Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:144551931-144552216 | Rare:92 | ||||
chr1:144560827-144561124 | Common:1; Rare:77 | ||||
chr1:145280815-145281116 | Common:7; Rare:101 | ||||
chr1:146052242-146052542 | Common:6; Rare:82 | ||||
chr1:148522297-148522601 | Common:4; Rare:74 | ||||
chr1:149636472-149636760 | Common:6; Rare:85 | ||||
chr1:155983197-155983477 | Rare:39 | ||||
chr1:158009803-158009941 | Rare:25 | ||||
chr1:161727025-161727193 | Common:4; Rare:33 | ||||
chr1:178037948-178038065 | Rare:42 | ||||
chr1:193115725-193115896 | Rare:37 | ||||
chr1:197201250-197201606 | Common:1; Rare:126 | ||||
chr1:211382653-211382858 | Common:2; Rare:81 | ||||
chr1:223992564-223992775 | Common:3; Rare:78 | ||||
chr1:244863774-244863877 | Rare:39; Clinvar:2; Clinvar (benign):1 |