| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:168915639-168915942 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:168924092-168924420 | Rare:81; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:173167980-173168213 | Common:3; Rare:36 | ||||
| chr4:182894607-182894814 | Common:1; Rare:35 | ||||
| chr4:183765682-183765913 | Common:3; Rare:40 | ||||
| chr4:184815076-184815250 | Common:2; Rare:41 | ||||
| chr4:184988734-184989013 | Common:6; Rare:51 | ||||
| chr5:91931-92201 | Rare:97 | ||||
| chr5:476598-476855 | Common:4; Rare:100; Clinvar:1 | ||||
| chr5:1594455-1594731 | Common:3; Rare:97 | ||||
| chr5:4511958-4512259 | Common:1; Rare:62 | ||||
| chr5:5138462-5138579 | Common:1; Rare:20 | ||||
| chr5:8457537-8457751 | Common:2; Rare:79 | ||||
| chr5:21459263-21459556 | Common:3; Rare:97 | ||||
| chr5:31195191-31195254 | Rare:8 |