| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32843982-32844119 | Rare:32; Clinvar:1 | ||||
| chr6:32844270-32844821 | Common:1; Rare:126 | ||||
| chr6:32853646-32853814 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):4 | ||||
| chr6:32854019-32854226 | Common:2; Rare:54 | ||||
| chr6:32968395-32968652 | Common:3; Rare:75 | ||||
| chr6:33200656-33200952 | Common:3; Rare:89 | ||||
| chr6:33271629-33272094 | Common:3; Rare:155 | ||||
| chr6:33289525-33289636 | Rare:27 | ||||
| chr6:33299408-33299489 | Common:1; Rare:15 | ||||
| chr6:33322898-33323272 | Common:5; Rare:116 | ||||
| chr6:34696738-34696975 | Common:1; Rare:55 | ||||
| chr6:34757290-34757556 | Common:1; Rare:74 | ||||
| chr6:35921047-35921253 | Common:1; Rare:86 | ||||
| chr6:36678419-36678832 | Common:1; Rare:100 | ||||
| chr6:36874792-36874882 | Rare:31 |