Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:140647594-140647919 | Common:5; Rare:131; Clinvar:4; Clinvar (benign):3 | ||||
chr5:140691300-140691646 | Common:1; Rare:125; Clinvar:11; Clinvar (benign):1 | ||||
chr5:141320742-141320920 | Common:1; Rare:62 | ||||
chr5:141636824-141637011 | Common:1; Rare:72 | ||||
chr5:141923684-141923909 | Common:1; Rare:70 | ||||
chr5:141968956-141969275 | Common:3; Rare:101 | ||||
chr5:142012970-142013133 | Rare:52 | ||||
chr5:142108685-142108989 | Common:3; Rare:99 | ||||
chr5:142324973-142325218 | Rare:84 | ||||
chr5:143404419-143404604 | Common:2; Rare:44 | ||||
chr5:144170564-144170731 | Common:1; Rare:69 | ||||
chr5:147234846-147235100 | Common:2; Rare:69 | ||||
chr5:148383777-148384022 | Rare:73 | ||||
chr5:149063020-149063335 | Rare:72; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr5:149141369-149141579 | Rare:56 |