| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:181243690-181243940 | Common:4; Rare:92 | ||||
| chr5:181260640-181260863 | Rare:76 | ||||
| chr5:181261065-181261303 | Rare:78 | ||||
| chr6:292449-292533 | Rare:26 | ||||
| chr6:693054-693228 | Rare:56 | ||||
| chr6:2245567-2245817 | Rare:85 | ||||
| chr6:2971269-2971576 | Common:4; Rare:74 | ||||
| chr6:2971592-2971717 | Common:1; Rare:36 | ||||
| chr6:2988621-2988673 | Common:1; Rare:9 | ||||
| chr6:2999653-2999893 | Common:10; Rare:47 | ||||
| chr6:3063814-3063967 | Common:1; Rare:61 | ||||
| chr6:3118575-3118742 | Common:2; Rare:55 | ||||
| chr6:3157405-3157690 | Common:7; Rare:89; Clinvar (benign):1 | ||||
| chr6:3227485-3227590 | Rare:19 | ||||
| chr6:3227592-3228018 | Rare:106 |