| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:99141514-99141740 | Common:2; Rare:85 | ||||
| chr2:99154883-99155079 | Common:2; Rare:76; Clinvar (benign):3 | ||||
| chr2:99180985-99181226 | Common:2; Rare:71 | ||||
| chr2:101002140-101002318 | Rare:70 | ||||
| chr2:102736857-102736936 | Common:1; Rare:27 | ||||
| chr2:105337468-105337610 | Common:1; Rare:70 | ||||
| chr2:105398950-105399240 | Common:2; Rare:103 | ||||
| chr2:106194243-106194568 | Common:6; Rare:138 | ||||
| chr2:108449047-108449277 | Rare:95 | ||||
| chr2:108534172-108534504 | Common:7; Rare:132 | ||||
| chr2:108719388-108719558 | Common:2; Rare:70 | ||||
| chr2:110115806-110115949 | Common:2; Rare:33 | ||||
| chr2:111884140-111884237 | Rare:29 | ||||
| chr2:111898305-111898630 | Common:2; Rare:71 | ||||
| chr2:112584374-112584633 | Common:1; Rare:71 |