Variant report

Variant	nsv975951
Chromosome Location	chr11:77440719-77446428
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:123)
CpG islands
(count:246)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:123 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr11:77441723-77442240	K562	blood:	n/a	n/a
2	CBX3	chr11:77441791-77442117	K562	blood:	n/a	n/a
3	CCNT2	chr11:77446058-77446258	K562	blood:	n/a	chr11:77446198-77446207
4	CEBPB	chr11:77440380-77440768	IMR90	lung:	n/a	chr11:77440504-77440515 chr11:77440746-77440759 chr11:77440503-77440516
5	CEBPB	chr11:77445421-77445721	K562	blood:	n/a	n/a
6	CEBPB	chr11:77440324-77440763	HepG2	liver:	n/a	chr11:77440504-77440515 chr11:77440746-77440759 chr11:77440503-77440516
7	CEBPB	chr11:77444875-77445075	A549	lung:	n/a	n/a
8	CTCF	chr11:77442988-77443033	MCF-7	breast:	n/a	n/a
9	CTCF	chr11:77442964-77443033	MCF-7	breast:	n/a	n/a
10	CTCF	chr11:77442840-77442990	HEK293	kidney:	n/a	n/a
11	CTCF	chr11:77442966-77443044	HepG2	liver:	n/a	n/a
12	CTCF	chr11:77442951-77443033	ProgFib	skin:	n/a	n/a
13	CTCF	chr11:77442974-77443057	MCF-7	breast:	n/a	n/a
14	CTCF	chr11:77443060-77443210	A549	lung:	n/a	n/a
15	CTCF	chr11:77442860-77443010	GM12871	blood:	n/a	n/a
16	FOXA1	chr11:77443135-77443499	HepG2	liver:	n/a	n/a
17	FOXA1	chr11:77443192-77443526	HepG2	liver:	n/a	n/a
18	FOXA1	chr11:77443177-77443550	HepG2	liver:	n/a	n/a
19	FOXA2	chr11:77443189-77443444	HepG2	liver:	n/a	n/a
20	GATA2	chr11:77445341-77445796	K562	blood:	n/a	n/a
21	HEY1	chr11:77445513-77445733	HepG2	liver:	n/a	n/a
22	HEY1	chr11:77446011-77446315	K562	blood:	n/a	n/a
23	HEY1	chr11:77446005-77446321	HepG2	liver:	n/a	n/a
24	HEY1	chr11:77446144-77446303	K562	blood:	n/a	n/a
25	HEY1	chr11:77445334-77445923	K562	blood:	n/a	n/a
26	HEY1	chr11:77446162-77446285	HepG2	liver:	n/a	n/a
27	IRF4	chr11:77445519-77445903	GM12878	blood:	n/a	n/a
28	JUN	chr11:77446323-77446382	HepG2	liver:	n/a	chr11:77446353-77446362 chr11:77446349-77446362
29	JUND	chr11:77446334-77446386	HepG2	liver:	n/a	chr11:77446353-77446362
30	JUND	chr11:77446170-77446280	HepG2	liver:	n/a	n/a
31	KAP1	chr11:77441547-77442091	K562	blood:	n/a	n/a
32	MYC	chr11:77446071-77446113	MCF-7	breast:	n/a	n/a
33	MYC	chr11:77446123-77446133	MCF-7	breast:	n/a	n/a
34	MYC	chr11:77444706-77444765	MCF-7	breast:	n/a	n/a
35	MYC	chr11:77444717-77444786	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr11:77445959-77446096	A549	lung:	n/a	n/a
37	POLR2A	chr11:77445359-77446408	GM12892	blood:	n/a	n/a
38	POLR2A	chr11:77442957-77443284	GM12878	blood:	n/a	n/a
39	POLR2A	chr11:77445353-77445792	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr11:77442422-77442596	GM12878	blood:	n/a	n/a
41	POLR2A	chr11:77446142-77446265	HepG2	liver:	n/a	n/a
42	POLR2A	chr11:77442912-77443650	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr11:77445394-77446359	GM12892	blood:	n/a	n/a
44	POLR2A	chr11:77446102-77446321	GM12892	blood:	n/a	n/a
