| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171433955-171434246 | Common:2; Rare:73 | ||||
| chr2:171687666-171687802 | Rare:44 | ||||
| chr2:171999833-171999972 | Common:1; Rare:57 | ||||
| chr2:174248468-174248751 | Common:1; Rare:87 | ||||
| chr2:174395644-174395794 | Common:1; Rare:52 | ||||
| chr2:176002232-176002398 | Common:2; Rare:69 | ||||
| chr2:176104356-176104535 | Common:1; Rare:39 | ||||
| chr2:176129586-176129735 | Rare:85 | ||||
| chr2:177212422-177212802 | Common:4; Rare:154 | ||||
| chr2:177264630-177264874 | Common:2; Rare:78 | ||||
| chr2:177392669-177393005 | Common:2; Rare:119; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:181891665-181891981 | Common:4; Rare:127 | ||||
| chr2:183124314-183124460 | Rare:56 | ||||
| chr2:186486110-186486344 | Common:3; Rare:76 | ||||
| chr2:189784276-189784537 | Common:4; Rare:93; Clinvar:8; Clinvar (benign):2 |