| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:32444647-32445040 | Common:3; Rare:123 | ||||
| chr5:32531750-32531865 | Common:1; Rare:24 | ||||
| chr5:33440632-33441038 | Common:4; Rare:106 | ||||
| chr5:34915472-34915764 | Common:1; Rare:80 | ||||
| chr5:36151880-36152111 | Rare:64 | ||||
| chr5:36876650-36876894 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371053-37371218 | Rare:56 | ||||
| chr5:40679673-40679955 | Common:2; Rare:69 | ||||
| chr5:40798144-40798259 | Rare:51 | ||||
| chr5:40835189-40835326 | Common:1; Rare:57 | ||||
| chr5:41904025-41904358 | Common:1; Rare:99 | ||||
| chr5:41925078-41925305 | Common:1; Rare:85 | ||||
| chr5:43064960-43065158 | Common:1; Rare:52 | ||||
| chr5:43121372-43121626 | Common:1; Rare:97 | ||||
| chr5:43295734-43295764 | Rare:7 |