| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119498745-119498916 | Rare:61 | ||||
| chr3:119660872-119661077 | Rare:34 | ||||
| chr3:119677318-119677517 | Common:1; Rare:71 | ||||
| chr3:120093472-120093893 | Rare:116 | ||||
| chr3:120094414-120094749 | Common:4; Rare:107 | ||||
| chr3:120349296-120349491 | Common:2; Rare:72 | ||||
| chr3:120450791-120451097 | Common:2; Rare:103 | ||||
| chr3:120451172-120451489 | Common:1; Rare:78 | ||||
| chr3:120742503-120742782 | Common:2; Rare:78 | ||||
| chr3:121749467-121749482 | |||||
| chr3:121749488-121749515 | Rare:5 | ||||
| chr3:121749633-121749812 | Rare:38 | ||||
| chr3:121834966-121835237 | Common:3; Rare:85; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383192-122383338 | Common:1; Rare:44 | ||||
| chr3:122384064-122384268 | Rare:75 |