Variant report

Variant	nsv523020
Chromosome Location	chr2:50871418-50938959
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:218)
CpG islands
(count:184)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:218 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr2:50919242-50919552	HepG2	liver:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
2	CEBPB	chr2:50890728-50891191	HepG2	liver:	n/a	chr2:50890749-50890760 chr2:50891044-50891055
3	CEBPB	chr2:50919241-50919557	IMR90	lung:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
4	CEBPB	chr2:50919262-50919518	K562	blood:	n/a	chr2:50919400-50919413 chr2:50919400-50919411
5	CTCF	chr2:50889583-50889671	GM19238	blood:	n/a	n/a
6	CTCF	chr2:50901960-50902110	RPTEC	kidney:	n/a	n/a
7	CTCF	chr2:50902140-50902290	WERI-Rb-1	eye:	n/a	n/a
8	CTCF	chr2:50902100-50902250	HCPEpiC	choroid plexus:	n/a	n/a
9	CTCF	chr2:50902180-50902330	GM12878	blood:	n/a	n/a
10	CTCF	chr2:50902182-50902235	LNCaP	prostate:	n/a	n/a
11	CTCF	chr2:50902163-50902293	Gliobla	brain:	n/a	n/a
12	CTCF	chr2:50902146-50902299	GM19238	blood:	n/a	n/a
13	CTCF	chr2:50902100-50902250	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr2:50902081-50902284	HepG2	liver:	n/a	n/a
15	CTCF	chr2:50902120-50902270	GM12866	blood:	n/a	n/a
16	CTCF	chr2:50902140-50902290	GM12872	blood:	n/a	n/a
17	CTCF	chr2:50902100-50902250	GM12872	blood:	n/a	n/a
18	CTCF	chr2:50902116-50902324	GM12892	blood:	n/a	n/a
19	CTCF	chr2:50902100-50902250	HCT-116	colon:	n/a	n/a
20	CTCF	chr2:50902320-50902470	A549	lung:	n/a	n/a
21	CTCF	chr2:50902180-50902330	HA-sp	spinal cord:	n/a	n/a
22	CTCF	chr2:50902120-50902270	A549	lung:	n/a	n/a
23	CTCF	chr2:50902080-50902230	GM12869	blood:	n/a	n/a
24	CTCF	chr2:50902173-50902283	HepG2	liver:	n/a	n/a
25	CTCF	chr2:50902140-50902290	GM12865	blood:	n/a	n/a
26	CTCF	chr2:50902200-50902350	GM12869	blood:	n/a	n/a
27	CTCF	chr2:50889589-50889673	MCF-7	breast:	n/a	n/a
28	CTCF	chr2:50889605-50889670	MCF-7	breast:	n/a	n/a
29	CTCF	chr2:50902046-50902364	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr2:50902100-50902250	NHEK	skin:	n/a	n/a
31	CTCF	chr2:50902145-50902298	MCF-7	breast:	n/a	n/a
32	CTCF	chr2:50902100-50902250	GM12874	blood:	n/a	n/a
33	CTCF	chr2:50902140-50902290	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr2:50902120-50902270	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr2:50902060-50902290	GM12864	blood:	n/a	n/a
36	CTCF	chr2:50902200-50902350	HRE	kidney:	n/a	n/a
37	CTCF	chr2:50902080-50902230	GM12873	blood:	n/a	n/a
38	CTCF	chr2:50902155-50902284	GM13977	blood:	n/a	n/a
39	CTCF	chr2:50902138-50902315	NHEK	skin:	n/a	n/a
40	CTCF	chr2:50889603-50889665	GM19240	blood:	n/a	n/a
41	CTCF	chr2:50889610-50889663	GM12891	blood:	n/a	n/a
42	CTCF	chr2:50902189-50902272	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:50902140-50902290	HMEC	breast:	n/a	n/a
44	CTCF	chr2:50902140-50902290	NB4	blood:	n/a	n/a
45	CTCF	chr2:50902035-50902240	K562	blood:	n/a	n/a
46	CTCF	chr2:50902080-50902230	GM06990	blood:	n/a	n/a
47	CTCF	chr2:50902100-50902250	HMF	breast:	n/a	n/a
48	CTCF	chr2:50902100-50902250	GM12870	blood:	n/a	n/a
49	CTCF	chr2:50902176-50902276	GM10248	blood:	n/a	n/a
50	CTCF	chr2:50902119-50902292	GM19240	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:50884693-50884743	GM06990	blood:	n/a
2	chr2:50884693-50884743	GM06990	blood:	n/a
3	chr2:50876837-50876887	AG04449	skin:	fetal
4	chr2:50884693-50884743	Caco-2	colon:	n/a
5	chr2:50876837-50876887	HUVEC	blood vessel:	n/a
6	chr2:50884252-50884302	Hepatocyte	liver:	n/a
7	chr2:50876837-50876887	RPTEC	kidney:	n/a
8	chr2:50884693-50884743	GM12891	blood:	n/a
9	chr2:50884252-50884302	MCF10A-Er-Src	breast:	n/a
10	chr2:50884252-50884302	ECC-1	luminal epithelium:	n/a
11	chr2:50884693-50884743	HEEpiC	esophagus:	n/a
12	chr2:50884693-50884743	SK-N-SH_RA	brain:	n/a
13	chr2:50884693-50884743	HL-60	blood:	n/a
14	chr2:50876837-50876887	HRCEpiC	kidney:	n/a
15	chr2:50884693-50884743	Jurkat	blood:	n/a
16	chr2:50876837-50876887	Caco-2	colon:	n/a
17	chr2:50884252-50884302	AG09309	skin:	n/a
18	chr2:50876837-50876887	NHDF-neo	bronchial:	n/a
19	chr2:50884252-50884302	CMK	blood:	n/a
20	chr2:50876837-50876887	HCM	heart:	n/a
21	chr2:50884252-50884302	AG04450	lung:	fetal
22	chr2:50884252-50884302	HEK293	kidney:	embryo
23	chr2:50884252-50884302	AG10803	skin:	n/a
24	chr2:50884693-50884743	HPAEpiC	pulmonary alveolar:	n/a
25	chr2:50884252-50884302	HNPCEpiC	eye:	n/a
26	chr2:50884252-50884302	BE2_C	brain:	n/a
27	chr2:50876837-50876887	Hepatocyte	liver:	n/a
28	chr2:50876837-50876887	H1-hESC	embryonic stem cell:	embryo
29	chr2:50884693-50884743	ECC-1	luminal epithelium:	n/a
30	chr2:50884693-50884743	HCT-116	colon:	n/a
31	chr2:50884252-50884302	PFSK-1	brain:	n/a
32	chr2:50884252-50884302	NT2-D1	testis:	n/a
33	chr2:50876837-50876887	SK-N-MC	brain:	n/a
34	chr2:50884252-50884302	AoSMC	blood vessel:	n/a
35	chr2:50884252-50884302	ProgFib	skin:	n/a
36	chr2:50884252-50884302	PrEC	prostate:	n/a
37	chr2:50884252-50884302	HepG2	liver:	n/a
38	chr2:50876837-50876887	NT2-D1	testis:	n/a
