Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:113841976-113842116 | Common:13; Rare:38 | ||||
chr14:22432665-22432888 | Rare:40 | ||||
chr14:22771171-22771347 | Rare:60 | ||||
chr14:34873880-34874198 | Common:2; Rare:64 | ||||
chr14:35401479-35401555 | Rare:17 | ||||
chr14:49633949-49634113 | Common:1; Rare:77; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:49862861-49863075 | Rare:71 | ||||
chr14:50515750-50516030 | Common:1; Rare:42 | ||||
chr14:58265904-58265927 | Rare:5 | ||||
chr14:70186895-70187157 | Common:1; Rare:68 | ||||
chr14:73099406-73099690 | Common:2; Rare:44 | ||||
chr14:75126271-75126346 | Rare:16 | ||||
chr14:75258876-75259384 | Common:2; Rare:128 | ||||
chr14:75277094-75277447 | Common:1; Rare:73 | ||||
chr14:75294193-75294458 | Common:1; Rare:71 |