| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:51879211-51879287 | Common:1; Rare:21 | ||||
| chr1:52055149-52055282 | Common:1; Rare:32 | ||||
| chr1:52056070-52056359 | Common:2; Rare:78 | ||||
| chr1:52141986-52142259 | Rare:61 | ||||
| chr1:52366106-52366509 | Common:4; Rare:113 | ||||
| chr1:52404381-52404633 | Common:1; Rare:72 | ||||
| chr1:52552941-52553387 | Common:4; Rare:134 | ||||
| chr1:52553436-52553697 | Common:3; Rare:74 | ||||
| chr1:52698318-52698476 | Common:2; Rare:52 | ||||
| chr1:53196640-53196792 | Common:1; Rare:50; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:53220563-53220712 | Common:2; Rare:75 | ||||
| chr1:53238414-53238602 | Common:1; Rare:70 | ||||
| chr1:53238619-53238754 | Rare:34 | ||||
| chr1:53327908-53328257 | Common:2; Rare:92 | ||||
| chr1:53838251-53838416 | Rare:51 |