| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:85595558-85595757 | Common:1; Rare:59 | ||||
| chr2:85612030-85612091 | Rare:18 | ||||
| chr2:86105855-86106182 | Common:2; Rare:79 | ||||
| chr2:86195395-86195683 | Common:8; Rare:93 | ||||
| chr2:95165651-95165817 | Rare:49 | ||||
| chr2:95207450-95207558 | Rare:40 | ||||
| chr2:96208252-96208403 | Rare:78 | ||||
| chr2:96208817-96208888 | Common:2; Rare:24 | ||||
| chr2:96265978-96266311 | Common:2; Rare:97 | ||||
| chr2:96305473-96305627 | Common:2; Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:96857915-96858243 | Common:2; Rare:119 | ||||
| chr2:98608420-98608636 | Common:1; Rare:93; Clinvar (benign):1 | ||||
| chr2:99141554-99141740 | Common:2; Rare:62 | ||||
| chr2:99154933-99155040 | Common:1; Rare:46; Clinvar (benign):2 | ||||
| chr2:99180985-99181208 | Common:2; Rare:67 |