| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219597716-219597884 | Common:1; Rare:60 | ||||
| chr2:221572271-221572528 | Common:6; Rare:92 | ||||
| chr2:222671422-222671658 | Common:1; Rare:71 | ||||
| chr2:223957248-223957475 | Common:4; Rare:87 | ||||
| chr2:226799811-226799994 | Rare:65 | ||||
| chr2:226835918-226836117 | Common:1; Rare:80 | ||||
| chr2:227164477-227164621 | Rare:29; Clinvar:2 | ||||
| chr2:227325184-227325425 | Common:5; Rare:85 | ||||
| chr2:227717949-227718165 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:229921924-229922516 | Common:3; Rare:205 | ||||
| chr2:230219917-230220075 | Rare:24 | ||||
| chr2:230225605-230225748 | Rare:28 | ||||
| chr2:230327093-230327235 | Rare:33 | ||||
| chr2:230416104-230416262 | Rare:49 | ||||
| chr2:231124997-231125043 | Rare:6 |