| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46173909-46174140 | Common:1; Rare:55 | ||||
| chr18:46917391-46917647 | Common:2; Rare:109 | ||||
| chr18:47150413-47150570 | Common:4; Rare:59 | ||||
| chr18:47929805-47929936 | Common:1; Rare:28 | ||||
| chr18:47930204-47930280 | Rare:23 | ||||
| chr18:47930291-47930571 | Common:1; Rare:122 | ||||
| chr18:47930787-47931018 | Rare:73 | ||||
| chr18:47931120-47931353 | Common:1; Rare:81 | ||||
| chr18:47931527-47931683 | Rare:43 | ||||
| chr18:48538927-48539208 | Common:1; Rare:67 | ||||
| chr18:48539251-48539295 | Common:1; Rare:9 | ||||
| chr18:49460621-49460832 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:49487079-49487328 | Common:3; Rare:90 | ||||
| chr18:49490452-49490939 | Common:1; Rare:119 | ||||
| chr18:49492241-49492603 | Common:3; Rare:138 |