| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6202059-6202316 | Common:1; Rare:59 | ||||
| chr12:6235191-6235593 | Common:2; Rare:128 | ||||
| chr12:6447958-6448148 | Common:1; Rare:35 | ||||
| chr12:6450856-6451097 | Rare:82; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6501935-6501948 | Rare:3 | ||||
| chr12:6537882-6538194 | Common:3; Rare:113 | ||||
| chr12:6600045-6600387 | Common:1; Rare:73 | ||||
| chr12:6601674-6602159 | Common:3; Rare:151 | ||||
| chr12:6655981-6656150 | Rare:23 | ||||
| chr12:6662204-6662503 | Common:2; Rare:47 | ||||
| chr12:6730782-6731137 | Common:5; Rare:104 | ||||
| chr12:6743475-6743501 | Rare:4 | ||||
| chr12:6770159-6770528 | Rare:105 | ||||
| chr12:6827349-6827607 | Common:2; Rare:76 | ||||
| chr12:6837728-6838019 | Rare:106 |