Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:1570012-1570102 | Common:1; Rare:26 | ||||
chr7:2242178-2242268 | Common:2; Rare:52 | ||||
chr7:6009030-6009287 | Common:3; Rare:99; Clinvar:3; Clinvar (benign):13 | ||||
chr7:17940484-17940592 | Common:2; Rare:37 | ||||
chr7:20331728-20331757 | Rare:6 | ||||
chr7:22727296-22727472 | Rare:67 | ||||
chr7:23105647-23105792 | Common:2; Rare:71; Clinvar:1 | ||||
chr7:23181824-23182068 | Common:2; Rare:93 | ||||
chr7:23470362-23470560 | Rare:58 | ||||
chr7:23531972-23532119 | Rare:55 | ||||
chr7:24980157-24980465 | Common:10; Rare:120 | ||||
chr7:25125249-25125643 | Rare:155; Clinvar:3 | ||||
chr7:26201369-26201555 | Rare:70 | ||||
chr7:26201619-26201805 | Common:1; Rare:99 | ||||
chr7:26864551-26864840 | Common:3; Rare:88 |