| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161131922-161132705 | Common:3; Rare:186 | ||||
| chr1:161153698-161153848 | Rare:33 | ||||
| chr1:161160252-161160300 | Rare:14 | ||||
| chr1:161162805-161163081 | Common:2; Rare:71 | ||||
| chr1:161166259-161166541 | Common:3; Rare:71; Clinvar:5; Clinvar (benign):1 | ||||
| chr1:161197190-161197459 | Common:3; Rare:47 | ||||
| chr1:161199041-161199329 | Rare:45 | ||||
| chr1:161202005-161202097 | Rare:18 | ||||
| chr1:161213366-161213718 | Rare:94; Clinvar:5; Clinvar (pathogenic):1 | ||||
| chr1:161314264-161314434 | Common:3; Rare:69; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr1:161749470-161749835 | Common:2; Rare:95 | ||||
| chr1:161749846-161750131 | Rare:102 | ||||
| chr1:161750207-161750562 | Common:1; Rare:71 | ||||
| chr1:161766133-161766440 | Common:4; Rare:99 | ||||
| chr1:161766706-161766824 | Common:1; Rare:18 |