Variant report

Variant	nsv975205
Chromosome Location	chr11:77628075-77671380
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:115)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:115 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:77641398-77641717	K562	blood:	n/a	n/a
2	ATF1	chr11:77670535-77670626	K562	blood:	n/a	n/a
3	ATF1	chr11:77641440-77641752	K562	blood:	n/a	n/a
4	ATF1	chr11:77669656-77669978	K562	blood:	n/a	n/a
5	ATF1	chr11:77640902-77640912	K562	blood:	n/a	n/a
6	BATF	chr11:77653561-77653797	GM12878	blood:	n/a	chr11:77653715-77653726 chr11:77653656-77653667
7	BATF	chr11:77653598-77653788	GM12878	blood:	n/a	chr11:77653715-77653726 chr11:77653656-77653667
8	CEBPB	chr11:77670427-77670742	IMR90	lung:	n/a	n/a
9	CEBPB	chr11:77641436-77641668	Hela-S3	cervix:	n/a	chr11:77641529-77641546
10	CEBPB	chr11:77653642-77653684	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr11:77653478-77653849	IMR90	lung:	n/a	chr11:77653512-77653523
12	CEBPD	chr11:77669508-77670023	K562	blood:	n/a	n/a
13	CEBPD	chr11:77641374-77641826	K562	blood:	n/a	n/a
14	CTCF	chr11:77667797-77667921	LNCaP	prostate:	n/a	n/a
15	CTCF	chr11:77646233-77646311	LNCaP	prostate:	n/a	n/a
16	CTCF	chr11:77654373-77654423	GM13976	blood:	n/a	n/a
17	CTCF	chr11:77657199-77657280	GM13976	blood:	n/a	n/a
18	CTCF	chr11:77639111-77639165	GM13976	blood:	n/a	n/a
19	CTCF	chr11:77665803-77665887	GM10248	blood:	n/a	n/a
20	CTCF	chr11:77669534-77669609	GM10248	blood:	n/a	n/a
21	CTCF	chr11:77653058-77653097	GM13976	blood:	n/a	n/a
22	CTCF	chr11:77654704-77654823	GM13976	blood:	n/a	n/a
23	CTCF	chr11:77667287-77667296	GM10248	blood:	n/a	n/a
24	CTCF	chr11:77669885-77669976	GM20000	blood:	n/a	n/a
25	CTCF	chr11:77667121-77667250	GM10248	blood:	n/a	n/a
26	CTCF	chr11:77669702-77669758	GM10248	blood:	n/a	n/a
27	CTCF	chr11:77649902-77650016	GM10248	blood:	n/a	n/a
28	CTCF	chr11:77639475-77639519	Medullo	brain:	n/a	n/a
29	CTCF	chr11:77639866-77639928	GM20000	blood:	n/a	n/a
30	CTCF	chr11:77640592-77640674	LNCaP	prostate:	n/a	n/a
31	CUX1	chr11:77641510-77641713	K562	blood:	n/a	n/a
32	EGR1	chr11:77669579-77669945	K562	blood:	n/a	n/a
33	EGR1	chr11:77669625-77669870	K562	blood:	n/a	n/a
34	EP300	chr11:77641404-77641658	K562	blood:	n/a	n/a
35	EP300	chr11:77669611-77669989	K562	blood:	n/a	n/a
36	FOS	chr11:77653605-77653800	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr11:77641385-77641741	HUVEC	blood vessel:	n/a	chr11:77641543-77641554 chr11:77641544-77641554 chr11:77641545-77641553
38	FOS	chr11:77652831-77652868	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr11:77653611-77653795	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr11:77663695-77663780	MCF10A-Er-Src	breast:	n/a	chr11:77663736-77663744
41	FOS	chr11:77652824-77652868	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr11:77652824-77652855	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr11:77652734-77652934	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr11:77653648-77653663	MCF10A-Er-Src	breast:	n/a	n/a
45	FOXA2	chr11:77645080-77645406	A549	lung:	n/a	n/a
46	GATA1	chr11:77641429-77641889	K562	blood:	n/a	n/a
47	GATA1	chr11:77669442-77670378	K562	blood:	n/a	chr11:77669953-77669961 chr11:77669950-77669963
48	GATA2	chr11:77654248-77654658	HUVEC	blood vessel:	n/a	n/a
49	GATA2	chr11:77670334-77670656	K562	blood:	n/a	n/a
50	GATA2	chr11:77641323-77641822	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:77644765-77644815	HMEC	breast:	n/a
2	chr11:77644765-77644815	NB4	blood:	n/a
3	chr11:77644765-77644815	AG09309	skin:	n/a
4	chr11:77644765-77644815	Hepatocyte	liver:	n/a
5	chr11:77644765-77644815	AG04450	lung:	fetal
6	chr11:77644765-77644815	HRPEpiC	eye:	n/a
7	chr11:77644765-77644815	HL-60	blood:	n/a
8	chr11:77644765-77644815	T-47D	breast:	n/a
9	chr11:77644765-77644815	SK-N-MC	brain:	n/a
10	chr11:77644765-77644815	PANC-1	pancreas:	n/a
11	chr11:77644765-77644815	HCT-116	colon:	n/a
12	chr11:77644765-77644815	Hela-S3	cervix:	n/a
13	chr11:77644765-77644815	GM12892	blood:	n/a
14	chr11:77644765-77644815	HRE	kidney:	n/a
15	chr11:77644765-77644815	SAEC	small airway:	n/a
16	chr11:77644765-77644815	BJ	skin:	n/a
17	chr11:77644765-77644815	HCM	heart:	n/a
18	chr11:77644765-77644815	HIPEpiC	eye:	n/a
19	chr11:77644765-77644815	HNPCEpiC	eye:	n/a
20	chr11:77644765-77644815	NHBE	bronchial:	n/a
21	chr11:77644765-77644815	H1-hESC	embryonic stem cell:	embryo
22	chr11:77644765-77644815	K562	blood:	n/a
23	chr11:77644765-77644815	HEEpiC	esophagus:	n/a
24	chr11:77644765-77644815	SK-N-SH_RA	brain:	n/a
25	chr11:77644765-77644815	HRCEpiC	kidney:	n/a
26	chr11:77644765-77644815	HCF	heart:	n/a
27	chr11:77644765-77644815	GM06990	blood:	n/a
28	chr11:77644765-77644815	HUVEC	blood vessel:	n/a
29	chr11:77644765-77644815	SK-N-SH	brain:	n/a
30	chr11:77644765-77644815	LNCaP	prostate:	n/a
31	chr11:77644765-77644815	SKMC	muscle:	n/a
