| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:53196640-53196916 | Common:1; Rare:103; Clinvar:6; Clinvar (benign):1 | ||||
| chr1:53220505-53220728 | Common:3; Rare:105 | ||||
| chr1:53238381-53238566 | Rare:57 | ||||
| chr1:53327976-53328281 | Common:2; Rare:74 | ||||
| chr1:53328395-53328497 | Common:1; Rare:16 | ||||
| chr1:53838204-53838596 | Rare:124 | ||||
| chr1:53945684-53946092 | Common:7; Rare:107 | ||||
| chr1:53946259-53946969 | Common:4; Rare:186 | ||||
| chr1:54053161-54053713 | Common:6; Rare:180 | ||||
| chr1:54199963-54200290 | Rare:97 | ||||
| chr1:54406366-54406529 | Common:3; Rare:62 | ||||
| chr1:54542587-54542707 | Common:1; Rare:26 | ||||
| chr1:54886893-54886931 | Rare:9 | ||||
| chr1:54886944-54887450 | Common:3; Rare:167; Clinvar:5; Clinvar (benign):2 | ||||
| chr1:55039348-55039623 | Common:2; Rare:64; Clinvar:4; Clinvar (benign):1 |