| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:181088494-181088772 | Common:1; Rare:105 | ||||
| chr1:181088792-181088943 | Common:1; Rare:54 | ||||
| chr1:182391334-182391480 | Rare:32 | ||||
| chr1:182789641-182789776 | Common:2; Rare:43 | ||||
| chr1:182839164-182839412 | Common:1; Rare:108 | ||||
| chr1:182839576-182839744 | Common:2; Rare:75 | ||||
| chr1:183023079-183023283 | Common:4; Rare:49 | ||||
| chr1:183134632-183135180 | Common:3; Rare:131 | ||||
| chr1:183186013-183186109 | Common:2; Rare:28; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:183186111-183186306 | Common:2; Rare:36; Clinvar (benign):2 | ||||
| chr1:183472255-183472522 | Common:2; Rare:93 | ||||
| chr1:183635515-183636079 | Common:3; Rare:163 | ||||
| chr1:184051612-184051853 | Common:4; Rare:94 | ||||
| chr1:184386728-184387082 | Common:3; Rare:109 | ||||
| chr1:185156900-185157226 | Common:2; Rare:86 |