Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:94418128-94418453 | Common:2; Rare:110 | ||||
chr1:94926961-94927450 | Common:4; Rare:154 | ||||
chr1:95072839-95072973 | Common:1; Rare:55; Clinvar (benign):2 | ||||
chr1:95234059-95234231 | Common:1; Rare:56 | ||||
chr1:98661610-98661885 | Common:2; Rare:95 | ||||
chr1:99646182-99646335 | Rare:39 | ||||
chr1:99849996-99850130 | Common:1; Rare:49 | ||||
chr1:99969949-99970062 | Rare:28 | ||||
chr1:100038006-100038165 | Common:1; Rare:66 | ||||
chr1:100132902-100133237 | Common:2; Rare:129 | ||||
chr1:100266114-100266420 | Common:3; Rare:107 | ||||
chr1:100894652-100894916 | Common:2; Rare:63 | ||||
chr1:100895921-100896149 | Rare:62 | ||||
chr1:101025754-101025937 | Common:1; Rare:54 | ||||
chr1:101236604-101237063 | Common:5; Rare:95 |