| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102408884-102409851 | Common:2; Rare:275 | ||||
| chr10:102420714-102420956 | Rare:88 | ||||
| chr10:102420945-102421274 | Common:2; Rare:341 | ||||
| chr10:102421290-102421710 | Common:3; Rare:297 | ||||
| chr10:102432485-102432839 | Common:4; Rare:230 | ||||
| chr10:102461180-102461485 | Rare:146 | ||||
| chr10:102501986-102502419 | Common:7; Rare:237 | ||||
| chr10:102502652-102502871 | Rare:75 | ||||
| chr10:102503769-102504341 | Common:4; Rare:219; Clinvar:17; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr10:102643637-102644048 | Rare:165 | ||||
| chr10:102644185-102644539 | Common:2; Rare:185 | ||||
| chr10:102644882-102645199 | Rare:139 | ||||
| chr10:102713917-102714066 | Rare:50 | ||||
| chr10:102713970-102714764 | Common:9; Rare:569 | ||||
| chr10:102714764-102715201 | Common:4; Rare:135 |