| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7637002-7637143 | Common:2; Rare:48; Clinvar (benign):1 | ||||
| chr19:7943641-7943990 | Rare:92 | ||||
| chr19:8005498-8005829 | Common:1; Rare:118 | ||||
| chr19:8321322-8321703 | Common:2; Rare:153 | ||||
| chr19:8390077-8390412 | Common:1; Rare:97 | ||||
| chr19:8444800-8445055 | Common:3; Rare:117 | ||||
| chr19:8514154-8514222 | Common:1; Rare:19 | ||||
| chr19:9140304-9140428 | Common:1; Rare:32 | ||||
| chr19:9324123-9324319 | Common:3; Rare:102 | ||||
| chr19:9435512-9435602 | Rare:36 | ||||
| chr19:9538574-9538728 | Common:1; Rare:44 | ||||
| chr19:9621192-9621555 | Common:3; Rare:102 | ||||
| chr19:9818811-9818866 | Rare:23 | ||||
| chr19:9827799-9827963 | Common:1; Rare:62 | ||||
| chr19:10333511-10333709 | Rare:66 |