| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38661992-38662392 | Common:7; Rare:245 | ||||
| chr19:38666108-38666411 | Common:1; Rare:70 | ||||
| chr19:38676568-38676799 | Common:2; Rare:35 | ||||
| chr19:38683003-38683425 | Common:1; Rare:121 | ||||
| chr19:38683511-38684002 | Common:6; Rare:128 | ||||
| chr19:38686237-38686459 | Rare:31 | ||||
| chr19:38700430-38701060 | Common:5; Rare:240; Clinvar (benign):1 | ||||
| chr19:38714254-38715064 | Common:16; Rare:392; Clinvar (benign):2 | ||||
| chr19:38799580-38799960 | Common:2; Rare:101 | ||||
| chr19:38835397-38835675 | Common:4; Rare:61 | ||||
| chr19:38989100-38989630 | Common:6; Rare:81 | ||||
| chr19:38993334-38993577 | Common:5; Rare:37 | ||||
| chr19:39033411-39033896 | Common:10; Rare:136 | ||||
| chr19:39038202-39038602 | Common:5; Rare:102 | ||||
| chr19:39046116-39046516 | Common:4; Rare:138 |