39	chr2:50884252-50884302	HCF	heart:	n/a
40	chr2:50876837-50876887	HIPEpiC	eye:	n/a
41	chr2:50884693-50884743	MCF-7	breast:	n/a
42	chr2:50884252-50884302	HEEpiC	esophagus:	n/a
43	chr2:50876837-50876887	HCPEpiC	choroid plexus:	n/a
44	chr2:50884693-50884743	NHDF-neo	bronchial:	n/a
45	chr2:50884693-50884743	Hela-S3	cervix:	n/a
46	chr2:50884252-50884302	IMR90	lung:	fetal
47	chr2:50876837-50876887	AG04450	lung:	fetal
48	chr2:50884252-50884302	K562	blood:	n/a
49	chr2:50884693-50884743	GM12892	blood:	n/a
50	chr2:50884693-50884743	HepG2	liver:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:50909775..50912434-chr2:50920496..50923402,2	MCF-7	breast:
2	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:
3	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:
4	chr2:50884111..50885778-chr2:50886770..50888521,2	MCF-7	breast:
5	chr2:50883231..50884999-chr2:50887642..50889397,2	MCF-7	breast:
6	chr2:50884335..50886694-chr2:50887318..50889235,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000216191	TF binding region
NRXN1	TF binding region
ENSG00000216191	CpG island
NRXN1	CpG island
ENSG00000179915	chromatin interactions
ENSG00000216191	chromatin interactions

Extended variants
information (count: 2445 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2445 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10182729	chr2:50871418-50871419	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs74535999	chr2:50871438-50871439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562278771	chr2:50871467-50871468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530435142	chr2:50871488-50871489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548838357	chr2:50871576-50871577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183124966	chr2:50871584-50871585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552300242	chr2:50871615-50871616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537640855	chr2:50871646-50871647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558413356	chr2:50871678-50871679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570503258	chr2:50871701-50871702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540097855	chr2:50871702-50871703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534350404	chr2:50871727-50871728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530757766	chr2:50871743-50871744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186024491	chr2:50871744-50871745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574065502	chr2:50871779-50871780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531172157	chr2:50871786-50871787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2194388	chr2:50871821-50871822	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs557180652	chr2:50871869-50871870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561648139	chr2:50871889-50871890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs575391010	chr2:50871932-50871933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545975428	chr2:50871946-50871947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565263674	chr2:50871947-50871948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567156592	chr2:50871950-50871951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149713684	chr2:50871971-50871972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541506137	chr2:50871979-50871980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559809534	chr2:50872000-50872001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200943916	chr2:50872007-50872008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2216786	chr2:50872014-50872015	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs191223991	chr2:50872061-50872062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372632720	chr2:50872107-50872108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374337869	chr2:50872113-50872114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368204890	chr2:50872121-50872122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145662014	chr2:50872138-50872139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369211884	chr2:50872140-50872141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564002107	chr2:50872223-50872224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575678261	chr2:50872239-50872240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531036972	chr2:50872273-50872274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201309772	chr2:50872276-50872277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552722004	chr2:50872308-50872309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538685964	chr2:50872347-50872348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575155068	chr2:50872374-50872375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373473295	chr2:50872378-50872379	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183223750	chr2:50872401-50872402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376467031	chr2:50872421-50872422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552166064	chr2:50872441-50872442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371306302	chr2:50872455-50872456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534432775	chr2:50872465-50872466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546241188	chr2:50872470-50872471	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187914713	chr2:50872492-50872493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565511348	chr2:50872524-50872525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Breast cancer	21364760	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
