| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3575046-3575506 | Common:3; Rare:128; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:3703681-3703881 | Common:2; Rare:48 | ||||
| chr2:3704134-3704287 | Common:6; Rare:42 | ||||
| chr2:5692110-5692502 | Rare:90 | ||||
| chr2:6865452-6865625 | Rare:45 | ||||
| chr2:6865634-6865862 | Common:2; Rare:71 | ||||
| chr2:6865872-6865920 | Rare:16 | ||||
| chr2:6865998-6866039 | Rare:9 | ||||
| chr2:6866053-6866115 | Common:1; Rare:22 | ||||
| chr2:6917269-6917534 | Common:1; Rare:92 | ||||
| chr2:6917617-6917672 | Common:1; Rare:18 | ||||
| chr2:8678722-8678975 | Common:3; Rare:101 | ||||
| chr2:8679188-8679391 | Rare:75 | ||||
| chr2:8681859-8682208 | Common:2; Rare:162 | ||||
| chr2:8682242-8682281 | Common:1; Rare:18 |