| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:48859781-48859902 | Rare:34 | ||||
| chr18:48949897-48950030 | Rare:51 | ||||
| chr18:49459774-49460433 | Common:19; Rare:281; Clinvar (benign):1 | ||||
| chr18:49460510-49460880 | Common:2; Rare:108; Clinvar:7; Clinvar (benign):1 | ||||
| chr18:49487165-49487372 | Common:3; Rare:80 | ||||
| chr18:49491657-49491968 | Common:1; Rare:113 | ||||
| chr18:49492435-49492571 | Common:1; Rare:58 | ||||
| chr18:49560941-49561341 | Common:3; Rare:114 | ||||
| chr18:49561503-49561661 | Rare:34 | ||||
| chr18:49561729-49562107 | Common:2; Rare:101 | ||||
| chr18:49562424-49562824 | Common:6; Rare:125 | ||||
| chr18:49812564-49813196 | Common:4; Rare:176 | ||||
| chr18:49813337-49813488 | Common:3; Rare:30 | ||||
| chr18:49813826-49814061 | Common:1; Rare:103 | ||||
| chr18:50266340-50266740 | Common:1; Rare:149; Clinvar:1; Clinvar (benign):1 |