Basal cell lymphoma	21115979	CNVD
Cognitive impairment	21505072	CNVD
Psychiatric disorder	19734545	CNVD
Autism	20844286	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Autism	19218893	CNVD
Autism	22209245	CNVD
Neuropsychiatric disorder	21827697	CNVD
Schizophrenia	22118685	CNVD
Autism	20663923	CNVD
Schizophrenia	21285140	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21990379	CNVD
Schizophrenia	22885689	CNVD
Autism	20964600	CNVD
Schizophrenia	19521646	CNVD
Attention deficit hyperactivity disorder	22214315	CNVD
Chronic motor tic disorder	22214315	CNVD
Schizophrenia	22214315	CNVD
Mental retardation	19896112	CNVD
Acute myeloid leukemia	20729466	CNVD
Bipolar disorder	19114987	CNVD
Autism	20841430	CNVD

Chromatin state (count:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:50868600-50872200	Weak transcription	Fetal Brain Male	brain
2	chr2:50869000-50875600	Weak transcription	Fetal Muscle Leg	muscle
3	chr2:50872200-50877800	Enhancers	Fetal Brain Male	brain
4	chr2:50872600-50873200	Enhancers	Fetal Brain Female	brain
5	chr2:50872800-50873400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr2:50873000-50873200	Enhancers	Brain Cingulate Gyrus	brain
7	chr2:50873000-50873400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr2:50873000-50873400	Enhancers	Brain Substantia Nigra	brain
9	chr2:50873200-50874000	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr2:50873200-50875600	Weak transcription	Fetal Brain Female	brain
11	chr2:50873200-50875800	Weak transcription	Fetal Kidney	kidney
12	chr2:50873400-50874800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr2:50873400-50875400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr2:50873400-50875400	Weak transcription	Brain Substantia Nigra	brain
15	chr2:50873600-50873800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr2:50873800-50876800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr2:50874000-50875600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr2:50874800-50878000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr2:50875200-50876000	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr2:50875400-50876000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr2:50875400-50876000	Enhancers	Brain Substantia Nigra	brain
22	chr2:50875400-50877800	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr2:50875600-50876000	Enhancers	H1 Cell Line	embryonic stem cell
24	chr2:50875600-50876000	Enhancers	Brain Hippocampus Middle	brain
25	chr2:50875600-50876000	Enhancers	Fetal Brain Female	brain
26	chr2:50875600-50876000	Enhancers	Fetal Muscle Leg	muscle
27	chr2:50875600-50876200	Enhancers	Brain Cingulate Gyrus	brain
28	chr2:50875600-50878000	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr2:50875800-50877000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr2:50875800-50877600	Enhancers	HSMMtube	muscle
31	chr2:50875800-50878000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr2:50876000-50876400	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr2:50876000-50877000	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr2:50876000-50877000	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr2:50876000-50877000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr2:50876000-50877000	Enhancers	NHEK	skin
37	chr2:50876000-50878800	Weak transcription	Brain Hippocampus Middle	brain
38	chr2:50876000-50878800	Weak transcription	Brain Substantia Nigra	brain
39	chr2:50876000-50878800	Weak transcription	Fetal Brain Female	brain
40	chr2:50876200-50879200	Weak transcription	Brain Cingulate Gyrus	brain
41	chr2:50876400-50878200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr2:50876400-50879800	Enhancers	HMEC	breast
43	chr2:50876600-50877200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:50876600-50877600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr2:50876600-50877800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr2:50876600-50877800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr2:50876800-50877400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr2:50876800-50877400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr2:50876800-50878000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:50876800-50878000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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