Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:108218333-108218520 | Rare:75 | ||||
chr13:110307087-110307494 | Common:6; Rare:133; Clinvar:1; Clinvar (benign):8 | ||||
chr13:113208188-113208274 | Common:2; Rare:15 | ||||
chr13:113208620-113208747 | Rare:78 | ||||
chr13:113209470-113209633 | Common:3; Rare:50 | ||||
chr13:113297037-113297379 | Common:2; Rare:119 | ||||
chr13:113321426-113321632 | Common:8; Rare:72 | ||||
chr13:113490672-113491167 | Common:5; Rare:187 | ||||
chr13:113759147-113759216 | Rare:19 | ||||
chr13:113863936-113864203 | Common:2; Rare:67 | ||||
chr14:20454783-20455338 | Common:7; Rare:143 | ||||
chr14:20684443-20684662 | Common:2; Rare:39; Clinvar (benign):2 | ||||
chr14:21476619-21476766 | Rare:65 | ||||
chr14:21476868-21477246 | Common:1; Rare:117 | ||||
chr14:22589144-22589495 | Common:4; Rare:111 |