| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:36067293-36067784 | Common:6; Rare:491 | ||||
| chr18:36129223-36129623 | Common:11; Rare:503 | ||||
| chr18:36129654-36130633 | Common:16; Rare:700 | ||||
| chr18:36187250-36187648 | Common:21; Rare:407 | ||||
| chr18:36187686-36188113 | Common:3; Rare:251 | ||||
| chr18:36818773-36819173 | Common:6; Rare:133 | ||||
| chr18:36828390-36828578 | Common:1; Rare:35 | ||||
| chr18:36828691-36829725 | Common:22; Rare:1621 | ||||
| chr18:37253857-37254301 | Common:4; Rare:421 | ||||
| chr18:41954939-41955370 | Common:5; Rare:339 | ||||
| chr18:41955729-41956129 | Common:3; Rare:58 | ||||
| chr18:45967189-45967939 | Common:3; Rare:834; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr18:46039690-46040332 | Common:1; Rare:213 | ||||
| chr18:46071969-46072463 | Common:6; Rare:214 | ||||
| chr18:46097422-46097822 | Common:1; Rare:79 |