Variant report

Variant	nsv8841
Chromosome Location	chr11:77641044-77692578
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:143)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:143 , 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	chr11:77641440-77641752	K562	blood:	n/a	n/a
3	ATF1	chr11:77670535-77670626	K562	blood:	n/a	n/a
4	ATF1	chr11:77669656-77669978	K562	blood:	n/a	n/a
5	BATF	chr11:77653598-77653788	GM12878	blood:	n/a	chr11:77653715-77653726 chr11:77653656-77653667
6	BATF	chr11:77653561-77653797	GM12878	blood:	n/a	chr11:77653715-77653726 chr11:77653656-77653667
7	CBX3	chr11:77684643-77685007	K562	blood:	n/a	n/a
8	CEBPB	chr11:77692430-77692753	IMR90	lung:	n/a	n/a
9	CEBPB	chr11:77692481-77692693	K562	blood:	n/a	n/a
10	CEBPB	chr11:77674619-77674936	K562	blood:	n/a	chr11:77674785-77674796
11	CEBPB	chr11:77653642-77653684	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr11:77674647-77674848	HepG2	liver:	n/a	chr11:77674785-77674796
13	CEBPB	chr11:77674676-77674915	K562	blood:	n/a	chr11:77674785-77674796
14	CEBPB	chr11:77641436-77641668	Hela-S3	cervix:	n/a	chr11:77641529-77641546
15	CEBPB	chr11:77670427-77670742	IMR90	lung:	n/a	n/a
16	CEBPB	chr11:77692456-77692714	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr11:77653478-77653849	IMR90	lung:	n/a	chr11:77653512-77653523
18	CEBPB	chr11:77678765-77679076	MCF-7	breast:	n/a	chr11:77678968-77678979
19	CEBPB	chr11:77678853-77679048	IMR90	lung:	n/a	chr11:77678968-77678979
20	CEBPB	chr11:77692486-77692697	A549	lung:	n/a	n/a
21	CEBPB	chr11:77678865-77679043	HepG2	liver:	n/a	chr11:77678968-77678979
22	CEBPD	chr11:77669508-77670023	K562	blood:	n/a	n/a
23	CEBPD	chr11:77641374-77641826	K562	blood:	n/a	n/a
24	CTCF	chr11:77685719-77685783	Fibrobl	skin:	n/a	n/a
25	CTCF	chr11:77649902-77650016	GM10248	blood:	n/a	n/a
26	CTCF	chr11:77684968-77685029	Lung_OC	lung:	n/a	n/a
27	CTCF	chr11:77653058-77653097	GM13976	blood:	n/a	n/a
28	CTCF	chr11:77657199-77657280	GM13976	blood:	n/a	n/a
29	CTCF	chr11:77667287-77667296	GM10248	blood:	n/a	n/a
30	CTCF	chr11:77654373-77654423	GM13976	blood:	n/a	n/a
31	CTCF	chr11:77665803-77665887	GM10248	blood:	n/a	n/a
32	CTCF	chr11:77669534-77669609	GM10248	blood:	n/a	n/a
33	CTCF	chr11:77667797-77667921	LNCaP	prostate:	n/a	n/a
34	CTCF	chr11:77669885-77669976	GM20000	blood:	n/a	n/a
35	CTCF	chr11:77654704-77654823	GM13976	blood:	n/a	n/a
36	CTCF	chr11:77667121-77667250	GM10248	blood:	n/a	n/a
37	CTCF	chr11:77669702-77669758	GM10248	blood:	n/a	n/a
38	CTCF	chr11:77646233-77646311	LNCaP	prostate:	n/a	n/a
39	CUX1	chr11:77641510-77641713	K562	blood:	n/a	n/a
40	EGR1	chr11:77669579-77669945	K562	blood:	n/a	n/a
41	EGR1	chr11:77669625-77669870	K562	blood:	n/a	n/a
42	ELF1	chr11:77676748-77676992	K562	blood:	n/a	chr11:77676881-77676894
43	EP300	chr11:77641404-77641658	K562	blood:	n/a	n/a
44	EP300	chr11:77669611-77669989	K562	blood:	n/a	n/a
45	FOS	chr11:77641385-77641741	HUVEC	blood vessel:	n/a	chr11:77641543-77641554 chr11:77641544-77641554 chr11:77641545-77641553
46	FOS	chr11:77652824-77652855	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr11:77663695-77663780	MCF10A-Er-Src	breast:	n/a	chr11:77663736-77663744
48	FOS	chr11:77652831-77652868	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr11:77653648-77653663	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr11:77653611-77653795	MCF10A-Er-Src	breast:	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	ProgFib	skin:	n/a
2	chr11:77644765-77644815	HNPCEpiC	eye:	n/a
3	chr11:77644765-77644815	HRCEpiC	kidney:	n/a
4	chr11:77644765-77644815	Jurkat	blood:	n/a
5	chr11:77644765-77644815	NHDF-neo	bronchial:	n/a
6	chr11:77644765-77644815	Hepatocyte	liver:	n/a
7	chr11:77644765-77644815	SKMC	muscle:	n/a
8	chr11:77644765-77644815	GM12878	blood:	n/a
9	chr11:77644765-77644815	PrEC	prostate:	n/a
10	chr11:77644765-77644815	HL-60	blood:	n/a
11	chr11:77644765-77644815	U87	brain:	n/a
12	chr11:77644765-77644815	K562	blood:	n/a
13	chr11:77644765-77644815	HMEC	breast:	n/a
14	chr11:77644765-77644815	H1-hESC	embryonic stem cell:	embryo
15	chr11:77644765-77644815	ECC-1	luminal epithelium:	n/a
16	chr11:77644765-77644815	CMK	blood:	n/a
17	chr11:77644765-77644815	MCF10A-Er-Src	breast:	n/a
18	chr11:77644765-77644815	AG09309	skin:	n/a
19	chr11:77644765-77644815	GM19239	blood:	n/a
20	chr11:77644765-77644815	RPTEC	kidney:	n/a
21	chr11:77644765-77644815	MCF-7	breast:	n/a
22	chr11:77644765-77644815	HPAEpiC	pulmonary alveolar:	n/a
23	chr11:77644765-77644815	A549	lung:	n/a
24	chr11:77644765-77644815	HRPEpiC	eye:	n/a
25	chr11:77644765-77644815	HEEpiC	esophagus:	n/a
26	chr11:77644765-77644815	Hela-S3	cervix:	n/a
27	chr11:77644765-77644815	GM12891	blood:	n/a
28	chr11:77644765-77644815	SK-N-SH_RA	brain:	n/a
29	chr11:77644765-77644815	T-47D	breast:	n/a
30	chr11:77644765-77644815	BJ	skin:	n/a
31	chr11:77644765-77644815	AG09319	gingival:	n/a
32	chr11:77644765-77644815	PANC-1	pancreas:	n/a
33	chr11:77644765-77644815	HRE	kidney:	n/a
34	chr11:77644765-77644815	LNCaP	prostate:	n/a
