Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:36187419-36187534 | Common:2; Rare:46 | ||||
chr18:36828772-36829131 | Common:3; Rare:131 | ||||
chr18:46104135-46104409 | Common:4; Rare:80; Clinvar (benign):1 | ||||
chr18:49813832-49814026 | Common:1; Rare:79 | ||||
chr18:50878951-50879169 | Common:4; Rare:74 | ||||
chr18:62186987-62187292 | Common:5; Rare:86 | ||||
chr18:68715036-68715255 | Common:3; Rare:101 | ||||
chr19:1103801-1104104 | Common:4; Rare:127 | ||||
chr19:2328552-2328693 | Rare:65 | ||||
chr19:2944926-2945187 | Common:5; Rare:89 | ||||
chr19:4723761-4723853 | Common:1; Rare:31 | ||||
chr19:5622737-5623128 | Common:5; Rare:148 | ||||
chr19:7629538-7629831 | Common:5; Rare:102; Clinvar (benign):1 | ||||
chr19:7920213-7920360 | Rare:59 | ||||
chr19:7943652-7943988 | Rare:85 |