| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4271189-4271447 | Common:6; Rare:136 | ||||
| chr16:4271752-4272060 | Common:1; Rare:196 | ||||
| chr16:4273905-4274350 | Common:6; Rare:155 | ||||
| chr16:4293595-4294190 | Common:8; Rare:244 | ||||
| chr16:4299120-4299500 | Common:6; Rare:209 | ||||
| chr16:4307501-4308123 | Common:10; Rare:369 | ||||
| chr16:4315523-4316126 | Common:9; Rare:361 | ||||
| chr16:4334797-4335363 | Common:1; Rare:256; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr16:4372614-4373337 | Common:10; Rare:252 | ||||
| chr16:4373945-4374349 | Common:3; Rare:144 | ||||
| chr16:4374930-4375410 | Common:1; Rare:164 | ||||
| chr16:4392950-4393200 | Common:3; Rare:73 | ||||
| chr16:4737498-4737898 | Common:2; Rare:237 | ||||
| chr16:4768576-4768960 | Common:3; Rare:277 | ||||
| chr16:4900685-4901683 | Common:5; Rare:477 |