Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:108215502-108215729 | Common:1; Rare:59 | ||||
chr13:108218267-108218639 | Common:1; Rare:132 | ||||
chr13:110305548-110305750 | Rare:31 | ||||
chr13:110306955-110307528 | Common:7; Rare:177; Clinvar:3; Clinvar (benign):10 | ||||
chr13:110506186-110506605 | Common:3; Rare:125; Clinvar:1; Clinvar (benign):5 | ||||
chr13:110561346-110561427 | Rare:33 | ||||
chr13:110561585-110561913 | Common:5; Rare:108 | ||||
chr13:110615408-110615671 | Common:2; Rare:91 | ||||
chr13:110712436-110712542 | Rare:52 | ||||
chr13:110713018-110713268 | Common:2; Rare:110 | ||||
chr13:110713481-110713657 | Common:2; Rare:75 | ||||
chr13:110715351-110715637 | Common:1; Rare:119 | ||||
chr13:110914366-110914796 | Common:7; Rare:179 | ||||
chr13:110914891-110915238 | Common:3; Rare:149 | ||||
chr13:111153614-111153724 | Common:2; Rare:49 |