Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:81512735-81513111 | Common:7; Rare:196; Clinvar (benign):14 | ||||
chr17:81666558-81666782 | Common:1; Rare:101 | ||||
chr17:81683745-81684052 | Common:4; Rare:144 | ||||
chr17:81703283-81703475 | Common:2; Rare:55; Clinvar (benign):2 | ||||
chr17:81833257-81833343 | Rare:35 | ||||
chr17:81891582-81891809 | Common:3; Rare:112 | ||||
chr17:81937246-81937441 | Rare:78 | ||||
chr17:82273688-82273816 | Common:1; Rare:39 | ||||
chr17:82450716-82450911 | Common:2; Rare:73 | ||||
chr18:268015-268283 | Common:1; Rare:74 | ||||
chr18:712599-712859 | Common:1; Rare:95 | ||||
chr18:812203-812437 | Common:3; Rare:81 | ||||
chr18:2571482-2571618 | Rare:36 | ||||
chr18:3013107-3013380 | Common:3; Rare:99 | ||||
chr18:3247347-3247530 | Common:1; Rare:53 |