| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:186191442-186191870 | Common:7; Rare:136; Clinvar:3; Clinvar (benign):5 | ||||
| chr4:186723754-186723952 | Common:5; Rare:80 | ||||
| chr4:189940588-189940991 | Common:13; Rare:135 | ||||
| chr5:191353-191514 | Common:1; Rare:40 | ||||
| chr5:218087-218446 | Common:4; Rare:139; Clinvar:11; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr5:443084-443289 | Common:10; Rare:97 | ||||
| chr5:693289-693586 | Common:6; Rare:88 | ||||
| chr5:850604-850756 | Common:4; Rare:58 | ||||
| chr5:892540-892941 | Common:5; Rare:124 | ||||
| chr5:1799778-1799993 | Common:8; Rare:101 | ||||
| chr5:1801286-1801498 | Common:4; Rare:113; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:5422311-5422677 | Common:3; Rare:124 | ||||
| chr5:6378476-6378686 | Rare:88 | ||||
| chr5:6633012-6633398 | Common:8; Rare:123; Clinvar:9; Clinvar (benign):3 | ||||
| chr5:7868991-7869209 | Common:2; Rare:112; Clinvar (benign):1 |