| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:160284109-160284390 | Common:1; Rare:61 | ||||
| chr1:160343147-160343399 | Rare:97 | ||||
| chr1:160355678-160355889 | Rare:43 | ||||
| chr1:160647035-160647093 | Rare:9 | ||||
| chr1:161020322-161020638 | Common:2; Rare:56 | ||||
| chr1:161021012-161021279 | Common:5; Rare:88 | ||||
| chr1:161045860-161046057 | Common:1; Rare:51 | ||||
| chr1:161118009-161118155 | Rare:77 | ||||
| chr1:161118492-161118570 | Common:1; Rare:16 | ||||
| chr1:161132426-161132882 | Common:2; Rare:141 | ||||
| chr1:161159404-161159517 | Common:1; Rare:31 | ||||
| chr1:161166247-161166522 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:161199014-161199304 | Rare:45 | ||||
| chr1:161225746-161226082 | Common:10; Rare:49 | ||||
| chr1:161314201-161314417 | Common:3; Rare:80; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 |