| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40477087-40477179 | Common:1; Rare:24 | ||||
| chr3:40506002-40506137 | Rare:26 | ||||
| chr3:40524815-40525013 | Common:1; Rare:58 | ||||
| chr3:41194835-41195303 | Common:1; Rare:78 | ||||
| chr3:42149076-42149456 | Common:1; Rare:89 | ||||
| chr3:42159937-42160199 | Common:1; Rare:50 | ||||
| chr3:42581900-42582145 | Common:3; Rare:74 | ||||
| chr3:42590671-42590958 | Common:3; Rare:88 | ||||
| chr3:42600358-42600777 | Common:2; Rare:161 | ||||
| chr3:42773187-42773345 | Common:1; Rare:47 | ||||
| chr3:42804302-42804663 | Common:2; Rare:100 | ||||
| chr3:42936290-42936435 | Common:1; Rare:41 | ||||
| chr3:43286449-43286654 | Common:2; Rare:91 | ||||
| chr3:43621835-43622316 | Common:2; Rare:139; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690792-43691028 | Common:4; Rare:128; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 |