| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127629431-127629882 | Common:1; Rare:130 | ||||
| chr2:127630643-127630907 | Common:1; Rare:73 | ||||
| chr2:127631102-127631375 | Common:2; Rare:104 | ||||
| chr2:127633020-127633361 | Common:4; Rare:100 | ||||
| chr2:131682413-131682528 | Common:2; Rare:34 | ||||
| chr2:132347354-132347503 | Common:1; Rare:38 | ||||
| chr2:133480657-133480757 | Common:1; Rare:13 | ||||
| chr2:135174233-135174284 | Common:1; Rare:14 | ||||
| chr2:161244645-161244841 | Common:1; Rare:58 | ||||
| chr2:168834137-168834313 | Common:2; Rare:37 | ||||
| chr2:171534689-171534944 | Common:1; Rare:46 | ||||
| chr2:172481704-172481860 | Common:2; Rare:31 | ||||
| chr2:172487136-172487441 | Common:3; Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:172489231-172489490 | Common:1; Rare:53 | ||||
| chr2:172614361-172614432 | Rare:12 |