Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:131390870-131391091 | Common:1; Rare:63 | ||||
chr5:135368494-135368658 | Rare:17 | ||||
chr5:137837138-137837315 | Rare:29 | ||||
chr5:137870229-137870321 | Common:3; Rare:14 | ||||
chr5:138611553-138611691 | Rare:30 | ||||
chr5:138928995-138929374 | Common:1; Rare:86; Clinvar:1 | ||||
chr5:138933587-138933981 | Common:1; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
chr5:138962191-138962377 | Rare:34 | ||||
chr5:140243054-140243368 | Common:1; Rare:68 | ||||
chr5:140250516-140250681 | Common:1; Rare:17 | ||||
chr5:140651716-140652121 | Common:1; Rare:87 | ||||
chr5:140654517-140654726 | Rare:51 | ||||
chr5:141956182-141956495 | Rare:97 | ||||
chr5:142403602-142403918 | Rare:42 | ||||
chr5:146047408-146047640 | Common:2; Rare:45 |