| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:102773766-102773852 | Rare:36 | ||||
| chr13:102845719-102846073 | Common:8; Rare:96; Clinvar:2; Clinvar (benign):4 | ||||
| chr13:106568085-106568215 | Rare:47 | ||||
| chr13:110915006-110915238 | Common:3; Rare:96 | ||||
| chr13:113208620-113208741 | Rare:73 | ||||
| chr13:114281480-114281637 | Common:1; Rare:75 | ||||
| chr13:114281808-114282102 | Common:6; Rare:146 | ||||
| chr14:20343230-20343655 | Common:11; Rare:241 | ||||
| chr14:20454815-20455281 | Common:6; Rare:120 | ||||
| chr14:20684470-20684618 | Common:1; Rare:24; Clinvar (benign):1 | ||||
| chr14:21025740-21025954 | Common:2; Rare:33 | ||||
| chr14:21476925-21477278 | Common:1; Rare:104 | ||||
| chr14:21511257-21511534 | Rare:83 | ||||
| chr14:21526207-21526466 | Rare:53 | ||||
| chr14:22766513-22766710 | Common:1; Rare:102 |