| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:36993117-36993559 | Common:2; Rare:138; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37176324-37176393 | Rare:17 | ||||
| chr3:38024484-38024674 | Common:1; Rare:70 | ||||
| chr3:38029616-38029864 | Common:1; Rare:50 | ||||
| chr3:39051983-39052050 | Common:1; Rare:27 | ||||
| chr3:39107574-39107723 | Common:3; Rare:45 | ||||
| chr3:39383288-39383432 | Common:1; Rare:25; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:39383547-39383693 | Rare:35; Clinvar:2 | ||||
| chr3:40309506-40309827 | Common:8; Rare:115 | ||||
| chr3:40457204-40457396 | Common:3; Rare:97 | ||||
| chr3:40524821-40524965 | Common:1; Rare:36 | ||||
| chr3:41224661-41224991 | Common:1; Rare:69; Clinvar (pathogenic):1 | ||||
| chr3:42581932-42582077 | Common:2; Rare:43 | ||||
| chr3:42600358-42600777 | Common:2; Rare:161 | ||||
| chr3:42773214-42773357 | Common:1; Rare:38 |