| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49104720-49104919 | Rare:86; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:49120773-49120997 | Rare:66 | ||||
| chr3:49132979-49133143 | Rare:35; Clinvar:1 | ||||
| chr3:49166289-49166426 | Common:1; Rare:36 | ||||
| chr3:49171332-49171636 | Common:3; Rare:60 | ||||
| chr3:49199423-49199537 | Rare:22 | ||||
| chr3:49340013-49340122 | Common:2; Rare:53 | ||||
| chr3:49358285-49358486 | Common:2; Rare:108 | ||||
| chr3:49411886-49412423 | Common:2; Rare:195 | ||||
| chr3:49429262-49429440 | Common:1; Rare:40 | ||||
| chr3:49470029-49470319 | Common:1; Rare:85 | ||||
| chr3:49674220-49674395 | Common:1; Rare:64 | ||||
| chr3:49689460-49689613 | Rare:47 | ||||
| chr3:49723949-49724139 | Common:4; Rare:63 | ||||
| chr3:49786501-49786781 | Rare:88 |