| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:181040121-181040334 | Rare:40 | ||||
| chr5:181223115-181223313 | Rare:68 | ||||
| chr5:181224497-181224615 | Common:1; Rare:35 | ||||
| chr5:181243690-181243727 | Rare:8 | ||||
| chr5:181261063-181261234 | Rare:59 | ||||
| chr6:693050-693209 | Rare:51 | ||||
| chr6:1626145-1626250 | Rare:26 | ||||
| chr6:2245418-2245831 | Common:1; Rare:137 | ||||
| chr6:2971533-2971715 | Common:1; Rare:51 | ||||
| chr6:3068491-3068570 | Common:1; Rare:21 | ||||
| chr6:3157530-3157669 | Common:6; Rare:51 | ||||
| chr6:3751339-3751603 | Common:1; Rare:118 | ||||
| chr6:4021218-4021445 | Rare:103 | ||||
| chr6:5004006-5004124 | Common:1; Rare:54 | ||||
| chr6:5260696-5261039 | Common:5; Rare:117; Clinvar (benign):4 |