| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:30559055-30559214 | Common:2; Rare:61 | ||||
| chr14:30622076-30622350 | Rare:77 | ||||
| chr14:31025536-31025656 | Common:1; Rare:28 | ||||
| chr14:31420514-31420763 | Common:3; Rare:78 | ||||
| chr14:31561083-31561491 | Common:4; Rare:112; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:32076556-32077043 | Common:3; Rare:136 | ||||
| chr14:33951052-33951210 | Common:1; Rare:53 | ||||
| chr14:34462203-34462585 | Common:1; Rare:134 | ||||
| chr14:34539649-34539856 | Rare:56 | ||||
| chr14:34629932-34630252 | Common:5; Rare:127 | ||||
| chr14:34714545-34714768 | Common:3; Rare:81 | ||||
| chr14:34875271-34875444 | Rare:70 | ||||
| chr14:34982372-34982709 | Common:1; Rare:136 | ||||
| chr14:35046097-35046586 | Common:2; Rare:168 | ||||
| chr14:35122200-35122687 | Common:1; Rare:135 |