Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16366967-16367296 | Common:1; Rare:104 | ||||
chr1:17053948-17054166 | Common:3; Rare:79; Clinvar:16; Clinvar (benign):11 | ||||
chr1:17438532-17438810 | Common:1; Rare:103 | ||||
chr1:17439542-17439918 | Rare:114 | ||||
chr1:18956664-18956948 | Common:2; Rare:76 | ||||
chr1:19210234-19210538 | Common:1; Rare:98 | ||||
chr1:19251502-19251866 | Common:6; Rare:120 | ||||
chr1:19312074-19312356 | Common:7; Rare:131 | ||||
chr1:19485437-19485736 | Common:1; Rare:100 | ||||
chr1:19596747-19597096 | Common:3; Rare:130 | ||||
chr1:20485630-20485883 | Rare:50 | ||||
chr1:20508069-20508193 | Common:2; Rare:46 | ||||
chr1:20588924-20589076 | Common:4; Rare:27 | ||||
chr1:20786183-20786453 | Common:6; Rare:78 | ||||
chr1:21176825-21177126 | Rare:88 |