| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32165636-32165902 | Common:1; Rare:105 | ||||
| chr2:33599212-33599432 | Common:1; Rare:86 | ||||
| chr2:37084312-37084551 | Common:3; Rare:88 | ||||
| chr2:37231551-37231702 | Common:4; Rare:85; Clinvar (benign):3 | ||||
| chr2:38076142-38076283 | Rare:36 | ||||
| chr2:38751348-38751595 | Common:3; Rare:108 | ||||
| chr2:38875886-38876047 | Common:1; Rare:58 | ||||
| chr2:39437085-39437447 | Common:4; Rare:128 | ||||
| chr2:43595978-43596158 | Common:1; Rare:57 | ||||
| chr2:44361767-44362002 | Common:1; Rare:69 | ||||
| chr2:45009647-45009939 | Common:3; Rare:70 | ||||
| chr2:46617025-46617262 | Common:7; Rare:103 | ||||
| chr2:46915733-46915908 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916033-46916089 | Common:1; Rare:15 | ||||
| chr2:47402910-47403197 | Common:1; Rare:129; Clinvar:43; Clinvar (benign):27 |