| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:42658028-42658074 | Rare:11 | ||||
| chr1:42658220-42658718 | Common:3; Rare:128 | ||||
| chr1:42659027-42659129 | Common:1; Rare:23 | ||||
| chr1:42681941-42682707 | Common:3; Rare:252 | ||||
| chr1:42682731-42682898 | Rare:56 | ||||
| chr1:42682962-42683208 | Common:1; Rare:119 | ||||
| chr1:42766561-42766653 | Rare:27; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:42766946-42767368 | Common:6; Rare:150; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:42767543-42767627 | Rare:31 | ||||
| chr1:42816611-42816753 | Rare:25 | ||||
| chr1:42816875-42817404 | Common:1; Rare:174 | ||||
| chr1:42846325-42846743 | Common:1; Rare:116 | ||||
| chr1:42847016-42847053 | Rare:6 | ||||
| chr1:42958339-42958696 | Common:1; Rare:101; Clinvar (benign):6 | ||||
| chr1:42958728-42959261 | Common:6; Rare:129; Clinvar:8; Clinvar (benign):5 |