Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:6444249-6444466 | Common:2; Rare:70 | ||||
chr17:6640645-6641121 | Common:7; Rare:153 | ||||
chr17:6651553-6651720 | Common:1; Rare:63 | ||||
chr17:6755902-6756085 | Common:3; Rare:46 | ||||
chr17:7012301-7012705 | Rare:135 | ||||
chr17:7023816-7024116 | Common:1; Rare:106 | ||||
chr17:7035773-7036086 | Rare:73 | ||||
chr17:7043006-7043132 | Common:3; Rare:55 | ||||
chr17:7241778-7241906 | Common:1; Rare:25 | ||||
chr17:7251963-7252325 | Common:1; Rare:141 | ||||
chr17:7315063-7315411 | Common:4; Rare:120 | ||||
chr17:7352062-7352237 | Rare:60 | ||||
chr17:7484208-7484371 | Common:1; Rare:67 | ||||
chr17:7583547-7583872 | Common:1; Rare:130; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:7627805-7627988 | Common:2; Rare:57 |