| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74507673-74507789 | Rare:24 | ||||
| chr2:74529665-74529952 | Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74958546-74958673 | Common:1; Rare:44 | ||||
| chr2:75560894-75561051 | Rare:32 | ||||
| chr2:75561258-75561445 | Common:2; Rare:23 | ||||
| chr2:84459234-84459581 | Common:3; Rare:87; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:84905532-84905890 | Common:1; Rare:106 | ||||
| chr2:85327924-85328080 | Common:2; Rare:72 | ||||
| chr2:85354526-85354790 | Common:1; Rare:85 | ||||
| chr2:85561431-85561581 | Rare:56; Clinvar:4 | ||||
| chr2:85595555-85595757 | Common:2; Rare:60 | ||||
| chr2:85612027-85612098 | Rare:19 | ||||
| chr2:85616048-85616275 | Common:1; Rare:90 | ||||
| chr2:86105855-86106259 | Common:3; Rare:112 | ||||
| chr2:86195387-86195666 | Common:5; Rare:91 |