| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:388521-389398 | Common:12; Rare:579 | ||||
| chr12:389357-389753 | Common:31; Rare:545 | ||||
| chr12:401303-402028 | Common:9; Rare:573 | ||||
| chr12:610200-610660 | Common:4; Rare:117 | ||||
| chr12:642968-643957 | Common:25; Rare:661 | ||||
| chr12:752234-752664 | Common:6; Rare:582 | ||||
| chr12:752930-753500 | Common:11; Rare:274; Clinvar:7; Clinvar (benign):16 | ||||
| chr12:949340-949910 | Common:21; Rare:414 | ||||
| chr12:949880-950140 | Common:5; Rare:99 | ||||
| chr12:989790-990094 | Rare:101 | ||||
| chr12:990350-990750 | Common:2; Rare:135 | ||||
| chr12:990710-990980 | Common:6; Rare:252 | ||||
| chr12:991007-991407 | Common:19; Rare:658 | ||||
| chr12:991450-991750 | Common:2; Rare:95 | ||||
| chr12:1529960-1530410 | Common:7; Rare:215 |