| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:10723318-10723459 | Common:3; Rare:39 | ||||
| chr12:11171158-11171256 | Common:2; Rare:41 | ||||
| chr12:11171553-11171666 | Common:2; Rare:35 | ||||
| chr12:12350193-12350290 | Rare:23 | ||||
| chr12:12356970-12357188 | Common:4; Rare:114 | ||||
| chr12:12611769-12612153 | Common:3; Rare:110 | ||||
| chr12:12891283-12891619 | Common:1; Rare:69 | ||||
| chr12:13000196-13000441 | Common:1; Rare:83 | ||||
| chr12:14365488-14365719 | Common:1; Rare:74 | ||||
| chr12:14567677-14567747 | Common:1; Rare:24 | ||||
| chr12:14774184-14774668 | Common:3; Rare:155 | ||||
| chr12:14803403-14803699 | Common:2; Rare:80 | ||||
| chr12:14885731-14885980 | Common:3; Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:15882329-15882682 | Common:1; Rare:106 | ||||
| chr12:16606067-16606182 | Common:3; Rare:20 |