| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39383151-39383422 | Rare:48; Clinvar:1 | ||||
| chr3:39383568-39383651 | Rare:19 | ||||
| chr3:42581896-42582128 | Common:2; Rare:72 | ||||
| chr3:42773202-42773332 | Common:1; Rare:41 | ||||
| chr3:43690782-43690939 | Common:1; Rare:68; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:44477652-44477802 | Common:1; Rare:28 | ||||
| chr3:44624950-44625045 | Common:1; Rare:23 | ||||
| chr3:44761610-44761774 | Common:2; Rare:58 | ||||
| chr3:44861669-44861917 | Common:3; Rare:91 | ||||
| chr3:44976122-44976283 | Common:2; Rare:69 | ||||
| chr3:45689177-45689471 | Common:1; Rare:98 | ||||
| chr3:45995814-45995875 | Rare:15; Clinvar:1 | ||||
| chr3:47380816-47381084 | Rare:86 | ||||
| chr3:48301386-48301490 | Common:1; Rare:20 | ||||
| chr3:48440048-48440269 | Common:1; Rare:68 |