| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:33891986-33892289 | Rare:71 | ||||
| chr5:34656032-34656478 | Common:4; Rare:123 | ||||
| chr5:34915486-34915898 | Common:2; Rare:124 | ||||
| chr5:34929554-34929908 | Rare:132 | ||||
| chr5:36151881-36152220 | Rare:106 | ||||
| chr5:36242126-36242226 | Rare:22 | ||||
| chr5:36876611-36876907 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371018-37371377 | Common:2; Rare:95 | ||||
| chr5:38845712-38846139 | Common:2; Rare:107 | ||||
| chr5:39074335-39074558 | Common:1; Rare:108 | ||||
| chr5:40755731-40756001 | Common:1; Rare:58 | ||||
| chr5:40798140-40798299 | Rare:67 | ||||
| chr5:40834179-40834565 | Common:3; Rare:114 | ||||
| chr5:40835144-40835398 | Common:2; Rare:108 | ||||
| chr5:43064975-43065147 | Common:1; Rare:48 |