| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:22436948-22437077 | Rare:47 | ||||
| chr16:22437189-22437308 | Rare:36 | ||||
| chr16:22437496-22437701 | Common:2; Rare:53 | ||||
| chr16:23452725-23452803 | Rare:28 | ||||
| chr16:23453127-23453231 | Rare:31 | ||||
| chr16:23557298-23557631 | Common:3; Rare:122; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:23641246-23641533 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:23678725-23678939 | Common:4; Rare:67 | ||||
| chr16:24729622-24729789 | Common:7; Rare:78 | ||||
| chr16:25111468-25111803 | Common:2; Rare:91 | ||||
| chr16:27214788-27214953 | Rare:39 | ||||
| chr16:27268713-27268872 | Common:1; Rare:57 | ||||
| chr16:27313371-27313601 | Common:2; Rare:50 | ||||
| chr16:27313792-27313985 | Common:2; Rare:56 | ||||
| chr16:27549838-27550167 | Common:2; Rare:125 |