Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:82839926-82840056 | Rare:26 | ||||
chr17:82840197-82840221 | Rare:5 | ||||
chr17:82840262-82840486 | Common:1; Rare:45 | ||||
chr18:812216-812409 | Common:1; Rare:71 | ||||
chr18:2571497-2571581 | Rare:24 | ||||
chr18:2655589-2655889 | Common:4; Rare:123 | ||||
chr18:3247351-3247929 | Common:1; Rare:167 | ||||
chr18:3261820-3262236 | Common:6; Rare:131 | ||||
chr18:3449402-3449751 | Common:2; Rare:89 | ||||
chr18:3450063-3450238 | Common:1; Rare:50 | ||||
chr18:9102469-9102772 | Common:2; Rare:127; Clinvar:6; Clinvar (benign):2 | ||||
chr18:9136497-9136908 | Rare:156 | ||||
chr18:9474892-9475100 | Common:2; Rare:50 | ||||
chr18:9475295-9475719 | Common:5; Rare:111 | ||||
chr18:11908279-11908442 | Rare:47 |