| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185535341-185535632 | Common:2; Rare:106; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:185775777-185776162 | Common:4; Rare:64 | ||||
| chr4:186191472-186191836 | Common:6; Rare:120; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:186723769-186723917 | Common:5; Rare:59 | ||||
| chr4:189940585-189941000 | Common:15; Rare:138 | ||||
| chr5:191356-191499 | Common:1; Rare:33 | ||||
| chr5:218114-218415 | Common:3; Rare:121; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr5:443095-443283 | Common:9; Rare:87 | ||||
| chr5:693289-693570 | Common:6; Rare:82 | ||||
| chr5:892625-892917 | Common:5; Rare:96 | ||||
| chr5:1799791-1799986 | Common:4; Rare:91 | ||||
| chr5:1801286-1801473 | Common:4; Rare:97; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:5422375-5422677 | Common:2; Rare:100 | ||||
| chr5:7868991-7869209 | Common:2; Rare:112; Clinvar (benign):1 | ||||
| chr5:9546037-9546360 | Common:8; Rare:77 |