| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7488997-7489103 | Rare:48 | ||||
| chr19:7534054-7534187 | Common:3; Rare:35; Clinvar (benign):1 | ||||
| chr19:7629528-7629848 | Common:5; Rare:115; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7874300-7874503 | Rare:50 | ||||
| chr19:7925459-7925735 | Common:2; Rare:73 | ||||
| chr19:7943627-7943988 | Rare:102 | ||||
| chr19:8005498-8005821 | Common:1; Rare:113 | ||||
| chr19:8308297-8308661 | Common:3; Rare:113 | ||||
| chr19:8321316-8321675 | Common:2; Rare:150 | ||||
| chr19:8390042-8390412 | Common:1; Rare:105 | ||||
| chr19:8444800-8445084 | Common:3; Rare:128; Clinvar (benign):1 | ||||
| chr19:8514154-8514222 | Common:1; Rare:19 | ||||
| chr19:9140311-9140422 | Rare:30 | ||||
| chr19:9538603-9538718 | Common:1; Rare:33 | ||||
| chr19:9621184-9621529 | Common:3; Rare:98 |