| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190319310-190319388 | Common:1; Rare:20 | ||||
| chr2:190319676-190320113 | Common:5; Rare:139; Clinvar (benign):6 | ||||
| chr2:190344078-190344361 | Common:3; Rare:70 | ||||
| chr2:190359950-190360157 | Common:1; Rare:40 | ||||
| chr2:190407716-190407974 | Rare:50 | ||||
| chr2:190407981-190408146 | Common:1; Rare:53 | ||||
| chr2:190408152-190408481 | Common:3; Rare:87 | ||||
| chr2:190408614-190408901 | Common:4; Rare:64 | ||||
| chr2:190468992-190469270 | Common:2; Rare:45 | ||||
| chr2:190533910-190534086 | Common:3; Rare:35 | ||||
| chr2:190534212-190534946 | Common:11; Rare:218 | ||||
| chr2:190534969-190535144 | Common:2; Rare:36 | ||||
| chr2:190648663-190649128 | Common:3; Rare:157 | ||||
| chr2:190649293-190649629 | Common:1; Rare:88 | ||||
| chr2:190880283-190880418 | Common:1; Rare:29 |