| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2004403-2004669 | Common:2; Rare:93 | ||||
| chr12:2795059-2795183 | Rare:51 | ||||
| chr12:2812516-2812713 | Common:1; Rare:47 | ||||
| chr12:2877031-2877254 | Rare:68 | ||||
| chr12:3873355-3873535 | Common:1; Rare:40 | ||||
| chr12:4273560-4273826 | Rare:76 | ||||
| chr12:4320991-4321236 | Common:3; Rare:88 | ||||
| chr12:4538444-4538896 | Common:1; Rare:97 | ||||
| chr12:4649005-4649171 | Common:2; Rare:56; Clinvar (benign):2 | ||||
| chr12:6375370-6375566 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:6493234-6493386 | Common:6; Rare:42 | ||||
| chr12:6493793-6494119 | Common:2; Rare:98 | ||||
| chr12:6534625-6534847 | Common:3; Rare:89 | ||||
| chr12:6568260-6568382 | Rare:46 | ||||
| chr12:6663097-6663403 | Common:2; Rare:85 |