| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48918702-48918912 | Common:2; Rare:105 | ||||
| chr3:49007181-49007432 | Common:2; Rare:98 | ||||
| chr3:49021503-49021650 | Rare:40 | ||||
| chr3:49029382-49029541 | Common:2; Rare:106 | ||||
| chr3:49104738-49104910 | Rare:69; Clinvar (benign):3 | ||||
| chr3:49132979-49133161 | Rare:38; Clinvar:1 | ||||
| chr3:49358285-49358458 | Common:2; Rare:93 | ||||
| chr3:49411822-49412379 | Common:2; Rare:190 | ||||
| chr3:49674225-49674395 | Common:1; Rare:64 | ||||
| chr3:49689460-49689613 | Rare:47 | ||||
| chr3:49723922-49724241 | Common:9; Rare:117 | ||||
| chr3:49786486-49786769 | Rare:90 | ||||
| chr3:50088805-50088980 | Rare:47 | ||||
| chr3:50350714-50350897 | Common:1; Rare:27 | ||||
| chr3:50569400-50569521 | Rare:26 |