Variant report

Variant	nsv1005938
Chromosome Location	chr2:10043181-10074384
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:459)
CpG islands
(count:61)
Chromatin interactive
region (count:31)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:459 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:10054894-10055193	K562	blood:	n/a	n/a
2	ARID3A	chr2:10052615-10052989	HepG2	liver:	n/a	n/a
3	ATF1	chr2:10054776-10055157	K562	blood:	n/a	n/a
4	ATF2	chr2:10054670-10055232	GM12878	blood:	n/a	n/a
5	ATF2	chr2:10054747-10055187	GM12878	blood:	n/a	n/a
6	ATF3	chr2:10054816-10055044	K562	blood:	n/a	n/a
7	ATF3	chr2:10054734-10055092	K562	blood:	n/a	n/a
8	BACH1	chr2:10054880-10055075	K562	blood:	n/a	n/a
9	BATF	chr2:10054796-10055100	GM12878	blood:	n/a	n/a
10	BATF	chr2:10054687-10055086	GM12878	blood:	n/a	n/a
11	BCL11A	chr2:10054773-10055070	GM12878	blood:	n/a	n/a
12	BCL3	chr2:10054744-10055096	GM12878	blood:	n/a	n/a
13	BCLAF1	chr2:10054741-10055071	GM12878	blood:	n/a	n/a
14	BHLHE40	chr2:10054761-10055119	A549	lung:	n/a	n/a
15	BHLHE40	chr2:10054804-10055053	HepG2	liver:	n/a	n/a
16	BHLHE40	chr2:10054509-10055197	K562	blood:	n/a	n/a
17	BHLHE40	chr2:10054533-10055280	GM12878	blood:	n/a	n/a
18	BRCA1	chr2:10044919-10045008	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr2:10054772-10055123	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr2:10054734-10055156	K562	blood:	n/a	n/a
21	CBX3	chr2:10054764-10055086	K562	blood:	n/a	n/a
22	CCNT2	chr2:10054838-10055031	K562	blood:	n/a	n/a
23	CEBPB	chr2:10060444-10060687	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:10054817-10055151	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr2:10054773-10055111	K562	blood:	n/a	n/a
26	CEBPB	chr2:10054834-10055111	K562	blood:	n/a	n/a
27	CEBPB	chr2:10060478-10060651	IMR90	lung:	n/a	n/a
28	CEBPB	chr2:10054862-10055052	GM12878	blood:	n/a	n/a
29	CHD1	chr2:10054874-10054885	GM12878	blood:	n/a	n/a
30	CHD2	chr2:10054814-10055202	GM12878	blood:	n/a	n/a
31	CHD2	chr2:10054819-10055146	Hela-S3	cervix:	n/a	n/a
32	CREB1	chr2:10054777-10055105	A549	lung:	n/a	n/a
33	CREB1	chr2:10054701-10055231	GM12878	blood:	n/a	n/a
34	CTCF	chr2:10054920-10055070	GM12868	blood:	n/a	n/a
35	CTCF	chr2:10054900-10055050	GM12866	blood:	n/a	n/a
36	CTCF	chr2:10054911-10055068	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:10054960-10055110	HMEC	breast:	n/a	n/a
38	CTCF	chr2:10054912-10055061	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:10054887-10055108	GM13977	blood:	n/a	n/a
40	CTCF	chr2:10054860-10055217	K562	blood:	n/a	n/a
41	CTCF	chr2:10054912-10055045	Fibrobl	skin:	n/a	n/a
42	CTCF	chr2:10054920-10055070	GM12874	blood:	n/a	n/a
43	CTCF	chr2:10072800-10072950	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr2:10054940-10055090	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr2:10054872-10055124	GM12891	blood:	n/a	n/a
46	CTCF	chr2:10054913-10055076	MCF-7	breast:	n/a	n/a
47	CTCF	chr2:10054743-10055168	A549	lung:	n/a	n/a
48	CTCF	chr2:10054900-10055050	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr2:10054920-10055070	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr2:10054940-10055090	HEEpiC	esophagus:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:10054883-10054933	AG09309	skin:	n/a
2	chr2:10054883-10054933	LNCaP	prostate:	n/a
3	chr2:10054883-10054933	HNPCEpiC	eye:	n/a
4	chr2:10054883-10054933	H1-hESC	embryonic stem cell:	embryo
5	chr2:10054883-10054933	HCM	heart:	n/a
6	chr2:10054883-10054933	HIPEpiC	eye:	n/a
7	chr2:10054883-10054933	AG04449	skin:	fetal
8	chr2:10054883-10054933	AG10803	skin:	n/a
9	chr2:10054883-10054933	GM12891	blood:	n/a
10	chr2:10054883-10054933	HRPEpiC	eye:	n/a
11	chr2:10054883-10054933	HEK293	kidney:	embryo
12	chr2:10054883-10054933	SK-N-SH	brain:	n/a
13	chr2:10054883-10054933	ECC-1	luminal epithelium:	n/a
14	chr2:10054883-10054933	PrEC	prostate:	n/a
15	chr2:10054883-10054933	IMR90	lung:	fetal
16	chr2:10054883-10054933	RPTEC	kidney:	n/a
17	chr2:10054883-10054933	HMEC	breast:	n/a
18	chr2:10054883-10054933	AG04450	lung:	fetal
19	chr2:10054883-10054933	ovcar-3	ovarian:	n/a
