| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:162344230-162344521 | Common:3; Rare:219 | ||||
| chr2:163735207-163735558 | Common:5; Rare:135 | ||||
| chr2:163735835-163736398 | Common:5; Rare:319 | ||||
| chr2:164620870-164621314 | Rare:228 | ||||
| chr2:164621367-164621691 | Common:4; Rare:177 | ||||
| chr2:164621909-164622562 | Common:6; Rare:132 | ||||
| chr2:164841038-164841697 | Rare:361 | ||||
| chr2:164841735-164842530 | Common:12; Rare:449 | ||||
| chr2:164955250-164955890 | Common:1; Rare:135 | ||||
| chr2:165793201-165793404 | Common:1; Rare:35 | ||||
| chr2:165793974-165794524 | Common:8; Rare:315; Clinvar:18; Clinvar (benign):3 | ||||
| chr2:165794665-165794871 | Common:2; Rare:65 | ||||
| chr2:165953702-165954094 | Common:7; Rare:360; Clinvar:24; Clinvar (benign):5 | ||||
| chr2:166375780-166376360 | Common:5; Rare:140; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:168247310-168248010 | Common:19; Rare:557 |