Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:4947890-4948082 | Rare:54 | ||||
chr17:4948920-4949212 | Common:2; Rare:96 | ||||
chr17:4949300-4949569 | Rare:70 | ||||
chr17:4949830-4950163 | Common:1; Rare:76 | ||||
chr17:4950641-4951137 | Common:2; Rare:117; Clinvar (benign):1 | ||||
chr17:4967793-4967889 | Rare:40 | ||||
chr17:4987621-4987794 | Common:1; Rare:59 | ||||
chr17:4997518-4997742 | Common:1; Rare:89 | ||||
chr17:5006995-5007313 | Common:1; Rare:89; Clinvar:1; Clinvar (benign):2 | ||||
chr17:5123087-5123233 | Rare:43 | ||||
chr17:5191823-5192112 | Common:2; Rare:89 | ||||
chr17:5282084-5282502 | Common:14; Rare:182 | ||||
chr17:5419633-5419878 | Common:3; Rare:75 | ||||
chr17:5420098-5420225 | Rare:51 | ||||
chr17:5438887-5439211 | Common:2; Rare:119 |