| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171434710-171434751 | Rare:14 | ||||
| chr2:171522291-171522525 | Common:3; Rare:54 | ||||
| chr2:171687702-171687816 | Rare:41 | ||||
| chr2:171894201-171894342 | Rare:65; Clinvar:2 | ||||
| chr2:171922283-171922506 | Rare:83 | ||||
| chr2:171999823-172000051 | Common:1; Rare:87 | ||||
| chr2:172084663-172084809 | Rare:32 | ||||
| chr2:172102747-172103053 | Common:3; Rare:76 | ||||
| chr2:172427489-172427732 | Common:4; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:172859919-172860176 | Rare:43 | ||||
| chr2:173354557-173354973 | Common:1; Rare:128 | ||||
| chr2:173965351-173965540 | Common:2; Rare:80 | ||||
| chr2:173965828-173965972 | Rare:53 | ||||
| chr2:174248456-174248751 | Common:1; Rare:91 | ||||
| chr2:174395629-174395840 | Common:1; Rare:71 |