| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:106146429-106146725 | Common:3; Rare:59 | ||||
| chr13:106529420-106529573 | Rare:24 | ||||
| chr13:109265157-109265431 | Common:4; Rare:62 | ||||
| chr13:110308513-110308622 | Common:1; Rare:21 | ||||
| chr13:110449511-110449786 | Common:4; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:112996735-112997060 | Common:4; Rare:73 | ||||
| chr13:113822030-113822341 | Common:2; Rare:101 | ||||
| chr13:113848637-113848902 | Common:1; Rare:34 | ||||
| chr13:113854474-113854669 | Rare:48 | ||||
| chr14:20456855-20457119 | Common:2; Rare:103; Clinvar:1 | ||||
| chr14:21088584-21088851 | Common:1; Rare:62 | ||||
| chr14:22769602-22769802 | Common:1; Rare:31; Clinvar (pathogenic):1 | ||||
| chr14:23061452-23061756 | Common:3; Rare:88 | ||||
| chr14:23959843-23959947 | Common:1; Rare:45 | ||||
| chr14:24036343-24036520 | Common:3; Rare:72 |