35	chr11:77644765-77644815	AoSMC	blood vessel:	n/a
36	chr11:77644765-77644815	PFSK-1	brain:	n/a
37	chr11:77644765-77644815	HCPEpiC	choroid plexus:	n/a
38	chr11:77644765-77644815	SAEC	small airway:	n/a
39	chr11:77644765-77644815	AG04450	lung:	fetal
40	chr11:77644765-77644815	NT2-D1	testis:	n/a
41	chr11:77644765-77644815	ovcar-3	ovarian:	n/a
42	chr11:77644765-77644815	HCT-116	colon:	n/a
43	chr11:77644765-77644815	GM06990	blood:	n/a
44	chr11:77644765-77644815	HCM	heart:	n/a
45	chr11:77644765-77644815	HepG2	liver:	n/a
46	chr11:77644765-77644815	HCF	heart:	n/a
47	chr11:77644765-77644815	SK-N-MC	brain:	n/a
48	chr11:77644765-77644815	HUVEC	blood vessel:	n/a
49	chr11:77644765-77644815	Caco-2	colon:	n/a
50	chr11:77644765-77644815	HAEpiC	amniotic membrane:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:77684778..77687771-chr11:77687903..77690145,2	K562	blood:
2	chr11:77675552..77677954-chr11:77679431..77681605,2	K562	blood:
3	chr11:77692487..77694366-chr11:77703526..77705740,2	K562	blood:
4	chr11:77668893..77671876-chr11:77671949..77673818,2	K562	blood:
5	chr11:77668893..77671876-chr11:77671949..77673818,2	K562	blood:
6	chr11:77683720..77686593-chr11:77691250..77693756,3	K562	blood:
7	chr11:77675552..77677954-chr11:77679431..77681605,2	K562	blood:
8	chr11:77680388..77683002-chr11:77686892..77688723,2	K562	blood:
9	chr11:77683720..77686593-chr11:77691250..77693756,3	K562	blood:
10	chr11:77684778..77687771-chr11:77687903..77690145,2	K562	blood:
11	chr11:77680388..77683002-chr11:77686892..77688723,2	K562	blood:
12	chr11:77691216..77693251-chr11:77709176..77711368,2	MCF-7	breast:

No data

Variant related genes	Relation type
INTS4	TF binding region
INTS4	CpG island
ENSG00000149262	chromatin interactions

Extended variants
information (count: 1936 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1936 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547600063	chr11:77641073-77641074	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs148058278	chr11:77641159-77641160	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs3018411	chr11:77641161-77641162	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs554961230	chr11:77641233-77641234	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555260062	chr11:77641271-77641272	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs11606971	chr11:77641273-77641274	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs540343393	chr11:77641295-77641296	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537797786	chr11:77641327-77641328	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs112779117	chr11:77641355-77641356	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs60509203	chr11:77641359-77641360	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs371403623	chr11:77641399-77641400	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576787564	chr11:77641436-77641437	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs3018167	chr11:77641465-77641466	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs140104448	chr11:77641481-77641482	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531889248	chr11:77641565-77641566	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553474585	chr11:77641572-77641573	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548797706	chr11:77641611-77641612	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368325779	chr11:77641648-77641649	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562107878	chr11:77641693-77641694	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs527402506	chr11:77641706-77641707	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547467522	chr11:77641737-77641738	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372052311	chr11:77641749-77641750	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185048852	chr11:77641764-77641765	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191079835	chr11:77641765-77641766	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569959043	chr11:77641781-77641782	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34535040	chr11:77641797-77641798	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535355741	chr11:77641810-77641811	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555560868	chr11:77641812-77641813	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565692421	chr11:77641813-77641814	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192459988	chr11:77641843-77641844	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34885173	chr11:77641863-77641864	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs398016770	chr11:77641870-77641871	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534312142	chr11:77641872-77641873	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553889821	chr11:77641885-77641886	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184376762	chr11:77641910-77641911	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542226375	