Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:208240437-208240489 | Rare:17 | ||||
chr1:208241278-208241681 | Common:1; Rare:98 | ||||
chr1:208242491-208242738 | Common:3; Rare:25 | ||||
chr1:209267663-209267856 | Common:2; Rare:39 | ||||
chr1:209794347-209794640 | Common:1; Rare:43 | ||||
chr1:209796512-209796603 | Common:1; Rare:18; Clinvar (benign):1 | ||||
chr1:209800788-209801039 | Common:1; Rare:43 | ||||
chr1:209804242-209804339 | Rare:11 | ||||
chr1:209823596-209823890 | Common:3; Rare:45 | ||||
chr1:209839960-209840333 | Rare:65 | ||||
chr1:209859313-209859339 | Rare:4 | ||||
chr1:210231479-210231559 | Rare:13 | ||||
chr1:210231594-210232000 | Rare:86 | ||||
chr1:210233636-210233961 | Common:2; Rare:112 | ||||
chr1:210234077-210234334 | Common:3; Rare:58 |