| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7395022-7395218 | Common:4; Rare:60 | ||||
| chr19:7629524-7629843 | Common:5; Rare:115; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636984-7637152 | Common:2; Rare:51; Clinvar (benign):1 | ||||
| chr19:7920149-7920364 | Rare:75 | ||||
| chr19:7943638-7943990 | Rare:94 | ||||
| chr19:8005536-8005829 | Common:1; Rare:105 | ||||
| chr19:8308282-8308638 | Common:3; Rare:117; Clinvar (benign):1 | ||||
| chr19:8321308-8321664 | Common:2; Rare:151 | ||||
| chr19:8390077-8390449 | Common:2; Rare:107 | ||||
| chr19:8444807-8445110 | Common:2; Rare:137; Clinvar (benign):1 | ||||
| chr19:8514145-8514232 | Common:1; Rare:24 | ||||
| chr19:9140294-9140442 | Common:2; Rare:39 | ||||
| chr19:9324058-9324280 | Common:5; Rare:104 | ||||
| chr19:9538561-9538716 | Common:1; Rare:45 | ||||
| chr19:9621181-9621548 | Common:3; Rare:103 |