Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:72727559-72727972 | Common:7; Rare:162 | ||||
chr13:72781836-72782269 | Common:1; Rare:153 | ||||
chr13:75482359-75482639 | Common:3; Rare:61 | ||||
chr13:75549429-75549860 | Common:8; Rare:114 | ||||
chr13:75635769-75635868 | Common:1; Rare:23 | ||||
chr13:76991975-76992181 | Common:2; Rare:96; Clinvar:17; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr13:77027137-77027307 | Common:6; Rare:57 | ||||
chr13:79405795-79406112 | Rare:94 | ||||
chr13:79406217-79406314 | Common:1; Rare:29 | ||||
chr13:79480947-79481480 | Common:3; Rare:201 | ||||
chr13:93227058-93227402 | Common:1; Rare:72; Clinvar:5; Clinvar (benign):1 | ||||
chr13:94596132-94596348 | Common:2; Rare:70 | ||||
chr13:94601596-94601939 | Common:3; Rare:109 | ||||
chr13:95301417-95301543 | Rare:36 | ||||
chr13:95676894-95677218 | Common:3; Rare:118 |