| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219498691-219498925 | Common:2; Rare:49 | ||||
| chr2:219597737-219597884 | Common:1; Rare:50 | ||||
| chr2:226835933-226836108 | Common:1; Rare:69 | ||||
| chr2:227325191-227325341 | Common:4; Rare:52 | ||||
| chr2:227717958-227718165 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:229921904-229922515 | Common:4; Rare:211 | ||||
| chr2:229923171-229923476 | Common:1; Rare:68 | ||||
| chr2:230326918-230327253 | Common:1; Rare:76 | ||||
| chr2:230416128-230416262 | Rare:43 | ||||
| chr2:230462349-230462518 | Common:1; Rare:50 | ||||
| chr2:231125041-231125086 | Rare:7 | ||||
| chr2:231460150-231460560 | Common:1; Rare:145 | ||||
| chr2:231464337-231464727 | Common:3; Rare:134 | ||||
| chr2:231710268-231710551 | Common:2; Rare:141 | ||||
| chr2:231781247-231781439 | Rare:54 |