| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47402915-47403189 | Common:1; Rare:123; Clinvar:38; Clinvar (benign):26 | ||||
| chr2:47905507-47905636 | Common:3; Rare:74 | ||||
| chr2:48440619-48440851 | Common:8; Rare:110 | ||||
| chr2:51032030-51032297 | Rare:65; Clinvar:3 | ||||
| chr2:51032420-51032601 | Common:7; Rare:44; Clinvar:4 | ||||
| chr2:53767559-53767881 | Common:5; Rare:114 | ||||
| chr2:53786842-53787164 | Rare:119 | ||||
| chr2:53970788-53971141 | Common:11; Rare:121 | ||||
| chr2:54115525-54115696 | Rare:62 | ||||
| chr2:54115895-54115977 | Common:2; Rare:33 | ||||
| chr2:55050296-55050391 | Rare:39 | ||||
| chr2:55050441-55050867 | Common:7; Rare:133 | ||||
| chr2:55232242-55232726 | Common:3; Rare:136 | ||||
| chr2:55269188-55269301 | Common:2; Rare:33 | ||||
| chr2:55419851-55420186 | Common:5; Rare:134 |