Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:130342557-130342926 | Common:7; Rare:117 | ||||
chr2:131105233-131105365 | Common:1; Rare:63 | ||||
chr2:131493043-131493113 | Common:1; Rare:20 | ||||
chr2:134918704-134918875 | Rare:71 | ||||
chr2:135531172-135531514 | Common:1; Rare:72 | ||||
chr2:135741723-135741944 | Common:1; Rare:87 | ||||
chr2:135985435-135985721 | Common:4; Rare:122; Clinvar (benign):1 | ||||
chr2:138501661-138502026 | Common:2; Rare:131 | ||||
chr2:144517724-144517796 | Common:1; Rare:9 | ||||
chr2:144520311-144520528 | Common:4; Rare:40; Clinvar (benign):1 | ||||
chr2:148020681-148021096 | Common:2; Rare:97; Clinvar (benign):2 | ||||
chr2:148021571-148021652 | Rare:17 | ||||
chr2:149038639-149038783 | Common:2; Rare:55 | ||||
chr2:149330350-149330624 | Common:1; Rare:118 | ||||
chr2:149587320-149587415 | Common:1; Rare:20 |