| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49580521-49580736 | Common:1; Rare:63 | ||||
| chr19:49665760-49666021 | Common:3; Rare:127; Clinvar (pathogenic):1 | ||||
| chr19:49690977-49691150 | Common:2; Rare:40 | ||||
| chr19:49813106-49813350 | Rare:103 | ||||
| chr19:49818272-49818344 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:49851001-49851039 | Rare:20 | ||||
| chr19:49851083-49851120 | Rare:15 | ||||
| chr19:49867217-49867345 | Common:1; Rare:46; Clinvar (benign):2 | ||||
| chr19:49867539-49867648 | Common:2; Rare:35 | ||||
| chr19:49877268-49877730 | Common:2; Rare:118 | ||||
| chr19:49929404-49929556 | Common:4; Rare:56 | ||||
| chr19:49929918-49930219 | Common:1; Rare:72 | ||||
| chr19:50025325-50025443 | Common:3; Rare:45 | ||||
| chr19:50384028-50384384 | Common:2; Rare:150; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:50476234-50476542 | Common:1; Rare:142 |