| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:50666419-50666720 | Common:3; Rare:81 | ||||
| chr5:50666889-50666972 | Common:1; Rare:26 | ||||
| chr5:50667342-50667570 | Common:1; Rare:71 | ||||
| chr5:51383239-51383460 | Common:2; Rare:89 | ||||
| chr5:52787803-52787971 | Common:1; Rare:35 | ||||
| chr5:52788024-52788339 | Common:1; Rare:73 | ||||
| chr5:52989171-52989370 | Common:4; Rare:57; Clinvar (benign):1 | ||||
| chr5:53109710-53109890 | Common:1; Rare:91; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr5:54310434-54310714 | Common:1; Rare:84 | ||||
| chr5:55024101-55024257 | Common:2; Rare:22 | ||||
| chr5:55307604-55308073 | Common:5; Rare:172 | ||||
| chr5:55534588-55534869 | Common:3; Rare:84 | ||||
| chr5:55534949-55535181 | Common:1; Rare:80 | ||||
| chr5:55994797-55995215 | Rare:153 | ||||
| chr5:56909490-56909652 | Common:2; Rare:47 |