Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:47501826-47502121 | Common:1; Rare:94 | ||||
chr20:47786558-47786667 | Common:2; Rare:16 | ||||
chr20:49046148-49046346 | Common:3; Rare:58 | ||||
chr20:49219281-49219538 | Rare:117 | ||||
chr20:49278036-49278278 | Rare:67 | ||||
chr20:49812765-49812926 | Common:3; Rare:44 | ||||
chr20:49915492-49915801 | Common:4; Rare:89 | ||||
chr20:50113124-50113244 | Common:5; Rare:59 | ||||
chr20:50153639-50153928 | Common:2; Rare:116 | ||||
chr20:50190584-50190833 | Rare:69 | ||||
chr20:50691493-50691775 | Rare:39 | ||||
chr20:50958490-50958850 | Common:1; Rare:123; Clinvar:1; Clinvar (benign):3 | ||||
chr20:53593790-53593894 | Common:1; Rare:38 | ||||
chr20:56392203-56392468 | Common:1; Rare:79 | ||||
chr20:58309417-58309715 | Common:2; Rare:118 |