Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:46398281-46398419 | Common:3; Rare:56 | ||||
chr10:49539023-49539213 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
chr10:49941922-49942118 | Rare:58 | ||||
chr10:50067817-50067987 | Common:4; Rare:74 | ||||
chr10:50623887-50624092 | Common:1; Rare:79 | ||||
chr10:52314073-52314298 | Common:1; Rare:55 | ||||
chr10:56361232-56361494 | Common:5; Rare:89 | ||||
chr10:58268915-58269274 | Common:6; Rare:111 | ||||
chr10:59709579-59709776 | Rare:51 | ||||
chr10:60733428-60733549 | Rare:38 | ||||
chr10:63465958-63466128 | Rare:78 | ||||
chr10:63521204-63521506 | Common:7; Rare:109 | ||||
chr10:68331913-68332168 | Common:2; Rare:106 | ||||
chr10:68332890-68332957 | Common:1; Rare:20 | ||||
chr10:68407193-68407339 | Common:3; Rare:40 |