| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:55589701-55589996 | Common:2; Rare:94 | ||||
| chr18:56651122-56651421 | Common:4; Rare:79 | ||||
| chr18:56651610-56651714 | Common:3; Rare:25 | ||||
| chr18:57622171-57622282 | Common:3; Rare:23 | ||||
| chr18:58863023-58863134 | Rare:28 | ||||
| chr18:59139689-59140027 | Common:3; Rare:92 | ||||
| chr18:59899827-59899997 | Common:3; Rare:54 | ||||
| chr18:62186920-62187340 | Common:5; Rare:116 | ||||
| chr18:62187621-62187791 | Common:2; Rare:49 | ||||
| chr18:62522842-62523076 | Common:4; Rare:78 | ||||
| chr18:63367131-63367360 | Common:1; Rare:87 | ||||
| chr18:63422336-63422716 | Common:2; Rare:111 | ||||
| chr18:63969882-63970139 | Common:2; Rare:50 | ||||
| chr18:68714982-68715388 | Common:7; Rare:160 | ||||
| chr18:70205644-70205783 | Common:3; Rare:57; Clinvar (benign):2 |