Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:9102475-9102758 | Common:2; Rare:113; Clinvar:5; Clinvar (benign):2 | ||||
chr18:9136498-9136872 | Rare:142 | ||||
chr18:9334488-9334905 | Common:1; Rare:101 | ||||
chr18:10525814-10526108 | Common:2; Rare:111 | ||||
chr18:11851322-11851427 | Rare:31 | ||||
chr18:11908276-11908466 | Common:2; Rare:58 | ||||
chr18:12307920-12308284 | Common:7; Rare:135 | ||||
chr18:12702678-12703084 | Common:3; Rare:166 | ||||
chr18:12884165-12884418 | Common:4; Rare:123 | ||||
chr18:12947688-12948098 | Common:3; Rare:116 | ||||
chr18:12991137-12991378 | Common:1; Rare:87 | ||||
chr18:13726515-13726726 | Common:3; Rare:79 | ||||
chr18:21612202-21612435 | Common:1; Rare:70 | ||||
chr18:22933821-22933902 | Common:1; Rare:28 | ||||
chr18:23453172-23453345 | Rare:59 |