| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:183544648-183545048 | Common:2; Rare:140 | ||||
| chr3:183555615-183556067 | Common:8; Rare:315 | ||||
| chr3:183635326-183637171 | Common:55; Rare:1479 | ||||
| chr3:183697624-183697873 | Common:4; Rare:189 | ||||
| chr3:183698021-183698145 | Rare:45 | ||||
| chr3:183884223-183884431 | Common:2; Rare:36 | ||||
| chr3:183884417-183885057 | Common:7; Rare:371 | ||||
| chr3:183885057-183885457 | Common:4; Rare:82 | ||||
| chr3:184016710-184017700 | Common:12; Rare:415 | ||||
| chr3:184017810-184018180 | Common:10; Rare:556 | ||||
| chr3:184018200-184018510 | Common:7; Rare:106 | ||||
| chr3:184134200-184134676 | Common:2; Rare:134 | ||||
| chr3:184135137-184135862 | Common:14; Rare:675; Clinvar:38; Clinvar (pathogenic):4 | ||||
| chr3:184154358-184155004 | Common:2; Rare:183 | ||||
| chr3:184155110-184155707 | Common:3; Rare:642 |