| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:2652455-2652655 | Common:8; Rare:66 | ||||
| chr20:2664175-2664329 | Common:4; Rare:67 | ||||
| chr20:2840627-2840768 | Common:1; Rare:54 | ||||
| chr20:2841132-2841302 | Common:3; Rare:35 | ||||
| chr20:3045800-3046098 | Common:3; Rare:79 | ||||
| chr20:3209433-3209542 | Common:1; Rare:37 | ||||
| chr20:3767730-3767985 | Common:3; Rare:80 | ||||
| chr20:3889171-3889387 | Common:1; Rare:108; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:4686240-4686498 | Common:1; Rare:55; Clinvar (benign):1 | ||||
| chr20:5112954-5113194 | Rare:102 | ||||
| chr20:5119894-5120185 | Common:1; Rare:98 | ||||
| chr20:5610933-5611208 | Common:2; Rare:103 | ||||
| chr20:5950401-5950753 | Common:8; Rare:111 | ||||
| chr20:10218638-10218928 | Rare:69 | ||||
| chr20:10640887-10641028 | Rare:39; Clinvar:1 |