| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:189940579-189941000 | Common:15; Rare:139 | ||||
| chr5:218104-218403 | Common:4; Rare:121; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr5:321577-321768 | Common:2; Rare:39 | ||||
| chr5:443059-443289 | Common:10; Rare:105 | ||||
| chr5:612211-612359 | Rare:59 | ||||
| chr5:693289-693502 | Common:4; Rare:60 | ||||
| chr5:892507-893001 | Common:5; Rare:161 | ||||
| chr5:1799785-1799988 | Common:7; Rare:96 | ||||
| chr5:1801300-1801509 | Common:4; Rare:111; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:2751835-2752139 | Common:1; Rare:99 | ||||
| chr5:5422185-5422700 | Common:3; Rare:172 | ||||
| chr5:6378479-6378674 | Rare:81 | ||||
| chr5:6632927-6633318 | Common:9; Rare:122; Clinvar:8; Clinvar (benign):6 | ||||
| chr5:6633651-6633722 | Common:1; Rare:27 | ||||
| chr5:7868987-7869209 | Common:2; Rare:115; Clinvar (benign):1 |