| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47402971-47403189 | Common:1; Rare:98; Clinvar:31; Clinvar (benign):25 | ||||
| chr2:47782844-47783189 | Common:3; Rare:143; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:47905497-47905877 | Common:3; Rare:185 | ||||
| chr2:48440614-48440824 | Common:6; Rare:91 | ||||
| chr2:53767768-53767879 | Common:2; Rare:45 | ||||
| chr2:53786842-53787090 | Rare:88 | ||||
| chr2:53970762-53971163 | Common:12; Rare:150 | ||||
| chr2:54115512-54115723 | Common:1; Rare:78 | ||||
| chr2:54457056-54457274 | Common:1; Rare:91 | ||||
| chr2:54457659-54457778 | Common:2; Rare:39 | ||||
| chr2:55050302-55050407 | Common:1; Rare:42 | ||||
| chr2:55050428-55050784 | Common:4; Rare:108 | ||||
| chr2:55112598-55112727 | Rare:30 | ||||
| chr2:55232241-55232719 | Common:3; Rare:131 | ||||
| chr2:55269167-55269310 | Common:2; Rare:42 |