| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:612178-612357 | Rare:73 | ||||
| chr5:892503-893005 | Common:5; Rare:162 | ||||
| chr5:1799764-1800002 | Common:9; Rare:112 | ||||
| chr5:1801281-1801460 | Common:4; Rare:90; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:5422360-5422682 | Common:2; Rare:106 | ||||
| chr5:6378479-6378706 | Rare:95 | ||||
| chr5:6633284-6633398 | Common:2; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:6712755-6713102 | Common:5; Rare:120 | ||||
| chr5:7868977-7869209 | Common:2; Rare:120; Clinvar (benign):1 | ||||
| chr5:10249767-10250445 | Common:19; Rare:321; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10353518-10353913 | Common:4; Rare:149 | ||||
| chr5:11903182-11903261 | Rare:13 | ||||
| chr5:14581658-14581881 | Rare:103 | ||||
| chr5:14664506-14664914 | Common:4; Rare:174 | ||||
| chr5:16465709-16465921 | Common:1; Rare:42 |