| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35455049-35455210 | Common:1; Rare:56 | ||||
| chr20:35556030-35556266 | Rare:73 | ||||
| chr20:35664880-35665047 | Common:1; Rare:42 | ||||
| chr20:35699305-35699475 | Rare:59; Clinvar (benign):3 | ||||
| chr20:35742161-35742685 | Common:6; Rare:171 | ||||
| chr20:36236440-36236491 | Rare:9 | ||||
| chr20:36573383-36573597 | Rare:88 | ||||
| chr20:36605532-36605784 | Common:1; Rare:89 | ||||
| chr20:36746062-36746305 | Common:2; Rare:87 | ||||
| chr20:36773732-36773965 | Common:3; Rare:80 | ||||
| chr20:37178865-37179220 | Rare:105 | ||||
| chr20:37289545-37289669 | Common:1; Rare:36 | ||||
| chr20:37297201-37297345 | Rare:25 | ||||
| chr20:37527834-37528191 | Common:5; Rare:125 | ||||
| chr20:38033407-38033775 | Common:2; Rare:107 |