| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:236281909-236282352 | Common:7; Rare:126 | ||||
| chr1:236523723-236523773 | Rare:6 | ||||
| chr1:236523831-236524098 | Common:3; Rare:79 | ||||
| chr1:236524411-236524764 | Common:2; Rare:84 | ||||
| chr1:236604398-236604717 | Common:5; Rare:94 | ||||
| chr1:236604778-236604968 | Rare:41 | ||||
| chr1:236686274-236686552 | Rare:111 | ||||
| chr1:236794942-236795504 | Common:7; Rare:205; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:236795794-236795877 | Rare:17 | ||||
| chr1:237041901-237042247 | Common:4; Rare:95 | ||||
| chr1:241519460-241519504 | Rare:15 | ||||
| chr1:241519678-241520042 | Common:2; Rare:106; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr1:241532349-241532398 | Rare:17 | ||||
| chr1:241640201-241640594 | Common:7; Rare:142 | ||||
| chr1:241847762-241847889 | Rare:43 |