32	chr11:77644765-77644815	PFSK-1	brain:	n/a
33	chr11:77644765-77644815	Caco-2	colon:	n/a
34	chr11:77644765-77644815	HAEpiC	amniotic membrane:	n/a
35	chr11:77644765-77644815	CMK	blood:	n/a
36	chr11:77644765-77644815	HCPEpiC	choroid plexus:	n/a
37	chr11:77644765-77644815	AG10803	skin:	n/a
38	chr11:77644765-77644815	GM12891	blood:	n/a
39	chr11:77644765-77644815	U87	brain:	n/a
40	chr11:77644765-77644815	A549	lung:	n/a
41	chr11:77644765-77644815	Jurkat	blood:	n/a
42	chr11:77644765-77644815	NT2-D1	testis:	n/a
43	chr11:77644765-77644815	RPTEC	kidney:	n/a
44	chr11:77644765-77644815	HepG2	liver:	n/a
45	chr11:77644765-77644815	HPAEpiC	pulmonary alveolar:	n/a
46	chr11:77644765-77644815	AG04449	skin:	fetal
47	chr11:77644765-77644815	PrEC	prostate:	n/a
48	chr11:77644765-77644815	ECC-1	luminal epithelium:	n/a
49	chr11:77644765-77644815	GM12878	blood:	n/a
50	chr11:77644765-77644815	ProgFib	skin:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:77668893..77671876-chr11:77671949..77673818,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000255115	TF binding region
INTS4	TF binding region
ENSG00000255115	CpG island
INTS4	CpG island

Extended variants
information (count: 1613 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1613 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138819913	chr11:77628108-77628109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564653293	chr11:77628140-77628141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530858109	chr11:77628237-77628238	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371047109	chr11:77628252-77628253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182517205	chr11:77628265-77628266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2511453	chr11:77628311-77628312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573351402	chr11:77628340-77628341	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187916907	chr11:77628342-77628343	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540759565	chr11:77628359-77628360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561829810	chr11:77628365-77628366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs59309476	chr11:77628366-77628367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113356411	chr11:77628373-77628374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs397939338	chr11:77628377-77628378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566197071	chr11:77628402-77628403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192204101	chr11:77628412-77628413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201272871	chr11:77628450-77628451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs398076053	chr11:77628451-77628452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558151420	chr11:77628462-77628463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145636860	chr11:77628474-77628475	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544137182	chr11:77628563-77628564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557640317	chr11:77628564-77628565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138234017	chr11:77628603-77628604	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183622444	chr11:77628608-77628609	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs373585849	chr11:77628656-77628657	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184360555	chr11:77628675-77628676	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188906529	chr11:77628731-77628732	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563257163	chr11:77628748-77628749	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs148762573	chr11:77628811-77628812	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs530793536	chr11:77628910-77628911	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs564914859	chr11:77628947-77628948	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs55962013	chr11:77628968-77628969	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs145073695	chr11:77629053-77629054	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs192451282	chr11:77629069-77629070	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs529919921	chr11:77629118-77629119	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs60400274	chr11:77629132-77629133	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs397702235	chr11:77629133-77629134	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs368331961	chr11:77629163-77629164	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566518328	chr11:77629180-77629181	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184498221	chr11:77629248-77629249	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557929411	chr11:77629254-77629255	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568143396	