| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:143450609-143450961 | Common:1; Rare:132; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143677864-143678024 | Common:1; Rare:38 | ||||
| chr6:143843176-143843465 | Common:2; Rare:96 | ||||
| chr6:144095494-144095831 | Common:6; Rare:101 | ||||
| chr6:145736006-145736302 | Common:3; Rare:52 | ||||
| chr6:145814655-145815060 | Common:2; Rare:165 | ||||
| chr6:145963989-145964121 | Common:4; Rare:29 | ||||
| chr6:145964198-145964630 | Common:1; Rare:137 | ||||
| chr6:149546001-149546153 | Rare:63 | ||||
| chr6:149566138-149566412 | Common:1; Rare:84 | ||||
| chr6:149648478-149648849 | Common:3; Rare:93 | ||||
| chr6:149718058-149718187 | Common:2; Rare:48 | ||||
| chr6:149746480-149746684 | Common:3; Rare:100 | ||||
| chr6:149749617-149749811 | Rare:102 | ||||
| chr6:150866330-150866512 | Rare:70 |