Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:116909719-116910084 | Common:1; Rare:101 | ||||
chr1:116910464-116910592 | Rare:44 | ||||
chr1:117059883-117060369 | Common:7; Rare:125 | ||||
chr1:117121867-117122027 | Common:1; Rare:45 | ||||
chr1:117367294-117367557 | Common:5; Rare:95 | ||||
chr1:117605731-117606070 | Common:2; Rare:103 | ||||
chr1:117929550-117929850 | Common:4; Rare:91 | ||||
chr1:119140599-119140778 | Common:1; Rare:66; Clinvar (pathogenic):1 | ||||
chr1:119648177-119648600 | Common:5; Rare:127 | ||||
chr1:119711821-119711970 | Common:2; Rare:41; Clinvar:2; Clinvar (benign):2 | ||||
chr1:120176364-120176656 | Common:1; Rare:56 | ||||
chr1:120723770-120723951 | Rare:7 | ||||
chr1:144460894-144461658 | Common:15; Rare:444 | ||||
chr1:145214489-145214719 | Rare:22 | ||||
chr1:145823843-145824275 | Rare:155 |