| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190881509-190881761 | Common:1; Rare:103 | ||||
| chr2:191013916-191014610 | Common:6; Rare:185; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:191020221-191020692 | Common:3; Rare:154 | ||||
| chr2:191020971-191021135 | Common:1; Rare:27 | ||||
| chr2:191150934-191151144 | Rare:32 | ||||
| chr2:191245251-191245463 | Common:1; Rare:70 | ||||
| chr2:191677759-191678236 | Common:4; Rare:130 | ||||
| chr2:195656795-195656870 | Rare:26 | ||||
| chr2:195656999-195657458 | Common:1; Rare:123 | ||||
| chr2:196068766-196068956 | Common:1; Rare:59 | ||||
| chr2:196171240-196171384 | Common:2; Rare:37 | ||||
| chr2:196171496-196171936 | Common:1; Rare:134 | ||||
| chr2:196176182-196176448 | Rare:42 | ||||
| chr2:196639465-196639818 | Rare:118 | ||||
| chr2:196639867-196639924 | Rare:13 |