| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:193059907-193060240 | Common:1; Rare:109 | ||||
| chr1:193105102-193105207 | Common:1; Rare:17 | ||||
| chr1:193105343-193105725 | Common:3; Rare:152 | ||||
| chr1:193121649-193122207 | Common:3; Rare:198; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr1:193122209-193122281 | Rare:18; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr1:193122399-193122531 | Rare:47 | ||||
| chr1:193186600-193186654 | Rare:10 | ||||
| chr1:196608488-196608551 | Rare:16 | ||||
| chr1:196608756-196609108 | Common:2; Rare:69 | ||||
| chr1:196652034-196652078 | Common:1; Rare:10; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:197146205-197146305 | Common:1; Rare:30; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:197146381-197146488 | Rare:43; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr1:197146533-197146899 | Common:1; Rare:96; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:197200650-197200924 | Common:3; Rare:49 | ||||
| chr1:197200935-197201017 | Rare:20 |