| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:220748589-220748797 | Common:1; Rare:69 | ||||
| chr1:222644127-222644441 | Common:2; Rare:96 | ||||
| chr1:222663834-222664099 | Rare:61 | ||||
| chr1:222712459-222712864 | Common:3; Rare:145 | ||||
| chr1:223821261-223821517 | Rare:72 | ||||
| chr1:224183151-224183289 | Common:2; Rare:70 | ||||
| chr1:224330116-224330439 | Common:6; Rare:101 | ||||
| chr1:225427971-225428280 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):3 | ||||
| chr1:225777716-225777895 | Common:3; Rare:53 | ||||
| chr1:225848937-225849095 | Rare:54 | ||||
| chr1:225882302-225882460 | Rare:48 | ||||
| chr1:225999308-225999616 | Common:2; Rare:104 | ||||
| chr1:226062058-226062094 | Rare:10 | ||||
| chr1:226062458-226062807 | Rare:125 | ||||
| chr1:226186677-226186786 | Rare:43 |