Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:111859663-111859875 | Rare:79 | ||||
chr3:112561597-112561699 | Rare:36 | ||||
chr3:113746150-113746366 | Rare:91 | ||||
chr3:114056481-114056825 | Common:2; Rare:131 | ||||
chr3:114624915-114625015 | Rare:17 | ||||
chr3:119463585-119463780 | Common:5; Rare:57 | ||||
chr3:119468864-119469015 | Rare:61 | ||||
chr3:120742503-120742772 | Common:2; Rare:76 | ||||
chr3:121749637-121750002 | Common:1; Rare:83 | ||||
chr3:121835036-121835229 | Common:2; Rare:63; Clinvar:4; Clinvar (benign):1 | ||||
chr3:122383192-122383323 | Common:1; Rare:41 | ||||
chr3:122384122-122384260 | Rare:55 | ||||
chr3:122416075-122416229 | Rare:42 | ||||
chr3:122564244-122564443 | Common:3; Rare:62 | ||||
chr3:123201693-123201967 | Common:1; Rare:77 |