| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:1118458-1118692 | Common:4; Rare:73 | ||||
| chr20:1392933-1393205 | Common:1; Rare:100 | ||||
| chr20:1894148-1894309 | Common:2; Rare:44 | ||||
| chr20:2652434-2652658 | Common:8; Rare:78 | ||||
| chr20:2664174-2664241 | Rare:32 | ||||
| chr20:2840631-2840777 | Common:1; Rare:60 | ||||
| chr20:3209429-3209557 | Common:1; Rare:44 | ||||
| chr20:3470872-3471077 | Common:2; Rare:103 | ||||
| chr20:3767728-3768051 | Common:4; Rare:102 | ||||
| chr20:3889160-3889420 | Common:1; Rare:135; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr20:4148549-4148890 | Rare:91 | ||||
| chr20:4686413-4686511 | Rare:16; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:5119914-5120179 | Common:1; Rare:88 | ||||
| chr20:5126530-5127120 | Common:4; Rare:184 | ||||
| chr20:5950355-5950701 | Common:8; Rare:108 |