| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185470944-185471651 | Common:75; Rare:620 | ||||
| chr4:186190647-186191047 | Common:4; Rare:87 | ||||
| chr4:186191110-186191375 | Common:10; Rare:131 | ||||
| chr4:186191340-186192021 | Common:43; Rare:944; Clinvar:18; Clinvar (benign):35; Clinvar (pathogenic):2 | ||||
| chr4:186204075-186204535 | Common:127; Rare:549 | ||||
| chr4:186722980-186723380 | Common:6; Rare:84 | ||||
| chr4:186723666-186724066 | Common:33; Rare:503 | ||||
| chr4:186726555-186726955 | Common:16; Rare:275 | ||||
| chr4:189940532-189940996 | Common:77; Rare:951 | ||||
| chr4:189940920-189941320 | Common:12; Rare:167 | ||||
| chr5:169470-169900 | Common:5; Rare:120 | ||||
| chr5:218037-218441 | Common:24; Rare:848; Clinvar:64; Clinvar (benign):55; Clinvar (pathogenic):14 | ||||
| chr5:270998-271735 | Common:15; Rare:608 | ||||
| chr5:272622-273438 | Common:7; Rare:222 | ||||
| chr5:443000-443330 | Common:69; Rare:692 |