| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46104135-46104414 | Common:4; Rare:82; Clinvar (benign):1 | ||||
| chr18:46173990-46174146 | Common:1; Rare:40 | ||||
| chr18:46174251-46174320 | Rare:23 | ||||
| chr18:46518995-46519185 | Rare:37 | ||||
| chr18:46520689-46520835 | Rare:25 | ||||
| chr18:46555371-46555450 | Rare:11 | ||||
| chr18:46556715-46556939 | Rare:41 | ||||
| chr18:46559269-46559424 | Common:1; Rare:29 | ||||
| chr18:46917095-46917228 | Rare:37 | ||||
| chr18:46917412-46917652 | Common:2; Rare:100 | ||||
| chr18:46920109-46920282 | Rare:28 | ||||
| chr18:46946528-46946845 | Common:3; Rare:74 | ||||
| chr18:47035584-47035722 | Rare:51 | ||||
| chr18:47150362-47150580 | Common:4; Rare:78 | ||||
| chr18:47930781-47931094 | Rare:111 |