Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11805905-11806276 | Common:2; Rare:102; Clinvar:1 | ||||
chr1:11934486-11934754 | Common:5; Rare:88; Clinvar:5; Clinvar (benign):1 | ||||
chr1:11980081-11980473 | Common:6; Rare:125; Clinvar:1; Clinvar (benign):4 | ||||
chr1:12409755-12409855 | Common:1; Rare:24 | ||||
chr1:12618174-12618419 | Common:2; Rare:51 | ||||
chr1:13749143-13749439 | Common:2; Rare:98 | ||||
chr1:15526600-15526914 | Common:2; Rare:100 | ||||
chr1:15584882-15584931 | Common:1; Rare:17 | ||||
chr1:16352434-16352608 | Common:3; Rare:94 | ||||
chr1:16440602-16440761 | Rare:49 | ||||
chr1:17618188-17618402 | Common:2; Rare:46 | ||||
chr1:19210079-19210519 | Rare:146 | ||||
chr1:19251494-19251873 | Common:6; Rare:127 | ||||
chr1:19311988-19312343 | Common:8; Rare:167 | ||||
chr1:19485439-19485762 | Common:1; Rare:120 |