| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:179882459-179882651 | Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:179882664-179882871 | Rare:94; Clinvar:6 | ||||
| chr1:179882971-179883183 | Common:3; Rare:79; Clinvar (benign):1 | ||||
| chr1:179954441-179955145 | Common:4; Rare:161 | ||||
| chr1:179955189-179955463 | Common:1; Rare:73 | ||||
| chr1:180154415-180154595 | Common:1; Rare:68 | ||||
| chr1:180154635-180154920 | Common:3; Rare:92 | ||||
| chr1:180229878-180230060 | Common:4; Rare:78 | ||||
| chr1:180502287-180502461 | Rare:53 | ||||
| chr1:180502516-180502774 | Common:2; Rare:107 | ||||
| chr1:180502815-180503186 | Common:1; Rare:129 | ||||
| chr1:180631821-180632171 | Common:6; Rare:128 | ||||
| chr1:181022839-181023296 | Common:26; Rare:204 | ||||
| chr1:181033832-181034008 | Rare:46 | ||||
| chr1:181088463-181088925 | Common:2; Rare:173 |