chr11:77629267-77629268	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs201084439	chr11:77629272-77629273	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571617997	chr11:77629286-77629287	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs76262866	chr11:77629314-77629315	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs75169853	chr11:77629315-77629316	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537488968	chr11:77629320-77629321	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557381877	chr11:77629328-77629329	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs367618437	chr11:77629352-77629353	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188752759	chr11:77629359-77629360	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372140943	chr11:77629417-77629418	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	20932292	CNVD
Cancer	20164920	CNVD
Ovarian cancer	20844748	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Colorectal cancer	16912164	CNVD
Mental retardation	17847001	CNVD
Melanoma	19509136	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Ovarian cancer	21720365	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:77577400-77630800	Weak transcription	Fetal Heart	heart
2	chr11:77583400-77670600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr11:77583400-77690000	Weak transcription	Colonic Mucosa	Colon
4	chr11:77591800-77650400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr11:77592800-77690000	Weak transcription	Small Intestine	intestine
6	chr11:77595800-77671000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr11:77597600-77629400	Weak transcription	Brain Germinal Matrix	brain
8	chr11:77597800-77629000	Weak transcription	Aorta	Aorta
9	chr11:77597800-77633800	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr11:77597800-77644200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr11:77597800-77644400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr11:77597800-77669800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr11:77597800-77671000	Weak transcription	Fetal Brain Male	brain
14	chr11:77597800-77678200	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr11:77597800-77690000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr11:77597800-77690000	Weak transcription	Esophagus	oesophagus
17	chr11:77597800-77690000	Weak transcription	Gastric	stomach
18	chr11:77601800-77629800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr11:77602000-77640600	Weak transcription	K562	blood
20	chr11:77602600-77644200	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr11:77602800-77690000	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr11:77603000-77637400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr11:77603200-77650200	Weak transcription	Fetal Brain Female	brain
24	chr11:77604800-77644200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr11:77612600-77637000	Weak transcription	Brain Anterior Caudate	brain
26	chr11:77614600-77629200	Weak transcription	Lung	lung
27	chr11:77614800-77638800	Weak transcription	Brain Angular Gyrus	brain
28	chr11:77614800-77700200	Weak transcription	Psoas Muscle	Psoas
29	chr11:77615000-77644200	Weak transcription	Spleen	Spleen
30	chr11:77615000-77656400	Weak transcription	Right Ventricle	heart
31	chr11:77615200-77637400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr11:77618200-77668200	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr11:77618400-77629000	Weak transcription	Left Ventricle	heart
34	chr11:77618800-77629000	Weak transcription	Fetal Muscle Leg	muscle
35	chr11:77618800-77635000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr11:77618800-77637200	Weak transcription	Brain Cingulate Gyrus	brain
37	chr11:77618800-77644200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr11:77619000-77628200	Weak transcription	Fetal Thymus	thymus
39	chr11:77619000-77636600	Weak transcription	Placenta	Placenta
40	chr11:77619000-77667000	Weak transcription	Fetal Kidney	kidney
41	chr11:77619000-77668000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr11:77619200-77637200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr11:77619200-77637400	Weak transcription	GM12878-XiMat	blood
44	chr11:77620800-77628600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr11:77620800-77642000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr11:77621800-77631200	Strong transcription	Primary monocytes fromperipheralblood	blood
47	chr11:77622200-77630200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr11:77622200-77635600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr11:77622600-77636800	Weak transcription	Primary B cells from cord blood	blood
50	chr11:77622800-77634000	Weak transcription	Fetal Intestine Large	intestine

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