| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:159904648-159904863 | Rare:64 | ||||
| chr2:160062474-160062763 | Common:5; Rare:73 | ||||
| chr2:161308334-161308497 | Common:1; Rare:40 | ||||
| chr2:162317912-162318229 | Rare:106; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:162343791-162344215 | Common:2; Rare:134 | ||||
| chr2:163736001-163736130 | Rare:24 | ||||
| chr2:164841195-164841520 | Rare:92 | ||||
| chr2:164841817-164841977 | Common:1; Rare:49 | ||||
| chr2:164955478-164955643 | Rare:39 | ||||
| chr2:165794122-165794323 | Common:2; Rare:57; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:165794693-165794795 | Common:1; Rare:16 | ||||
| chr2:165795149-165795470 | Common:1; Rare:55 | ||||
| chr2:166494121-166494380 | Common:1; Rare:44 | ||||
| chr2:168247535-168247763 | Common:4; Rare:86 | ||||
| chr2:168456544-168456614 | Rare:23 |