| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:401446-401669 | Rare:60 | ||||
| chr12:2877027-2877262 | Rare:70 | ||||
| chr12:2959843-2959958 | Common:1; Rare:29 | ||||
| chr12:4320949-4321247 | Common:4; Rare:112 | ||||
| chr12:4538444-4538930 | Common:3; Rare:110 | ||||
| chr12:4648982-4649154 | Common:2; Rare:57; Clinvar (benign):1 | ||||
| chr12:6200239-6200452 | Common:3; Rare:63 | ||||
| chr12:6493212-6493376 | Common:6; Rare:45 | ||||
| chr12:6493778-6494140 | Common:2; Rare:108 | ||||
| chr12:6534421-6534860 | Common:8; Rare:184 | ||||
| chr12:6568234-6568382 | Rare:55 | ||||
| chr12:6723970-6724158 | Rare:45 | ||||
| chr12:6724193-6724295 | Rare:23 | ||||
| chr12:6753057-6753232 | Common:4; Rare:63 | ||||
| chr12:6851238-6851470 | Rare:55 |