| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:189053901-189054192 | Common:3; Rare:79; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:189056964-189057282 | Common:2; Rare:55; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:189103350-189103677 | Common:7; Rare:51 | ||||
| chr2:189160482-189160790 | Rare:46 | ||||
| chr2:189177292-189177560 | Rare:52 | ||||
| chr2:189443073-189443226 | Rare:30 | ||||
| chr2:189448289-189448434 | Rare:41 | ||||
| chr2:189457284-189457420 | Rare:34 | ||||
| chr2:189575160-189575454 | Rare:62 | ||||
| chr2:189577723-189577951 | Common:2; Rare:46 | ||||
| chr2:189667223-189667946 | Common:1; Rare:215 | ||||
| chr2:189670197-189670591 | Rare:85 | ||||
| chr2:189727296-189727561 | Common:5; Rare:25 | ||||
| chr2:189751975-189752040 | Rare:13 | ||||
| chr2:189766439-189766709 | Common:2; Rare:63 |