Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7012323-7012685 | Rare:123 | ||||
chr17:7251967-7252314 | Common:1; Rare:133 | ||||
chr17:7479579-7479713 | Rare:20 | ||||
chr17:7484247-7484371 | Common:1; Rare:51 | ||||
chr17:7583564-7583864 | Common:1; Rare:121; Clinvar:3; Clinvar (benign):3 | ||||
chr17:7627799-7627994 | Common:2; Rare:63 | ||||
chr17:7857170-7857363 | Common:1; Rare:104 | ||||
chr17:7857460-7857735 | Common:2; Rare:86 | ||||
chr17:7885200-7885351 | Rare:49 | ||||
chr17:7931906-7932189 | Common:5; Rare:83 | ||||
chr17:8176354-8176431 | Rare:23 | ||||
chr17:8248042-8248171 | Common:3; Rare:55; Clinvar:2; Clinvar (benign):2 | ||||
chr17:8435710-8436034 | Common:4; Rare:123 | ||||
chr17:10697471-10697653 | Common:3; Rare:85; Clinvar:5; Clinvar (benign):3 | ||||
chr17:14069440-14069573 | Common:2; Rare:55; Clinvar:2; Clinvar (benign):3 |