| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:182789661-182789786 | Common:2; Rare:42 | ||||
| chr1:182839194-182839451 | Common:1; Rare:103 | ||||
| chr1:182839559-182839725 | Common:2; Rare:76 | ||||
| chr1:183134655-183135180 | Common:3; Rare:122 | ||||
| chr1:183472261-183472525 | Common:2; Rare:92 | ||||
| chr1:183635515-183636146 | Common:5; Rare:181 | ||||
| chr1:184051676-184051771 | Common:2; Rare:38 | ||||
| chr1:184386886-184387213 | Common:1; Rare:81 | ||||
| chr1:185156878-185157306 | Common:2; Rare:122 | ||||
| chr1:186375178-186375472 | Rare:73 | ||||
| chr1:186375653-186375960 | Common:1; Rare:82 | ||||
| chr1:186680403-186680756 | Common:3; Rare:80 | ||||
| chr1:192808793-192809170 | Common:4; Rare:159; Clinvar:1 | ||||
| chr1:193059185-193059770 | Common:1; Rare:252 | ||||
| chr1:193122041-193122206 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 |