| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184734028-184734450 | Common:10; Rare:165 | ||||
| chr4:185143135-185143383 | Common:3; Rare:81; Clinvar:1; Clinvar (benign):4 | ||||
| chr4:185203827-185204097 | Common:4; Rare:83 | ||||
| chr4:185396563-185396642 | Rare:20 | ||||
| chr4:185425892-185426299 | Common:4; Rare:121 | ||||
| chr4:185956229-185956488 | Common:2; Rare:64 | ||||
| chr4:186191459-186191826 | Common:6; Rare:124; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:186723796-186723906 | Common:2; Rare:40 | ||||
| chr4:186726655-186726929 | Common:4; Rare:93 | ||||
| chr4:189940560-189941060 | Common:18; Rare:171 | ||||
| chr5:218087-218392 | Common:4; Rare:125; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr5:443084-443263 | Common:9; Rare:81 | ||||
| chr5:612201-612358 | Rare:62 | ||||
| chr5:693286-693538 | Common:6; Rare:73 | ||||
| chr5:892519-892867 | Common:5; Rare:98 |