| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:5238006-5238148 | Common:1; Rare:54 | ||||
| chr18:14642492-14642695 | Rare:55 | ||||
| chr18:31724609-31724940 | Common:2; Rare:42 | ||||
| chr18:36128334-36128720 | Common:1; Rare:67 | ||||
| chr18:55452285-55452525 | Common:2; Rare:34 | ||||
| chr18:55840312-55840518 | Common:1; Rare:30 | ||||
| chr18:57662592-57662783 | Common:1; Rare:35; Clinvar (pathogenic):1 | ||||
| chr18:58251724-58252049 | Rare:64; Clinvar (benign):1 | ||||
| chr18:59053458-59053643 | Rare:24 | ||||
| chr18:59066590-59066883 | Common:3; Rare:51 | ||||
| chr18:76491470-76491654 | Common:3; Rare:79 | ||||
| chr19:622659-622865 | Common:1; Rare:106 | ||||
| chr19:1876164-1876283 | Common:1; Rare:43 | ||||
| chr19:5207932-5208239 | Common:2; Rare:100 | ||||
| chr19:5212120-5212415 | Common:3; Rare:102 |