| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39107562-39107697 | Common:3; Rare:44 | ||||
| chr3:39383272-39383457 | Common:2; Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383570-39383686 | Rare:25; Clinvar:1 | ||||
| chr3:39406555-39406776 | Common:6; Rare:88 | ||||
| chr3:40309448-40309813 | Common:9; Rare:125 | ||||
| chr3:40457201-40457388 | Common:3; Rare:91 | ||||
| chr3:40505971-40506168 | Rare:37 | ||||
| chr3:40524812-40525006 | Common:1; Rare:55 | ||||
| chr3:41199908-41200148 | Common:1; Rare:64 | ||||
| chr3:41962277-41962592 | Common:3; Rare:81 | ||||
| chr3:42160063-42160222 | Common:1; Rare:33 | ||||
| chr3:42581900-42582204 | Common:3; Rare:89 | ||||
| chr3:42600337-42600778 | Common:3; Rare:170 | ||||
| chr3:42600880-42601000 | Rare:44 | ||||
| chr3:42633415-42633636 | Common:1; Rare:49 |