| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184185861-184186210 | Common:5; Rare:131 | ||||
| chr3:184248877-184249041 | Common:2; Rare:83; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184261262-184261690 | Common:1; Rare:101 | ||||
| chr3:184298941-184299296 | Common:4; Rare:114 | ||||
| chr3:184314412-184314664 | Common:3; Rare:74 | ||||
| chr3:184335852-184336066 | Rare:71 | ||||
| chr3:184336188-184336300 | Rare:23 | ||||
| chr3:184711608-184711747 | Common:2; Rare:46 | ||||
| chr3:184711831-184712184 | Common:1; Rare:122 | ||||
| chr3:184812031-184812231 | Common:2; Rare:59 | ||||
| chr3:185152768-185153067 | Common:4; Rare:112 | ||||
| chr3:185282803-185283045 | Common:1; Rare:66 | ||||
| chr3:185498885-185499162 | Rare:98 | ||||
| chr3:185585935-185586392 | Common:1; Rare:107 | ||||
| chr3:185824889-185825150 | Rare:78 |