| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6199515-6199827 | Common:11; Rare:98 | ||||
| chr19:7395022-7395185 | Common:4; Rare:50 | ||||
| chr19:7489006-7489166 | Common:2; Rare:73 | ||||
| chr19:7534046-7534202 | Common:3; Rare:38; Clinvar (benign):1 | ||||
| chr19:7629534-7629848 | Common:5; Rare:111; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7668954-7669093 | Common:2; Rare:40 | ||||
| chr19:7874304-7874469 | Rare:45 | ||||
| chr19:7925496-7925727 | Common:2; Rare:62 | ||||
| chr19:7943641-7943990 | Rare:92 | ||||
| chr19:8308308-8308655 | Common:3; Rare:106 | ||||
| chr19:8321328-8321567 | Common:2; Rare:112 | ||||
| chr19:8390032-8390419 | Common:1; Rare:108 | ||||
| chr19:8444832-8445046 | Common:2; Rare:99 | ||||
| chr19:8514149-8514207 | Common:1; Rare:15 | ||||
| chr19:9140311-9140428 | Rare:31 |