20	chr2:10054883-10054933	SAEC	small airway:	n/a
21	chr2:10054883-10054933	HUVEC	blood vessel:	n/a
22	chr2:10054883-10054933	HCF	heart:	n/a
23	chr2:10054883-10054933	GM06990	blood:	n/a
24	chr2:10054883-10054933	SK-N-MC	brain:	n/a
25	chr2:10054883-10054933	SK-N-SH_RA	brain:	n/a
26	chr2:10054883-10054933	NHDF-neo	bronchial:	n/a
27	chr2:10054883-10054933	HCPEpiC	choroid plexus:	n/a
28	chr2:10054883-10054933	ProgFib	skin:	n/a
29	chr2:10054883-10054933	MCF-7	breast:	n/a
30	chr2:10054883-10054933	PFSK-1	brain:	n/a
31	chr2:10054883-10054933	PANC-1	pancreas:	n/a
32	chr2:10054883-10054933	SKMC	muscle:	n/a
33	chr2:10054883-10054933	Hela-S3	cervix:	n/a
34	chr2:10054883-10054933	GM12892	blood:	n/a
35	chr2:10054883-10054933	Hepatocyte	liver:	n/a
36	chr2:10054883-10054933	GM19239	blood:	n/a
37	chr2:10054883-10054933	NT2-D1	testis:	n/a
38	chr2:10054883-10054933	HRCEpiC	kidney:	n/a
39	chr2:10054883-10054933	AoSMC	blood vessel:	n/a
40	chr2:10054883-10054933	A549	lung:	n/a
41	chr2:10054883-10054933	HRE	kidney:	n/a
42	chr2:10054883-10054933	Jurkat	blood:	n/a
43	chr2:10054883-10054933	BE2_C	brain:	n/a
44	chr2:10054883-10054933	HPAEpiC	pulmonary alveolar:	n/a
45	chr2:10054883-10054933	HAEpiC	amniotic membrane:	n/a
46	chr2:10054883-10054933	NH-A	brain:	n/a
47	chr2:10054883-10054933	HepG2	liver:	n/a
48	chr2:10054883-10054933	HEEpiC	esophagus:	n/a
49	chr2:10054883-10054933	GM12878	blood:	n/a
50	chr2:10054883-10054933	NB4	blood:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:10053405..10055914-chr2:10061703..10065567,3	K562	blood:
2	chr2:10045085..10047212-chr2:10048163..10049823,2	K562	blood:
3	chr2:10045085..10047212-chr2:10048163..10049823,2	K562	blood:
4	chr2:9940167..9943661-chr2:10053697..10057580,3	MCF-7	breast:
5	chr2:10053405..10055914-chr2:10061703..10065567,3	K562	blood:
6	chr2:10036313..10038528-chr2:10044301..10045845,2	MCF-7	breast:
7	chr2:10053405..10055914-chr2:10061703..10064557,2	K562	blood:
8	chr2:10054070..10056636-chr2:10061535..10064977,4	MCF-7	breast:
9	chr2:10039201..10042198-chr2:10045779..10048080,2	MCF-7	breast:
10	chr2:10054861..10056659-chr2:10057768..10060141,2	K562	blood:
11	chr2:10058951..10060878-chr2:10081099..10082615,2	K562	blood:
12	chr2:10037949..10040040-chr2:10055239..10057291,2	MCF-7	breast:
13	chr2:10037952..10040907-chr2:10047681..10050214,2	K562	blood:
14	chr2:10053405..10055914-chr2:10061703..10064557,2	K562	blood:
15	chr2:10049796..10051308-chr2:10053649..10056131,2	K562	blood:
16	chr2:9985747..9988019-chr2:10062440..10064881,2	MCF-7	breast:
17	chr2:10036109..10038742-chr2:10044743..10047677,2	K562	blood:
18	chr2:10037000..10039031-chr2:10044234..10045895,2	MCF-7	breast:
19	chr2:9940189..9942989-chr2:10049056..10050927,2	MCF-7	breast:
20	chr2:10040912..10043798-chr2:10089997..10091829,3	MCF-7	breast:
21	chr2:10045993..10047524-chr2:10050988..10053341,2	K562	blood:
22	chr2:10054070..10056636-chr2:10061535..10064977,4	MCF-7	breast:
23	chr2:10049796..10051308-chr2:10053649..10056131,2	K562	blood:
24	chr2:10045993..10047524-chr2:10050988..10053341,2	K562	blood:
25	chr2:10055984..10058361-chr2:10061943..10063449,2	MCF-7	breast:
26	chr2:10045831..10047655-chr2:10091725..10093739,2	MCF-7	breast:
27	chr2:10055984..10058361-chr2:10061943..10063449,2	MCF-7	breast:
28	chr2:10047372..10050689-chr2:10052531..10055799,4	MCF-7	breast:
29	chr2:9983243..9984795-chr2:10042473..10044081,2	K562	blood:
30	chr2:10047372..10050689-chr2:10052531..10055799,4	MCF-7	breast:
31	chr2:10054861..10056659-chr2:10057768..10060141,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYS1-8	chr2:10067190-10067461	l_1772_chr2:10062860-10067461_breast
2	lnc-CYS1-8	chr2:10066971-10067181	l_1772_chr2:10062860-10067461_breast
3	lnc-CYS1-8	chr2:10062861-10063502	l_1772_chr2:10062860-10067461_breast

No data

Variant related genes	Relation type
ENSG00000269973	TF binding region
ENSG00000269973	CpG island
ENSG00000134317	chromatin interactions
ENSG00000115750	chromatin interactions

Extended variants
