Variant report

Variant	nsv933564
Chromosome Location	chr11:71148635-71152521
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:78)
CpG islands
(count:305)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:78 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr11:71148913-71149171	K562	blood:	n/a	n/a
2	CTCF	chr11:71149005-71149167	GM12878	blood:	n/a	n/a
3	CTCF	chr11:71148980-71149130	HCPEpiC	choroid plexus:	n/a	n/a
4	CTCF	chr11:71149037-71149117	MCF-7	breast:	n/a	n/a
5	CTCF	chr11:71149005-71149144	GM13977	blood:	n/a	n/a
6	CTCF	chr11:71149016-71149137	Spleen_OC	spleen:	n/a	n/a
7	CTCF	chr11:71149037-71149153	MCF-7	breast:	n/a	n/a
8	CTCF	chr11:71149018-71149134	GM19239	blood:	n/a	n/a
9	CTCF	chr11:71149020-71149170	HBMEC	blood vessel:	n/a	n/a
10	CTCF	chr11:71149005-71149103	GM13976	blood:	n/a	n/a
11	CTCF	chr11:71149069-71149097	GM10248	blood:	n/a	n/a
12	CTCF	chr11:71149009-71149160	GM19240	blood:	n/a	n/a
13	CTCF	chr11:71148980-71149130	GM06990	blood:	n/a	n/a
14	CTCF	chr11:71148980-71149130	Caco-2	colon:	n/a	n/a
15	CTCF	chr11:71149140-71149290	MCF-7	breast:	n/a	n/a
16	CTCF	chr11:71149013-71149162	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr11:71149080-71149230	GM06990	blood:	n/a	n/a
18	CTCF	chr11:71149000-71149150	GM12875	blood:	n/a	n/a
19	CTCF	chr11:71148991-71149173	GM12892	blood:	n/a	n/a
20	CTCF	chr11:71149052-71149142	K562	blood:	n/a	n/a
21	CTCF	chr11:71148980-71149130	HL-60	blood:	n/a	n/a
22	CTCF	chr11:71148970-71149196	GM12891	blood:	n/a	n/a
23	CTCF	chr11:71149000-71149150	K562	blood:	n/a	n/a
24	CTCF	chr11:71148977-71149196	GM19238	blood:	n/a	n/a
25	CTCF	chr11:71149071-71149111	Gliobla	brain:	n/a	n/a
26	CTCF	chr11:71149059-71149141	K562	blood:	n/a	n/a
27	MAZ	chr11:71149018-71149132	K562	blood:	n/a	n/a
28	MYC	chr11:71151501-71151515	MCF-7	breast:	n/a	n/a
29	MYC	chr11:71151438-71151494	MCF-7	breast:	n/a	n/a
30	MYC	chr11:71151433-71151520	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr11:71148888-71149641	HepG2	liver:	n/a	n/a
32	POLR2A	chr11:71152197-71152233	K562	blood:	n/a	n/a
33	POLR2A	chr11:71152240-71152597	K562	blood:	n/a	n/a
34	POLR2A	chr11:71147942-71151728	K562	blood:	n/a	n/a
35	POLR2A	chr11:71148698-71149476	HL-60	blood:	n/a	n/a
36	POLR2A	chr11:71151267-71151350	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr11:71152343-71152665	K562	blood:	n/a	n/a
38	POLR2A	chr11:71152016-71153031	HepG2	liver:	n/a	n/a
39	POLR2A	chr11:71148233-71150150	K562	blood:	n/a	n/a
40	POLR2A	chr11:71148432-71148702	HepG2	liver:	n/a	n/a
41	POLR2A	chr11:71151377-71151397	Hela-S3	cervix:	n/a	n/a
42	POLR2A	chr11:71149350-71149560	K562	blood:	n/a	n/a
43	POLR2A	chr11:71148793-71148828	HepG2	liver:	n/a	n/a
44	POLR2A	chr11:71150850-71151968	HepG2	liver:	n/a	n/a
45	POLR2A	chr11:71152008-71152193	K562	blood:	n/a	n/a
46	POLR2A	chr11:71152445-71152468	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr11:71151551-71151614	MCF-7	breast:	n/a	n/a
