| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:229625641-229625854 | Rare:47 | ||||
| chr1:229625927-229626284 | Rare:117 | ||||
| chr1:230642232-230642609 | Common:1; Rare:130 | ||||
| chr1:230747127-230747423 | Common:4; Rare:60 | ||||
| chr1:230868357-230868553 | Rare:79 | ||||
| chr1:230868837-230868968 | Rare:21 | ||||
| chr1:230869026-230869055 | Rare:5 | ||||
| chr1:230978739-230979122 | Common:2; Rare:147 | ||||
| chr1:231241107-231241367 | Common:2; Rare:128; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:231337003-231337317 | Common:2; Rare:84 | ||||
| chr1:231337455-231337533 | Rare:13 | ||||
| chr1:231337775-231338319 | Common:5; Rare:174 | ||||
| chr1:231528540-231528798 | Common:2; Rare:96 | ||||
| chr1:232805295-232805440 | Common:2; Rare:82 | ||||
| chr1:232950476-232950651 | Common:3; Rare:60 |