| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34363164-34363325 | Rare:43 | ||||
| chr20:34677086-34677318 | Rare:59 | ||||
| chr20:34872821-34872973 | Rare:54 | ||||
| chr20:35092783-35092948 | Common:2; Rare:74 | ||||
| chr20:35147302-35147437 | Rare:39 | ||||
| chr20:35284501-35284870 | Common:3; Rare:109 | ||||
| chr20:35455051-35455311 | Common:1; Rare:90 | ||||
| chr20:35664874-35665045 | Common:1; Rare:46 | ||||
| chr20:35699298-35699456 | Rare:52; Clinvar (benign):3 | ||||
| chr20:36461133-36461486 | Common:1; Rare:102 | ||||
| chr20:36746065-36746192 | Common:2; Rare:58 | ||||
| chr20:37095955-37096018 | Rare:28 | ||||
| chr20:37178861-37179165 | Rare:88 | ||||
| chr20:37289577-37289669 | Common:1; Rare:28 | ||||
| chr20:37521112-37521278 | Common:1; Rare:42 |