| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:90256455-90256607 | Common:2; Rare:47 | ||||
| chr14:90331894-90332167 | Common:1; Rare:80 | ||||
| chr14:90396870-90397183 | Common:5; Rare:152 | ||||
| chr14:90397186-90397241 | Rare:19; Clinvar (benign):2 | ||||
| chr14:91114010-91114118 | Rare:36 | ||||
| chr14:91244681-91244794 | Common:2; Rare:16 | ||||
| chr14:91510406-91510655 | Common:1; Rare:80 | ||||
| chr14:91836421-91836687 | Common:12; Rare:45 | ||||
| chr14:92040026-92040132 | Common:2; Rare:31; Clinvar (benign):1 | ||||
| chr14:92121655-92122005 | Common:5; Rare:121 | ||||
| chr14:92748510-92748783 | Rare:67 | ||||
| chr14:92793953-92794408 | Rare:149 | ||||
| chr14:93184817-93185020 | Rare:74 | ||||
| chr14:93206985-93207288 | Common:2; Rare:147 | ||||
| chr14:93430586-93430984 | Rare:77 |