| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35046134-35046707 | Common:2; Rare:203 | ||||
| chr14:35121808-35121860 | Rare:12 | ||||
| chr14:35121955-35122351 | Common:2; Rare:105 | ||||
| chr14:35122436-35122772 | Common:2; Rare:103 | ||||
| chr14:35292198-35292611 | Common:5; Rare:137; Clinvar:1 | ||||
| chr14:35402741-35403242 | Common:5; Rare:160; Clinvar (benign):4 | ||||
| chr14:35404422-35404854 | Common:3; Rare:141; Clinvar:1; Clinvar (benign):5 | ||||
| chr14:35826187-35826502 | Common:1; Rare:88 | ||||
| chr14:35826698-35826970 | Common:1; Rare:76 | ||||
| chr14:36320561-36320772 | Common:4; Rare:77 | ||||
| chr14:37197832-37198103 | Common:3; Rare:88 | ||||
| chr14:38256067-38256307 | Common:1; Rare:60 | ||||
| chr14:39103591-39103825 | Common:2; Rare:48 | ||||
| chr14:39114259-39114341 | Common:2; Rare:36 | ||||
| chr14:39170203-39170450 | Common:3; Rare:59 |