| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49029378-49029472 | Common:1; Rare:64 | ||||
| chr3:49104738-49104919 | Rare:73; Clinvar (benign):3 | ||||
| chr3:49120754-49121018 | Rare:77 | ||||
| chr3:49132991-49133161 | Rare:35; Clinvar:1 | ||||
| chr3:49166289-49166442 | Common:1; Rare:40 | ||||
| chr3:49340013-49340124 | Common:2; Rare:53 | ||||
| chr3:49358274-49358499 | Common:2; Rare:122 | ||||
| chr3:49429250-49429429 | Rare:44 | ||||
| chr3:49674225-49674395 | Common:1; Rare:64 | ||||
| chr3:49689460-49689631 | Rare:50 | ||||
| chr3:49723949-49724092 | Common:2; Rare:47 | ||||
| chr3:49869827-49870029 | Common:1; Rare:50 | ||||
| chr3:49929850-49929903 | Rare:19 | ||||
| chr3:50267404-50267658 | Common:2; Rare:84 | ||||
| chr3:50299355-50299656 | Common:1; Rare:75 |