45	POLR2A	chr11:77442987-77442996	MCF-7	breast:	n/a	n/a
46	POLR2A	chr11:77444708-77444737	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr11:77446164-77446264	A549	lung:	n/a	n/a
48	POLR2A	chr11:77445413-77445575	GM12878	blood:	n/a	n/a
49	POLR2A	chr11:77445971-77446374	GM12891	blood:	n/a	n/a
50	POLR2A	chr11:77446010-77446412	GM12891	blood:	n/a	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:77443626-77443676	T-47D	breast:	n/a
2	chr11:77443626-77443676	HRCEpiC	kidney:	n/a
3	chr11:77443626-77443676	T-47D	breast:	n/a
4	chr11:77443626-77443676	HRCEpiC	kidney:	n/a
5	chr11:77443626-77443676	NHDF-neo	bronchial:	n/a
6	chr11:77443626-77443676	GM12878	blood:	n/a
7	chr11:77446159-77446209	HMEC	breast:	n/a
8	chr11:77443626-77443676	SK-N-MC	brain:	n/a
9	chr11:77443626-77443676	HNPCEpiC	eye:	n/a
10	chr11:77446074-77446124	K562	blood:	n/a
11	chr11:77446074-77446124	SKMC	muscle:	n/a
12	chr11:77445972-77446022	HEEpiC	esophagus:	n/a
13	chr11:77443626-77443676	HUVEC	blood vessel:	n/a
14	chr11:77446074-77446124	HIPEpiC	eye:	n/a
15	chr11:77446074-77446124	RPTEC	kidney:	n/a
16	chr11:77446159-77446209	NT2-D1	testis:	n/a
17	chr11:77446159-77446209	HAEpiC	amniotic membrane:	n/a
18	chr11:77446159-77446209	AG04449	skin:	fetal
19	chr11:77443626-77443676	HCM	heart:	n/a
20	chr11:77443626-77443676	IMR90	lung:	fetal
21	chr11:77446074-77446124	HRCEpiC	kidney:	n/a
22	chr11:77446074-77446124	AG04450	lung:	fetal
23	chr11:77445972-77446022	HRCEpiC	kidney:	n/a
24	chr11:77446074-77446124	PrEC	prostate:	n/a
25	chr11:77445972-77446022	HCT-116	colon:	n/a
26	chr11:77446159-77446209	HRCEpiC	kidney:	n/a
27	chr11:77446074-77446124	HCT-116	colon:	n/a
28	chr11:77443626-77443676	SAEC	small airway:	n/a
29	chr11:77446159-77446209	BE2_C	brain:	n/a
30	chr11:77445972-77446022	AG04450	lung:	fetal
31	chr11:77446074-77446124	HEEpiC	esophagus:	n/a
32	chr11:77445972-77446022	ovcar-3	ovarian:	n/a
33	chr11:77443626-77443676	GM19239	blood:	n/a
34	chr11:77446159-77446209	HCPEpiC	choroid plexus:	n/a
35	chr11:77445972-77446022	AG10803	skin:	n/a
36	chr11:77446074-77446124	ECC-1	luminal epithelium:	n/a
37	chr11:77445972-77446022	Hepatocyte	liver:	n/a
38	chr11:77446159-77446209	Jurkat	blood:	n/a
39	chr11:77446159-77446209	A549	lung:	n/a
40	chr11:77445972-77446022	AG09309	skin:	n/a
41	chr11:77443626-77443676	HCF	heart:	n/a
42	chr11:77446159-77446209	LNCaP	prostate:	n/a
43	chr11:77446074-77446124	HepG2	liver:	n/a
44	chr11:77446074-77446124	SK-N-SH	brain:	n/a
45	chr11:77443626-77443676	AG09309	skin:	n/a
46	chr11:77445972-77446022	NHDF-neo	bronchial:	n/a
47	chr11:77446159-77446209	MCF-7	breast:	n/a
48	chr11:77446159-77446209	H1-hESC	embryonic stem cell:	embryo
49	chr11:77446159-77446209	HCM	heart:	n/a
50	chr11:77443626-77443676	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:77440760..77442573-chr11:77444032..77446751,2	K562	blood:
2	chr11:77435507..77439532-chr11:77440099..77442814,3	K562	blood:

