| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36151794-36152270 | Rare:134 | ||||
| chr5:36242162-36242334 | Common:1; Rare:44 | ||||
| chr5:36876625-36876889 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37249308-37249591 | Common:1; Rare:95; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37370985-37371389 | Common:2; Rare:110 | ||||
| chr5:37379059-37379360 | Common:3; Rare:69 | ||||
| chr5:39074373-39074502 | Common:1; Rare:53 | ||||
| chr5:40679299-40679419 | Common:1; Rare:25 | ||||
| chr5:40679668-40679929 | Common:2; Rare:60 | ||||
| chr5:40755889-40756018 | Rare:35 | ||||
| chr5:40798166-40798435 | Common:1; Rare:104 | ||||
| chr5:40835171-40835406 | Common:2; Rare:93 | ||||
| chr5:40909366-40909592 | Rare:50 | ||||
| chr5:41870372-41870556 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:41904003-41904368 | Common:1; Rare:107 |