Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7223305-7223354 | Rare:14 | ||||
chr17:7223656-7223937 | Rare:88; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):6 | ||||
chr17:7224038-7224388 | Rare:123; Clinvar:9; Clinvar (benign):9; Clinvar (pathogenic):5 | ||||
chr17:7234260-7234551 | Rare:114 | ||||
chr17:7237735-7237958 | Common:1; Rare:65 | ||||
chr17:7238223-7238371 | Rare:15 | ||||
chr17:7238560-7238657 | Common:2; Rare:7 | ||||
chr17:7242266-7242665 | Common:2; Rare:118 | ||||
chr17:7246026-7246316 | Rare:55 | ||||
chr17:7251530-7252317 | Common:5; Rare:257 | ||||
chr17:7252780-7252921 | Common:1; Rare:52 | ||||
chr17:7262087-7262676 | Rare:123 | ||||
chr17:7306863-7307066 | Common:1; Rare:64 | ||||
chr17:7307226-7307684 | Common:6; Rare:120 | ||||
chr17:7308218-7308455 | Rare:89 |