Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:113746161-113746318 | Rare:65 | ||||
chr3:114056524-114056815 | Common:2; Rare:103 | ||||
chr3:119498354-119498674 | Common:5; Rare:106 | ||||
chr3:120742503-120742782 | Common:2; Rare:78 | ||||
chr3:121749640-121749769 | Rare:33 | ||||
chr3:121834966-121835237 | Common:3; Rare:85; Clinvar:6; Clinvar (benign):2 | ||||
chr3:122416043-122416215 | Rare:56 | ||||
chr3:122564251-122564421 | Common:2; Rare:51 | ||||
chr3:123066949-123067161 | Rare:54 | ||||
chr3:123585032-123585317 | Common:1; Rare:86 | ||||
chr3:126084099-126084188 | Common:1; Rare:31 | ||||
chr3:127598217-127598466 | Common:3; Rare:76 | ||||
chr3:128052155-128052515 | Common:3; Rare:122 | ||||
chr3:128879417-128879627 | Common:2; Rare:94; Clinvar:2 | ||||
chr3:129183822-129184074 | Common:2; Rare:86 |