| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183504529-183504817 | Common:3; Rare:92 | ||||
| chr4:183659096-183659411 | Common:1; Rare:104 | ||||
| chr4:184474504-184474842 | Rare:78 | ||||
| chr4:184649413-184649803 | Common:4; Rare:126 | ||||
| chr4:184734058-184734394 | Common:5; Rare:119 | ||||
| chr4:184825931-184826274 | Common:7; Rare:106 | ||||
| chr4:185203891-185204095 | Rare:66 | ||||
| chr4:185395895-185396030 | Rare:42 | ||||
| chr4:185396563-185396853 | Rare:93 | ||||
| chr4:185396993-185397261 | Rare:96 | ||||
| chr4:185425866-185426255 | Common:4; Rare:118 | ||||
| chr4:185471060-185471412 | Common:10; Rare:43 | ||||
| chr4:185535341-185535668 | Common:2; Rare:118; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:185656829-185657361 | Common:3; Rare:101 | ||||
| chr4:185657557-185657767 | Common:1; Rare:51 |