| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:193058589-193058786 | Common:1; Rare:44 | ||||
| chr1:193059244-193059717 | Rare:219 | ||||
| chr1:193105096-193105233 | Common:1; Rare:29 | ||||
| chr1:193105360-193105627 | Common:3; Rare:113 | ||||
| chr1:193121639-193122224 | Common:3; Rare:209; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr1:197146129-197146273 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:197146630-197146899 | Rare:78; Clinvar:1 | ||||
| chr1:197775415-197775493 | Rare:19 | ||||
| chr1:197902556-197902695 | Common:1; Rare:47 | ||||
| chr1:197902814-197903051 | Common:2; Rare:118 | ||||
| chr1:198156866-198157099 | Common:4; Rare:91 | ||||
| chr1:198157491-198157762 | Common:1; Rare:99 | ||||
| chr1:198638935-198639115 | Common:1; Rare:23 | ||||
| chr1:200409956-200410244 | Rare:91 | ||||
| chr1:200620146-200620456 | Common:1; Rare:63 |