| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:113073332-113073497 | Rare:67 | ||||
| chr1:113073565-113073641 | Rare:32 | ||||
| chr1:113390152-113390567 | Common:2; Rare:108 | ||||
| chr1:113759398-113759666 | Common:4; Rare:82 | ||||
| chr1:113759752-113759828 | Rare:9 | ||||
| chr1:113759877-113759961 | Rare:17 | ||||
| chr1:113759970-113760007 | Rare:4 | ||||
| chr1:113811984-113812052 | Common:1; Rare:21 | ||||
| chr1:113812199-113812720 | Common:3; Rare:195 | ||||
| chr1:113904521-113904581 | Rare:19 | ||||
| chr1:113904734-113905394 | Common:7; Rare:196; Clinvar (benign):2 | ||||
| chr1:113905663-113905709 | Rare:13 | ||||
| chr1:113929052-113929150 | Rare:18 | ||||
| chr1:113929230-113929756 | Common:3; Rare:162 | ||||
| chr1:113929905-113930281 | Common:1; Rare:113 |