| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:34240245-34240555 | Common:1; Rare:54 | ||||
| chr3:34256348-34256453 | Rare:12 | ||||
| chr3:34268660-34268962 | Common:4; Rare:66 | ||||
| chr3:34297979-34298145 | Common:4; Rare:20 | ||||
| chr3:34334210-34334462 | Common:8; Rare:41 | ||||
| chr3:34437873-34437949 | Rare:13 | ||||
| chr3:34505324-34505388 | Rare:7 | ||||
| chr3:34527600-34527666 | Rare:3 | ||||
| chr3:34658003-34658032 | Rare:2 | ||||
| chr3:36987946-36988182 | Common:1; Rare:43 | ||||
| chr3:36989061-36989216 | Rare:23 | ||||
| chr3:37043110-37043399 | Common:1; Rare:60 | ||||
| chr3:37048290-37048574 | Common:1; Rare:64; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr3:37074939-37075156 | Common:1; Rare:48 | ||||
| chr3:37097108-37097340 | Common:1; Rare:53 |