Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:131170704-131170984 | Common:1; Rare:55 | ||||
chr5:132866505-132866698 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
chr5:133051856-133052091 | Rare:88 | ||||
chr5:134004662-134004838 | Common:1; Rare:69 | ||||
chr5:134738353-134738605 | Rare:98 | ||||
chr5:138543134-138543490 | Common:2; Rare:112 | ||||
chr5:140303059-140303164 | Common:1; Rare:35 | ||||
chr5:140647594-140647883 | Common:5; Rare:116; Clinvar:4; Clinvar (benign):3 | ||||
chr5:140691317-140691463 | Common:1; Rare:49; Clinvar:5 | ||||
chr5:149551369-149551622 | Rare:59 | ||||
chr5:151080958-151081197 | Common:1; Rare:79 | ||||
chr5:154038887-154039010 | Rare:42 | ||||
chr5:159263201-159263321 | Common:1; Rare:39 | ||||
chr5:173328411-173328602 | Rare:36 | ||||
chr5:176388569-176388792 | Common:4; Rare:83 |