Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:88684091-88684413 | Common:2; Rare:81 | ||||
chr1:88684455-88684600 | Common:1; Rare:38 | ||||
chr1:88832680-88832805 | Rare:17 | ||||
chr1:88992584-88992982 | Common:3; Rare:103 | ||||
chr1:89022820-89022947 | Rare:16 | ||||
chr1:89065179-89065440 | Common:1; Rare:41 | ||||
chr1:89198872-89199001 | Rare:15 | ||||
chr1:89820893-89821202 | Common:1; Rare:96 | ||||
chr1:89821787-89822006 | Rare:59 | ||||
chr1:89994981-89995226 | Common:2; Rare:94 | ||||
chr1:91021449-91021673 | Common:2; Rare:50 | ||||
chr1:91021963-91022186 | Rare:66 | ||||
chr1:92298945-92299076 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92832000-92832117 | Rare:76; Clinvar:7; Clinvar (benign):5 | ||||
chr1:92961430-92961581 | Rare:59 |