| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:57392535-57392776 | Common:1; Rare:62 | ||||
| chr20:57709892-57710183 | Rare:84 | ||||
| chr20:58309421-58309736 | Common:2; Rare:119 | ||||
| chr20:58651581-58651850 | Common:1; Rare:60; Clinvar:2; Clinvar (benign):3 | ||||
| chr20:58652313-58652413 | Common:2; Rare:44 | ||||
| chr20:58839538-58840103 | Common:3; Rare:124 | ||||
| chr20:58840120-58840156 | Rare:8 | ||||
| chr20:58840305-58840558 | Common:1; Rare:102; Clinvar:2 | ||||
| chr20:58840564-58840795 | Rare:83; Clinvar:1 | ||||
| chr20:58840894-58841191 | Common:3; Rare:66 | ||||
| chr20:58841531-58841867 | Common:4; Rare:74 | ||||
| chr20:58888826-58889224 | Common:1; Rare:129 | ||||
| chr20:58890893-58891109 | Common:2; Rare:88 | ||||
| chr20:58891317-58891839 | Common:3; Rare:211; Clinvar:4; Clinvar (pathogenic):2 | ||||
| chr20:58891860-58892181 | Common:6; Rare:169 |