| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7535564-7535783 | Common:3; Rare:78 | ||||
| chr19:7629531-7629871 | Common:5; Rare:120; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7637024-7637144 | Common:2; Rare:41; Clinvar (benign):1 | ||||
| chr19:7903747-7903921 | Rare:62 | ||||
| chr19:7920150-7920547 | Rare:144 | ||||
| chr19:7925556-7925735 | Common:2; Rare:48 | ||||
| chr19:7928575-7928829 | Common:1; Rare:43 | ||||
| chr19:7933507-7933870 | Common:3; Rare:106; Clinvar (benign):1 | ||||
| chr19:7943609-7943990 | Rare:112 | ||||
| chr19:8005504-8005829 | Common:1; Rare:115 | ||||
| chr19:8308288-8308661 | Common:4; Rare:119; Clinvar (benign):1 | ||||
| chr19:8320858-8320948 | Rare:36 | ||||
| chr19:8321301-8321653 | Common:2; Rare:153 | ||||
| chr19:8363948-8364167 | Common:1; Rare:54 | ||||
| chr19:8389897-8390432 | Common:4; Rare:152 |