Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:216723326-216723642 | Rare:84 | ||||
chr1:217078208-217078425 | Common:1; Rare:31 | ||||
chr1:217089572-217089927 | Common:1; Rare:76 | ||||
chr1:217090492-217090581 | Rare:16 | ||||
chr1:217630954-217631379 | Common:3; Rare:124 | ||||
chr1:218285178-218285352 | Common:2; Rare:84 | ||||
chr1:218345751-218345913 | Rare:41; Clinvar:1 | ||||
chr1:218345944-218346269 | Common:5; Rare:84; Clinvar:9; Clinvar (benign):3 | ||||
chr1:218346273-218346407 | Rare:23; Clinvar (benign):1 | ||||
chr1:218346471-218346783 | Common:1; Rare:81; Clinvar:2; Clinvar (benign):5 | ||||
chr1:218346893-218346963 | Rare:19; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:219173733-219174279 | Common:2; Rare:202 | ||||
chr1:220046398-220046748 | Common:1; Rare:109 | ||||
chr1:220272345-220272552 | Rare:59; Clinvar:5 | ||||
chr1:221742056-221742288 | Rare:60 |