| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35455059-35455310 | Common:1; Rare:88 | ||||
| chr20:35542020-35542109 | Common:2; Rare:51 | ||||
| chr20:35664843-35665015 | Common:1; Rare:46 | ||||
| chr20:35699344-35699475 | Rare:43 | ||||
| chr20:35742182-35742640 | Common:5; Rare:144 | ||||
| chr20:35771851-35772055 | Common:2; Rare:66 | ||||
| chr20:36236374-36236491 | Common:2; Rare:29 | ||||
| chr20:36461133-36461486 | Common:1; Rare:102 | ||||
| chr20:36746062-36746320 | Common:3; Rare:88 | ||||
| chr20:36951645-36951798 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:37095918-37096269 | Common:1; Rare:119 | ||||
| chr20:37178865-37179205 | Rare:101 | ||||
| chr20:37289357-37289669 | Common:1; Rare:78 | ||||
| chr20:37521077-37521285 | Common:1; Rare:55 | ||||
| chr20:37527821-37528196 | Common:5; Rare:136 |