| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:3247326-3247877 | Common:1; Rare:152 | ||||
| chr18:3261820-3262230 | Common:6; Rare:130 | ||||
| chr18:3450022-3450196 | Rare:49 | ||||
| chr18:9102504-9102766 | Common:2; Rare:106; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136522-9136837 | Rare:121 | ||||
| chr18:9475460-9475695 | Common:3; Rare:60 | ||||
| chr18:9914195-9914292 | Rare:47 | ||||
| chr18:12702671-12703084 | Common:3; Rare:166 | ||||
| chr18:12884163-12884425 | Common:4; Rare:127 | ||||
| chr18:12991137-12991417 | Common:2; Rare:102 | ||||
| chr18:13726439-13726720 | Common:3; Rare:111 | ||||
| chr18:21450995-21451029 | Rare:8 | ||||
| chr18:21600621-21600946 | Common:2; Rare:88 | ||||
| chr18:22933807-22933889 | Common:1; Rare:31 | ||||
| chr18:23453069-23453349 | Rare:98 |