| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:86668318-86668541 | Common:2; Rare:58 | ||||
| chr10:86756248-86756835 | Common:8; Rare:357; Clinvar:2 | ||||
| chr10:86958360-86958610 | Common:2; Rare:102 | ||||
| chr10:87094047-87094312 | Rare:78 | ||||
| chr10:87094765-87095260 | Common:2; Rare:246; Clinvar:6 | ||||
| chr10:87504786-87504984 | Common:2; Rare:157 | ||||
| chr10:87659570-87659924 | Common:7; Rare:122 | ||||
| chr10:87817804-87818376 | Common:4; Rare:339 | ||||
| chr10:87862630-87862880 | Rare:111 | ||||
| chr10:87863257-87863818 | Common:4; Rare:294; Clinvar:180; Clinvar (benign):18 | ||||
| chr10:87864340-87865130 | Common:3; Rare:250; Clinvar:26; Clinvar (benign):24; Clinvar (pathogenic):2 | ||||
| chr10:88879892-88880526 | Common:4; Rare:199 | ||||
| chr10:88880510-88881087 | Common:7; Rare:168 | ||||
| chr10:88990230-88990993 | Common:11; Rare:310; Clinvar:2; Clinvar (benign):10 | ||||
| chr10:88991265-88991470 | Common:5; Rare:71 |