Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7577056-7577278 | Common:1; Rare:51 | ||||
chr17:7583535-7583865 | Common:1; Rare:133; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:7627580-7627612 | Rare:10 | ||||
chr17:7717667-7717760 | Rare:20 | ||||
chr17:7803963-7804273 | Rare:75 | ||||
chr17:7843927-7844210 | Common:4; Rare:85 | ||||
chr17:7857382-7857735 | Common:3; Rare:113 | ||||
chr17:7857892-7858074 | Rare:65 | ||||
chr17:7931890-7932258 | Common:5; Rare:99 | ||||
chr17:8147743-8148023 | Rare:92 | ||||
chr17:8151166-8151498 | Common:3; Rare:82 | ||||
chr17:8151751-8151989 | Rare:45 | ||||
chr17:8152348-8152567 | Common:2; Rare:51 | ||||
chr17:8156542-8156879 | Common:4; Rare:96 | ||||
chr17:8162897-8163098 | Rare:71 |