| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:182839206-182839420 | Common:1; Rare:91 | ||||
| chr1:183186131-183186350 | Common:4; Rare:50; Clinvar:2; Clinvar (benign):4 | ||||
| chr1:183472306-183472525 | Common:2; Rare:76 | ||||
| chr1:183635666-183636100 | Common:4; Rare:124 | ||||
| chr1:184051600-184051761 | Common:3; Rare:60 | ||||
| chr1:184754812-184755171 | Common:1; Rare:87 | ||||
| chr1:184974396-184974670 | Rare:68 | ||||
| chr1:185045257-185045632 | Common:2; Rare:129 | ||||
| chr1:185156922-185157297 | Common:1; Rare:102 | ||||
| chr1:185157431-185157523 | Common:1; Rare:31 | ||||
| chr1:185316778-185317079 | Common:1; Rare:71 | ||||
| chr1:185317083-185317088 | Rare:2 | ||||
| chr1:185317091-185317491 | Common:2; Rare:111 | ||||
| chr1:186375038-186375928 | Common:1; Rare:254 | ||||
| chr1:186680323-186680690 | Common:3; Rare:80 |