Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:1275682-1276131 | Common:2; Rare:210 | ||||
chr19:1354735-1355014 | Common:3; Rare:122 | ||||
chr19:2328388-2328707 | Common:2; Rare:138 | ||||
chr19:2426889-2427194 | Common:3; Rare:112 | ||||
chr19:3539984-3540171 | Common:2; Rare:52 | ||||
chr19:3546080-3546411 | Common:7; Rare:192 | ||||
chr19:3547274-3547517 | Rare:114 | ||||
chr19:3572631-3573026 | Common:2; Rare:107 | ||||
chr19:3981991-3982409 | Common:2; Rare:158; Clinvar:1; Clinvar (benign):4 | ||||
chr19:4007500-4007759 | Common:3; Rare:102 | ||||
chr19:5293218-5293408 | Common:1; Rare:89 | ||||
chr19:5622729-5623194 | Common:5; Rare:183 | ||||
chr19:5680475-5680765 | Rare:88 | ||||
chr19:5978078-5978369 | Common:3; Rare:108 | ||||
chr19:6361772-6361810 | Rare:18 |