| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:165912950-165913183 | Common:1; Rare:44 | ||||
| chr2:165933629-165933671 | Rare:6 | ||||
| chr2:166222666-166222941 | Common:4; Rare:30 | ||||
| chr2:166544465-166544476 | |||||
| chr2:167711821-167711876 | Rare:11 | ||||
| chr2:168436262-168436515 | Rare:35 | ||||
| chr2:168995781-168995834 | Rare:12 | ||||
| chr2:169001176-169001343 | Common:1; Rare:28 | ||||
| chr2:169570502-169570665 | Rare:32 | ||||
| chr2:169585707-169585952 | Rare:48 | ||||
| chr2:169704813-169704879 | Rare:13 | ||||
| chr2:169717355-169717588 | Common:1; Rare:35 | ||||
| chr2:169720762-169720983 | Common:3; Rare:33 | ||||
| chr2:169810866-169811329 | Rare:120 | ||||
| chr2:169828136-169828352 | Common:3; Rare:29 |