| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:163735987-163736113 | Rare:24 | ||||
| chr2:164841202-164841529 | Rare:96 | ||||
| chr2:164955545-164955650 | Rare:28 | ||||
| chr2:165953703-165953955 | Common:2; Rare:106; Clinvar:9; Clinvar (benign):2 | ||||
| chr2:166000442-166000898 | Common:1; Rare:58 | ||||
| chr2:169362466-169362686 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:169479368-169479565 | Common:3; Rare:74; Clinvar (benign):1 | ||||
| chr2:169584755-169584809 | Rare:15 | ||||
| chr2:169694348-169694571 | Common:5; Rare:76 | ||||
| chr2:169798767-169798965 | Rare:51 | ||||
| chr2:169808363-169808481 | Common:3; Rare:32 | ||||
| chr2:170928970-170929334 | Common:4; Rare:117 | ||||
| chr2:171160346-171160595 | Rare:86 | ||||
| chr2:171433934-171434248 | Common:3; Rare:81 | ||||
| chr2:171434395-171434687 | Common:1; Rare:95; Clinvar:2 |