| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200864229-200864253 | Rare:6 | ||||
| chr2:200864591-200864784 | Common:1; Rare:71 | ||||
| chr2:200888974-200889424 | Common:2; Rare:144 | ||||
| chr2:200963604-200963868 | Common:1; Rare:69 | ||||
| chr2:201071586-201072047 | Rare:101 | ||||
| chr2:201116274-201116429 | Rare:29 | ||||
| chr2:201451444-201451874 | Common:3; Rare:108 | ||||
| chr2:201642637-201642722 | Rare:43 | ||||
| chr2:201780896-201781243 | Common:3; Rare:106; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:202238504-202238670 | Rare:57 | ||||
| chr2:202634666-202635009 | Common:5; Rare:115 | ||||
| chr2:202912127-202912322 | Common:2; Rare:65 | ||||
| chr2:203014552-203014925 | Common:1; Rare:119 | ||||
| chr2:203238854-203239040 | Rare:73 | ||||
| chr2:203239234-203239320 | Rare:30 |