| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:180809796-180810336 | Common:13; Rare:144 | ||||
| chr5:181223118-181223319 | Rare:68 | ||||
| chr5:181223500-181223745 | Common:4; Rare:64 | ||||
| chr5:181237820-181238378 | Common:5; Rare:143 | ||||
| chr5:181243653-181243969 | Common:4; Rare:111 | ||||
| chr5:181261093-181261277 | Rare:62 | ||||
| chr6:292000-292283 | Common:1; Rare:47 | ||||
| chr6:693054-693198 | Rare:47 | ||||
| chr6:2245550-2245835 | Rare:100 | ||||
| chr6:2765096-2765671 | Common:9; Rare:261 | ||||
| chr6:2841846-2841920 | Common:1; Rare:11 | ||||
| chr6:2988339-2988738 | Common:3; Rare:57 | ||||
| chr6:3068322-3068573 | Common:1; Rare:88 | ||||
| chr6:3118589-3118842 | Common:3; Rare:81 | ||||
| chr6:3157408-3157614 | Common:5; Rare:69; Clinvar (benign):1 |