| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:162073986-162074223 | Common:1; Rare:61 | ||||
| chr2:169584744-169584800 | Rare:9 | ||||
| chr2:170928908-170929331 | Common:5; Rare:124 | ||||
| chr2:171433951-171434234 | Common:2; Rare:72 | ||||
| chr2:171434753-171434827 | Rare:19 | ||||
| chr2:171687345-171687616 | Common:2; Rare:49 | ||||
| chr2:171894217-171894313 | Rare:52; Clinvar:1 | ||||
| chr2:171999833-171999967 | Common:1; Rare:57 | ||||
| chr2:173354606-173354923 | Common:1; Rare:98 | ||||
| chr2:173965357-173965531 | Common:1; Rare:74 | ||||
| chr2:174248454-174248764 | Common:1; Rare:96 | ||||
| chr2:174395624-174395794 | Common:2; Rare:56 | ||||
| chr2:176002254-176002398 | Common:1; Rare:54 | ||||
| chr2:176116626-176116861 | Rare:66; Clinvar:1 | ||||
| chr2:176116995-176117295 | Rare:94; Clinvar:2; Clinvar (benign):1 |