| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:180632139-180632210 | Rare:25 | ||||
| chr1:181482542-181482927 | Common:2; Rare:123 | ||||
| chr1:181483480-181483700 | Common:3; Rare:46 | ||||
| chr1:182391327-182391402 | Rare:17 | ||||
| chr1:182391769-182392045 | Common:4; Rare:92; Clinvar:4; Clinvar (benign):4 | ||||
| chr1:182604381-182604579 | Rare:44 | ||||
| chr1:182789642-182789778 | Common:2; Rare:44 | ||||
| chr1:182839246-182839430 | Common:1; Rare:79 | ||||
| chr1:182839553-182839723 | Common:2; Rare:75 | ||||
| chr1:183635666-183636146 | Common:5; Rare:134 | ||||
| chr1:183805114-183805238 | Rare:38 | ||||
| chr1:184386691-184387205 | Common:4; Rare:142 | ||||
| chr1:184754589-184754690 | Common:1; Rare:47 | ||||
| chr1:185156710-185156748 | Rare:20 | ||||
| chr1:185156886-185157306 | Common:2; Rare:119 |