| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43595931-43596191 | Common:1; Rare:88 | ||||
| chr2:43637100-43637356 | Common:2; Rare:81 | ||||
| chr2:44361479-44362115 | Common:4; Rare:210 | ||||
| chr2:46297173-46297444 | Common:4; Rare:102; Clinvar (benign):1 | ||||
| chr2:46297723-46297766 | Rare:13 | ||||
| chr2:46617016-46617276 | Common:7; Rare:114 | ||||
| chr2:46915722-46915953 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916026-46916175 | Common:2; Rare:51 | ||||
| chr2:47176186-47176237 | Rare:17 | ||||
| chr2:47344972-47345153 | Common:1; Rare:48 | ||||
| chr2:47369064-47369586 | Common:4; Rare:220; Clinvar:18; Clinvar (benign):6 | ||||
| chr2:47402893-47403200 | Common:1; Rare:141; Clinvar:46; Clinvar (benign):30 | ||||
| chr2:47905489-47905847 | Common:3; Rare:176 | ||||
| chr2:48440610-48440956 | Common:8; Rare:152 | ||||
| chr2:53767549-53767871 | Common:5; Rare:111 |