| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7488995-7489103 | Rare:48 | ||||
| chr19:7629529-7629844 | Common:5; Rare:113; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636996-7637143 | Common:2; Rare:50; Clinvar (benign):1 | ||||
| chr19:7943627-7943988 | Rare:102 | ||||
| chr19:8005498-8005821 | Common:1; Rare:113 | ||||
| chr19:8321324-8321703 | Common:2; Rare:153 | ||||
| chr19:8390042-8390449 | Common:2; Rare:115 | ||||
| chr19:8444790-8445109 | Common:4; Rare:142; Clinvar (benign):1 | ||||
| chr19:8514121-8514222 | Common:2; Rare:32 | ||||
| chr19:8526443-8526463 | Rare:6 | ||||
| chr19:9140304-9140437 | Common:1; Rare:37 | ||||
| chr19:9435479-9435641 | Common:1; Rare:62 | ||||
| chr19:9538591-9538731 | Common:1; Rare:43 | ||||
| chr19:9621181-9621534 | Common:3; Rare:100 | ||||
| chr19:9675035-9675164 | Rare:38 |