Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:60163886-60164118 | Common:1; Rare:62 | ||||
chr13:67230294-67230634 | Common:2; Rare:110 | ||||
chr13:72727595-72727973 | Common:4; Rare:145 | ||||
chr13:72781926-72782210 | Rare:98 | ||||
chr13:75549430-75549821 | Common:8; Rare:101 | ||||
chr13:77027142-77027275 | Common:5; Rare:41 | ||||
chr13:78659135-78659235 | Common:2; Rare:73 | ||||
chr13:100088921-100089139 | Rare:81; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:102596785-102597028 | Common:1; Rare:113 | ||||
chr13:102798895-102799180 | Common:1; Rare:59 | ||||
chr13:106568103-106568261 | Rare:50 | ||||
chr13:108218321-108218512 | Rare:73 | ||||
chr13:110307087-110307485 | Common:6; Rare:130; Clinvar:1; Clinvar (benign):8 | ||||
chr13:110915016-110915320 | Common:3; Rare:116 | ||||
chr13:112588107-112588261 | Rare:37 |