Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:109877310-109877590 | Rare:106 | ||||
chr1:110209940-110210490 | Common:3; Rare:265 | ||||
chr1:115062590-115062960 | Rare:133 | ||||
chr1:117366603-117366946 | Common:1; Rare:102 | ||||
chr1:119150251-119151001 | Common:7; Rare:248 | ||||
chr1:119712652-119712879 | Common:1; Rare:84 | ||||
chr1:119720901-119721337 | Common:7; Rare:210; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:120340962-120341067 | Common:1; Rare:36 | ||||
chr1:121518602-121519200 | Common:4; Rare:203 | ||||
chr1:121519144-121519544 | Common:2; Rare:166 | ||||
chr1:121519548-121519698 | Rare:53 | ||||
chr1:145215897-145216148 | Rare:67 | ||||
chr1:145425498-145425702 | Rare:171 | ||||
chr1:145979410-145979770 | Rare:110 | ||||
chr1:146037760-146038270 | Common:6; Rare:210 |