| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:46203151-46203384 | Rare:43 | ||||
| chr1:46247254-46247807 | Common:5; Rare:99 | ||||
| chr1:46303134-46303745 | Common:3; Rare:178 | ||||
| chr1:46339873-46340199 | Common:4; Rare:62 | ||||
| chr1:46340503-46340886 | Common:7; Rare:102 | ||||
| chr1:46340985-46341204 | Common:1; Rare:49 | ||||
| chr1:46603928-46604037 | Rare:19 | ||||
| chr1:46604063-46604495 | Common:2; Rare:120 | ||||
| chr1:46616370-46616596 | Common:2; Rare:49 | ||||
| chr1:46616597-46617007 | Common:3; Rare:81 | ||||
| chr1:46667909-46668180 | Common:1; Rare:83 | ||||
| chr1:46668282-46668688 | Common:3; Rare:119 | ||||
| chr1:46719047-46719457 | Common:3; Rare:148 | ||||
| chr1:47313514-47313608 | Common:1; Rare:13 | ||||
| chr1:47313927-47314557 | Common:6; Rare:134; Clinvar:3; Clinvar (benign):1 |