| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:131710784-131711119 | Rare:167 | ||||
| chr12:131929033-131929314 | Common:20; Rare:173; Clinvar:2 | ||||
| chr12:131929574-131929782 | Rare:137; Clinvar (benign):6 | ||||
| chr12:131949756-131950072 | Common:2; Rare:119 | ||||
| chr12:132084053-132084374 | Common:12; Rare:196 | ||||
| chr12:132144272-132144515 | Common:2; Rare:181 | ||||
| chr12:132489820-132490204 | Common:4; Rare:231 | ||||
| chr12:132559859-132560146 | Rare:170 | ||||
| chr12:132687288-132687669 | Common:6; Rare:268; Clinvar:16; Clinvar (benign):20; Clinvar (pathogenic):2 | ||||
| chr12:132710545-132710938 | Common:10; Rare:257 | ||||
| chr12:132761715-132762209 | Common:6; Rare:329 | ||||
| chr12:132829010-132829360 | Common:1; Rare:216 | ||||
| chr12:132887508-132887810 | Common:1; Rare:169 | ||||
| chr12:132955830-132956190 | Common:6; Rare:97 | ||||
| chr12:132956254-132956403 | Common:2; Rare:63 |