Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:2977294-2977590 | Common:2; Rare:104 | ||||
chr19:3982805-3983192 | Common:5; Rare:138; Clinvar:1; Clinvar (benign):3 | ||||
chr19:4007510-4007758 | Common:3; Rare:101 | ||||
chr19:4723747-4724012 | Common:2; Rare:87 | ||||
chr19:4831701-4831763 | Rare:16 | ||||
chr19:4867621-4867853 | Common:3; Rare:71 | ||||
chr19:5622742-5623181 | Common:5; Rare:168 | ||||
chr19:5680468-5680606 | Rare:43 | ||||
chr19:5978078-5978415 | Common:3; Rare:130 | ||||
chr19:6361739-6361835 | Rare:42; Clinvar:1 | ||||
chr19:7395037-7395185 | Common:4; Rare:47 | ||||
chr19:7629529-7629836 | Common:5; Rare:109; Clinvar (benign):2 | ||||
chr19:8005514-8005821 | Common:1; Rare:108 | ||||
chr19:8321322-8321563 | Common:2; Rare:111 | ||||
chr19:8390038-8390419 | Common:1; Rare:107 |