Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:132887548-132887845 | Rare:87 | ||||
chr12:132956252-132956437 | Common:1; Rare:39 | ||||
chr12:132986269-132986428 | Rare:35 | ||||
chr12:133080238-133080459 | Common:5; Rare:66 | ||||
chr12:133130232-133130652 | Common:7; Rare:139 | ||||
chr13:19863538-19863852 | Common:5; Rare:114 | ||||
chr13:19958455-19958751 | Common:5; Rare:141 | ||||
chr13:20525778-20525915 | Common:1; Rare:58 | ||||
chr13:21061517-21061705 | Common:1; Rare:58 | ||||
chr13:21140408-21140678 | Rare:117 | ||||
chr13:21176529-21176711 | Common:1; Rare:86 | ||||
chr13:21670961-21671156 | Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
chr13:23579233-23579405 | Common:3; Rare:55 | ||||
chr13:23889289-23889591 | Common:1; Rare:104 | ||||
chr13:24160581-24160790 | Common:1; Rare:64 |