Variant report

Variant	nsv898859
Chromosome Location	chr12:20950737-21082276
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:20961418-20961995	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:20983563-20983814	HepG2	liver:	n/a	n/a
3	BATF	chr12:21021928-21022137	GM12878	blood:	n/a	chr12:21022019-21022030
4	BCL3	chr12:20983287-20983862	A549	lung:	n/a	n/a
5	BHLHE40	chr12:21017099-21017177	GM12878	blood:	n/a	n/a
6	BRCA1	chr12:20975364-20975513	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr12:21071557-21071721	A549	lung:	n/a	n/a
8	CEBPB	chr12:20961578-20961819	HepG2	liver:	n/a	chr12:20961744-20961757
9	CEBPB	chr12:21037942-21038507	A549	lung:	n/a	n/a
10	CEBPB	chr12:21036282-21036646	Hela-S3	cervix:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
11	CEBPB	chr12:20961462-20961896	HepG2	liver:	n/a	chr12:20961744-20961757
12	CEBPB	chr12:20982280-20982503	HepG2	liver:	n/a	chr12:20982413-20982424
13	CEBPB	chr12:21036286-21036659	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
14	CEBPB	chr12:20982312-20982493	IMR90	lung:	n/a	chr12:20982413-20982424
15	CEBPB	chr12:20975351-20976142	A549	lung:	n/a	n/a
16	CEBPB	chr12:21038060-21038439	A549	lung:	n/a	n/a
17	CEBPB	chr12:20983497-20983867	A549	lung:	n/a	chr12:20983711-20983722
18	CEBPB	chr12:21015510-21015751	A549	lung:	n/a	n/a
19	CEBPB	chr12:21036268-21036667	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
20	CEBPB	chr12:20983564-20983877	HepG2	liver:	n/a	chr12:20983711-20983722
21	CEBPB	chr12:21065012-21065124	HepG2	liver:	n/a	chr12:21065034-21065045
22	CEBPB	chr12:21036323-21036549	HepG2	liver:	n/a	chr12:21036463-21036474
23	CEBPB	chr12:21036155-21036832	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
24	CEBPB	chr12:21056070-21056238	HepG2	liver:	n/a	n/a
25	CEBPB	chr12:20983601-20983801	Hela-S3	cervix:	n/a	chr12:20983711-20983722
26	CEBPB	chr12:20961440-20961862	HepG2	liver:	n/a	chr12:20961744-20961757
27	CEBPB	chr12:20983561-20984147	A549	lung:	n/a	chr12:20983711-20983722
28	CEBPB	chr12:20991943-20992076	A549	lung:	n/a	chr12:20992038-20992049
29	CEBPB	chr12:20975368-20976107	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr12:20983420-20984015	A549	lung:	n/a	chr12:20983711-20983722
31	CEBPB	chr12:20991877-20992081	HepG2	liver:	n/a	chr12:20992038-20992049
32	CEBPB	chr12:21038089-21038427	A549	lung:	n/a	n/a
33	CEBPB	chr12:20982284-20982555	A549	lung:	n/a	chr12:20982413-20982424
34	CHD2	chr12:20975360-20975559	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr12:20951600-20951750	MCF-7	breast:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
36	CTCF	chr12:20951636-20951776	GM12878	blood:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
37	CTCF	chr12:20951488-20951864	H1-hESC	embryonic stem cell:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
38	CTCF	chr12:21022151-21022264	GM19240	blood:	n/a	n/a
39	CTCF	chr12:21022146-21022257	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr12:20951640-20951790	HRE	kidney:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
41	CTCF	chr12:20951680-20951830	NHDF-neo	bronchial:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
42	CTCF	chr12:21022130-21022264	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr12:20951580-20951781	T-47D	breast:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
44	CTCF	chr12:20951660-20951810	AG09319	gingival:	n/a	chr12:20951705-20951723 chr12:20951700-20951721
45	CTCF	chr12:21022158-21022249	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr12:20951500-20951650	BE2_C	brain:	n/a	n/a
47	CTCF	chr12:21016151-21016207	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr12:21022131-21022252	MCF-7	breast:	n/a	n/a
49	CTCF	chr12:20951560-20951710	HCT-116	colon:	n/a	n/a
50	CTCF	chr12:21016018-21016303	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:20960446-20960496	AG10803	skin:	n/a
2	chr12:20960446-20960496	AG10803	skin:	n/a
3	chr12:20962423-20962473	MCF10A-Er-Src	breast:	n/a
4	chr12:20966439-20966489	NB4	blood:	n/a
5	chr12:20983111-20983161	CMK	blood:	n/a
6	chr12:20966439-20966489	HUVEC	blood vessel:	n/a
7	chr12:20966439-20966489	LNCaP	prostate:	n/a
8	chr12:21014317-21014367	BE2_C	brain:	n/a
9	chr12:21014317-21014367	HepG2	liver:	n/a
10	chr12:20960446-20960496	Hepatocyte	liver:	n/a
11	chr12:21014317-21014367	GM19239	blood:	n/a
12	chr12:20966439-20966489	HCT-116	colon:	n/a
13	chr12:21015340-21015390	PFSK-1	brain:	n/a
14	chr12:21015340-21015390	Caco-2	colon:	n/a
15	chr12:20966524-20966574	Hela-S3	cervix:	n/a
16	chr12:20966524-20966574	Caco-2	colon:	n/a
17	chr12:20960446-20960496	GM06990	blood:	n/a
18	chr12:21015340-21015390	RPTEC	kidney:	n/a
19	chr12:20960446-20960496	HIPEpiC	eye:	n/a
20	chr12:20960446-20960496	HAEpiC	amniotic membrane:	n/a
21	chr12:21015340-21015390	MCF-7	breast:	n/a
22	chr12:21014317-21014367	NH-A	brain:	n/a
23	chr12:20960446-20960496	H1-hESC	embryonic stem cell:	embryo
