Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:138501675-138502017 | Common:2; Rare:118 | ||||
chr2:144517317-144517742 | Common:5; Rare:131; Clinvar:3; Clinvar (benign):5 | ||||
chr2:144518134-144518143 | |||||
chr2:144520111-144520528 | Common:4; Rare:75; Clinvar (benign):1 | ||||
chr2:148020681-148021098 | Common:2; Rare:97; Clinvar (benign):2 | ||||
chr2:148021544-148021658 | Rare:22 | ||||
chr2:149587306-149587364 | Rare:12 | ||||
chr2:149587685-149587826 | Common:1; Rare:40; Clinvar:1 | ||||
chr2:151289619-151289756 | Common:1; Rare:35 | ||||
chr2:152717829-152717964 | Rare:56 | ||||
chr2:152718002-152718315 | Common:1; Rare:104 | ||||
chr2:152718500-152718639 | Rare:51 | ||||
chr2:158968475-158968693 | Rare:69 | ||||
chr2:159615225-159615343 | Common:2; Rare:28 | ||||
chr2:159616418-159616741 | Common:2; Rare:61 |