Variant report

Variant	nsv874116
Chromosome Location	chr2:52582766-52685592
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	ATF2	chr2:52667276-52667711	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr2:52667277-52667714	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr2:52667354-52667508	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr2:52667333-52667627	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr2:52675296-52675528	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:52675363-52675413	K562	blood:	n/a	n/a
7	BRCA1	chr2:52656816-52657285	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr2:52666507-52666820	HepG2	liver:	n/a	chr2:52666669-52666680 chr2:52666671-52666680 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666671-52666682
9	CEBPB	chr2:52616319-52616570	HepG2	liver:	n/a	chr2:52616446-52616457 chr2:52616447-52616458 chr2:52616446-52616459
10	CEBPB	chr2:52666489-52666836	Hela-S3	cervix:	n/a	chr2:52666669-52666680 chr2:52666671-52666680 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666671-52666682
11	CEBPB	chr2:52669548-52669831	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:52657012-52657230	H1-hESC	embryonic stem cell:	n/a	chr2:52657151-52657160 chr2:52657086-52657099 chr2:52657149-52657162 chr2:52657151-52657162 chr2:52657151-52657160 chr2:52657149-52657162 chr2:52657151-52657160 chr2:52657151-52657160 chr2:52657149-52657160
13	CEBPB	chr2:52682200-52682504	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:52669525-52669824	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:52667357-52667802	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr2:52650929-52651105	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr2:52623783-52624296	HepG2	liver:	n/a	chr2:52624106-52624117
18	CEBPB	chr2:52650239-52651116	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr2:52669548-52669834	A549	lung:	n/a	n/a
20	CEBPB	chr2:52683698-52683958	A549	lung:	n/a	n/a
21	CEBPB	chr2:52683689-52684029	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:52682169-52682476	IMR90	lung:	n/a	n/a
23	CEBPB	chr2:52679211-52679275	A549	lung:	n/a	n/a
24	CEBPB	chr2:52656987-52657341	HepG2	liver:	n/a	chr2:52657151-52657160 chr2:52657086-52657099 chr2:52657149-52657162 chr2:52657151-52657162 chr2:52657151-52657160 chr2:52657149-52657162 chr2:52657151-52657160 chr2:52657151-52657160 chr2:52657149-52657160
25	CEBPB	chr2:52656730-52657359	IMR90	lung:	n/a	chr2:52657151-52657160 chr2:52657086-52657099 chr2:52657149-52657162 chr2:52657151-52657162 chr2:52657151-52657160 chr2:52657149-52657162 chr2:52657151-52657160 chr2:52657151-52657160 chr2:52657149-52657160
26	CEBPB	chr2:52656984-52657337	A549	lung:	n/a	chr2:52657151-52657160 chr2:52657086-52657099 chr2:52657149-52657162 chr2:52657151-52657162 chr2:52657151-52657160 chr2:52657149-52657162 chr2:52657151-52657160 chr2:52657151-52657160 chr2:52657149-52657160
27	CEBPB	chr2:52666378-52666692	H1-hESC	embryonic stem cell:	n/a	chr2:52666669-52666680 chr2:52666671-52666680 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666671-52666682
28	CEBPB	chr2:52682177-52682409	A549	lung:	n/a	n/a
29	CEBPB	chr2:52656477-52657495	Hela-S3	cervix:	n/a	chr2:52657151-52657160 chr2:52657086-52657099 chr2:52657149-52657162 chr2:52657151-52657162 chr2:52657151-52657160 chr2:52657149-52657162 chr2:52657151-52657160 chr2:52657434-52657447 chr2:52657151-52657160 chr2:52657149-52657160
30	CEBPB	chr2:52682180-52682454	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr2:52666595-52666817	K562	blood:	n/a	chr2:52666669-52666680 chr2:52666671-52666680 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666669-52666682 chr2:52666671-52666682
32	CEBPB	chr2:52667215-52667804	Hela-S3	cervix:	n/a	n/a
33	CHD1	chr2:52640945-52640985	GM12878	blood:	n/a	n/a
34	CHD2	chr2:52667317-52667650	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr2:52638167-52638367	K562	blood:	n/a	n/a
36	CTCF	chr2:52643460-52643610	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:52643480-52643630	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr2:52643600-52643750	HEK293	kidney:	n/a	chr2:52643676-52643694
39	CTCF	chr2:52643591-52643705	LNCaP	prostate:	n/a	chr2:52643676-52643694
40	CTCF	chr2:52643640-52643790	Caco-2	colon:	n/a	chr2:52643676-52643694
41	CTCF	chr2:52643576-52643817	H1-hESC	embryonic stem cell:	n/a	chr2:52643676-52643694
42	CTCF	chr2:52643600-52643750	SAEC	small airway:	n/a	chr2:52643676-52643694
43	CTCF	chr2:52655380-52655530	A549	lung:	n/a	chr2:52655506-52655519
44	CTCF	chr2:52684738-52684835	GM10248	blood:	n/a	n/a
45	CTCF	chr2:52636448-52636746	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr2:52643671-52643710	GM12878	blood:	n/a	chr2:52643676-52643694
47	CTCF	chr2:52643580-52643730	HA-sp	spinal cord:	n/a	chr2:52643676-52643694
48	CTCF	chr2:52643603-52643735	HepG2	liver:	n/a	chr2:52643676-52643694
49	CTCF	chr2:52643680-52643830	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr2:52643680-52643830	HEEpiC	esophagus:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52614831-52614881	PANC-1	pancreas:	n/a
2	chr2:52614831-52614881	HPAEpiC	pulmonary alveolar:	n/a
3	chr2:52614831-52614881	AG09309	skin:	n/a
4	chr2:52656979-52657029	ECC-1	luminal epithelium:	n/a
5	chr2:52656979-52657029	HCPEpiC	choroid plexus:	n/a
6	chr2:52656979-52657029	PFSK-1	brain:	n/a
