Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:925586-925762 | Common:1; Rare:54 | ||||
chr1:945362-945656 | Common:1; Rare:125 | ||||
chr1:959225-959349 | Common:1; Rare:82 | ||||
chr1:1000164-1000519 | Common:6; Rare:111 | ||||
chr1:1231895-1232265 | Rare:126; Clinvar (benign):2 | ||||
chr1:1273768-1274021 | Common:1; Rare:102 | ||||
chr1:1307826-1307999 | Rare:34 | ||||
chr1:1308337-1308652 | Common:8; Rare:135 | ||||
chr1:1324598-1324849 | Common:3; Rare:135 | ||||
chr1:1375127-1375608 | Common:7; Rare:139 | ||||
chr1:1399272-1399603 | Common:1; Rare:154 | ||||
chr1:1407126-1407411 | Common:1; Rare:125 | ||||
chr1:1435559-1435766 | Rare:77 | ||||
chr1:1574490-1574736 | Common:1; Rare:85 | ||||
chr1:1574852-1574947 | Rare:42 |