Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:4545496-4545593 | Common:3; Rare:29 | ||||
chr17:4555312-4555503 | Common:3; Rare:88 | ||||
chr17:4704107-4704216 | Rare:62 | ||||
chr17:4806996-4807192 | Common:4; Rare:65 | ||||
chr17:4939892-4940348 | Common:2; Rare:134 | ||||
chr17:4947952-4948227 | Common:1; Rare:94 | ||||
chr17:4948943-4949290 | Common:2; Rare:101 | ||||
chr17:4967155-4967432 | Common:2; Rare:64 | ||||
chr17:4987634-4987718 | Common:1; Rare:35 | ||||
chr17:5007260-5007536 | Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
chr17:5078369-5078547 | Common:4; Rare:52 | ||||
chr17:5191831-5192077 | Common:1; Rare:80 | ||||
chr17:5234825-5234976 | Rare:30 | ||||
chr17:5419540-5420216 | Common:6; Rare:229 | ||||
chr17:5486127-5486627 | Common:6; Rare:173 |