| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24398730-24399520 | Common:11; Rare:545 | ||||
| chr14:24429477-24430140 | Common:27; Rare:720 | ||||
| chr14:24430060-24430982 | Common:6; Rare:386 | ||||
| chr14:24442123-24442523 | Common:5; Rare:267 | ||||
| chr14:24442579-24443084 | Common:36; Rare:719 | ||||
| chr14:24443253-24443653 | Common:5; Rare:73 | ||||
| chr14:26598220-26598540 | Common:1; Rare:85 | ||||
| chr14:29650530-29651050 | Common:15; Rare:213 | ||||
| chr14:29927760-29928130 | Common:2; Rare:114 | ||||
| chr14:30558900-30559250 | Common:12; Rare:390 | ||||
| chr14:30559494-30559894 | Common:1; Rare:86 | ||||
| chr14:30621275-30621693 | Common:8; Rare:172 | ||||
| chr14:30621970-30623133 | Common:8; Rare:777 | ||||
| chr14:30873860-30874120 | Common:3; Rare:49 | ||||
| chr14:30874140-30875774 | Common:36; Rare:1308; Clinvar:3; Clinvar (benign):2 |