| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28844531-28844981 | Common:2; Rare:136; Clinvar:2; Clinvar (benign):7 | ||||
| chr16:28844993-28845339 | Rare:91; Clinvar:1 | ||||
| chr16:28846264-28846696 | Common:2; Rare:142; Clinvar:6; Clinvar (benign):5 | ||||
| chr16:28863306-28863565 | Common:1; Rare:54 | ||||
| chr16:28863713-28864010 | Common:3; Rare:77 | ||||
| chr16:28879811-28880072 | Common:3; Rare:77 | ||||
| chr16:28925172-28925254 | Rare:22 | ||||
| chr16:28936569-28936832 | Rare:68 | ||||
| chr16:28974647-28974792 | Common:1; Rare:60 | ||||
| chr16:29790448-29790816 | Common:2; Rare:135; Clinvar (benign):2 | ||||
| chr16:29805376-29805894 | Common:2; Rare:220 | ||||
| chr16:29805910-29805964 | Rare:24 | ||||
| chr16:29805977-29806155 | Rare:31 | ||||
| chr16:29806194-29806702 | Common:4; Rare:121 | ||||
| chr16:29806744-29807063 | Rare:131 |