| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39383269-39383676 | Common:3; Rare:87; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:39406596-39406776 | Common:2; Rare:70 | ||||
| chr3:39406963-39407009 | Rare:17 | ||||
| chr3:40309506-40309968 | Common:8; Rare:161 | ||||
| chr3:40309971-40310107 | Common:2; Rare:48 | ||||
| chr3:40310365-40310568 | Common:3; Rare:34 | ||||
| chr3:40387058-40387245 | Common:2; Rare:59 | ||||
| chr3:40457201-40457463 | Common:6; Rare:120 | ||||
| chr3:40505930-40506182 | Rare:53 | ||||
| chr3:40524795-40525004 | Common:1; Rare:59 | ||||
| chr3:41238952-41239289 | Rare:104 | ||||
| chr3:41962040-41962568 | Common:6; Rare:129 | ||||
| chr3:42149059-42149390 | Rare:73 | ||||
| chr3:42581878-42582211 | Common:3; Rare:99 | ||||
| chr3:42590662-42590959 | Common:3; Rare:91 |