| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24195461-24195831 | Common:2; Rare:98 | ||||
| chr14:24213093-24213201 | Rare:21 | ||||
| chr14:24213280-24213624 | Common:3; Rare:109 | ||||
| chr14:24215442-24215842 | Common:2; Rare:200 | ||||
| chr14:24215979-24216192 | Common:1; Rare:65 | ||||
| chr14:24232319-24232454 | Common:6; Rare:34 | ||||
| chr14:24232510-24232730 | Rare:51 | ||||
| chr14:24242235-24242436 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:24242586-24242824 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24242970-24243147 | Common:1; Rare:31 | ||||
| chr14:24271131-24271310 | Rare:50 | ||||
| chr14:24271410-24271770 | Common:3; Rare:104 | ||||
| chr14:24299734-24299890 | Common:4; Rare:49 | ||||
| chr14:24366621-24366876 | Common:1; Rare:64 | ||||
| chr14:24367369-24367523 | Rare:31 |