| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:243255207-243255438 | Common:1; Rare:58 | ||||
| chr1:243255721-243256128 | Common:1; Rare:113; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:246566147-246566587 | Common:2; Rare:151 | ||||
| chr1:247104334-247104530 | Common:2; Rare:57 | ||||
| chr10:988305-988485 | Common:1; Rare:72 | ||||
| chr10:1048880-1049095 | Common:2; Rare:110 | ||||
| chr10:5813364-5813634 | Common:2; Rare:106 | ||||
| chr10:7787950-7788222 | Common:1; Rare:113 | ||||
| chr10:12195789-12195973 | Rare:46 | ||||
| chr10:13300059-13300192 | Rare:45; Clinvar:1 | ||||
| chr10:14838035-14838328 | Common:2; Rare:77 | ||||
| chr10:15097321-15097395 | Common:1; Rare:33 | ||||
| chr10:17233583-17233929 | Common:3; Rare:110; Clinvar (benign):1 | ||||
| chr10:17643877-17644286 | Common:2; Rare:122 | ||||
| chr10:18659265-18659491 | Common:2; Rare:81 |