Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:16215385-16215650 | Common:2; Rare:108 | ||||
chr17:16217058-16217247 | Rare:52; Clinvar:1 | ||||
chr17:16381022-16381465 | Common:4; Rare:191 | ||||
chr17:17237133-17237433 | Common:4; Rare:91; Clinvar (benign):2 | ||||
chr17:17496393-17496519 | Rare:33 | ||||
chr17:17591389-17591485 | Rare:33 | ||||
chr17:17591664-17591902 | Common:1; Rare:64 | ||||
chr17:17836949-17837042 | Common:2; Rare:22 | ||||
chr17:18039095-18039424 | Common:4; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
chr17:18314921-18315332 | Common:1; Rare:117 | ||||
chr17:19648662-19648972 | Common:3; Rare:106 | ||||
chr17:19977820-19977958 | Common:1; Rare:45 | ||||
chr17:20009086-20009389 | Common:2; Rare:82 | ||||
chr17:21214128-21214349 | Common:2; Rare:101 | ||||
chr17:27293981-27294122 | Common:1; Rare:59 |