| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:45689150-45689455 | Common:2; Rare:103 | ||||
| chr3:46979572-46979839 | Common:1; Rare:59; Clinvar:1 | ||||
| chr3:47164087-47164256 | Rare:43 | ||||
| chr3:47380690-47381053 | Rare:115 | ||||
| chr3:47781814-47782054 | Rare:97 | ||||
| chr3:48301348-48301490 | Common:1; Rare:37 | ||||
| chr3:48440035-48440276 | Common:1; Rare:73 | ||||
| chr3:48473051-48473287 | Common:2; Rare:47 | ||||
| chr3:48918813-48918900 | Common:2; Rare:50 | ||||
| chr3:49007066-49007427 | Common:2; Rare:134 | ||||
| chr3:49021503-49021764 | Rare:60; Clinvar:1 | ||||
| chr3:49022011-49022174 | Rare:55; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49132946-49133143 | Rare:37; Clinvar:2 | ||||
| chr3:49340010-49340102 | Common:1; Rare:48 | ||||
| chr3:49411917-49412445 | Common:2; Rare:196 |