| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:47781682-47781723 | Rare:9 | ||||
| chr3:47781784-47782054 | Rare:107 | ||||
| chr3:47803080-47803203 | Rare:30 | ||||
| chr3:48088804-48089065 | Rare:88 | ||||
| chr3:48301323-48301490 | Common:1; Rare:50 | ||||
| chr3:48301499-48301599 | Common:2; Rare:36 | ||||
| chr3:48439997-48440324 | Common:3; Rare:125 | ||||
| chr3:48504126-48504297 | Common:2; Rare:55 | ||||
| chr3:48570637-48570941 | Rare:92; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr3:48600460-48600730 | Common:1; Rare:86 | ||||
| chr3:48847658-48847965 | Common:1; Rare:83 | ||||
| chr3:48918701-48918993 | Common:2; Rare:148 | ||||
| chr3:48926800-48926919 | Common:2; Rare:21 | ||||
| chr3:48989734-48989892 | Rare:41 | ||||
| chr3:48990969-48991072 | Rare:14 |