| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48241027-48241108 | Rare:21 | ||||
| chr3:48301340-48301622 | Common:3; Rare:89 | ||||
| chr3:48440120-48440323 | Common:1; Rare:85 | ||||
| chr3:48473015-48473249 | Common:1; Rare:54 | ||||
| chr3:48504069-48504319 | Common:2; Rare:78 | ||||
| chr3:48847682-48847955 | Common:1; Rare:77 | ||||
| chr3:48918702-48918944 | Common:2; Rare:126 | ||||
| chr3:49021503-49021720 | Rare:55; Clinvar:1 | ||||
| chr3:49029378-49029564 | Common:2; Rare:131 | ||||
| chr3:49094023-49094148 | Rare:24 | ||||
| chr3:49104708-49104910 | Rare:88; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:49339984-49340289 | Common:3; Rare:112 | ||||
| chr3:49358232-49358522 | Common:4; Rare:145 | ||||
| chr3:49411862-49412445 | Common:2; Rare:210 | ||||
| chr3:49689482-49689605 | Rare:38 |