| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123633613-123633869 | Common:2; Rare:125; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123671030-123671129 | Common:1; Rare:21 | ||||
| chr12:123712216-123712513 | Common:3; Rare:107; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:124914820-124915057 | Common:3; Rare:99 | ||||
| chr12:130871735-130872129 | Common:4; Rare:162 | ||||
| chr12:131710779-131711132 | Common:1; Rare:102 | ||||
| chr12:131929074-131929296 | Common:9; Rare:63; Clinvar:1 | ||||
| chr12:132887553-132887794 | Rare:74 | ||||
| chr12:132956265-132956421 | Common:1; Rare:34 | ||||
| chr12:133080724-133080932 | Rare:67 | ||||
| chr12:133130217-133130652 | Common:7; Rare:146 | ||||
| chr13:19633373-19633751 | Common:1; Rare:142 | ||||
| chr13:19782927-19783088 | Common:2; Rare:57 | ||||
| chr13:21140223-21140670 | Rare:172 | ||||
| chr13:21176389-21176706 | Common:4; Rare:134 |