| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:169584315-169584630 | Common:1; Rare:121 | ||||
| chr2:169584760-169584825 | Rare:21 | ||||
| chr2:169694323-169694579 | Common:6; Rare:94 | ||||
| chr2:170928929-170929338 | Common:4; Rare:125 | ||||
| chr2:171433905-171434324 | Common:3; Rare:111 | ||||
| chr2:171434742-171434832 | Rare:20 | ||||
| chr2:171999818-171999985 | Common:1; Rare:69 | ||||
| chr2:172427349-172427595 | Common:8; Rare:77 | ||||
| chr2:172427634-172427963 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:173354828-173354979 | Rare:54 | ||||
| chr2:173964054-173964370 | Rare:139 | ||||
| chr2:173965276-173965500 | Common:1; Rare:79 | ||||
| chr2:174248503-174248828 | Common:2; Rare:107 | ||||
| chr2:174395639-174395880 | Common:1; Rare:82 | ||||
| chr2:174487022-174487328 | Common:1; Rare:73 |