Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:197499826-197500135 | Rare:110; Clinvar:1; Clinvar (benign):1 | ||||
chr2:197500216-197500427 | Common:1; Rare:88 | ||||
chr2:197515873-197516107 | Common:1; Rare:90 | ||||
chr2:200510040-200510262 | Common:1; Rare:68 | ||||
chr2:200864606-200864807 | Common:1; Rare:79 | ||||
chr2:200889050-200889424 | Common:2; Rare:121 | ||||
chr2:201071608-201072043 | Rare:93 | ||||
chr2:201451548-201451867 | Common:3; Rare:82 | ||||
chr2:201642660-201642770 | Rare:58 | ||||
chr2:201643449-201643561 | Rare:29; Clinvar:3 | ||||
chr2:202912151-202912291 | Common:1; Rare:51 | ||||
chr2:203014672-203014931 | Common:1; Rare:78 | ||||
chr2:203239240-203239308 | Rare:25 | ||||
chr2:205682356-205682510 | Rare:27 | ||||
chr2:206086281-206086445 | Rare:32 |