| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:240091737-240091944 | Common:3; Rare:87 | ||||
| chr1:241848100-241848205 | Common:1; Rare:25 | ||||
| chr1:243255055-243255433 | Common:1; Rare:91 | ||||
| chr1:243255741-243256161 | Common:1; Rare:122; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:244451915-244452219 | Common:1; Rare:100 | ||||
| chr1:244856493-244856763 | Common:1; Rare:65; Clinvar (benign):2 | ||||
| chr1:246566141-246566634 | Common:3; Rare:160 | ||||
| chr10:134539-134838 | Rare:72 | ||||
| chr10:988327-988490 | Common:1; Rare:68 | ||||
| chr10:1048884-1049095 | Common:2; Rare:108 | ||||
| chr10:1049344-1049504 | Common:5; Rare:72 | ||||
| chr10:1056701-1056835 | Common:2; Rare:52 | ||||
| chr10:5813373-5813506 | Common:2; Rare:54 | ||||
| chr10:5889912-5890297 | Common:5; Rare:138 | ||||
| chr10:7787863-7788258 | Common:1; Rare:162 |