| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:106193939-106194092 | Rare:51 | ||||
| chr2:106194099-106194189 | Common:1; Rare:24 | ||||
| chr2:106194191-106194640 | Common:6; Rare:192 | ||||
| chr2:108377890-108378153 | Common:1; Rare:45 | ||||
| chr2:108448541-108448789 | Common:4; Rare:51 | ||||
| chr2:108448927-108449338 | Common:1; Rare:155 | ||||
| chr2:108449399-108449567 | Common:3; Rare:63 | ||||
| chr2:108449829-108449891 | Common:3; Rare:17 | ||||
| chr2:108533859-108534653 | Common:11; Rare:282 | ||||
| chr2:108534759-108534907 | Rare:41 | ||||
| chr2:108534949-108535097 | Common:1; Rare:33 | ||||
| chr2:108719264-108719743 | Common:4; Rare:210; Clinvar (benign):3 | ||||
| chr2:108786366-108786458 | Rare:24 | ||||
| chr2:108786549-108786932 | Common:8; Rare:168 | ||||
| chr2:108786983-108787086 | Common:1; Rare:36 |