| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:51029997-51030299 | Rare:242; Clinvar:6 | ||||
| chr18:51030560-51030860 | Common:2; Rare:172; Clinvar:4; Clinvar (benign):8 | ||||
| chr18:51196340-51196740 | Rare:182 | ||||
| chr18:51196760-51197210 | Common:10; Rare:256 | ||||
| chr18:51197428-51198124 | Rare:327 | ||||
| chr18:54224239-54225051 | Common:9; Rare:430 | ||||
| chr18:54269260-54269908 | Common:16; Rare:467 | ||||
| chr18:54269910-54270300 | Common:4; Rare:182 | ||||
| chr18:54357814-54358043 | Common:17; Rare:139 | ||||
| chr18:54828285-54828628 | Rare:132 | ||||
| chr18:54959374-54959540 | Common:2; Rare:45 | ||||
| chr18:56637778-56638178 | Common:5; Rare:118 | ||||
| chr18:56651111-56651444 | Common:11; Rare:225 | ||||
| chr18:57435100-57435540 | Common:1; Rare:202 | ||||
| chr18:57444224-57444639 | Common:3; Rare:93 |