Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:543656-543879 | Rare:82 | ||||
chr20:675937-676129 | Rare:49 | ||||
chr20:676259-676344 | Rare:25 | ||||
chr20:676447-676512 | Common:1; Rare:16 | ||||
chr20:676606-676822 | Common:2; Rare:50 | ||||
chr20:1118419-1118677 | Common:4; Rare:88 | ||||
chr20:1266165-1266344 | Common:3; Rare:39 | ||||
chr20:1325254-1325445 | Rare:49 | ||||
chr20:1392934-1393240 | Common:2; Rare:118 | ||||
chr20:1994054-1994228 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):2 | ||||
chr20:2102090-2102385 | Common:2; Rare:90 | ||||
chr20:2103336-2103413 | Common:1; Rare:34 | ||||
chr20:2470677-2471006 | Common:4; Rare:113 | ||||
chr20:2508863-2509236 | Common:2; Rare:82 | ||||
chr20:2652420-2652679 | Common:8; Rare:103 |