| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40444188-40444910 | Common:16; Rare:534 | ||||
| chr19:40465593-40466220 | Common:11; Rare:532 | ||||
| chr19:40570560-40571170 | Common:7; Rare:276; Clinvar (pathogenic):1 | ||||
| chr19:40576653-40576932 | Common:11; Rare:212 | ||||
| chr19:40596910-40597280 | Common:1; Rare:267 | ||||
| chr19:40601214-40601616 | Common:1; Rare:179; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:40609750-40610310 | Common:11; Rare:195; Clinvar (benign):3 | ||||
| chr19:40613725-40614215 | Common:7; Rare:300; Clinvar:6; Clinvar (benign):6 | ||||
| chr19:40614640-40614829 | Common:4; Rare:84 | ||||
| chr19:40690568-40690961 | Common:9; Rare:242 | ||||
| chr19:40714970-40715214 | Rare:145 | ||||
| chr19:40715591-40715967 | Common:7; Rare:110 | ||||
| chr19:40716070-40716449 | Common:3; Rare:51 | ||||
| chr19:40716684-40717416 | Common:7; Rare:501 | ||||
| chr19:40718219-40718334 | Common:1; Rare:32; Clinvar:1 |