| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:71773330-71773820 | Common:23; Rare:520 | ||||
| chr10:71850847-71851247 | Common:2; Rare:146; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr10:71851181-71851525 | Common:33; Rare:731; Clinvar:25; Clinvar (benign):52; Clinvar (pathogenic):6 | ||||
| chr10:71964010-71964270 | Common:1; Rare:72 | ||||
| chr10:71964290-71964490 | Common:1; Rare:51 | ||||
| chr10:72215318-72216206 | Common:4; Rare:684 | ||||
| chr10:72216202-72216640 | Common:11; Rare:530 | ||||
| chr10:72216760-72217172 | Common:6; Rare:271 | ||||
| chr10:72273105-72274440 | Common:6; Rare:1097 | ||||
| chr10:72274371-72274854 | Common:3; Rare:252 | ||||
| chr10:72353942-72355213 | Common:22; Rare:1360 | ||||
| chr10:72625978-72626414 | Common:9; Rare:471 | ||||
| chr10:72691855-72692255 | Common:3; Rare:248 | ||||
| chr10:72692306-72692706 | Rare:119 | ||||
| chr10:73096310-73097252 | Common:28; Rare:908 |