24	chr12:20983111-20983161	HCT-116	colon:	n/a
25	chr12:20960446-20960496	NH-A	brain:	n/a
26	chr12:20960409-20960459	HPAEpiC	pulmonary alveolar:	n/a
27	chr12:20960446-20960496	GM19239	blood:	n/a
28	chr12:21014317-21014367	SK-N-MC	brain:	n/a
29	chr12:20960409-20960459	Hepatocyte	liver:	n/a
30	chr12:20983111-20983161	Caco-2	colon:	n/a
31	chr12:20962423-20962473	HRCEpiC	kidney:	n/a
32	chr12:20983111-20983161	HIPEpiC	eye:	n/a
33	chr12:20983111-20983161	HCM	heart:	n/a
34	chr12:20962423-20962473	AG04450	lung:	fetal
35	chr12:20966439-20966489	BE2_C	brain:	n/a
36	chr12:20966524-20966574	IMR90	lung:	fetal
37	chr12:20960446-20960496	SK-N-MC	brain:	n/a
38	chr12:20966439-20966489	HepG2	liver:	n/a
39	chr12:20962423-20962473	H1-hESC	embryonic stem cell:	embryo
40	chr12:20966524-20966574	SK-N-SH	brain:	n/a
41	chr12:21015340-21015390	AG04450	lung:	fetal
42	chr12:21015340-21015390	SK-N-SH	brain:	n/a
43	chr12:20983111-20983161	HEK293	kidney:	embryo
44	chr12:20983111-20983161	AoSMC	blood vessel:	n/a
45	chr12:21015340-21015390	Jurkat	blood:	n/a
46	chr12:21015340-21015390	GM12878	blood:	n/a
47	chr12:21014317-21014367	HL-60	blood:	n/a
48	chr12:20966524-20966574	AG09319	gingival:	n/a
49	chr12:21015340-21015390	GM06990	blood:	n/a
50	chr12:20966524-20966574	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:20639028..20639571-chr12:20951385..20952022,2	MCF-7	breast:
2	chr12:20798864..20799798-chr12:20951213..20952118,4	MCF-7	breast:
3	chr12:20798899..20799416-chr12:20951641..20952181,2	MCF-7	breast:

Variant related genes	Relation type
SLCO1B3	TF binding region
ENSG00000256157	TF binding region
ENSG00000257046	TF binding region
SLCO1B7	TF binding region
SLCO1B3	CpG island
ENSG00000256157	CpG island
ENSG00000257046	CpG island
SLCO1B7	CpG island

Extended variants
information (count: 6067 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:6067 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11613314	chr12:20950737-20950738	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552004526	chr12:20950759-20950760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs199622474	chr12:20950760-20950761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs55676640	chr12:20950766-20950767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374720176	chr12:20950768-20950769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs61921587	chr12:20950769-20950770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537687028	chr12:20950809-20950810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143663310	chr12:20950811-20950812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146818462	chr12:20950815-20950816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs190202691	chr12:20950816-20950817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527947698	chr12:20950821-20950822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553747567	chr12:20950858-20950859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11045506	chr12:20950865-20950866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576881374	chr12:20950897-20950898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371436371	chr12:20950948-20950949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546523661	chr12:20950966-20950967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548057484	chr12:20951047-20951048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556857024	chr12:20951048-20951049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs117875604	chr12:20951071-20951072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542457398	chr12:20951166-20951167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562126439	chr12:20951198-20951199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79645867	chr12:20951254-20951255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7309696	chr12:20951307-20951308	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs142919560	chr12:20951314-20951315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182621781	chr12:20951332-20951333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549753053	chr12:20951339-20951340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113091088	chr12:20951366-20951367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533562785	chr12:20951457-20951458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186941087	chr12:20951531-20951532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78915301	chr12:20951536-20951537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568130226	chr12:20951539-20951540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4141474	chr12:20951540-20951541	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs150280357	chr12:20951543-20951544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570473224	chr12:20951564-20951565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375090477	chr12:20951566-20951567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7138918	