| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24213572-24213646 | Common:1; Rare:22 | ||||
| chr14:24232256-24232936 | Common:9; Rare:165 | ||||
| chr14:24242268-24242408 | Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:24242562-24242769 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24299749-24299862 | Common:1; Rare:32 | ||||
| chr14:24429855-24429954 | Rare:24 | ||||
| chr14:24442680-24443013 | Common:5; Rare:107 | ||||
| chr14:25049890-25050218 | Common:3; Rare:100 | ||||
| chr14:31101318-31101505 | Rare:48 | ||||
| chr14:31123035-31123299 | Common:1; Rare:41 | ||||
| chr14:31207611-31207944 | Common:2; Rare:114 | ||||
| chr14:31420528-31420756 | Common:3; Rare:69 | ||||
| chr14:32076128-32076312 | Rare:53 | ||||
| chr14:32076536-32077051 | Common:3; Rare:141 | ||||
| chr14:34462214-34462575 | Common:1; Rare:127 |