| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48241071-48241115 | Rare:13 | ||||
| chr3:48440120-48440324 | Common:1; Rare:86 | ||||
| chr3:48473043-48473257 | Common:2; Rare:49 | ||||
| chr3:48504152-48504353 | Common:2; Rare:53 | ||||
| chr3:48556789-48557173 | Common:1; Rare:86 | ||||
| chr3:48918757-48918900 | Common:2; Rare:84 | ||||
| chr3:49029378-49029564 | Common:2; Rare:131 | ||||
| chr3:49104738-49104910 | Rare:69; Clinvar (benign):3 | ||||
| chr3:49132987-49133150 | Rare:35; Clinvar:1 | ||||
| chr3:49166294-49166426 | Common:1; Rare:33 | ||||
| chr3:49340010-49340289 | Common:3; Rare:98 | ||||
| chr3:49411839-49412213 | Common:1; Rare:124 | ||||
| chr3:49412240-49412423 | Common:1; Rare:67 | ||||
| chr3:49674225-49674402 | Common:1; Rare:70 | ||||
| chr3:49689460-49689573 | Rare:29 |