| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:185156900-185157324 | Common:2; Rare:119 | ||||
| chr1:185316996-185317324 | Common:2; Rare:97 | ||||
| chr1:185317333-185317600 | Common:1; Rare:67 | ||||
| chr1:186375009-186375951 | Common:1; Rare:267 | ||||
| chr1:190477622-190477753 | Common:2; Rare:38 | ||||
| chr1:190477878-190478353 | Rare:108 | ||||
| chr1:190478490-190478579 | Common:1; Rare:12 | ||||
| chr1:190478683-190478993 | Common:6; Rare:79 | ||||
| chr1:192808828-192809125 | Common:4; Rare:137 | ||||
| chr1:193059253-193059779 | Common:1; Rare:246 | ||||
| chr1:193105391-193105525 | Common:2; Rare:53 | ||||
| chr1:193121759-193122203 | Common:2; Rare:159; Clinvar:5; Clinvar (benign):4 | ||||
| chr1:193186510-193186698 | Common:2; Rare:33 | ||||
| chr1:196608736-196609027 | Common:1; Rare:57 | ||||
| chr1:197902535-197902644 | Rare:33 |