Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20508052-20508200 | Common:2; Rare:54 | ||||
chr1:20661350-20661705 | Common:3; Rare:127; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786573-20786870 | Rare:110 | ||||
chr1:21176852-21177087 | Rare:64 | ||||
chr1:21345448-21345655 | Common:3; Rare:76 | ||||
chr1:21783086-21783279 | Common:2; Rare:69 | ||||
chr1:21874614-21874949 | Common:2; Rare:98; Clinvar (benign):1 | ||||
chr1:22451760-22451879 | Rare:45 | ||||
chr1:22636551-22636707 | Common:1; Rare:36 | ||||
chr1:23344219-23344532 | Common:2; Rare:106 | ||||
chr1:23368188-23368523 | Common:1; Rare:96 | ||||
chr1:23368892-23369251 | Common:3; Rare:100 | ||||
chr1:23424693-23424843 | Rare:39 | ||||
chr1:23559413-23559671 | Common:2; Rare:113 | ||||
chr1:23778247-23778639 | Common:10; Rare:156 |