| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1801300-1801447 | Common:4; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:5422360-5422693 | Common:2; Rare:107 | ||||
| chr5:6378498-6378678 | Rare:71 | ||||
| chr5:7869000-7869200 | Common:2; Rare:100; Clinvar (benign):1 | ||||
| chr5:9545971-9546361 | Common:10; Rare:97 | ||||
| chr5:10353597-10353901 | Common:3; Rare:111 | ||||
| chr5:14498203-14498603 | Common:2; Rare:129; Clinvar:1 | ||||
| chr5:14716801-14717006 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:16465515-16465902 | Rare:106 | ||||
| chr5:31532052-31532332 | Common:3; Rare:76 | ||||
| chr5:32174271-32174389 | Common:1; Rare:45 | ||||
| chr5:32710533-32710702 | Common:1; Rare:38 | ||||
| chr5:32712238-32712277 | Rare:8 | ||||
| chr5:33440632-33441095 | Common:7; Rare:128 | ||||
| chr5:34656111-34656475 | Common:3; Rare:99 |