| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96335719-96335813 | Common:1; Rare:30 | ||||
| chr2:96638292-96638538 | Common:1; Rare:64 | ||||
| chr2:96857934-96858258 | Common:2; Rare:116 | ||||
| chr2:97094820-97094935 | Common:1; Rare:24 | ||||
| chr2:97645780-97646122 | Common:3; Rare:107 | ||||
| chr2:97663926-97664262 | Common:1; Rare:103 | ||||
| chr2:98608420-98608665 | Common:1; Rare:106; Clinvar (benign):1 | ||||
| chr2:99154883-99155008 | Common:1; Rare:49 | ||||
| chr2:99180935-99181239 | Common:2; Rare:95 | ||||
| chr2:99337253-99337485 | Rare:84 | ||||
| chr2:100562759-100563309 | Common:3; Rare:193 | ||||
| chr2:100924818-100925178 | Rare:59 | ||||
| chr2:101002156-101002324 | Rare:64 | ||||
| chr2:102142670-102142936 | Common:4; Rare:83 | ||||
| chr2:102736821-102736944 | Common:1; Rare:62 |