| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31945835-31946456 | Common:4; Rare:93; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:31949002-31949556 | Common:4; Rare:122; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:31949990-31950440 | Common:1; Rare:127; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:31958885-31959214 | Rare:110; Clinvar:8 | ||||
| chr6:32109275-32109482 | Rare:33 | ||||
| chr6:32127722-32127910 | Rare:49 | ||||
| chr6:32128194-32128517 | Common:3; Rare:77 | ||||
| chr6:32154371-32154492 | Rare:14 | ||||
| chr6:32176054-32176282 | Common:1; Rare:47 | ||||
| chr6:32177042-32177407 | Common:1; Rare:62 | ||||
| chr6:32178204-32178523 | Common:2; Rare:56 | ||||
| chr6:32190161-32190367 | Rare:36 | ||||
| chr6:32192509-32192667 | Rare:32 | ||||
| chr6:32838683-32839125 | Common:7; Rare:68 | ||||
| chr6:32843992-32844156 | Rare:36; Clinvar:1 |