889-49022185 | Rare:88; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr3:49025210-49025450 | Common:1; Rare:50 | ||||
| chr3:49104477-49104599 | Rare:43; Clinvar (benign):1 | ||||
| chr3:49104708-49104881 | Rare:76; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:49120783-49120987 | Rare:62 | ||||
| chr3:49340029-49340314 | Common:3; Rare:92 | ||||
| chr3:49358285-49358458 | Common:2; Rare:93 | ||||
| chr3:49411916-49412402 | Common:2; Rare:182 | ||||
| chr3:49429262-49429461 | Common:1; Rare:40 | ||||
| chr3:49674225-49674395 | Common:1; Rare:64 | ||||
| chr3:49689460-49689599 | Rare:43 | ||||
| chr3:49723930-49724254 | Common:10; Rare:116 | ||||
| chr3:49786515-49786749 | Rare:74 | ||||
| chr3:49803148-49803283 | Rare:49 | ||||
| chr3:49856513-49856737 | Common:2; Rare:68 |