| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32175985-32176258 | Common:2; Rare:106 | ||||
| chr6:32177045-32177560 | Common:3; Rare:136 | ||||
| chr6:32178074-32178469 | Common:5; Rare:112 | ||||
| chr6:32189630-32190080 | Common:6; Rare:177 | ||||
| chr6:32190170-32190364 | Rare:60 | ||||
| chr6:32196400-32196850 | Common:4; Rare:198 | ||||
| chr6:32838030-32838460 | Common:5; Rare:164; Clinvar (benign):5 | ||||
| chr6:32838687-32838851 | Common:5; Rare:30 | ||||
| chr6:32843979-32844141 | Rare:69; Clinvar:2 | ||||
| chr6:32844303-32844491 | Rare:77 | ||||
| chr6:32844569-32844850 | Common:2; Rare:113 | ||||
| chr6:32853642-32853831 | Common:2; Rare:167; Clinvar:4; Clinvar (benign):8 | ||||
| chr6:32853970-32854216 | Common:2; Rare:56 | ||||
| chr6:32968445-32968672 | Common:6; Rare:96 | ||||
| chr6:32968690-32969020 | Common:11; Rare:169 |