| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:45688300-45689195 | Common:11; Rare:301 | ||||
| chr1:45750406-45750900 | Common:2; Rare:372 | ||||
| chr1:45803415-45803689 | Common:6; Rare:288 | ||||
| chr1:46132431-46132782 | Common:9; Rare:245 | ||||
| chr1:46132840-46133543 | Common:10; Rare:420 | ||||
| chr1:46174501-46174845 | Rare:122 | ||||
| chr1:46183118-46183468 | Common:6; Rare:138 | ||||
| chr1:46183697-46183839 | Common:1; Rare:26 | ||||
| chr1:46197657-46198195 | Rare:211; Clinvar:11; Clinvar (benign):7 | ||||
| chr1:46198321-46198618 | Common:16; Rare:356; Clinvar:3; Clinvar (benign):3 | ||||
| chr1:46247227-46248001 | Common:16; Rare:332 | ||||
| chr1:46303093-46303777 | Common:9; Rare:565 | ||||
| chr1:46339873-46340234 | Common:8; Rare:134 | ||||
| chr1:46340371-46340907 | Common:15; Rare:278 | ||||
| chr1:46340936-46341142 | Common:1; Rare:58 |