Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:56468559-56468695 | Rare:63 | ||||
chr20:58389860-58390034 | Common:1; Rare:51 | ||||
chr20:58515201-58515521 | Common:3; Rare:58 | ||||
chr20:58651092-58651298 | Common:2; Rare:46; Clinvar (benign):1 | ||||
chr20:58651591-58651847 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
chr20:58839530-58839830 | Common:1; Rare:65 | ||||
chr20:58840309-58840347 | Rare:15 | ||||
chr20:58840398-58840737 | Common:1; Rare:130; Clinvar:3 | ||||
chr20:58852708-58852748 | Rare:10 | ||||
chr20:58852801-58852986 | Common:1; Rare:46 | ||||
chr20:58854168-58854342 | Rare:75; Clinvar:2 | ||||
chr20:59940213-59940518 | Rare:112 | ||||
chr20:62182909-62183049 | Rare:49 | ||||
chr20:62386938-62387136 | Common:3; Rare:88 | ||||
chr20:62937875-62938209 | Common:2; Rare:120 |