| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:5043778-5044044 | Common:3; Rare:68; Clinvar (benign):1 | ||||
| chr12:6124489-6124607 | Rare:20; Clinvar:2 | ||||
| chr12:6200005-6200420 | Common:3; Rare:116 | ||||
| chr12:6375340-6375654 | Common:3; Rare:80; Clinvar:1; Clinvar (benign):6 | ||||
| chr12:6383991-6384262 | Common:1; Rare:59 | ||||
| chr12:6493107-6493386 | Common:7; Rare:87 | ||||
| chr12:6493746-6494107 | Common:2; Rare:108 | ||||
| chr12:6534232-6534602 | Common:6; Rare:142 | ||||
| chr12:6568249-6568388 | Rare:53 | ||||
| chr12:6688876-6689118 | Rare:74 | ||||
| chr12:6689467-6689732 | Common:1; Rare:65 | ||||
| chr12:6723895-6724172 | Common:1; Rare:63 | ||||
| chr12:6724196-6724296 | Rare:21 | ||||
| chr12:6851877-6852180 | Rare:81 | ||||
| chr12:6870119-6870476 | Common:1; Rare:119; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 |