Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:235073590-235073813 | Common:1; Rare:45 | ||||
chr1:235255661-235255935 | Rare:52 | ||||
chr1:236547823-236548078 | Common:4; Rare:73 | ||||
chr1:243101689-243101913 | Common:11; Rare:138 | ||||
chr1:243730153-243730259 | Rare:19 | ||||
chr1:244325134-244325179 | Rare:11 | ||||
chr1:244451144-244451257 | Common:2; Rare:32 | ||||
chr1:244863679-244863954 | Rare:94; Clinvar:5; Clinvar (benign):5 | ||||
chr1:244970945-244971078 | Rare:34 | ||||
chr1:246569797-246569909 | Rare:20 | ||||
chr1:247201688-247201871 | Common:2; Rare:28 | ||||
chr1:248863317-248863355 | Rare:12 | ||||
chr10:307007-307166 | Rare:33 | ||||
chr10:485144-485328 | Rare:60 | ||||
chr10:621771-621926 | Rare:34 |