| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:176319720-176320143 | Common:5; Rare:131 | ||||
| chr4:177442376-177442479 | Rare:61; Clinvar:1 | ||||
| chr4:183444549-183444654 | Rare:45 | ||||
| chr4:183659162-183659327 | Rare:50 | ||||
| chr4:184649420-184649775 | Common:4; Rare:117 | ||||
| chr4:185396489-185396855 | Rare:120 | ||||
| chr4:185397014-185397246 | Rare:83 | ||||
| chr4:185425933-185426260 | Common:2; Rare:90 | ||||
| chr4:185471083-185471415 | Common:10; Rare:33 | ||||
| chr4:186726644-186726797 | Common:4; Rare:51 | ||||
| chr5:218114-218343 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:443074-443278 | Common:10; Rare:92 | ||||
| chr5:892546-892896 | Common:5; Rare:106 | ||||
| chr5:1799778-1799961 | Common:8; Rare:90 | ||||
| chr5:1801352-1801415 | Common:1; Rare:21; Clinvar (benign):1 |