48	POLR2A	chr11:71150534-71150746	K562	blood:	n/a	n/a
49	POLR2A	chr11:71148729-71148732	HepG2	liver:	n/a	n/a
50	POLR2A	chr11:71150511-71150709	HepG2	liver:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71150315-71150365	GM19239	blood:	n/a
2	chr11:71150200-71150250	IMR90	lung:	fetal
3	chr11:71150247-71150297	NHDF-neo	bronchial:	n/a
4	chr11:71150200-71150250	HUVEC	blood vessel:	n/a
5	chr11:71150200-71150250	GM12878	blood:	n/a
6	chr11:71150200-71150250	Hepatocyte	liver:	n/a
7	chr11:71150247-71150297	ProgFib	skin:	n/a
8	chr11:71150247-71150297	SK-N-SH	brain:	n/a
9	chr11:71150315-71150365	HL-60	blood:	n/a
10	chr11:71150020-71150070	HCT-116	colon:	n/a
11	chr11:71150020-71150070	HCPEpiC	choroid plexus:	n/a
12	chr11:71149985-71150035	SK-N-SH	brain:	n/a
13	chr11:71150247-71150297	HMEC	breast:	n/a
14	chr11:71150200-71150250	SK-N-MC	brain:	n/a
15	chr11:71150020-71150070	AG09319	gingival:	n/a
16	chr11:71149985-71150035	SK-N-SH_RA	brain:	n/a
17	chr11:71149985-71150035	RPTEC	kidney:	n/a
18	chr11:71149985-71150035	HepG2	liver:	n/a
19	chr11:71150315-71150365	HCPEpiC	choroid plexus:	n/a
20	chr11:71150315-71150365	GM12892	blood:	n/a
21	chr11:71150315-71150365	GM12878	blood:	n/a
22	chr11:71150200-71150250	AG04449	skin:	fetal
23	chr11:71150020-71150070	BE2_C	brain:	n/a
24	chr11:71150020-71150070	AG04449	skin:	fetal
25	chr11:71150020-71150070	AG10803	skin:	n/a
26	chr11:71150200-71150250	LNCaP	prostate:	n/a
27	chr11:71150020-71150070	H1-hESC	embryonic stem cell:	embryo
28	chr11:71150200-71150250	AoSMC	blood vessel:	n/a
29	chr11:71150315-71150365	AG09309	skin:	n/a
30	chr11:71150020-71150070	SK-N-SH_RA	brain:	n/a
31	chr11:71150315-71150365	NHBE	bronchial:	n/a
32	chr11:71149985-71150035	HRCEpiC	kidney:	n/a
33	chr11:71150020-71150070	AoSMC	blood vessel:	n/a
34	chr11:71150200-71150250	PFSK-1	brain:	n/a
35	chr11:71150200-71150250	NH-A	brain:	n/a
36	chr11:71150200-71150250	AG04450	lung:	fetal
37	chr11:71150020-71150070	GM19239	blood:	n/a
38	chr11:71149985-71150035	PANC-1	pancreas:	n/a
39	chr11:71150200-71150250	T-47D	breast:	n/a
40	chr11:71149985-71150035	AoSMC	blood vessel:	n/a
41	chr11:71150315-71150365	HEK293	kidney:	embryo
42	chr11:71150200-71150250	NB4	blood:	n/a
43	chr11:71149985-71150035	ProgFib	skin:	n/a
44	chr11:71150200-71150250	K562	blood:	n/a
45	chr11:71150020-71150070	HRCEpiC	kidney:	n/a
46	chr11:71150315-71150365	HCM	heart:	n/a
47	chr11:71150315-71150365	HRCEpiC	kidney:	n/a
48	chr11:71150020-71150070	PrEC	prostate:	n/a
49	chr11:71150247-71150297	ovcar-3	ovarian:	n/a
50	chr11:71150200-71150250	HCPEpiC	choroid plexus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:71145861..71148478-chr11:71150680..71152334,2	K562	blood:
2	chr11:71150692..71153685-chr11:71157371..71159231,2	K562	blood:
3	chr11:71139536..71142433-chr11:71147657..71149469,2	K562	blood:

