| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:105744677-105744937 | Common:1; Rare:103 | ||||
| chr2:105745293-105745355 | Rare:16 | ||||
| chr2:105745617-105745723 | Rare:27 | ||||
| chr2:106193926-106194053 | Rare:41 | ||||
| chr2:106194212-106194643 | Common:6; Rare:185 | ||||
| chr2:108448514-108448569 | Common:3; Rare:8 | ||||
| chr2:108448956-108449307 | Common:1; Rare:139 | ||||
| chr2:108533853-108534497 | Common:9; Rare:242 | ||||
| chr2:108534853-108534898 | Rare:6 | ||||
| chr2:108621188-108621261 | Rare:7 | ||||
| chr2:108719298-108719587 | Common:3; Rare:127; Clinvar (benign):2 | ||||
| chr2:108719636-108719860 | Common:1; Rare:77; Clinvar (benign):1 | ||||
| chr2:108786549-108786829 | Common:6; Rare:130 | ||||
| chr2:109129014-109129217 | Rare:88 | ||||
| chr2:109613835-109614036 | Common:2; Rare:71 |