Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:34441686-34441870 | Common:1; Rare:36 | ||||
chr14:34453232-34453383 | Common:1; Rare:12 | ||||
chr14:34453896-34454046 | Common:1; Rare:24 | ||||
chr14:34459260-34459548 | Common:6; Rare:49 | ||||
chr14:34515787-34516050 | Rare:46 | ||||
chr14:34971945-34972091 | Rare:25 | ||||
chr14:35103733-35103960 | Rare:27 | ||||
chr14:36306063-36306146 | Common:1; Rare:12 | ||||
chr14:39085659-39085802 | Common:11; Rare:42 | ||||
chr14:39175833-39176133 | Common:4; Rare:77 | ||||
chr14:44963257-44963559 | Rare:94 | ||||
chr14:44980772-44980839 | Rare:12 | ||||
chr14:49622706-49622871 | Rare:35 | ||||
chr14:49633932-49634113 | Common:1; Rare:83; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr14:49634299-49634490 | Common:1; Rare:95; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):1 |