| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:169584325-169584656 | Common:1; Rare:125 | ||||
| chr2:169584703-169584862 | Rare:44 | ||||
| chr2:169694319-169694615 | Common:6; Rare:110 | ||||
| chr2:169798795-169798973 | Rare:45 | ||||
| chr2:169805481-169805766 | Rare:65 | ||||
| chr2:169805908-169806284 | Common:2; Rare:73 | ||||
| chr2:170928797-170929421 | Common:7; Rare:177 | ||||
| chr2:171160557-171160598 | Common:1; Rare:9 | ||||
| chr2:171433941-171434338 | Common:3; Rare:107 | ||||
| chr2:171434546-171434706 | Rare:48; Clinvar:1 | ||||
| chr2:171434746-171434824 | Rare:18 | ||||
| chr2:171522551-171522714 | Rare:51 | ||||
| chr2:171687096-171687828 | Common:3; Rare:155 | ||||
| chr2:171687989-171688053 | Rare:15 | ||||
| chr2:171688071-171688140 | Rare:23 |