| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:24138909-24139072 | Common:2; Rare:53 | ||||
| chr18:24271239-24271349 | Common:2; Rare:13 | ||||
| chr18:24397033-24397346 | Common:1; Rare:61 | ||||
| chr18:24397712-24398112 | Common:2; Rare:132 | ||||
| chr18:24426593-24426808 | Common:3; Rare:81 | ||||
| chr18:25231051-25231246 | Rare:40 | ||||
| chr18:25231491-25231534 | Rare:9 | ||||
| chr18:25352092-25352426 | Common:2; Rare:137 | ||||
| chr18:26090565-26090982 | Common:5; Rare:161 | ||||
| chr18:26091123-26091299 | Common:2; Rare:46 | ||||
| chr18:26657460-26657494 | Rare:5 | ||||
| chr18:31943098-31943397 | Common:7; Rare:100 | ||||
| chr18:32018457-32019000 | Common:4; Rare:174; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:32041103-32041490 | Common:1; Rare:58 | ||||
| chr18:32041616-32041973 | Common:6; Rare:55 |