| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48446630-48446743 | Rare:40 | ||||
| chr3:48504144-48504288 | Common:2; Rare:42 | ||||
| chr3:48556778-48557173 | Common:1; Rare:91 | ||||
| chr3:48561106-48561295 | Rare:49 | ||||
| chr3:48563766-48563821 | Rare:9 | ||||
| chr3:48847781-48847965 | Rare:64 | ||||
| chr3:48918724-48918930 | Common:2; Rare:115 | ||||
| chr3:48989721-48989870 | Rare:39 | ||||
| chr3:49007028-49007429 | Common:2; Rare:139 | ||||
| chr3:49018517-49018618 | Rare:42 | ||||
| chr3:49021500-49021725 | Rare:55; Clinvar:1 | ||||
| chr3:49022009-49022174 | Rare:55; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49029346-49029512 | Common:1; Rare:119 | ||||
| chr3:49104615-49104880 | Common:1; Rare:108; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49120847-49121187 | Rare:93; Clinvar:1 |