| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:8697740-8698033 | Common:1; Rare:119 | ||||
| chr12:8823487-8823801 | Common:1; Rare:92; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:8913534-8913948 | Common:1; Rare:75 | ||||
| chr12:8914286-8914868 | Common:7; Rare:164 | ||||
| chr12:8915167-8915456 | Common:2; Rare:68 | ||||
| chr12:8949551-8949856 | Common:1; Rare:63 | ||||
| chr12:8949975-8950095 | Common:1; Rare:33 | ||||
| chr12:10613508-10613688 | Common:1; Rare:70 | ||||
| chr12:11170918-11171265 | Common:4; Rare:92 | ||||
| chr12:11171567-11171677 | Common:2; Rare:35 | ||||
| chr12:12356970-12357165 | Common:4; Rare:104 | ||||
| chr12:12611687-12612088 | Common:2; Rare:115 | ||||
| chr12:12717207-12717408 | Rare:67 | ||||
| chr12:13000196-13000453 | Common:1; Rare:84 | ||||
| chr12:14365490-14365767 | Common:1; Rare:86 |