| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3796030-3796602 | Common:7; Rare:286 | ||||
| chr20:3819663-3820424 | Common:6; Rare:254 | ||||
| chr20:3820371-3821106 | Common:6; Rare:565 | ||||
| chr20:3846500-3846957 | Common:8; Rare:390 | ||||
| chr20:3847220-3847620 | Common:3; Rare:137 | ||||
| chr20:3888236-3888929 | Common:6; Rare:297 | ||||
| chr20:3889006-3889466 | Common:12; Rare:1176; Clinvar:48; Clinvar (benign):19; Clinvar (pathogenic):8 | ||||
| chr20:3889482-3889977 | Common:25; Rare:560; Clinvar:7; Clinvar (benign):11; Clinvar (pathogenic):9 | ||||
| chr20:3890111-3890778 | Common:4; Rare:147 | ||||
| chr20:3891188-3891588 | Common:2; Rare:79 | ||||
| chr20:4014874-4015842 | Common:37; Rare:1032 | ||||
| chr20:4148562-4148962 | Rare:311 | ||||
| chr20:4221485-4221885 | Rare:140 | ||||
| chr20:4222445-4222845 | Common:15; Rare:93 | ||||
| chr20:4686191-4687232 | Common:8; Rare:455; Clinvar:3; Clinvar (benign):5 |