| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:95577416-95577576 | Common:5; Rare:48 | ||||
| chr6:96521687-96521863 | Common:6; Rare:83 | ||||
| chr6:96897667-96898083 | Common:5; Rare:150; Clinvar:4; Clinvar (benign):4 | ||||
| chr6:97283107-97283318 | Common:2; Rare:60 | ||||
| chr6:99394133-99394247 | Common:2; Rare:37 | ||||
| chr6:99425216-99425446 | Common:2; Rare:69 | ||||
| chr6:100881062-100881501 | Common:7; Rare:141 | ||||
| chr6:105137149-105137288 | Rare:54 | ||||
| chr6:105179916-105180017 | Common:3; Rare:25 | ||||
| chr6:105403049-105403256 | Common:2; Rare:78 | ||||
| chr6:106086149-106086411 | Rare:70 | ||||
| chr6:106325401-106325437 | Common:1; Rare:14 | ||||
| chr6:106325524-106325868 | Common:1; Rare:108 | ||||
| chr6:106629432-106629624 | Common:2; Rare:44 | ||||
| chr6:107028084-107028381 | Common:2; Rare:101 |