Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:70163502-70163802 | Common:4; Rare:56 | ||||
chr10:70170411-70170749 | Common:4; Rare:108 | ||||
chr10:70233281-70233494 | Common:6; Rare:84; Clinvar (benign):1 | ||||
chr10:70404507-70404545 | Rare:13 | ||||
chr10:71819465-71819896 | Common:1; Rare:172; Clinvar:5; Clinvar (benign):4 | ||||
chr10:71851183-71851427 | Common:5; Rare:106; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72216215-72216311 | Rare:45 | ||||
chr10:72273693-72274148 | Common:2; Rare:128 | ||||
chr10:72626009-72626253 | Common:1; Rare:55 | ||||
chr10:73096729-73097121 | Common:5; Rare:109 | ||||
chr10:73167868-73168386 | Common:1; Rare:145 | ||||
chr10:73229790-73229873 | Rare:13 | ||||
chr10:73252544-73252817 | Common:2; Rare:79; Clinvar:5; Clinvar (benign):2 | ||||
chr10:73433722-73433870 | Common:1; Rare:33 | ||||
chr10:73495553-73495771 | Rare:47 |