| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41500626-41500790 | Common:1; Rare:31 | ||||
| chr19:41888074-41888240 | Common:2; Rare:48 | ||||
| chr19:42287363-42287685 | Rare:91; Clinvar:1 | ||||
| chr19:42408069-42408254 | Common:1; Rare:70 | ||||
| chr19:46860833-46861121 | Common:3; Rare:94 | ||||
| chr19:46981733-46981923 | Common:4; Rare:41 | ||||
| chr19:47051732-47052114 | Common:11; Rare:42 | ||||
| chr19:47271001-47271099 | Common:1; Rare:27 | ||||
| chr19:48966402-48966745 | Common:1; Rare:118; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:49637068-49637250 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:49720490-49720758 | Common:2; Rare:56 | ||||
| chr19:53865263-53865369 | Rare:20 | ||||
| chr2:887709-887819 | Common:2; Rare:25 | ||||
| chr2:9495226-9495330 | Rare:18 | ||||
| chr2:12715893-12716088 | Common:2; Rare:37 |