| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:40691378-40691859 | Common:3; Rare:196 | ||||
| chr1:40692015-40692257 | Common:2; Rare:80 | ||||
| chr1:40979362-40979822 | Common:5; Rare:139 | ||||
| chr1:40980480-40980534 | Rare:16 | ||||
| chr1:42335160-42335355 | Common:3; Rare:100 | ||||
| chr1:42658295-42658464 | Common:2; Rare:51 | ||||
| chr1:42682158-42682424 | Common:2; Rare:68 | ||||
| chr1:42682570-42682723 | Common:1; Rare:64 | ||||
| chr1:42766505-42766645 | Rare:38; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:42766976-42767386 | Common:7; Rare:145; Clinvar (benign):1 | ||||
| chr1:42816938-42817139 | Common:1; Rare:58 | ||||
| chr1:42817193-42817567 | Rare:121 | ||||
| chr1:42846392-42846652 | Common:1; Rare:73 | ||||
| chr1:42958635-42959104 | Common:4; Rare:118; Clinvar:6; Clinvar (benign):8 | ||||
| chr1:42959110-42959532 | Common:3; Rare:97; Clinvar:2; Clinvar (benign):1 |