| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7629502-7629848 | Common:7; Rare:128; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7637007-7637149 | Common:2; Rare:47; Clinvar (benign):1 | ||||
| chr19:7680741-7680895 | Common:1; Rare:52 | ||||
| chr19:7888416-7888577 | Common:1; Rare:37 | ||||
| chr19:7903484-7903923 | Common:2; Rare:148 | ||||
| chr19:7920240-7920364 | Rare:57 | ||||
| chr19:7943606-7944017 | Rare:127 | ||||
| chr19:8005498-8005826 | Common:1; Rare:116 | ||||
| chr19:8321308-8321711 | Common:2; Rare:161 | ||||
| chr19:8364018-8364162 | Common:1; Rare:37 | ||||
| chr19:8390032-8390449 | Common:2; Rare:116 | ||||
| chr19:8444800-8445109 | Common:3; Rare:139; Clinvar (benign):1 | ||||
| chr19:8514116-8514274 | Common:2; Rare:46 | ||||
| chr19:8832231-8832348 | Rare:39 | ||||
| chr19:9140304-9140444 | Common:2; Rare:38 |