Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1048510-1048750 | Common:7; Rare:85 | ||||
chr16:1125420-1125760 | Rare:92 | ||||
chr16:1152180-1152365 | Common:1; Rare:45 | ||||
chr16:1408181-1408429 | Common:6; Rare:103 | ||||
chr16:1430907-1431080 | Common:1; Rare:48 | ||||
chr16:1445530-1445930 | Common:7; Rare:183; Clinvar:3; Clinvar (benign):7 | ||||
chr16:1585140-1585420 | Common:2; Rare:50 | ||||
chr16:2023220-2023481 | Common:4; Rare:76 | ||||
chr16:2158809-2159209 | Common:1; Rare:116 | ||||
chr16:2501581-2501698 | Common:1; Rare:19; Clinvar:1; Clinvar (benign):1 | ||||
chr16:2593310-2593930 | Common:3; Rare:132 | ||||
chr16:2603279-2603488 | Common:2; Rare:88 | ||||
chr16:2673362-2673715 | Common:10; Rare:124 | ||||
chr16:2721290-2721670 | Common:2; Rare:117 | ||||
chr16:2904222-2904403 | Common:2; Rare:42 |