| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:98608305-98608636 | Common:1; Rare:136; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:98731062-98731285 | Common:3; Rare:80 | ||||
| chr2:98869253-98869403 | Common:1; Rare:37 | ||||
| chr2:99141147-99141484 | Common:1; Rare:120 | ||||
| chr2:99141512-99141735 | Common:2; Rare:84 | ||||
| chr2:99154877-99155101 | Common:2; Rare:90; Clinvar (benign):3 | ||||
| chr2:99180985-99181227 | Common:2; Rare:71 | ||||
| chr2:99337197-99337456 | Rare:83 | ||||
| chr2:100006933-100007242 | Rare:87 | ||||
| chr2:100562871-100563046 | Common:2; Rare:57 | ||||
| chr2:101002162-101002318 | Rare:61 | ||||
| chr2:101002508-101002805 | Rare:70 | ||||
| chr2:101252646-101252907 | Common:5; Rare:88 | ||||
| chr2:101308680-101308785 | Rare:41 | ||||
| chr2:102142593-102142934 | Common:4; Rare:99 |