| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7561811-7562126 | Common:3; Rare:87 | ||||
| chr17:7583520-7583868 | Common:1; Rare:137; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7857444-7858003 | Common:4; Rare:183 | ||||
| chr17:7931880-7932253 | Common:5; Rare:98 | ||||
| chr17:10697505-10697631 | Common:3; Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:14069472-14069563 | Common:2; Rare:34; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:15999590-15999851 | Common:3; Rare:135; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:18039158-18039420 | Common:4; Rare:68; Clinvar (benign):1 | ||||
| chr17:18314913-18315332 | Common:1; Rare:119 | ||||
| chr17:19977801-19977952 | Common:1; Rare:49 | ||||
| chr17:21214135-21214344 | Common:2; Rare:91 | ||||
| chr17:28318942-28319206 | Common:3; Rare:87 | ||||
| chr17:28335345-28335784 | Common:1; Rare:106 | ||||
| chr17:28357450-28357667 | Common:5; Rare:108 | ||||
| chr17:28599004-28599150 | Common:2; Rare:37 |