| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7629531-7629848 | Common:5; Rare:113; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636981-7637143 | Common:2; Rare:51; Clinvar (benign):1 | ||||
| chr19:7943647-7943967 | Rare:79 | ||||
| chr19:8321361-8321703 | Common:2; Rare:130 | ||||
| chr19:8363883-8364162 | Common:2; Rare:64 | ||||
| chr19:8390048-8390419 | Common:1; Rare:105 | ||||
| chr19:8444812-8445052 | Common:2; Rare:111 | ||||
| chr19:8514121-8514222 | Common:2; Rare:32 | ||||
| chr19:9140311-9140432 | Rare:33 | ||||
| chr19:9324074-9324319 | Common:5; Rare:117 | ||||
| chr19:9538596-9538707 | Common:1; Rare:32 | ||||
| chr19:9621184-9621529 | Common:3; Rare:98 | ||||
| chr19:9675035-9675130 | Rare:24 | ||||
| chr19:9700653-9700705 | Rare:9 | ||||
| chr19:9818811-9818856 | Rare:17 |