| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49018739-49018877 | Rare:60 | ||||
| chr12:49131355-49131617 | Common:2; Rare:95 | ||||
| chr12:49188488-49188590 | Common:1; Rare:14 | ||||
| chr12:49188981-49189281 | Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49367159-49367524 | Common:1; Rare:103 | ||||
| chr12:49568104-49568234 | Common:2; Rare:41 | ||||
| chr12:49623284-49623575 | Common:1; Rare:81 | ||||
| chr12:49828404-49828544 | Rare:47 | ||||
| chr12:50085067-50085364 | Common:1; Rare:79 | ||||
| chr12:50167298-50167695 | Common:3; Rare:107 | ||||
| chr12:50200796-50201133 | Common:1; Rare:69 | ||||
| chr12:50283452-50283664 | Common:2; Rare:64 | ||||
| chr12:50400795-50400968 | Rare:55 | ||||
| chr12:50763925-50764338 | Common:1; Rare:112 | ||||
| chr12:51173061-51173235 | Rare:32 |