| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129226494-129226720 | Common:2; Rare:41 | ||||
| chr3:129279560-129279910 | Rare:147 | ||||
| chr3:129314857-129315271 | Common:8; Rare:269 | ||||
| chr3:129399337-129399997 | Common:15; Rare:401 | ||||
| chr3:129485630-129486266 | Rare:293 | ||||
| chr3:129486350-129486815 | Rare:149 | ||||
| chr3:129499090-129499580 | Common:4; Rare:87 | ||||
| chr3:129505928-129506890 | Common:4; Rare:487; Clinvar:10; Clinvar (benign):1 | ||||
| chr3:129507540-129507725 | Rare:132; Clinvar:1 | ||||
| chr3:129605285-129605475 | Common:1; Rare:63 | ||||
| chr3:129605531-129605754 | Rare:74 | ||||
| chr3:129605908-129606315 | Rare:201 | ||||
| chr3:129623530-129623850 | Common:5; Rare:117 | ||||
| chr3:129625940-129626220 | Rare:78 | ||||
| chr3:129626713-129626974 | Common:11; Rare:166 |