| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:133347211-133347411 | Rare:39 | ||||
| chr10:133357601-133357836 | Common:2; Rare:65 | ||||
| chr10:133357926-133358228 | Common:8; Rare:157 | ||||
| chr10:133373316-133373517 | Common:2; Rare:143; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr10:133379001-133379307 | Common:36; Rare:110 | ||||
| chr10:133393986-133394417 | Common:4; Rare:320 | ||||
| chr11:207322-207753 | Common:17; Rare:277 | ||||
| chr11:208615-208856 | Rare:173 | ||||
| chr11:236321-236546 | Common:14; Rare:127 | ||||
| chr11:236895-237050 | Common:2; Rare:109 | ||||
| chr11:289016-289208 | Common:2; Rare:97 | ||||
| chr11:307801-308286 | Common:27; Rare:173 | ||||
| chr11:314313-314782 | Common:13; Rare:174 | ||||
| chr11:320746-321035 | Common:11; Rare:81; Clinvar:1 | ||||
| chr11:327260-327800 | Common:4; Rare:188 |