| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49007153-49007426 | Common:2; Rare:112 | ||||
| chr3:49021502-49021710 | Rare:52; Clinvar:1 | ||||
| chr3:49029372-49029564 | Common:2; Rare:136 | ||||
| chr3:49104708-49104878 | Rare:76; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:49132998-49133124 | Rare:30; Clinvar:1 | ||||
| chr3:49166286-49166443 | Common:1; Rare:41 | ||||
| chr3:49171470-49171636 | Common:2; Rare:37 | ||||
| chr3:49340013-49340129 | Common:2; Rare:53 | ||||
| chr3:49358217-49358486 | Common:4; Rare:144 | ||||
| chr3:49411839-49412215 | Common:1; Rare:125 | ||||
| chr3:49429269-49429419 | Rare:33 | ||||
| chr3:49674225-49674402 | Common:1; Rare:70 | ||||
| chr3:49689461-49689613 | Rare:47 | ||||
| chr3:49723922-49724219 | Common:9; Rare:103 | ||||
| chr3:49786501-49786769 | Rare:87 |