| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143816775-143816891 | Common:1; Rare:49 | ||||
| chr8:143937177-143937480 | Common:1; Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:144011315-144011462 | Rare:19 | ||||
| chr8:144019864-144020018 | Rare:26 | ||||
| chr8:144397570-144397813 | Common:1; Rare:102 | ||||
| chr8:144676146-144676457 | Rare:68 | ||||
| chr8:144685726-144686059 | Common:4; Rare:85 | ||||
| chr8:144700078-144700391 | Common:1; Rare:61 | ||||
| chr8:144700468-144700701 | Common:3; Rare:56 | ||||
| chr8:144735645-144735796 | Rare:33 | ||||
| chr8:144875879-144876184 | Common:2; Rare:51 | ||||
| chr8:145002821-145003062 | Common:2; Rare:89 | ||||
| chr9:10907-11098 | Common:1; Rare:38 | ||||
| chr9:114609-114752 | Common:1; Rare:40 | ||||
| chr9:127091-127148 | Common:1; Rare:17 |