| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142578699-142578976 | Rare:107; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142596280-142596470 | Common:2; Rare:49 | ||||
| chr3:142888852-142889257 | Common:4; Rare:96 | ||||
| chr3:143001177-143001672 | Common:5; Rare:141 | ||||
| chr3:143119649-143119785 | Rare:34 | ||||
| chr3:146160935-146161279 | Common:1; Rare:117; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:146544434-146544970 | Common:5; Rare:129 | ||||
| chr3:147409219-147409380 | Rare:63 | ||||
| chr3:148790943-148791111 | Rare:26 | ||||
| chr3:148991376-148991630 | Common:2; Rare:115; Clinvar (benign):1 | ||||
| chr3:149086467-149086720 | Rare:74 | ||||
| chr3:149129545-149129721 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149333220-149333636 | Common:4; Rare:100 | ||||
| chr3:149377593-149377942 | Common:1; Rare:72 | ||||
| chr3:149576140-149576512 | Common:1; Rare:55 |