| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:99154906-99155037 | Common:1; Rare:53; Clinvar (benign):1 | ||||
| chr2:99180985-99181239 | Common:2; Rare:72 | ||||
| chr2:100562714-100563046 | Common:3; Rare:105 | ||||
| chr2:101002142-101002318 | Rare:69 | ||||
| chr2:102736876-102736932 | Common:1; Rare:15 | ||||
| chr2:105337471-105337612 | Common:1; Rare:67 | ||||
| chr2:105398987-105399164 | Rare:60 | ||||
| chr2:106194243-106194568 | Common:6; Rare:138 | ||||
| chr2:108534152-108534477 | Common:7; Rare:131 | ||||
| chr2:108654905-108655046 | Rare:36 | ||||
| chr2:108719373-108719564 | Common:3; Rare:77; Clinvar (benign):1 | ||||
| chr2:108786625-108786804 | Common:6; Rare:94 | ||||
| chr2:111884135-111884249 | Rare:33 | ||||
| chr2:112584388-112584628 | Common:1; Rare:65 | ||||
| chr2:112645718-112645949 | Common:1; Rare:86 |