| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:229508192-229508491 | Common:2; Rare:203 | ||||
| chr1:229558646-229559044 | Common:3; Rare:183 | ||||
| chr1:229625631-229625868 | Rare:82 | ||||
| chr1:229626032-229626306 | Rare:192 | ||||
| chr1:230067048-230067451 | Common:2; Rare:228 | ||||
| chr1:230978797-230979130 | Common:2; Rare:225 | ||||
| chr1:231241089-231241367 | Common:2; Rare:207; Clinvar:7; Clinvar (benign):2 | ||||
| chr1:231337775-231338082 | Common:7; Rare:210 | ||||
| chr1:231528524-231528870 | Common:5; Rare:197 | ||||
| chr1:232950444-232950658 | Common:6; Rare:135 | ||||
| chr1:233294730-233295370 | Common:8; Rare:235 | ||||
| chr1:233295418-233295557 | Common:1; Rare:46 | ||||
| chr1:233327435-233327780 | Common:5; Rare:49 | ||||
| chr1:233613755-233614190 | Common:10; Rare:202 | ||||
| chr1:234373276-234373830 | Common:3; Rare:423; Clinvar (benign):15 |