| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:113515114-113515279 | Rare:52 | ||||
| chr3:113746156-113746389 | Rare:96 | ||||
| chr3:113746786-113747076 | Common:4; Rare:66 | ||||
| chr3:114056481-114056823 | Common:2; Rare:131 | ||||
| chr3:114624930-114625074 | Common:1; Rare:19 | ||||
| chr3:119463585-119463817 | Common:5; Rare:71 | ||||
| chr3:119468848-119469009 | Rare:61 | ||||
| chr3:120094414-120094569 | Common:2; Rare:64 | ||||
| chr3:120742489-120742783 | Common:2; Rare:85 | ||||
| chr3:121545962-121546059 | Common:1; Rare:27 | ||||
| chr3:121749646-121750011 | Common:1; Rare:84 | ||||
| chr3:121835032-121835209 | Common:2; Rare:57; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:122383192-122383323 | Common:1; Rare:41 | ||||
| chr3:122416041-122416229 | Rare:60 | ||||
| chr3:122514830-122515029 | Common:2; Rare:57 |