| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:12482421-12482821 | Common:4; Rare:79 | ||||
| chr10:12485020-12485500 | Common:2; Rare:161 | ||||
| chr10:12556359-12556869 | Common:11; Rare:110 | ||||
| chr10:12605740-12606340 | Common:9; Rare:123 | ||||
| chr10:12606360-12606670 | Rare:62 | ||||
| chr10:13108539-13109346 | Common:12; Rare:291; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr10:13288130-13288440 | Common:4; Rare:70; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr10:13348897-13349218 | Rare:56 | ||||
| chr10:13349930-13350330 | Common:2; Rare:100 | ||||
| chr10:13390594-13390994 | Common:4; Rare:132 | ||||
| chr10:13483356-13484321 | Common:7; Rare:196 | ||||
| chr10:13690647-13691047 | Common:14; Rare:151 | ||||
| chr10:13704326-13704719 | Common:5; Rare:120 | ||||
| chr10:13705185-13705333 | Common:5; Rare:62 | ||||
| chr10:13705614-13705845 | Common:2; Rare:43 |