Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99659364-99659539 | Rare:47 | ||||
chr10:99732076-99732322 | Rare:88; Clinvar:3 | ||||
chr10:100185914-100186076 | Rare:65 | ||||
chr10:100912770-100913011 | Common:1; Rare:69 | ||||
chr10:100969315-100969562 | Common:3; Rare:58 | ||||
chr10:100980713-100980855 | Rare:53 | ||||
chr10:100987429-100987575 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
chr10:101031097-101031326 | Common:1; Rare:49 | ||||
chr10:101588217-101588329 | Rare:47 | ||||
chr10:101818393-101818749 | Common:1; Rare:98 | ||||
chr10:102111268-102111492 | Rare:62 | ||||
chr10:102714271-102714627 | Common:2; Rare:119 | ||||
chr10:103396411-103396710 | Rare:106 | ||||
chr10:104032611-104032975 | Common:3; Rare:100; Clinvar:4 | ||||
chr10:104268974-104269190 | Common:2; Rare:49 |