| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110449670-110450070 | Common:4; Rare:106 | ||||
| chr12:110450294-110450497 | Common:1; Rare:61 | ||||
| chr12:110468176-110468489 | Common:3; Rare:101 | ||||
| chr12:110468590-110468930 | Rare:94 | ||||
| chr12:110469160-110469480 | Common:1; Rare:49 | ||||
| chr12:110502026-110502332 | Common:1; Rare:110 | ||||
| chr12:110583236-110583532 | Rare:82 | ||||
| chr12:110613923-110614181 | Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:110614374-110614774 | Common:2; Rare:109; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:110742861-110743257 | Common:2; Rare:125 | ||||
| chr12:111034380-111035000 | Rare:153 | ||||
| chr12:111369054-111369280 | Common:1; Rare:62 | ||||
| chr12:111405745-111405943 | Rare:60 | ||||
| chr12:111597462-111598053 | Rare:225 | ||||
| chr12:111598330-111598730 | Common:1; Rare:143 |