Variant report

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ESR1	chr10:25940018-25940694	T-47D	breast:	n/a	n/a

Variant related genes	Relation type
GPN3P1	TF binding region

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373281395	chr10:25940056-25940057	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs200763950	chr10:25940059-25940060	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs143587474	chr10:25940064-25940065	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs376680702	chr10:25940066-25940067	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs138194225	chr10:25940068-25940069	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs112345182	chr10:25940072-25940073	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs370129464	chr10:25940073-25940074	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs564307145	chr10:25940076-25940077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs529299794	chr10:25940078-25940079	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs112029604	chr10:25940079-25940080	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs551450587	chr10:25940080-25940081	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs199741122	chr10:25940082-25940083	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs377312266	chr10:25940083-25940084	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs57139341	chr10:25940085-25940086	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:39)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21525872	CNVD

Chromatin state (count:0 , 50 per page) page:

No data

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