| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:1231933-1232310 | Rare:142; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr1:1324630-1324796 | Common:2; Rare:87 | ||||
| chr1:1399305-1399558 | Common:1; Rare:105 | ||||
| chr1:1407229-1407363 | Common:1; Rare:56 | ||||
| chr1:1435595-1435724 | Rare:46 | ||||
| chr1:2391543-2391908 | Common:2; Rare:135 | ||||
| chr1:2556244-2556432 | Common:1; Rare:77 | ||||
| chr1:3624777-3625052 | Common:1; Rare:92 | ||||
| chr1:3857175-3857286 | Common:1; Rare:40 | ||||
| chr1:3900219-3900406 | Common:11; Rare:87 | ||||
| chr1:9943354-9943490 | Common:2; Rare:31 | ||||
| chr1:11654731-11654918 | Common:4; Rare:54 | ||||
| chr1:15410041-15410251 | Common:2; Rare:66 | ||||
| chr1:15526565-15526897 | Common:2; Rare:104 | ||||
| chr1:19210254-19210395 | Rare:53 |