| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:35290165-35290429 | Common:3; Rare:88 | ||||
| chr18:35344392-35344564 | Common:2; Rare:57 | ||||
| chr18:35497621-35497711 | Common:3; Rare:31 | ||||
| chr18:35972449-35972731 | Common:4; Rare:95 | ||||
| chr18:36067266-36067322 | Common:1; Rare:8 | ||||
| chr18:36129191-36129538 | Common:4; Rare:111 | ||||
| chr18:36129683-36129946 | Common:2; Rare:97 | ||||
| chr18:36187408-36187530 | Common:2; Rare:46 | ||||
| chr18:36828742-36829148 | Common:3; Rare:155 | ||||
| chr18:44680677-44680995 | Common:1; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:45967243-45967465 | Rare:83 | ||||
| chr18:46098214-46098581 | Common:11; Rare:108; Clinvar (benign):6 | ||||
| chr18:46104135-46104414 | Common:4; Rare:82; Clinvar (benign):1 | ||||
| chr18:46917412-46917665 | Common:2; Rare:104 | ||||
| chr18:47150419-47150575 | Common:4; Rare:59 |