| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:19787043-19787314 | Common:3; Rare:45 | ||||
| chr1:20650293-20650517 | Common:3; Rare:61; Clinvar (benign):1 | ||||
| chr1:20654345-20654633 | Common:4; Rare:86; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr1:20779823-20779980 | Common:1; Rare:48 | ||||
| chr1:21013060-21013196 | Common:2; Rare:23 | ||||
| chr1:21603811-21604081 | Common:3; Rare:76 | ||||
| chr1:21619032-21619329 | Common:2; Rare:78 | ||||
| chr1:21638778-21639001 | Common:1; Rare:46 | ||||
| chr1:21672179-21672463 | Common:4; Rare:54 | ||||
| chr1:21831461-21831672 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:21880434-21880715 | Common:3; Rare:88; Clinvar:6; Clinvar (benign):3 | ||||
| chr1:21884811-21885151 | Common:1; Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:23562236-23562332 | Rare:14 | ||||
| chr1:24110871-24111145 | Common:2; Rare:52 | ||||
| chr1:24515820-24515863 | Rare:6 |