| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171894210-171894336 | Rare:58; Clinvar:1 | ||||
| chr2:171922288-171922515 | Rare:85 | ||||
| chr2:171999827-171999985 | Common:1; Rare:65 | ||||
| chr2:172427440-172427967 | Common:7; Rare:160; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:172468901-172469176 | Common:3; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:172490768-172490975 | Rare:33 | ||||
| chr2:173354602-173354970 | Common:1; Rare:113 | ||||
| chr2:173963949-173964361 | Rare:167 | ||||
| chr2:173965241-173965529 | Common:1; Rare:102 | ||||
| chr2:173965828-173965987 | Rare:55 | ||||
| chr2:174248456-174248731 | Common:1; Rare:83 | ||||
| chr2:174395555-174395887 | Common:2; Rare:101 | ||||
| chr2:174486948-174487394 | Common:2; Rare:107 | ||||
| chr2:174597732-174597985 | Rare:29 | ||||
| chr2:174634539-174634724 | Rare:40 |