information (count: 1259 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1259 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568010151	chr2:10043193-10043194	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs528426166	chr2:10043215-10043216	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs408987	chr2:10043250-10043251	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs187721069	chr2:10043300-10043301	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs530571515	chr2:10043301-10043302	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs550658220	chr2:10043307-10043308	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs576623506	chr2:10043334-10043335	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs542277984	chr2:10043364-10043365	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs202192186	chr2:10043381-10043382	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs409920	chr2:10043404-10043405	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs552576946	chr2:10043415-10043416	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs34255995	chr2:10043442-10043443	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs566115049	chr2:10043465-10043466	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs535342533	chr2:10043501-10043502	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs554937171	chr2:10043503-10043504	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs67545243	chr2:10043504-10043505	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs4669486	chr2:10043505-10043506	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs392617	chr2:10043510-10043511	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs1709854	chr2:10043581-10043582	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs184809894	chr2:10043602-10043603	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs368691364	chr2:10043621-10043622	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs555643674	chr2:10043638-10043639	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs372105468	chr2:10043679-10043680	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs559823273	chr2:10043680-10043681	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs410121	chr2:10043707-10043708	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs6713616	chr2:10043774-10043775	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs138163355	chr2:10043876-10043877	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs372455771	chr2:10043880-10043881	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs189271603	chr2:10043960-10043961	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs550547358	chr2:10044054-10044055	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs114276447	chr2:10044156-10044157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75520790	chr2:10044201-10044202	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
33	rs417271	chr2:10044205-10044206	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs79538767	chr2:10044220-10044221	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535061036	chr2:10044334-10044335	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs417748	chr2:10044412-10044413	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs74624726	chr2:10044415-10044416	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
38	rs192361968	chr2:10044436-10044437	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs394308	chr2:10044440-10044441	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs184416650	chr2:10044481-10044482	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs577500176	chr2:10044516-10044517	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs394650	chr2:10044543-10044544	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs116413277	chr2:10044545-10044546	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571577181	chr2:10044560-10044561	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs115945880	chr2:10044562-10044563	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537305186	chr2:10044606-10044607	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575476763	chr2:10044665-10044666	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs544091965	chr2:10044794-10044795	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563948831	chr2:10044799-10044800	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564933	chr2:10044827-10044828	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
