| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52536330-52536752 | Common:3; Rare:135 | ||||
| chr3:52685586-52685795 | Common:1; Rare:51 | ||||
| chr3:52685798-52686181 | Common:3; Rare:143 | ||||
| chr3:52705587-52706252 | Common:4; Rare:219 | ||||
| chr3:53130398-53130577 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53347518-53347685 | Common:1; Rare:49 | ||||
| chr3:53494167-53494220 | Common:3; Rare:16 | ||||
| chr3:53846410-53846577 | Rare:56 | ||||
| chr3:53891804-53892033 | Common:2; Rare:69 | ||||
| chr3:56557086-56557230 | Common:2; Rare:56 | ||||
| chr3:56801903-56802084 | Common:1; Rare:65 | ||||
| chr3:57079241-57079382 | Common:2; Rare:48 | ||||
| chr3:57227604-57227913 | Common:3; Rare:106 | ||||
| chr3:57555987-57556321 | Rare:86 | ||||
| chr3:57597292-57597773 | Common:4; Rare:141 |