| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:185045253-185045632 | Common:2; Rare:131 | ||||
| chr1:185156922-185157303 | Common:1; Rare:106 | ||||
| chr1:185317183-185317686 | Common:2; Rare:134 | ||||
| chr1:186375018-186375945 | Common:1; Rare:262 | ||||
| chr1:190478154-190478365 | Common:1; Rare:56 | ||||
| chr1:190478723-190478981 | Common:3; Rare:71 | ||||
| chr1:192808729-192809077 | Common:4; Rare:139 | ||||
| chr1:193059269-193059762 | Common:1; Rare:236 | ||||
| chr1:193105348-193105549 | Common:3; Rare:88 | ||||
| chr1:193121737-193122203 | Common:2; Rare:171; Clinvar:5; Clinvar (benign):4 | ||||
| chr1:193186532-193186698 | Rare:29 | ||||
| chr1:196608395-196608504 | Common:2; Rare:25 | ||||
| chr1:196608517-196608552 | Rare:12 | ||||
| chr1:196608774-196609105 | Common:2; Rare:67 | ||||
| chr1:197146383-197146495 | Rare:43; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 |