| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:26937932-26938159 | Common:7; Rare:66 | ||||
| chr12:26938299-26938537 | Common:3; Rare:91 | ||||
| chr12:27523995-27524245 | Rare:61 | ||||
| chr12:28190378-28190506 | Common:1; Rare:40 | ||||
| chr12:29148892-29149332 | Common:3; Rare:127 | ||||
| chr12:30695810-30695925 | Common:1; Rare:35 | ||||
| chr12:30754768-30755064 | Common:1; Rare:120 | ||||
| chr12:31073722-31073920 | Common:8; Rare:69 | ||||
| chr12:31729000-31729296 | Common:1; Rare:92 | ||||
| chr12:31959276-31959488 | Common:2; Rare:68 | ||||
| chr12:32399221-32399607 | Common:5; Rare:103 | ||||
| chr12:32399790-32399955 | Common:1; Rare:50 | ||||
| chr12:32896760-32897001 | Common:3; Rare:81; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:38905517-38905914 | Common:7; Rare:110 | ||||
| chr12:42238169-42238471 | Common:1; Rare:99 |