| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6361751-6361897 | Rare:64; Clinvar (benign):1 | ||||
| chr19:6393379-6393530 | Common:1; Rare:44 | ||||
| chr19:6737276-6737314 | Rare:12 | ||||
| chr19:7395022-7395199 | Common:4; Rare:56 | ||||
| chr19:7629535-7629848 | Common:5; Rare:111; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7920240-7920364 | Rare:57 | ||||
| chr19:7943627-7943995 | Rare:103 | ||||
| chr19:8005514-8005821 | Common:1; Rare:108 | ||||
| chr19:8321322-8321702 | Common:2; Rare:153 | ||||
| chr19:8390056-8390348 | Common:1; Rare:72 | ||||
| chr19:8444807-8445108 | Common:2; Rare:136; Clinvar (benign):1 | ||||
| chr19:8514154-8514222 | Common:1; Rare:19 | ||||
| chr19:8832294-8832341 | Rare:18 | ||||
| chr19:9140311-9140439 | Common:1; Rare:36 | ||||
| chr19:9324066-9324290 | Common:5; Rare:110 |