Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:6144795-6144966 | Common:1; Rare:41 | ||||
chr10:7787929-7788250 | Common:1; Rare:136 | ||||
chr10:7818364-7818520 | Common:1; Rare:35 | ||||
chr10:8053475-8053653 | Rare:54 | ||||
chr10:12043165-12043387 | Common:2; Rare:66 | ||||
chr10:12068683-12069014 | Common:2; Rare:117 | ||||
chr10:12129483-12129685 | Rare:89 | ||||
chr10:12195783-12195984 | Rare:50 | ||||
chr10:13099978-13100205 | Common:2; Rare:58; Clinvar:2; Clinvar (benign):4 | ||||
chr10:13348003-13348370 | Rare:125 | ||||
chr10:13586810-13587037 | Common:2; Rare:74 | ||||
chr10:13707194-13707473 | Common:3; Rare:60 | ||||
chr10:13707557-13707738 | Rare:41 | ||||
chr10:14008157-14008386 | Rare:51 | ||||
chr10:14008421-14008477 | Rare:11 |