| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:25250435-25250558 | Rare:35 | ||||
| chr12:25250793-25251325 | Rare:155; Clinvar:5; Clinvar (benign):4 | ||||
| chr12:25648503-25648681 | Common:1; Rare:50 | ||||
| chr12:25648771-25649075 | Common:2; Rare:48 | ||||
| chr12:25958404-25958987 | Common:4; Rare:202 | ||||
| chr12:25958995-25959455 | Common:5; Rare:130 | ||||
| chr12:26122528-26122853 | Common:3; Rare:118 | ||||
| chr12:26123250-26123339 | Common:1; Rare:19 | ||||
| chr12:26124999-26125538 | Common:4; Rare:110 | ||||
| chr12:26832405-26832734 | Common:2; Rare:72 | ||||
| chr12:26832970-26833489 | Common:3; Rare:142 | ||||
| chr12:26937791-26938116 | Common:7; Rare:85 | ||||
| chr12:26938229-26938654 | Common:4; Rare:156 | ||||
| chr12:26938710-26938784 | Rare:24 | ||||
| chr12:26938828-26938940 | Rare:37 |