| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:131900861-131901098 | Rare:145 | ||||
| chr10:131981894-131982180 | Common:4; Rare:194 | ||||
| chr10:132307876-132308192 | Common:10; Rare:181 | ||||
| chr10:132331758-132332270 | Common:34; Rare:302 | ||||
| chr10:132396330-132396880 | Common:6; Rare:212 | ||||
| chr10:132397080-132397222 | Common:6; Rare:41 | ||||
| chr10:132537129-132538050 | Common:11; Rare:866 | ||||
| chr10:132710570-132710860 | Common:3; Rare:55 | ||||
| chr10:133308811-133308992 | Rare:141 | ||||
| chr10:133309096-133309394 | Common:4; Rare:212 | ||||
| chr10:133373317-133373504 | Common:2; Rare:127; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr10:133393975-133394325 | Common:4; Rare:285 | ||||
| chr11:207314-207740 | Common:17; Rare:276 | ||||
| chr11:208615-208850 | Rare:126 | ||||
| chr11:236316-236562 | Common:16; Rare:161 |