chr11:77641972-77641973	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142529736	chr11:77641979-77641980	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183872908	chr11:77641990-77641991	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556123575	chr11:77642077-77642078	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576689036	chr11:77642081-77642082	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375330081	chr11:77642154-77642155	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369898247	chr11:77642191-77642192	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142088248	chr11:77642207-77642208	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560504919	chr11:77642211-77642212	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs145823612	chr11:77642217-77642218	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563275122	chr11:77642316-77642317	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541626755	chr11:77642322-77642323	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564214268	chr11:77642407-77642408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188422236	chr11:77642412-77642413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376515195	chr11:77642428-77642429	Weak transcription Strong transcription	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:1028 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:77583400-77670600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr11:77583400-77690000	Weak transcription	Colonic Mucosa	Colon
3	chr11:77591800-77650400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr11:77592800-77690000	Weak transcription	Small Intestine	intestine
5	chr11:77595800-77671000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr11:77597800-77644200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:77597800-77644400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr11:77597800-77669800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr11:77597800-77671000	Weak transcription	Fetal Brain Male	brain
10	chr11:77597800-77678200	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr11:77597800-77690000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr11:77597800-77690000	Weak transcription	Esophagus	oesophagus
13	chr11:77597800-77690000	Weak transcription	Gastric	stomach
14	chr11:77602600-77644200	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr11:77602800-77690000	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr11:77603200-77650200	Weak transcription	Fetal Brain Female	brain
17	chr11:77604800-77644200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr11:77614800-77700200	Weak transcription	Psoas Muscle	Psoas
19	chr11:77615000-77644200	Weak transcription	Spleen	Spleen
20	chr11:77615000-77656400	Weak transcription	Right Ventricle	heart
21	chr11:77618200-77668200	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr11:77618800-77644200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr11:77619000-77667000	Weak transcription	Fetal Kidney	kidney
24	chr11:77619000-77668000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr11:77620800-77642000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:77625800-77665600	Weak transcription	HSMMtube	muscle
27	chr11:77625800-77697400	Weak transcription	Rectal Smooth Muscle	rectum
28	chr11:77626000-77666200	Weak transcription	Brain Substantia Nigra	brain
29	chr11:77626000-77690000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr11:77626200-77641600	Weak transcription	Osteobl	bone
31	chr11:77626200-77665400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr11:77626200-77689400	Weak transcription	Colon Smooth Muscle	Colon
33	chr11:77626600-77644800	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr11:77626600-77665600	Weak transcription	Ovary	ovary
35	chr11:77626600-77689600	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr11:77626600-77690000	Weak transcription	Pancreas	Pancrea
37	chr11:77627000-77642000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr11:77627000-77645200	Weak transcription	HepG2	liver
39	chr11:77627800-77684800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr11:77628000-77646000	Weak transcription	Primary T cells from cord blood	blood
41	chr11:77628000-77671000	Weak transcription	HSMM	muscle
42	chr11:77628400-77668000	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr11:77629400-77653400	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr11:77629400-77668000	Weak transcription	Aorta	Aorta
45	chr11:77630000-77648000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr11:77630000-77665400	Weak transcription	Lung	lung
47	chr11:77630200-77669600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr11:77630400-77641600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr11:77630400-77642600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr11:77630600-77665400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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