| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184185856-184186228 | Common:9; Rare:268 | ||||
| chr3:184248871-184249032 | Common:2; Rare:166; Clinvar:10; Clinvar (benign):4 | ||||
| chr3:184249432-184249783 | Common:2; Rare:196 | ||||
| chr3:184298939-184299391 | Common:10; Rare:257 | ||||
| chr3:184314394-184314736 | Common:4; Rare:97 | ||||
| chr3:184314931-184315365 | Common:1; Rare:214 | ||||
| chr3:184315632-184315835 | Rare:50 | ||||
| chr3:184361573-184361940 | Rare:164 | ||||
| chr3:184362650-184363030 | Rare:107 | ||||
| chr3:184377711-184378477 | Common:2; Rare:283; Clinvar:2 | ||||
| chr3:184711819-184712272 | Common:2; Rare:235 | ||||
| chr3:184812022-184812207 | Common:2; Rare:58 | ||||
| chr3:185152840-185153280 | Common:9; Rare:208 | ||||
| chr3:185254010-185254220 | Common:2; Rare:125; Clinvar:2 | ||||
| chr3:185282825-185283041 | Common:2; Rare:106 |