| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:211258916-211259404 | Common:3; Rare:177 | ||||
| chr1:211326536-211326651 | Common:2; Rare:26 | ||||
| chr1:211326715-211326862 | Common:3; Rare:39 | ||||
| chr1:211579129-211579412 | Rare:92 | ||||
| chr1:211675405-211675864 | Common:4; Rare:112; Clinvar (benign):1 | ||||
| chr1:211675997-211676150 | Common:1; Rare:28 | ||||
| chr1:211830130-211830670 | Common:4; Rare:143 | ||||
| chr1:211830706-211830974 | Common:1; Rare:62 | ||||
| chr1:212035131-212035393 | Rare:73 | ||||
| chr1:212035493-212035847 | Common:2; Rare:98 | ||||
| chr1:212284988-212285462 | Common:5; Rare:146 | ||||
| chr1:212414758-212415046 | Common:3; Rare:98 | ||||
| chr1:212432730-212432953 | Rare:65 | ||||
| chr1:212608286-212608769 | Common:4; Rare:121 | ||||
| chr1:212699088-212699463 | Common:4; Rare:93 |