| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:169798711-169798923 | Rare:64 | ||||
| chr2:169798943-169799090 | Common:1; Rare:36 | ||||
| chr2:169799460-169799492 | Rare:5 | ||||
| chr2:169824812-169825083 | Common:4; Rare:81 | ||||
| chr2:169827336-169827536 | Rare:58 | ||||
| chr2:170179883-170180171 | Common:2; Rare:47 | ||||
| chr2:170180360-170180478 | Common:2; Rare:19 | ||||
| chr2:170928861-170929352 | Common:5; Rare:142 | ||||
| chr2:170929823-170929905 | Rare:32 | ||||
| chr2:171160679-171161353 | Common:7; Rare:224 | ||||
| chr2:171433361-171433484 | Rare:25 | ||||
| chr2:171433754-171434410 | Common:4; Rare:174; Clinvar:3 | ||||
| chr2:171434516-171434702 | Rare:57; Clinvar:1 | ||||
| chr2:171434717-171434849 | Common:1; Rare:34 | ||||
| chr2:171521661-171521859 | Common:1; Rare:27 |