Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:12702627-12703147 | Common:3; Rare:203 | ||||
chr18:13726488-13726720 | Common:3; Rare:88 | ||||
chr18:21704759-21704889 | Rare:47 | ||||
chr18:24397780-24398076 | Common:2; Rare:110 | ||||
chr18:31943084-31943377 | Common:7; Rare:95 | ||||
chr18:35290182-35290384 | Common:2; Rare:72 | ||||
chr18:36129808-36130029 | Common:2; Rare:88 | ||||
chr18:36187320-36187663 | Common:5; Rare:101 | ||||
chr18:36828735-36828895 | Rare:62 | ||||
chr18:36828986-36829127 | Common:1; Rare:53 | ||||
chr18:46098244-46098614 | Common:11; Rare:103; Clinvar (benign):5 | ||||
chr18:46104275-46104362 | Common:1; Rare:17 | ||||
chr18:46917473-46917617 | Rare:60 | ||||
chr18:49813510-49814110 | Common:2; Rare:190 | ||||
chr18:50878996-50879276 | Common:4; Rare:89 |