Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:9182252-9182478 | Common:2; Rare:63 | ||||
chr1:9182887-9183028 | Rare:34 | ||||
chr1:9191926-9192061 | Common:1; Rare:18 | ||||
chr1:9293451-9293836 | Common:2; Rare:99 | ||||
chr1:9317863-9317882 | Common:1; Rare:1 | ||||
chr1:9321161-9321367 | Common:1; Rare:42 | ||||
chr1:9356584-9356769 | Common:2; Rare:33 | ||||
chr1:9356965-9357063 | Rare:13 | ||||
chr1:9428934-9429170 | Common:3; Rare:70 | ||||
chr1:9441877-9441952 | Common:1; Rare:13 | ||||
chr1:9739512-9739809 | Common:2; Rare:53 | ||||
chr1:9897839-9897902 | Common:1; Rare:13 | ||||
chr1:10132145-10132480 | Rare:74 | ||||
chr1:10321075-10321097 | Common:1; Rare:6 | ||||
chr1:10348525-10348736 | Rare:57; Clinvar:1; Clinvar (benign):1 |