| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:68774749-68774947 | Rare:34 | ||||
| chr2:69387083-69387384 | Common:1; Rare:83; Clinvar:3 | ||||
| chr2:69437401-69437669 | Common:1; Rare:129; Clinvar:6; Clinvar (benign):3 | ||||
| chr2:69643587-69643825 | Rare:81 | ||||
| chr2:69643934-69644275 | Common:7; Rare:58 | ||||
| chr2:69741989-69742169 | Common:1; Rare:41 | ||||
| chr2:69829524-69829760 | Common:1; Rare:90 | ||||
| chr2:69914484-69914642 | Rare:44 | ||||
| chr2:70086909-70087097 | Common:1; Rare:100 | ||||
| chr2:70087373-70087758 | Common:2; Rare:150 | ||||
| chr2:70190941-70191124 | Rare:44 | ||||
| chr2:70258007-70258249 | Common:2; Rare:88 | ||||
| chr2:71068526-71068681 | Rare:73 | ||||
| chr2:71129812-71129932 | Rare:26 | ||||
| chr2:71130216-71130698 | Common:7; Rare:141; Clinvar:1; Clinvar (benign):2 |