Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:13700164-13700279 | Rare:45 | ||||
chr1:15526553-15526885 | Common:2; Rare:102 | ||||
chr1:15758499-15758802 | Common:1; Rare:61 | ||||
chr1:16237148-16237319 | Rare:56 | ||||
chr1:16352401-16352591 | Common:3; Rare:105 | ||||
chr1:16440539-16440753 | Common:1; Rare:58 | ||||
chr1:16613486-16613660 | Common:1 | ||||
chr1:17054020-17054325 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):3 | ||||
chr1:19210220-19210523 | Rare:103 | ||||
chr1:19251502-19251913 | Common:9; Rare:144 | ||||
chr1:19312038-19312346 | Common:8; Rare:151 | ||||
chr1:19596871-19597064 | Common:2; Rare:90 | ||||
chr1:20486179-20486357 | Rare:39 | ||||
chr1:20508103-20508236 | Common:2; Rare:44 | ||||
chr1:20661346-20661718 | Common:3; Rare:134; Clinvar:4; Clinvar (benign):6 |