| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:13813490-13814060 | Common:3; Rare:181 | ||||
| chr6:15245140-15245630 | Common:6; Rare:205 | ||||
| chr6:16760004-16760287 | Common:2; Rare:121 | ||||
| chr6:16760360-16760671 | Rare:167 | ||||
| chr6:17311780-17312390 | Common:4; Rare:160 | ||||
| chr6:18257950-18258640 | Common:9; Rare:297 | ||||
| chr6:18265951-18266141 | Common:2; Rare:63 | ||||
| chr6:19804660-19805050 | Common:12; Rare:373 | ||||
| chr6:19838963-19839263 | Common:4; Rare:170 | ||||
| chr6:21258690-21258980 | Common:4; Rare:46 | ||||
| chr6:24504720-24504950 | Common:6; Rare:116; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):6 | ||||
| chr6:24771260-24771540 | Common:2; Rare:45 | ||||
| chr6:25835670-25836228 | Common:11; Rare:106 | ||||
| chr6:25992517-25992775 | Common:1; Rare:119 | ||||
| chr6:26055280-26055557 | Rare:203 |