| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:31207647-31207902 | Common:2; Rare:91 | ||||
| chr14:31420526-31420763 | Common:3; Rare:71 | ||||
| chr14:31457389-31457580 | Common:2; Rare:64 | ||||
| chr14:31561089-31561450 | Common:4; Rare:97; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:34462226-34462548 | Common:1; Rare:107 | ||||
| chr14:34539659-34539856 | Rare:53 | ||||
| chr14:34630118-34630260 | Common:5; Rare:66 | ||||
| chr14:34714580-34714819 | Common:4; Rare:89 | ||||
| chr14:34875313-34875480 | Rare:63 | ||||
| chr14:34982504-34982719 | Common:1; Rare:93 | ||||
| chr14:35046105-35046451 | Common:2; Rare:114 | ||||
| chr14:35121935-35122787 | Common:4; Rare:241 | ||||
| chr14:35292212-35292470 | Common:5; Rare:96; Clinvar:1 | ||||
| chr14:36320580-36320764 | Common:3; Rare:59 | ||||
| chr14:39103138-39103371 | Common:1; Rare:69 |