| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122384128-122384233 | Rare:44 | ||||
| chr3:122416055-122416225 | Rare:53 | ||||
| chr3:122564236-122564429 | Common:3; Rare:57 | ||||
| chr3:123585489-123585590 | Rare:20 | ||||
| chr3:123700942-123701306 | Rare:76; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:124730340-124730464 | Common:3; Rare:67; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:125375218-125375464 | Rare:71 | ||||
| chr3:125520146-125520307 | Rare:54 | ||||
| chr3:125595252-125595367 | Common:2; Rare:39 | ||||
| chr3:125595498-125595672 | Common:1; Rare:59 | ||||
| chr3:126084004-126084212 | Common:2; Rare:71 | ||||
| chr3:126704104-126704302 | Common:2; Rare:65 | ||||
| chr3:127628970-127629251 | Common:1; Rare:92 | ||||
| chr3:127672808-127673028 | Common:4; Rare:106 | ||||
| chr3:127822455-127822646 | Rare:40 |