No data

Variant related genes	Relation type
RSF1	TF binding region
FTH1P16	TF binding region
RSF1	CpG island
FTH1P16	CpG island
ENSG00000048649	chromatin interactions
ENSG00000227376	chromatin interactions

Extended variants
information (count: 233 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:233 , 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	rs368214780	chr11:77440821-77440822	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs532447204	chr11:77440831-77440832	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs546453222	chr11:77440875-77440876	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs563207418	chr11:77440929-77440930	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs558224162	chr11:77440940-77440941	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs398045289	chr11:77440968-77440969	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs188321626	chr11:77440974-77440975	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs548768182	chr11:77440998-77440999	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs568676904	chr11:77441010-77441011	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs527342211	chr11:77441022-77441023	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs142669780	chr11:77441032-77441033	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs570426211	chr11:77441046-77441047	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs370526040	chr11:77441053-77441054	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs539091955	chr11:77441058-77441059	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs556024362	chr11:77441061-77441062	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs569580097	chr11:77441073-77441074	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs35476484	chr11:77441081-77441082	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs146902381	chr11:77441084-77441085	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs372004070	chr11:77441095-77441096	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs77351563	chr11:77441118-77441119	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs572187068	chr11:77441137-77441138	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs529515111	chr11:77441182-77441183	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs554001072	chr11:77441205-77441206	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs118094644	chr11:77441302-77441303	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs562889813	chr11:77441313-77441314	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs531993637	chr11:77441321-77441322	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs542552229	chr11:77441330-77441331	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs562301273	chr11:77441340-77441341	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs7109199	chr11:77441382-77441383	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs547448697	chr11:77441428-77441429	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs570489884	chr11:77441429-77441430	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs375808938	chr11:77441447-77441448	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs549338725	chr11:77441485-77441486	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs114080355	chr11:77441569-77441570	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs535352606	chr11:77441571-77441572	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs2154988	chr11:77441591-77441592	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs575950341	chr11:77441646-77441647	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs191802917	chr11:77441658-77441659	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs543451327	chr11:77441691-77441692	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs183935648	chr11:77441711-77441712	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs186798851	chr11:77441718-77441719	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs3949117	chr11:77441721-77441722	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs557946365	chr11:77441722-77441723	ZNF genes & repeats Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs577237128	chr11:77441741-77441742	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs539939115	chr11:77441766-77441767	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs370728976	chr11:77441772-77441773	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs138688335	chr11:77441803-77441804	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs191270227	chr11:77441846-77441847	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs185708359	chr11:77441848-77441849	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs562274416	chr11:77441851-77441852	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
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	21240255	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
Breast cancer	17142309	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

Chromatin state (count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:77391600-77442000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr11:77394600-77441800	Weak transcription	Spleen	Spleen
3	chr11:77394600-77445600	Weak transcription	Esophagus	oesophagus
4	chr11:77394600-77458800	Weak transcription	Small Intestine	intestine
5	chr11:77394800-77462600	Weak transcription	Fetal Heart	heart
6	chr11:77403200-77442200	Weak transcription	Brain Anterior Caudate	brain
7	chr11:77404600-77441800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr11:77407200-77448000	Weak transcription	K562	blood
9	chr11:77409400-77441600	Weak transcription	Brain Hippocampus Middle	brain
10	chr11:77409600-77441800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr11:77409600-77453400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr11:77409600-77458800	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr11:77409600-77478200	Weak transcription	Brain Angular Gyrus	brain
14	chr11:77409800-77441600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:77409800-77441600	Weak transcription	Aorta	Aorta
16	chr11:77409800-77441800	Weak transcription	Colon Smooth Muscle	Colon
17	chr11:77410400-77477600	Weak transcription	Brain Substantia Nigra	brain
18	chr11:77412800-77441800	Weak transcription	Fetal Brain Male	brain
19	chr11:77416800-77441600	Weak transcription	HMEC	breast
20	chr11:77416800-77441800	Weak transcription	NHEK	skin
21	chr11:77417200-77442000	Weak transcription	HUVEC	blood vessel
22	chr11:77417800-77441600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr11:77418400-77441600	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr11:77422200-77441600	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr11:77424400-77442000	Weak transcription	Right Ventricle	heart
26	chr11:77428600-77442000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr11:77431600-77482400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr11:77433800-77441800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr11:77434800-77442200	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr11:77435000-77441200	Weak transcription	Hela-S3	cervix
31	chr11:77436000-77441600	Weak transcription	Fetal Intestine Small	intestine
32	chr11:77436000-77441800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr11:77436000-77441800	Weak transcription	Brain Germinal Matrix	brain
34	chr11:77436000-77441800	Weak transcription	Fetal Lung	lung
35	chr11:77436000-77441800	Weak transcription	Psoas Muscle	Psoas
36	chr11:77436000-77442200	Weak transcription	Fetal Stomach	stomach
37	chr11:77436000-77442600	Weak transcription	Pancreas	Pancrea
38	chr11:77436200-77441600	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr11:77436200-77441600	Weak transcription	Primary B cells from cord blood	blood
40	chr11:77436200-77441600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr11:77436200-77441600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr11:77436200-77441600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr11:77436200-77441600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr11:77436200-77441600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr11:77436200-77441600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr11:77436200-77441600	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr11:77436200-77441800	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr11:77436200-77441800	Weak transcription	Primary hematopoietic stem cells	blood
49	chr11:77436200-77441800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr11:77436200-77441800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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