Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:121834979-121835231 | Common:3; Rare:82; Clinvar:6; Clinvar (benign):2 | ||||
chr3:122383204-122383308 | Common:1; Rare:33 | ||||
chr3:122384046-122384260 | Rare:79 | ||||
chr3:122416075-122416218 | Rare:40 | ||||
chr3:122564243-122564429 | Common:3; Rare:56 | ||||
chr3:122564437-122564563 | Common:1; Rare:33 | ||||
chr3:122680746-122680874 | Rare:41 | ||||
chr3:122793802-122793920 | Common:2; Rare:26 | ||||
chr3:123700865-123701306 | Common:2; Rare:103; Clinvar:9; Clinvar (benign):5 | ||||
chr3:124730380-124730466 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
chr3:125375236-125375389 | Rare:41 | ||||
chr3:127598223-127598456 | Common:3; Rare:65 | ||||
chr3:128052202-128052485 | Common:2; Rare:95 | ||||
chr3:128879434-128879669 | Common:4; Rare:117; Clinvar:2; Clinvar (benign):2 | ||||
chr3:129183821-129184078 | Common:2; Rare:87 |