| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:71663800-71664061 | Common:1; Rare:78 | ||||
| chr12:71664292-71664477 | Rare:53 | ||||
| chr12:71686017-71686420 | Common:2; Rare:113 | ||||
| chr12:71686449-71686531 | Common:1; Rare:18 | ||||
| chr12:71839595-71839806 | Common:1; Rare:81 | ||||
| chr12:74537753-74537873 | Common:1; Rare:47 | ||||
| chr12:75390891-75391105 | Common:1; Rare:66 | ||||
| chr12:75480634-75480825 | Rare:31 | ||||
| chr12:75511511-75511723 | Rare:74 | ||||
| chr12:76031592-76031892 | Common:1; Rare:92 | ||||
| chr12:76053089-76053360 | Common:1; Rare:72 | ||||
| chr12:76083832-76084065 | Rare:64 | ||||
| chr12:76084566-76084823 | Common:1; Rare:81 | ||||
| chr12:76085015-76085062 | Common:2; Rare:10 | ||||
| chr12:76348351-76348468 | Common:1; Rare:46; Clinvar:3; Clinvar (benign):1 |