| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:34888625-34888972 | Common:1; Rare:121 | ||||
| chr21:35048757-35048985 | Common:1; Rare:68; Clinvar:4; Clinvar (benign):4 | ||||
| chr21:36059887-36060076 | Common:1; Rare:36 | ||||
| chr21:36060291-36060783 | Common:9; Rare:145 | ||||
| chr21:36069853-36070067 | Common:7; Rare:68 | ||||
| chr21:36070252-36070393 | Common:1; Rare:75 | ||||
| chr21:36319908-36320300 | Common:5; Rare:184 | ||||
| chr21:36320443-36320521 | Common:2; Rare:17 | ||||
| chr21:36320618-36320838 | Common:2; Rare:101 | ||||
| chr21:36385240-36385501 | Rare:96 | ||||
| chr21:36542764-36543003 | Common:1; Rare:47 | ||||
| chr21:36966282-36966498 | Common:2; Rare:62 | ||||
| chr21:36966572-36966696 | Common:1; Rare:46 | ||||
| chr21:36989776-36990072 | Common:6; Rare:94 | ||||
| chr21:36990199-36990374 | Common:4; Rare:56; Clinvar (benign):3 |