| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34112102-34112423 | Rare:104 | ||||
| chr20:34303277-34303363 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:34303369-34303464 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:34363164-34363331 | Rare:44 | ||||
| chr20:34516278-34516455 | Common:3; Rare:72 | ||||
| chr20:34677083-34677294 | Rare:55 | ||||
| chr20:34872821-34872885 | Rare:27 | ||||
| chr20:34955734-34955841 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:35147265-35147392 | Common:1; Rare:46 | ||||
| chr20:35284491-35284870 | Common:3; Rare:113 | ||||
| chr20:35411959-35412113 | Rare:54 | ||||
| chr20:35455034-35455210 | Common:1; Rare:58 | ||||
| chr20:35542359-35542517 | Rare:56 | ||||
| chr20:35616945-35617058 | Common:1; Rare:18 | ||||
| chr20:35631559-35631731 | Common:2; Rare:57 |