| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:17753721-17754168 | Common:4; Rare:142; Clinvar (benign):1 | ||||
| chr2:19901652-19902051 | Common:2; Rare:160 | ||||
| chr2:19990079-19990211 | Rare:34 | ||||
| chr2:20223974-20224010 | Common:1; Rare:8 | ||||
| chr2:20225061-20225240 | Common:1; Rare:49 | ||||
| chr2:20350828-20351071 | Common:1; Rare:104 | ||||
| chr2:20446877-20447126 | Common:3; Rare:102 | ||||
| chr2:20447239-20447546 | Common:2; Rare:103 | ||||
| chr2:20447548-20447990 | Common:1; Rare:120 | ||||
| chr2:20651050-20651276 | Rare:73 | ||||
| chr2:23926663-23926782 | Common:2; Rare:42 | ||||
| chr2:23927058-23927378 | Common:4; Rare:106 | ||||
| chr2:23940379-23940514 | Common:3; Rare:49 | ||||
| chr2:24049545-24049724 | Rare:48 | ||||
| chr2:24076242-24076574 | Rare:89 |