| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:169106064-169106368 | Common:6; Rare:108 | ||||
| chr1:169367722-169368290 | Common:4; Rare:122 | ||||
| chr1:169427305-169427534 | Common:2; Rare:48 | ||||
| chr1:169485762-169486194 | Common:1; Rare:115; Clinvar:5; Clinvar (benign):4 | ||||
| chr1:169794842-169795130 | Common:3; Rare:78 | ||||
| chr1:170532068-170532213 | Rare:79; Clinvar:1 | ||||
| chr1:171313892-171314185 | Common:1; Rare:61 | ||||
| chr1:171485315-171485740 | Common:1; Rare:130 | ||||
| chr1:171523225-171523520 | Rare:60 | ||||
| chr1:171741929-171742122 | Common:1; Rare:65 | ||||
| chr1:171781388-171781762 | Common:4; Rare:99 | ||||
| chr1:171841364-171841546 | Common:3; Rare:57 | ||||
| chr1:173476929-173477493 | Common:6; Rare:184 | ||||
| chr1:173669827-173669992 | Common:1; Rare:46 | ||||
| chr1:173714852-173715081 | Common:1; Rare:51 |