| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:174522464-174522666 | Rare:58; Clinvar:2 | ||||
| chr4:176319641-176320028 | Common:4; Rare:114 | ||||
| chr4:177442376-177442526 | Rare:90; Clinvar:2 | ||||
| chr4:183099016-183099151 | Rare:49 | ||||
| chr4:183504522-183504803 | Common:1; Rare:94 | ||||
| chr4:183659126-183659349 | Common:1; Rare:70 | ||||
| chr4:184474504-184474816 | Rare:69 | ||||
| chr4:184649440-184649770 | Common:4; Rare:106 | ||||
| chr4:184734088-184734376 | Common:5; Rare:96 | ||||
| chr4:184805509-184805819 | Common:1; Rare:56 | ||||
| chr4:185396569-185396845 | Rare:90 | ||||
| chr4:185425864-185426255 | Common:4; Rare:120 | ||||
| chr4:185471051-185471412 | Common:10; Rare:46 | ||||
| chr4:185657275-185657405 | Common:2; Rare:39 | ||||
| chr4:186191460-186191825 | Common:6; Rare:124; Clinvar:2; Clinvar (benign):5 |