| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96868561-96868804 | Rare:60 | ||||
| chr2:97094835-97094934 | Common:1; Rare:21 | ||||
| chr2:97113473-97113542 | Rare:15 | ||||
| chr2:97663912-97664261 | Common:1; Rare:106 | ||||
| chr2:98608381-98608690 | Common:1; Rare:125; Clinvar (benign):1 | ||||
| chr2:99141135-99141441 | Common:1; Rare:111 | ||||
| chr2:99154863-99155094 | Common:3; Rare:95; Clinvar (benign):3 | ||||
| chr2:99180920-99181246 | Common:2; Rare:105 | ||||
| chr2:99255643-99255737 | Rare:17 | ||||
| chr2:99337226-99337466 | Rare:84 | ||||
| chr2:100417374-100417694 | Rare:96 | ||||
| chr2:100562640-100563050 | Common:5; Rare:120 | ||||
| chr2:101002129-101002503 | Rare:130 | ||||
| chr2:101252658-101252907 | Common:5; Rare:82 | ||||
| chr2:101474656-101474821 | Common:1; Rare:28 |