Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:167554159-167554412 | Rare:38 | ||||
chr1:167721177-167721209 | Rare:3 | ||||
chr1:167721634-167722083 | Common:4; Rare:110 | ||||
chr1:167722413-167722633 | Common:5; Rare:54 | ||||
chr1:167935215-167935342 | Rare:28 | ||||
chr1:167935509-167935624 | Rare:18 | ||||
chr1:167935949-167936341 | Common:2; Rare:118 | ||||
chr1:167936426-167937094 | Common:2; Rare:229 | ||||
chr1:167937212-167937283 | Rare:14 | ||||
chr1:167937437-167937610 | Rare:43 | ||||
chr1:168136210-168136554 | Common:3; Rare:97; Clinvar (benign):1 | ||||
chr1:168136781-168137128 | Common:1; Rare:61 | ||||
chr1:168137154-168137404 | Rare:45 | ||||
chr1:168178657-168179082 | Common:4; Rare:126 | ||||
chr1:168179157-168179361 | Rare:49 |