| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105235639-105236039 | Common:1; Rare:243 | ||||
| chr12:105236047-105236490 | Common:12; Rare:737 | ||||
| chr12:106247800-106248200 | Common:1; Rare:114 | ||||
| chr12:106301608-106302060 | Common:7; Rare:133 | ||||
| chr12:106302140-106303051 | Common:47; Rare:559 | ||||
| chr12:106302967-106303401 | Common:12; Rare:252 | ||||
| chr12:106357510-106357840 | Common:7; Rare:128; Clinvar:5; Clinvar (benign):2 | ||||
| chr12:106357860-106358281 | Common:28; Rare:714; Clinvar:1 | ||||
| chr12:106358341-106358830 | Common:7; Rare:199 | ||||
| chr12:106773985-106775150 | Common:25; Rare:1155 | ||||
| chr12:106955029-106956321 | Common:18; Rare:1294 | ||||
| chr12:106956425-106957051 | Common:2; Rare:414 | ||||
| chr12:106957015-106957415 | Common:3; Rare:72 | ||||
| chr12:106985082-106986018 | Rare:363 | ||||
| chr12:106986990-106987410 | Common:25; Rare:397 |