| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179147963-179148205 | Common:4; Rare:77 | ||||
| chr3:179347573-179347804 | Common:1; Rare:58 | ||||
| chr3:179604620-179604921 | Common:3; Rare:120 | ||||
| chr3:180602032-180602389 | Common:1; Rare:125 | ||||
| chr3:180870071-180870084 | Rare:1 | ||||
| chr3:180933152-180933367 | Common:2; Rare:45 | ||||
| chr3:180989629-180989790 | Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:182793360-182793638 | Common:3; Rare:69 | ||||
| chr3:183099392-183099821 | Common:2; Rare:127; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:183884781-183885040 | Common:1; Rare:98 | ||||
| chr3:184017876-184018053 | Rare:50 | ||||
| chr3:184135221-184135392 | Common:2; Rare:52; Clinvar:5 | ||||
| chr3:184186032-184186233 | Common:2; Rare:85 | ||||
| chr3:184249531-184249689 | Rare:43 | ||||
| chr3:184298979-184299283 | Common:2; Rare:91 |