| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47028928-47029424 | Common:3; Rare:304; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:47043543-47044102 | Common:7; Rare:354 | ||||
| chr2:47069569-47069900 | Common:5; Rare:143 | ||||
| chr2:47076870-47077280 | Common:1; Rare:92 | ||||
| chr2:47159680-47159980 | Rare:79 | ||||
| chr2:47174926-47175411 | Common:9; Rare:175 | ||||
| chr2:47175441-47175761 | Common:1; Rare:103 | ||||
| chr2:47175719-47175824 | Common:2; Rare:38 | ||||
| chr2:47191872-47192107 | Common:4; Rare:92 | ||||
| chr2:47193090-47193667 | Common:11; Rare:221 | ||||
| chr2:47215909-47216309 | Common:16; Rare:273 | ||||
| chr2:47226179-47227048 | Common:5; Rare:320 | ||||
| chr2:47250610-47251030 | Common:9; Rare:148 | ||||
| chr2:47272130-47272700 | Common:5; Rare:265 | ||||
| chr2:47319732-47320132 | Common:8; Rare:139 |