Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:17439669-17439883 | Rare:69 | ||||
chr1:19210157-19210410 | Rare:96 | ||||
chr1:19251458-19251854 | Common:6; Rare:135 | ||||
chr1:19311997-19312346 | Common:8; Rare:165 | ||||
chr1:20486198-20486388 | Rare:46 | ||||
chr1:20508063-20508194 | Common:2; Rare:49 | ||||
chr1:20661340-20661730 | Common:3; Rare:140; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786614-20786867 | Rare:97 | ||||
chr1:20787230-20787460 | Rare:113 | ||||
chr1:21176848-21177109 | Rare:76 | ||||
chr1:21345454-21345676 | Common:2; Rare:81 | ||||
chr1:21782970-21783291 | Common:2; Rare:114 | ||||
chr1:22052559-22052790 | Common:2; Rare:79 | ||||
chr1:23344233-23344521 | Common:2; Rare:93 | ||||
chr1:23368227-23368502 | Common:1; Rare:82 |