| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46098007-46098148 | Common:2; Rare:54 | ||||
| chr18:46098161-46098634 | Common:55; Rare:512; Clinvar (benign):32 | ||||
| chr18:46104137-46104455 | Common:21; Rare:430; Clinvar (benign):2 | ||||
| chr18:46104396-46104796 | Common:4; Rare:96 | ||||
| chr18:46173210-46173700 | Common:3; Rare:212 | ||||
| chr18:46173720-46174350 | Common:8; Rare:398 | ||||
| chr18:46916804-46916943 | Rare:35 | ||||
| chr18:46916960-46917739 | Common:8; Rare:792 | ||||
| chr18:46918026-46918426 | Common:2; Rare:135 | ||||
| chr18:47149469-47150389 | Common:17; Rare:635 | ||||
| chr18:47150372-47150740 | Common:23; Rare:490 | ||||
| chr18:47176270-47176676 | Common:4; Rare:266; Clinvar (benign):3 | ||||
| chr18:47896587-47897150 | Common:3; Rare:175 | ||||
| chr18:47930330-47930830 | Common:6; Rare:722 | ||||
| chr18:47931020-47931450 | Common:6; Rare:469 |