Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:16883955-16884281 | Common:1; Rare:81 | ||||
chr3:17140761-17141029 | Rare:65 | ||||
chr3:29279996-29280066 | Rare:20 | ||||
chr3:31580009-31580199 | Rare:37 | ||||
chr3:37244171-37244181 | |||||
chr3:37244186-37244280 | Common:2; Rare:26 | ||||
chr3:40453163-40453417 | Common:6; Rare:56 | ||||
chr3:41225468-41225700 | Rare:48; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr3:42654377-42654630 | Rare:75 | ||||
chr3:48684546-48684761 | Rare:51 | ||||
chr3:49131407-49131604 | Common:1; Rare:64; Clinvar:2 | ||||
chr3:51393601-51393614 | Rare:4 | ||||
chr3:52235179-52235381 | Common:1; Rare:29 | ||||
chr3:57952311-57952557 | Rare:39 | ||||
chr3:61560849-61561037 | Common:3; Rare:52 |