Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:240256038-240256181 | Rare:32 | ||||
chr20:2795365-2795604 | Rare:68 | ||||
chr20:18793974-18794097 | Rare:40 | ||||
chr20:19757486-19757687 | Common:3; Rare:58 | ||||
chr20:19757919-19758306 | Common:5; Rare:130 | ||||
chr20:19974502-19974789 | Rare:86; Clinvar (benign):4 | ||||
chr20:23358098-23358227 | Common:1; Rare:37 | ||||
chr20:23981111-23981294 | Common:2; Rare:35 | ||||
chr20:24011452-24011654 | Common:4; Rare:37 | ||||
chr20:25853994-25854117 | Common:3; Rare:47 | ||||
chr20:26009678-26009866 | Common:1; Rare:45 | ||||
chr20:31604162-31604448 | Common:1; Rare:111 | ||||
chr20:36050204-36050262 | Rare:10 | ||||
chr20:36050322-36050732 | Common:2; Rare:142 | ||||
chr20:36105776-36105913 | Common:1; Rare:24 |