| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4007356-4007809 | Common:15; Rare:628 | ||||
| chr19:4008032-4008432 | Common:2; Rare:169 | ||||
| chr19:4064952-4065352 | Common:2; Rare:121 | ||||
| chr19:4065397-4065810 | Common:3; Rare:178 | ||||
| chr19:4065850-4066268 | Common:3; Rare:296 | ||||
| chr19:4066206-4067395 | Common:19; Rare:851 | ||||
| chr19:4123796-4124450 | Common:37; Rare:915; Clinvar:1; Clinvar (benign):47 | ||||
| chr19:4181437-4182356 | Common:4; Rare:287 | ||||
| chr19:4182354-4182777 | Common:7; Rare:556; Clinvar:5 | ||||
| chr19:4229230-4229660 | Common:3; Rare:149 | ||||
| chr19:4246772-4247323 | Common:16; Rare:632 | ||||
| chr19:4247290-4247590 | Common:12; Rare:92 | ||||
| chr19:4288291-4288691 | Common:7; Rare:187 | ||||
| chr19:4303929-4304760 | Common:11; Rare:284 | ||||
| chr19:4326868-4327018 | Common:1; Rare:47 |