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
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD

Chromatin state (count:835 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:9993800-10079600	Weak transcription	Gastric	stomach
2	chr2:9999200-10053800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr2:10014800-10045400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr2:10017800-10073000	Weak transcription	Right Ventricle	heart
5	chr2:10024400-10053800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr2:10024800-10047600	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr2:10024800-10051400	Weak transcription	Duodenum Mucosa	Duodenum
8	chr2:10025000-10047000	Weak transcription	Thymus	Thymus
9	chr2:10025000-10053800	Weak transcription	Fetal Muscle Trunk	muscle
10	chr2:10025000-10053800	Weak transcription	Ovary	ovary
11	chr2:10025000-10054400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr2:10025000-10054400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:10025000-10054400	Weak transcription	Spleen	Spleen
14	chr2:10025400-10052600	Weak transcription	Left Ventricle	heart
15	chr2:10026000-10072800	Weak transcription	Stomach Smooth Muscle	stomach
16	chr2:10027000-10047000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr2:10027400-10052200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr2:10027400-10053400	Weak transcription	Fetal Brain Male	brain
19	chr2:10027600-10052000	Weak transcription	Primary B cells from peripheral blood	blood
20	chr2:10028200-10051000	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr2:10028200-10053800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr2:10030400-10077200	Weak transcription	Aorta	Aorta
23	chr2:10030600-10080600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr2:10032600-10044600	Weak transcription	Primary T cells fromperipheralblood	blood
25	chr2:10032800-10044400	Weak transcription	Dnd41	blood
26	chr2:10033000-10044000	Weak transcription	Primary hematopoietic stem cells	blood
27	chr2:10033000-10044400	Weak transcription	Primary B cells from cord blood	blood
28	chr2:10033000-10052800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr2:10036000-10065800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr2:10036400-10047800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr2:10036400-10052200	Weak transcription	Liver	Liver
32	chr2:10036600-10047600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr2:10036600-10076200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr2:10036800-10051800	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr2:10036800-10073000	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr2:10037000-10047400	Weak transcription	Fetal Intestine Large	intestine
37	chr2:10037200-10044600	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr2:10037200-10044600	Weak transcription	Fetal Thymus	thymus
39	chr2:10037200-10047200	Weak transcription	Primary T cells from cord blood	blood
40	chr2:10037200-10051800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr2:10037200-10080400	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr2:10037600-10046000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr2:10037800-10045600	Weak transcription	HepG2	liver
44	chr2:10037800-10075600	Weak transcription	Brain Cingulate Gyrus	brain
45	chr2:10038000-10045000	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr2:10038000-10047000	Weak transcription	Fetal Intestine Small	intestine
47	chr2:10038000-10047000	Weak transcription	Fetal Muscle Leg	muscle
48	chr2:10038000-10049800	Weak transcription	K562	blood
49	chr2:10038000-10052600	Weak transcription	Fetal Kidney	kidney
50	chr2:10038000-10052800	Weak transcription	HUVEC	blood vessel

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