Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145823937-145824261 | Rare:115 | ||||
chr1:145927374-145927648 | Common:1; Rare:72; Clinvar (pathogenic):1 | ||||
chr1:145964573-145964742 | Rare:43 | ||||
chr1:145996552-145996808 | Rare:96 | ||||
chr1:147172436-147172730 | Common:1; Rare:77 | ||||
chr1:149842748-149842908 | Rare:3 | ||||
chr1:149850826-149851064 | Rare:1 | ||||
chr1:149886646-149887024 | Common:2; Rare:139 | ||||
chr1:149887894-149888217 | Rare:100 | ||||
chr1:149927767-149927917 | Common:1; Rare:54; Clinvar (benign):4 | ||||
chr1:150067646-150067860 | Rare:66 | ||||
chr1:150235937-150236374 | Common:1; Rare:101 | ||||
chr1:150282296-150282572 | Common:3; Rare:48 | ||||
chr1:150364581-150364709 | Rare:45 | ||||
chr1:150579208-150579271 | Rare:28 |