| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47345052-47345148 | Rare:26 | ||||
| chr2:47369095-47369607 | Common:4; Rare:214; Clinvar:19; Clinvar (benign):7 | ||||
| chr2:47402910-47403189 | Common:1; Rare:123; Clinvar:38; Clinvar (benign):26 | ||||
| chr2:47782946-47783190 | Common:2; Rare:104; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:47905489-47905847 | Common:3; Rare:176 | ||||
| chr2:48440619-48440962 | Common:8; Rare:150 | ||||
| chr2:48529242-48529376 | Common:1; Rare:38 | ||||
| chr2:51032095-51032293 | Rare:54; Clinvar:2 | ||||
| chr2:53767559-53767974 | Common:5; Rare:154 | ||||
| chr2:53786842-53787298 | Common:1; Rare:178 | ||||
| chr2:53970725-53971189 | Common:12; Rare:176 | ||||
| chr2:54115469-54115692 | Rare:80 | ||||
| chr2:54456070-54456423 | Common:2; Rare:135 | ||||
| chr2:54456588-54456707 | Common:1; Rare:37 | ||||
| chr2:54457093-54457290 | Common:1; Rare:81 |