chr12:20951579-20951580	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs557188369	chr12:20951596-20951597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575303873	chr12:20951603-20951604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147762487	chr12:20951640-20951641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35691363	chr12:20951651-20951652	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs58922711	chr12:20951674-20951675	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs555948052	chr12:20951736-20951737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572499387	chr12:20951739-20951740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141149984	chr12:20951789-20951790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11614888	chr12:20951845-20951846	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs577710763	chr12:20951858-20951859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4141475	chr12:20951861-20951862	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs189866023	chr12:20951902-20951903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146946360	chr12:20951932-20951933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113167124	chr12:20951978-20951979	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21364760	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:170 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:20942600-20961200	Weak transcription	A549	lung
2	chr12:20951200-20951600	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr12:20951200-20951600	Enhancers	Liver	Liver
4	chr12:20951200-20952000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr12:20951200-20953000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr12:20951400-20951600	Enhancers	Adipose Nuclei	Adipose
7	chr12:20951600-20952800	Weak transcription	Adipose Nuclei	Adipose
8	chr12:20951600-20953200	Weak transcription	Liver	Liver
9	chr12:20951800-20952200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr12:20952000-20953000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr12:20952800-20953400	Enhancers	Adipose Nuclei	Adipose
12	chr12:20953000-20953200	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr12:20953000-20953600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr12:20953000-20954600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr12:20953200-20953600	Enhancers	Liver	Liver
16	chr12:20953200-20958000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr12:20953600-20954600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr12:20954600-20957800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr12:20954600-20957800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr12:20957000-20957200	Enhancers	Primary hematopoietic stem cells	blood
21	chr12:20957200-20957800	Weak transcription	Primary hematopoietic stem cells	blood
22	chr12:20957800-20959800	Enhancers	Primary hematopoietic stem cells	blood
23	chr12:20957800-20961200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:20957800-20962400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr12:20958000-20960000	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr12:20959600-20959800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr12:20959800-20960800	Weak transcription	Primary hematopoietic stem cells	blood
28	chr12:20960000-20960800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr12:20960200-20961000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr12:20960800-20961000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr12:20960800-20961800	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr12:20960800-20962400	Enhancers	Primary hematopoietic stem cells	blood
33	chr12:20961000-20961400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr12:20961000-20961400	Enhancers	Liver	Liver
35	chr12:20961200-20962000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr12:20961200-20962000	Strong transcription	A549	lung
37	chr12:20961400-20961800	Enhancers	Fetal Kidney	kidney
38	chr12:20961400-20962200	Flanking Active TSS	Liver	Liver
39	chr12:20961400-20962400	Enhancers	HepG2	liver
40	chr12:20962000-20963000	Weak transcription	A549	lung
41	chr12:20962000-20965000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr12:20962200-20963000	Enhancers	Liver	Liver
43	chr12:20962400-20962800	Weak transcription	Primary hematopoietic stem cells	blood
44	chr12:20962400-20964000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr12:20963000-20963200	Flanking Active TSS	Liver	Liver
46	chr12:20963000-20964200	Enhancers	A549	lung
47	chr12:20963200-20964600	Active TSS	Liver	Liver
48	chr12:20964000-20964800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr12:20964200-20964600	Flanking Active TSS	A549	lung
50	chr12:20964400-20964600	Enhancers	Primary hematopoietic stem cells	blood

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