| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70087864-70088823 | Common:1; Rare:229 | ||||
| chr2:70293626-70293811 | Common:2; Rare:61 | ||||
| chr2:70301987-70302314 | Common:5; Rare:127 | ||||
| chr2:71068533-71068672 | Rare:64 | ||||
| chr2:71129812-71129891 | Rare:15 | ||||
| chr2:71130178-71130666 | Common:6; Rare:141; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71453493-71453708 | Common:1; Rare:43 | ||||
| chr2:73071685-73071863 | Common:2; Rare:71 | ||||
| chr2:73234250-73234381 | Common:1; Rare:47 | ||||
| chr2:73385689-73386059 | Common:4; Rare:179; Clinvar:16; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr2:73642349-73642431 | Rare:25 | ||||
| chr2:73737276-73737505 | Common:3; Rare:73 | ||||
| chr2:73828804-73829012 | Common:1; Rare:49 | ||||
| chr2:74147829-74148125 | Common:2; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74365966-74366250 | Rare:88; Clinvar (benign):1 |