| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:228406828-228406977 | Common:3; Rare:36 | ||||
| chr1:228457860-228458130 | Common:1; Rare:96 | ||||
| chr1:228735302-228735484 | Common:1; Rare:56 | ||||
| chr1:229271003-229271366 | Rare:115 | ||||
| chr1:229508215-229508481 | Common:1; Rare:106 | ||||
| chr1:229625938-229626266 | Rare:104 | ||||
| chr1:230747195-230747528 | Common:2; Rare:77 | ||||
| chr1:230978658-230979144 | Common:4; Rare:178 | ||||
| chr1:231241094-231241362 | Common:2; Rare:130; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:231337020-231337219 | Common:2; Rare:46 | ||||
| chr1:231337729-231338061 | Common:3; Rare:125 | ||||
| chr1:231338246-231338344 | Rare:21 | ||||
| chr1:231528492-231528823 | Common:2; Rare:110 | ||||
| chr1:232950520-232950664 | Common:1; Rare:54 | ||||
| chr1:233613895-233614186 | Common:5; Rare:89 |