| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:13638870-13639035 | Common:1; Rare:50 | ||||
| chr20:13784845-13785136 | Common:3; Rare:132; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:13995246-13995617 | Rare:106 | ||||
| chr20:14337442-14337680 | Rare:58 | ||||
| chr20:16573278-16573585 | Common:2; Rare:91 | ||||
| chr20:16729842-16730139 | Common:1; Rare:88 | ||||
| chr20:17569978-17570222 | Common:3; Rare:106 | ||||
| chr20:17968438-17968649 | Common:4; Rare:96 | ||||
| chr20:17968781-17969129 | Common:3; Rare:123 | ||||
| chr20:18137779-18137982 | Common:1; Rare:74 | ||||
| chr20:18288178-18288263 | Rare:23 | ||||
| chr20:18288491-18288568 | Rare:22 | ||||
| chr20:18466715-18466844 | Rare:30 | ||||
| chr20:18466923-18467444 | Common:1; Rare:115 | ||||
| chr20:18497165-18497308 | Common:1; Rare:54 |