Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:2664161-2664248 | Common:1; Rare:43 | ||||
chr20:2840672-2840777 | Common:1; Rare:50 | ||||
chr20:3173521-3173725 | Common:1; Rare:71 | ||||
chr20:3209439-3209543 | Rare:37 | ||||
chr20:3767720-3768040 | Common:3; Rare:101 | ||||
chr20:5112770-5113144 | Common:2; Rare:120 | ||||
chr20:5119907-5120168 | Common:1; Rare:88 | ||||
chr20:5126538-5126825 | Common:3; Rare:81 | ||||
chr20:5950358-5950680 | Common:8; Rare:94 | ||||
chr20:13784871-13785080 | Common:2; Rare:93; Clinvar (benign):3 | ||||
chr20:16573297-16573540 | Common:1; Rare:68 | ||||
chr20:17968375-17968633 | Common:5; Rare:109 | ||||
chr20:17968762-17969132 | Common:4; Rare:133 | ||||
chr20:17969543-17969570 | Rare:3 | ||||
chr20:18467148-18467459 | Common:2; Rare:63 |