7	chr2:52614831-52614881	ovcar-3	ovarian:	n/a
8	chr2:52656979-52657029	BJ	skin:	n/a
9	chr2:52614831-52614881	HUVEC	blood vessel:	n/a
10	chr2:52656979-52657029	GM06990	blood:	n/a
11	chr2:52656979-52657029	LNCaP	prostate:	n/a
12	chr2:52614831-52614881	LNCaP	prostate:	n/a
13	chr2:52614831-52614881	HEK293	kidney:	embryo
14	chr2:52614831-52614881	K562	blood:	n/a
15	chr2:52656979-52657029	HAEpiC	amniotic membrane:	n/a
16	chr2:52656979-52657029	K562	blood:	n/a
17	chr2:52614831-52614881	GM06990	blood:	n/a
18	chr2:52656979-52657029	HMEC	breast:	n/a
19	chr2:52614831-52614881	AoSMC	blood vessel:	n/a
20	chr2:52656979-52657029	AG04450	lung:	fetal
21	chr2:52614831-52614881	Jurkat	blood:	n/a
22	chr2:52614831-52614881	PFSK-1	brain:	n/a
23	chr2:52656979-52657029	T-47D	breast:	n/a
24	chr2:52614831-52614881	H1-hESC	embryonic stem cell:	embryo
25	chr2:52656979-52657029	HRPEpiC	eye:	n/a
26	chr2:52656979-52657029	ProgFib	skin:	n/a
27	chr2:52614831-52614881	NT2-D1	testis:	n/a
28	chr2:52614831-52614881	HL-60	blood:	n/a
29	chr2:52656979-52657029	Jurkat	blood:	n/a
30	chr2:52656979-52657029	Hepatocyte	liver:	n/a
31	chr2:52614831-52614881	BE2_C	brain:	n/a
32	chr2:52614831-52614881	IMR90	lung:	fetal
33	chr2:52614831-52614881	NHBE	bronchial:	n/a
34	chr2:52614831-52614881	NHDF-neo	bronchial:	n/a
35	chr2:52656979-52657029	SAEC	small airway:	n/a
36	chr2:52614831-52614881	GM12892	blood:	n/a
37	chr2:52656979-52657029	SKMC	muscle:	n/a
38	chr2:52614831-52614881	HCF	heart:	n/a
39	chr2:52614831-52614881	HAEpiC	amniotic membrane:	n/a
40	chr2:52656979-52657029	HCF	heart:	n/a
41	chr2:52656979-52657029	AG10803	skin:	n/a
42	chr2:52656979-52657029	HRE	kidney:	n/a
43	chr2:52656979-52657029	HepG2	liver:	n/a
44	chr2:52614831-52614881	SK-N-SH	brain:	n/a
45	chr2:52656979-52657029	NH-A	brain:	n/a
46	chr2:52614831-52614881	SKMC	muscle:	n/a
47	chr2:52656979-52657029	HCM	heart:	n/a
48	chr2:52656979-52657029	HNPCEpiC	eye:	n/a
49	chr2:52656979-52657029	HCT-116	colon:	n/a
50	chr2:52614831-52614881	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:52618576..52620644-chr2:52620820..52623618,2	MCF-7	breast:
2	chr2:52644535..52645157-chr2:52839947..52840842,2	MCF-7	breast:
3	chr2:52618576..52620644-chr2:52620820..52623618,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHAC2-3	chr2:52616601-52617150	XLOC_001468
2	lnc-CHAC2-4	chr2:52634116-52635055	ENSG00000231918.1
3	lnc-CHAC2-3	chr2:52600256-52600309	XLOC_001468

Variant related genes	Relation type
ENSG00000225444	TF binding region
ENSG00000225444	CpG island

Extended variants
information (count: 4254 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:4254 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10178558	chr2:52582766-52582767	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552427500	chr2:52582806-52582807	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149370452	chr2:52582810-52582811	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183074015	chr2:52582822-52582823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs34021617	chr2:52582871-52582872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566338359	chr2:52582898-52582899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552168899	chr2:52582932-52582933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs568114484	chr2:52582949-52582950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537104305	chr2:52582964-52582965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144801917	chr2:52583010-52583011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577362688	chr2:52583059-52583060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148556469	chr2:52583113-52583114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1364577	chr2:52583131-52583132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553613436	chr2:52583161-52583162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115092611	chr2:52583191-52583192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542562212	chr2:52583199-52583200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560827896	chr2:52583202-52583203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373150992	chr2:52583272-52583273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529756329	chr2:52583288-52583289	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs188019611	chr2:52583343-52583344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575469794	chr2:52583374-52583375	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201093284	chr2:52583454-52583455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563268190	chr2:52583455-52583456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs544556896	chr2:52583460-52583461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192994587	chr2:52583578-52583579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114023911	chr2:52583588-52583589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549280909	chr2:52583607-52583608	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373860701	chr2:52583612-52583613	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534632500	chr2:52583713-52583714	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183616049	chr2:52583747-52583748	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs77024910	chr2:52583758-52583759	