| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49903847-49904128 | Common:2; Rare:69 | ||||
| chr12:50025362-50025780 | Common:2; Rare:116 | ||||
| chr12:50085071-50085364 | Common:1; Rare:77 | ||||
| chr12:50167284-50167701 | Common:3; Rare:113 | ||||
| chr12:50222540-50222789 | Common:1; Rare:52 | ||||
| chr12:50283514-50283672 | Common:3; Rare:47 | ||||
| chr12:50400716-50401008 | Common:1; Rare:95 | ||||
| chr12:50763925-50764297 | Common:1; Rare:98 | ||||
| chr12:50764366-50764501 | Common:2; Rare:42 | ||||
| chr12:51026313-51026523 | Common:3; Rare:93; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51048065-51048359 | Common:2; Rare:97 | ||||
| chr12:51172725-51172877 | Common:3; Rare:31 | ||||
| chr12:51173020-51173243 | Rare:43 | ||||
| chr12:51238644-51238905 | Common:8; Rare:113 | ||||
| chr12:51239121-51239303 | Common:2; Rare:54 |