| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183659122-183659410 | Common:1; Rare:94 | ||||
| chr4:184474472-184474823 | Rare:79 | ||||
| chr4:184649396-184649796 | Common:5; Rare:130 | ||||
| chr4:184734066-184734403 | Common:5; Rare:115 | ||||
| chr4:184825917-184826265 | Common:7; Rare:108 | ||||
| chr4:185142981-185143284 | Common:3; Rare:81; Clinvar (benign):2 | ||||
| chr4:185395837-185396017 | Common:2; Rare:49 | ||||
| chr4:185396569-185396843 | Rare:88 | ||||
| chr4:185425866-185426036 | Common:2; Rare:64 | ||||
| chr4:186144727-186145013 | Common:3; Rare:82 | ||||
| chr4:186191460-186191818 | Common:6; Rare:118; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:186723765-186723967 | Common:6; Rare:81 | ||||
| chr4:189940588-189941012 | Common:16; Rare:145 | ||||
| chr5:216758-216994 | Rare:59 | ||||
| chr5:218106-218376 | Common:4; Rare:115; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):2 |