| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219278147-219278394 | Common:2; Rare:41 | ||||
| chr2:219278971-219279456 | Common:2; Rare:133 | ||||
| chr2:219279673-219279924 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:219279955-219280098 | Rare:27 | ||||
| chr2:219387505-219387847 | Common:2; Rare:117 | ||||
| chr2:219387866-219388128 | Common:2; Rare:42 | ||||
| chr2:219497922-219498115 | Common:1; Rare:52 | ||||
| chr2:219498471-219499014 | Common:3; Rare:119 | ||||
| chr2:219543037-219543246 | Common:2; Rare:52 | ||||
| chr2:219543304-219543488 | Rare:50 | ||||
| chr2:219543507-219543684 | Rare:52 | ||||
| chr2:219543701-219543815 | Rare:33 | ||||
| chr2:219543827-219544090 | Common:3; Rare:80 | ||||
| chr2:219552599-219552797 | Rare:74; Clinvar (benign):1 | ||||
| chr2:219597634-219597926 | Common:2; Rare:112 |