| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:77708427-77708486 | Rare:15 | ||||
| chr10:77711495-77711632 | Common:1; Rare:39 | ||||
| chr10:77836352-77836605 | Common:4; Rare:52 | ||||
| chr10:77837728-77837845 | Rare:23 | ||||
| chr10:77846764-77846971 | Rare:46 | ||||
| chr10:77925556-77925711 | Rare:30 | ||||
| chr10:77983850-77984017 | Common:1; Rare:44; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr10:77984171-77984411 | Rare:70; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr10:78043348-78043390 | Rare:10 | ||||
| chr10:78177612-78177811 | Common:1; Rare:39 | ||||
| chr10:78302861-78303105 | Rare:37 | ||||
| chr10:78303206-78303285 | Common:1; Rare:18 | ||||
| chr10:78303411-78303583 | Common:5; Rare:52 | ||||
| chr10:78357867-78357983 | Common:1; Rare:16 | ||||
| chr10:78402079-78402228 | Common:2; Rare:22 |