Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15847460-15848110 | Rare:206 | ||||
chr1:16155942-16156181 | Rare:56; Clinvar:2 | ||||
chr1:16206497-16206721 | Common:6; Rare:41 | ||||
chr1:16352418-16352578 | Common:2; Rare:87 | ||||
chr1:16366982-16367305 | Common:1; Rare:101 | ||||
chr1:16440549-16440846 | Common:2; Rare:97 | ||||
chr1:16613343-16613408 | Common:1 | ||||
chr1:16921842-16921966 | Rare:22 | ||||
chr1:16980590-16980878 | Common:5; Rare:83 | ||||
chr1:17053922-17054368 | Common:3; Rare:139; Clinvar:17; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
chr1:17438371-17438733 | Common:4; Rare:136 | ||||
chr1:17439207-17439363 | Common:2; Rare:43 | ||||
chr1:17439431-17439909 | Rare:127 | ||||
chr1:19081592-19081748 | Common:3; Rare:56 | ||||
chr1:19210083-19210558 | Common:1; Rare:153 |