No data

Variant related genes	Relation type
DHCR7	TF binding region
DHCR7	CpG island
ENSG00000172893	chromatin interactions

Extended variants
information (count: 237 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:237 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371380132	chr11:71148662-71148663	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs2852857	chr11:71148669-71148670	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs527861389	chr11:71148693-71148694	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552335947	chr11:71148724-71148725	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs34177783	chr11:71148770-71148771	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570575642	chr11:71148785-71148786	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs370045836	chr11:71148819-71148820	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376037564	chr11:71148828-71148829	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs111241376	chr11:71148829-71148830	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368368717	chr11:71148844-71148845	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200882823	chr11:71148852-71148853	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs200157761	chr11:71148864-71148865	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs370955781	chr11:71148893-71148894	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs149974099	chr11:71148894-71148895	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142808899	chr11:71148914-71148915	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs80338858	chr11:71148915-71148916	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs201574502	chr11:71148938-71148939	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs121909765	chr11:71148955-71148956	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565893436	chr11:71148959-71148960	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184297154	chr11:71148969-71148970	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs398123607	chr11:71148980-71148981	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148468879	chr11:71148981-71148982	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs121909766	chr11:71148982-71148983	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs80338863	chr11:71148990-71148991	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375043191	chr11:71149006-71149007	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368017833	chr11:71149020-71149021	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201362072	chr11:71149022-71149023	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544262288	chr11:71149040-71149041	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189115711	chr11:71149046-71149047	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142698584	chr11:71149048-71149049	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11233679	chr11:71149066-71149067	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs949176	chr11:71149069-71149070	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs527951276	chr11:71149132-71149133	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147611608	chr11:71149136-71149137	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1790326	chr11:71149137-71149138	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs531443406	chr11:71149139-71149140	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549890139	chr11:71149163-71149164	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557826567	chr11:71149179-71149180	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568092286	chr11:71149180-71149181	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142213908	chr11:71149203-71149204	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144287385	chr11:71149210-71149211	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs369593130	chr11:71149254-71149255	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs565859721	chr11:71149259-71149260	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373523169	chr11:71149285-71149286	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572860778	chr11:71149308-71149309	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181726776	chr11:71149321-71149322	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147807751	chr11:71149351-71149352	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569508380	chr11:71149384-71149385	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185517598	chr11:71149397-71149398	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537996768	chr11:71149403-71149404	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:161 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71135000-71150600	Weak transcription	NH-A	brain
2	chr11:71137200-71149600	Weak transcription	Primary B cells from peripheral blood	blood
3	chr11:71140600-71158200	Weak transcription	Fetal Brain Male	brain
4	chr11:71140800-71154000	Weak transcription	Fetal Lung	lung
5	chr11:71140800-71154000	Weak transcription	HSMM	muscle
6	chr11:71143000-71150600	Weak transcription	Osteobl	bone
7	chr11:71143600-71149400	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr11:71144000-71156200	Strong transcription	Fetal Brain Female	brain
9	chr11:71144200-71152000	Weak transcription	Fetal Thymus	thymus
10	chr11:71144200-71158200	Weak transcription	Small Intestine	intestine
11	chr11:71144400-71156200	Strong transcription	Primary T cells from cord blood	blood
12	chr11:71144600-71157800	Strong transcription	HUES6 Cell Line	embryonic stem cell
13	chr11:71144800-71149400	Weak transcription	Primary B cells from cord blood	blood
14	chr11:71144800-71156600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:71144800-71156800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr11:71144800-71156800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr11:71144800-71157800	Strong transcription	H9 Cell Line	embryonic stem cell
18	chr11:71145000-71148800	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr11:71145000-71149800	Weak transcription	Psoas Muscle	Psoas
20	chr11:71145000-71150800	Weak transcription	A549	lung
21	chr11:71145000-71155400	Strong transcription	Primary neutrophils fromperipheralblood	blood
22	chr11:71145000-71156400	Strong transcription	Brain Germinal Matrix	brain
23	chr11:71145000-71156600	Strong transcription	Fetal Stomach	stomach
24	chr11:71145000-71157000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr11:71145000-71157000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr11:71145000-71157400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr11:71145000-71157800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr11:71145000-71158600	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr11:71145200-71148800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr11:71145200-71156200	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr11:71145200-71157000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
32	chr11:71145200-71157000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr11:71145200-71157200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr11:71145200-71157400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
35	chr11:71145200-71157400	Strong transcription	HMEC	breast
36	chr11:71145200-71157800	Strong transcription	H1 Cell Line	embryonic stem cell
37	chr11:71145400-71149400	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr11:71145400-71149600	Weak transcription	Right Atrium	heart
39	chr11:71145400-71157800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr11:71145400-71158000	Weak transcription	Stomach Mucosa	stomach
41	chr11:71145600-71149200	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr11:71145600-71157000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr11:71145600-71157000	Strong transcription	HUES64 Cell Line	embryonic stem cell
44	chr11:71145600-71158000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr11:71145800-71155400	Strong transcription	Left Ventricle	heart
46	chr11:71145800-71156200	Strong transcription	Lung	lung
47	chr11:71145800-71156400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr11:71145800-71156600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr11:71145800-71156600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr11:71145800-71156800	Strong transcription	Duodenum Mucosa	Duodenum

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