Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:59173804-59174260 | Common:1; Rare:119; Clinvar (pathogenic):1 | ||||
chr15:60347949-60348264 | Common:1; Rare:49 | ||||
chr15:60394009-60394367 | Common:1; Rare:57 | ||||
chr15:60518903-60519084 | Common:1; Rare:33 | ||||
chr15:60525575-60525866 | Rare:67 | ||||
chr15:60546001-60546195 | Rare:37 | ||||
chr15:60578640-60578834 | Rare:39 | ||||
chr15:63348379-63348409 | Rare:5 | ||||
chr15:63364982-63365018 | Rare:5 | ||||
chr15:63570279-63570380 | Rare:21 | ||||
chr15:63590465-63590746 | Common:1; Rare:76 | ||||
chr15:64955011-64955269 | Common:5; Rare:55 | ||||
chr15:71341737-71341862 | Rare:32 | ||||
chr15:71972056-71972223 | Common:2; Rare:31 | ||||
chr15:72230239-72230548 | Common:2; Rare:93 |