| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:99154863-99155054 | Common:2; Rare:80; Clinvar (benign):2 | ||||
| chr2:99180979-99181242 | Common:2; Rare:74 | ||||
| chr2:99337226-99337464 | Rare:83 | ||||
| chr2:100105361-100105590 | Rare:60 | ||||
| chr2:100105622-100105978 | Rare:91 | ||||
| chr2:100417305-100417707 | Rare:115 | ||||
| chr2:100562847-100563050 | Common:3; Rare:65 | ||||
| chr2:101002162-101002577 | Rare:135 | ||||
| chr2:101252848-101252907 | Rare:12 | ||||
| chr2:102736821-102736932 | Common:1; Rare:57 | ||||
| chr2:105037859-105038095 | Common:3; Rare:81 | ||||
| chr2:105337208-105337620 | Common:5; Rare:143 | ||||
| chr2:106887085-106887316 | Rare:66 | ||||
| chr2:106887493-106887547 | Common:1; Rare:7 | ||||
| chr2:108449098-108449268 | Rare:68 |