Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:9615030-9615104 | Rare:21 | ||||
chr18:9914170-9914325 | Rare:64 | ||||
chr18:10525932-10526099 | Common:2; Rare:75 | ||||
chr18:11908274-11908442 | Rare:50 | ||||
chr18:12307937-12308349 | Common:6; Rare:150 | ||||
chr18:12702658-12703090 | Common:3; Rare:172 | ||||
chr18:12947703-12948061 | Common:3; Rare:83 | ||||
chr18:12991125-12991307 | Rare:66 | ||||
chr18:13726462-13726720 | Common:3; Rare:102 | ||||
chr18:21111709-21111958 | Common:2; Rare:90 | ||||
chr18:22933781-22933889 | Common:1; Rare:43 | ||||
chr18:23453176-23453349 | Rare:61 | ||||
chr18:23503278-23503576 | Common:2; Rare:115 | ||||
chr18:23586372-23586537 | Common:3; Rare:72; Clinvar:5; Clinvar (benign):2 | ||||
chr18:24426620-24426765 | Common:3; Rare:61 |