| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184474512-184474829 | Rare:73 | ||||
| chr4:184649413-184649805 | Common:4; Rare:127 | ||||
| chr4:185425875-185426242 | Common:3; Rare:110 | ||||
| chr4:185471090-185471412 | Common:10; Rare:31 | ||||
| chr4:189940626-189940993 | Common:11; Rare:134 | ||||
| chr5:218100-218369 | Common:4; Rare:111; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr5:443084-443281 | Common:10; Rare:91 | ||||
| chr5:892541-892984 | Common:5; Rare:140 | ||||
| chr5:1799785-1799993 | Common:7; Rare:98 | ||||
| chr5:1801281-1801432 | Common:4; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:6378466-6378718 | Rare:101 | ||||
| chr5:7869000-7869204 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr5:10249874-10250378 | Common:19; Rare:242; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10353590-10353896 | Common:3; Rare:113 | ||||
| chr5:16465709-16465887 | Rare:32 |