Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42924725-42925125 | Common:7; Rare:120 | ||||
chr1:42941080-42941189 | Rare:24 | ||||
chr1:42941889-42942019 | Rare:23 | ||||
chr1:42957853-42958317 | Common:11; Rare:258 | ||||
chr1:42962734-42962911 | Common:1; Rare:37 | ||||
chr1:42967165-42967327 | Common:3; Rare:27 | ||||
chr1:43007501-43007725 | Common:4; Rare:58 | ||||
chr1:43008468-43008785 | Rare:58 | ||||
chr1:43143513-43143830 | Common:2; Rare:50 | ||||
chr1:43206846-43207030 | Common:1; Rare:59 | ||||
chr1:43207032-43207150 | Rare:19 | ||||
chr1:43227290-43227550 | Common:4; Rare:50 | ||||
chr1:43330180-43330720 | Common:5; Rare:69 | ||||
chr1:43348503-43348670 | Common:1; Rare:32 | ||||
chr1:43348861-43349290 | Common:2; Rare:145; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 |