| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:193059253-193059683 | Rare:204 | ||||
| chr1:193105373-193105529 | Common:3; Rare:67 | ||||
| chr1:193121743-193122241 | Common:2; Rare:184; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr1:193186597-193186683 | Rare:14 | ||||
| chr1:197146579-197146829 | Rare:62; Clinvar:3 | ||||
| chr1:197902566-197902647 | Rare:27 | ||||
| chr1:197902850-197903024 | Common:2; Rare:91 | ||||
| chr1:200620698-200620957 | Common:1; Rare:73 | ||||
| chr1:200669809-200670107 | Common:12; Rare:96 | ||||
| chr1:201469156-201469370 | Common:3; Rare:72 | ||||
| chr1:201829036-201829209 | Rare:79 | ||||
| chr1:201888547-201888685 | Common:1; Rare:24 | ||||
| chr1:201955389-201955538 | Rare:45 | ||||
| chr1:202341894-202342146 | Common:1; Rare:65 | ||||
| chr1:202348506-202348715 | Common:1; Rare:46 |