Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:21526217-21526534 | Rare:60 | ||||
chr14:22588490-22588745 | Common:2; Rare:44 | ||||
chr14:22589067-22589575 | Common:4; Rare:149 | ||||
chr14:22589652-22589839 | Common:1; Rare:41 | ||||
chr14:22598196-22598595 | Common:1; Rare:128 | ||||
chr14:22766440-22766962 | Common:4; Rare:232 | ||||
chr14:22815751-22816030 | Common:1; Rare:56; Clinvar (benign):1 | ||||
chr14:22819702-22819978 | Common:4; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
chr14:22822552-22822939 | Common:3; Rare:77 | ||||
chr14:22823014-22823052 | Common:1; Rare:6 | ||||
chr14:22823253-22823534 | Common:2; Rare:48 | ||||
chr14:22829691-22829991 | Common:1; Rare:90 | ||||
chr14:22836606-22836646 | Rare:9 | ||||
chr14:22837295-22837382 | Rare:36 | ||||
chr14:22871111-22871178 | Common:1; Rare:15 |