| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49568104-49568216 | Common:2; Rare:37 | ||||
| chr12:49741423-49741611 | Rare:56 | ||||
| chr12:49758245-49758480 | Common:4; Rare:74 | ||||
| chr12:49828391-49828600 | Common:1; Rare:75 | ||||
| chr12:49903867-49904102 | Common:2; Rare:58 | ||||
| chr12:50025416-50025747 | Common:2; Rare:90 | ||||
| chr12:50085035-50085384 | Common:1; Rare:93 | ||||
| chr12:50103881-50104038 | Rare:35 | ||||
| chr12:50167269-50167451 | Common:2; Rare:61 | ||||
| chr12:50283481-50283672 | Common:3; Rare:61 | ||||
| chr12:50763925-50764161 | Common:1; Rare:64 | ||||
| chr12:51026319-51026510 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51048098-51048370 | Common:2; Rare:96 | ||||
| chr12:51083399-51083708 | Rare:118 | ||||
| chr12:51173074-51173256 | Rare:33 |