Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11979914-11980328 | Common:3; Rare:104; Clinvar:1; Clinvar (benign):1 | ||||
chr1:12617208-12617583 | Rare:92 | ||||
chr1:12617588-12617882 | Common:5; Rare:29 | ||||
chr1:12618202-12618445 | Rare:54 | ||||
chr1:13749082-13749455 | Common:2; Rare:128 | ||||
chr1:16352419-16352569 | Common:2; Rare:83 | ||||
chr1:16366982-16367281 | Common:1; Rare:94 | ||||
chr1:16613493-16613898 | Common:7; Rare:1 | ||||
chr1:17053954-17054395 | Common:3; Rare:132; Clinvar:16; Clinvar (benign):10 | ||||
chr1:17439707-17439875 | Rare:56 | ||||
chr1:17580050-17580193 | Common:1; Rare:18 | ||||
chr1:19210254-19210417 | Rare:63 | ||||
chr1:19251506-19251854 | Common:6; Rare:115 | ||||
chr1:19257602-19257856 | Common:1; Rare:64 | ||||
chr1:19288560-19288787 | Common:5; Rare:90 |