| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:197499811-197500431 | Common:1; Rare:238; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197515728-197516118 | Common:2; Rare:130 | ||||
| chr2:197675711-197675854 | Rare:25 | ||||
| chr2:200510040-200510122 | Rare:27 | ||||
| chr2:200526042-200526208 | Common:1; Rare:42 | ||||
| chr2:200811421-200811608 | Common:1; Rare:65 | ||||
| chr2:200864585-200864811 | Common:1; Rare:85 | ||||
| chr2:200888977-200889483 | Common:3; Rare:157 | ||||
| chr2:201071620-201072052 | Rare:90 | ||||
| chr2:201118489-201118792 | Rare:46 | ||||
| chr2:201451486-201451833 | Common:2; Rare:91 | ||||
| chr2:201642632-201642802 | Rare:77 | ||||
| chr2:201780896-201781001 | Common:2; Rare:30; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:202238443-202238625 | Rare:63; Clinvar:1 | ||||
| chr2:202911881-202912291 | Common:2; Rare:112 |