| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40348364-40348739 | Common:4; Rare:123 | ||||
| chr19:40377824-40378144 | Common:2; Rare:111; Clinvar (benign):1 | ||||
| chr19:40425975-40426136 | Common:1; Rare:49 | ||||
| chr19:40444233-40444517 | Common:3; Rare:91 | ||||
| chr19:40576679-40576902 | Common:3; Rare:63 | ||||
| chr19:40609560-40609854 | Common:1; Rare:94; Clinvar (benign):4 | ||||
| chr19:40714980-40715187 | Rare:49 | ||||
| chr19:40716876-40717112 | Common:1; Rare:73 | ||||
| chr19:40717581-40717874 | Rare:85 | ||||
| chr19:40718056-40718181 | Rare:43 | ||||
| chr19:40750365-40750639 | Common:5; Rare:81 | ||||
| chr19:40751076-40751357 | Common:3; Rare:77 | ||||
| chr19:40751762-40752078 | Common:2; Rare:73 | ||||
| chr19:40777921-40778303 | Common:1; Rare:105 | ||||
| chr19:41193105-41193368 | Common:1; Rare:94 |