Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:77124493-77124501 | Rare:1 | ||||
chr17:82875452-82875598 | Common:2; Rare:36 | ||||
chr18:3593941-3594127 | Common:3; Rare:30 | ||||
chr18:3603478-3603737 | Common:1; Rare:41 | ||||
chr18:5238030-5238130 | Common:1; Rare:40 | ||||
chr18:11850306-11850356 | Rare:3 | ||||
chr18:12288053-12288288 | Common:3; Rare:43 | ||||
chr18:29156585-29156863 | Common:3; Rare:62 | ||||
chr18:35478481-35478815 | Rare:51 | ||||
chr18:70048078-70048401 | Rare:66 | ||||
chr19:1032387-1032649 | Common:2; Rare:82 | ||||
chr19:3977327-3977553 | Common:3; Rare:81; Clinvar (benign):5 | ||||
chr19:4363849-4364127 | Common:2; Rare:90 | ||||
chr19:14565950-14566083 | Common:1; Rare:54 | ||||
chr19:16734208-16734267 | Rare:12 |