| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:164882841-164883076 | Common:1; Rare:46 | ||||
| chr3:166361742-166362021 | Common:3; Rare:56 | ||||
| chr3:166431996-166432264 | Common:1; Rare:47 | ||||
| chr3:169765032-169765194 | Rare:72; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:170741303-170741590 | Rare:43 | ||||
| chr3:170765613-170765685 | Rare:13 | ||||
| chr3:171002392-171002603 | Common:1; Rare:46 | ||||
| chr3:171569688-171569832 | Common:1; Rare:27 | ||||
| chr3:171776093-171776212 | Common:1; Rare:17 | ||||
| chr3:171777289-171777424 | Common:3; Rare:28 | ||||
| chr3:171778519-171778879 | Rare:66 | ||||
| chr3:171781770-171782275 | Common:2; Rare:83 | ||||
| chr3:172153401-172153574 | Rare:28 | ||||
| chr3:172648885-172649055 | Rare:29 | ||||
| chr3:173395121-173395273 | Common:1; Rare:33 |