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548085370	chr2:52583763-52583764	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568102102	chr2:52583764-52583765	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188269420	chr2:52583827-52583828	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369388400	chr2:52583904-52583905	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs202227052	chr2:52583908-52583909	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536798365	chr2:52583914-52583915	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79157513	chr2:52583925-52583926	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147744960	chr2:52583944-52583945	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373661874	chr2:52583947-52583948	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs578089432	chr2:52583968-52583969	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1424795	chr2:52583984-52583985	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs140974958	chr2:52583986-52583987	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553262643	chr2:52584001-52584002	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs74642840	chr2:52584036-52584037	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4971807	chr2:52584090-52584091	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs536989531	chr2:52584100-52584101	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574464499	chr2:52584106-52584107	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145039656	chr2:52584138-52584139	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192440087	chr2:52584153-52584154	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52567400-52583600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr2:52573200-52583800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr2:52574400-52585400	Strong transcription	HUES6 Cell Line	embryonic stem cell
4	chr2:52580200-52585800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr2:52581600-52584000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:52583600-52584000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:52583600-52584000	Enhancers	Colon Smooth Muscle	Colon
8	chr2:52583600-52584200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr2:52583800-52584000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr2:52583800-52584200	Enhancers	Fetal Lung	lung
11	chr2:52585400-52587800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
12	chr2:52585800-52586800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
13	chr2:52586200-52586600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr2:52586600-52590600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr2:52587800-52591000	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr2:52588600-52589800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr2:52589800-52592000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr2:52591000-52591600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
19	chr2:52591200-52591400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr2:52591400-52591600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr2:52591600-52591800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr2:52591600-52591800	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr2:52591800-52614800	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr2:52592000-52594200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr2:52595400-52596000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr2:52596400-52596600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr2:52607800-52615000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr2:52609400-52609800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr2:52610800-52614800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr2:52613600-52613800	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr2:52613600-52613800	Enhancers	Fetal Brain Female	brain
32	chr2:52613600-52614000	Enhancers	Fetal Brain Male	brain
33	chr2:52613600-52614400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr2:52613800-52614800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr2:52613800-52618800	Weak transcription	Fetal Brain Female	brain
36	chr2:52614000-52615600	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:52614200-52615400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr2:52614400-52614800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr2:52614800-52615200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr2:52614800-52615200	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr2:52614800-52615200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr2:52614800-52615400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr2:52614800-52615600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr2:52614800-52615800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr2:52614800-52616800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr2:52615000-52615600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr2:52615400-52618000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr2:52615800-52617200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr2:52616800-52619000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr2:52617600-52618200	Enhancers	Osteobl	bone

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