| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:22544476-22544502 | Common:1; Rare:9 | ||||
| chr12:22625023-22625230 | Rare:107 | ||||
| chr12:26937936-26938159 | Common:7; Rare:65 | ||||
| chr12:26938267-26938528 | Common:3; Rare:98 | ||||
| chr12:27523990-27524234 | Rare:59 | ||||
| chr12:27710754-27710884 | Common:2; Rare:60 | ||||
| chr12:28190354-28190483 | Common:1; Rare:41 | ||||
| chr12:31073732-31073902 | Common:8; Rare:61 | ||||
| chr12:31324092-31324316 | Rare:46 | ||||
| chr12:31326059-31326448 | Common:4; Rare:132 | ||||
| chr12:31729019-31729267 | Rare:72 | ||||
| chr12:31959282-31959461 | Common:2; Rare:54 | ||||
| chr12:32106668-32106884 | Common:3; Rare:62 | ||||
| chr12:32896764-32896966 | Common:1; Rare:63; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:38905583-38905722 | Common:3; Rare:38 |