| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:137219274-137219586 | Common:5; Rare:106; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:138773642-138773836 | Common:3; Rare:90 | ||||
| chr6:139374463-139374491 | Rare:10 | ||||
| chr6:139374519-139374660 | Rare:73 | ||||
| chr6:142147140-142147284 | Rare:51 | ||||
| chr6:143060723-143060928 | Common:7; Rare:73 | ||||
| chr6:143450660-143450936 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:144150292-144150529 | Common:5; Rare:68 | ||||
| chr6:144285223-144285378 | Common:2; Rare:40 | ||||
| chr6:145814664-145814921 | Common:1; Rare:115 | ||||
| chr6:145964305-145964737 | Rare:136 | ||||
| chr6:147204580-147204656 | Rare:23 | ||||
| chr6:148342902-148343178 | Common:1; Rare:100 | ||||
| chr6:149718067-149718158 | Common:2; Rare:32 | ||||
| chr6:149749617-149749800 | Rare:99 |