| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:102659397-102659527 | Common:1; Rare:33 | ||||
| chr1:102660706-102660836 | Common:1; Rare:31 | ||||
| chr1:102853819-102853901 | Rare:38 | ||||
| chr1:104072966-104073021 | Rare:12 | ||||
| chr1:104073639-104073860 | Common:2; Rare:48 | ||||
| chr1:104172907-104173167 | Common:5; Rare:59 | ||||
| chr1:104407954-104408221 | Common:7; Rare:86 | ||||
| chr1:105618893-105619058 | Common:1; Rare:30 | ||||
| chr1:105630546-105630700 | Common:1; Rare:38 | ||||
| chr1:105796136-105796366 | Common:3; Rare:80 | ||||
| chr1:105956522-105956751 | Common:1; Rare:41 | ||||
| chr1:106073141-106073231 | Common:2; Rare:18 | ||||
| chr1:106447949-106448092 | Common:3; Rare:25 | ||||
| chr1:107045630-107045756 | Rare:30 | ||||
| chr1:108901631-108901875 | Common:4; Rare:62; Clinvar:1; Clinvar (benign):1 |