Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:107674058-107674340 | Common:2; Rare:30 | ||||
chrX:107674709-107675024 | Rare:40 | ||||
chrX:107676946-107677165 | Rare:27 | ||||
chrX:107711095-107711333 | Common:1; Rare:19 | ||||
chrX:109732288-109732517 | Rare:28 | ||||
chrX:119606395-119606602 | Common:1; Rare:39 | ||||
chrX:125204309-125204623 | Rare:36 | ||||
chrX:126472545-126472616 | Common:1; Rare:11 | ||||
chrX:129813679-129813921 | Common:1; Rare:33; Clinvar (benign):1 | ||||
chrX:130074068-130074319 | Common:1; Rare:45 | ||||
chrX:134549639-134549811 | Common:1; Rare:39 | ||||
chrX:135032989-135033039 | Rare:7 | ||||
chrX:136030389-136030617 | Common:1; Rare:32 | ||||
chrX:136175354-136175631 | Common:1; Rare:30 | ||||
chrX:136202989-136203271 | Common:2; Rare:35 |