Variant report

Variant	nsv524537
Chromosome Location	chr11:77583266-77593221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:161)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr11:77591413-77591582	K562	blood:	n/a	n/a
2	CEBPB	chr11:77590230-77590605	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr11:77590271-77590494	IMR90	lung:	n/a	n/a
4	CTCF	chr11:77590360-77590510	HFF	foreskin:	n/a	n/a
5	CTCF	chr11:77590520-77590670	A549	lung:	n/a	n/a
6	CTCF	chr11:77590300-77590450	AoAF	blood vessel:	n/a	n/a
7	CTCF	chr11:77590480-77590630	GM12873	blood:	n/a	n/a
8	CTCF	chr11:77590420-77590570	BJ	skin:	n/a	n/a
9	CTCF	chr11:77590200-77590350	K562	blood:	n/a	n/a
10	CTCF	chr11:77590500-77590650	GM12872	blood:	n/a	n/a
11	CTCF	chr11:77590540-77590690	AG10803	skin:	n/a	n/a
12	CTCF	chr11:77590240-77590390	AG09319	gingival:	n/a	n/a
13	CTCF	chr11:77590240-77590390	GM12864	blood:	n/a	n/a
14	CTCF	chr11:77590220-77590370	AG04449	skin:	n/a	n/a
15	CTCF	chr11:77590460-77590610	BE2_C	brain:	n/a	n/a
16	CTCF	chr11:77590540-77590690	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr11:77590320-77590470	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr11:77590480-77590630	GM12874	blood:	n/a	n/a
19	CTCF	chr11:77590300-77590450	HCFaa	heart:	n/a	n/a
20	CTCF	chr11:77590600-77590750	AoAF	blood vessel:	n/a	n/a
21	CTCF	chr11:77590360-77590510	HMEC	breast:	n/a	n/a
22	CTCF	chr11:77590380-77590530	MCF-7	breast:	n/a	n/a
23	CTCF	chr11:77590440-77590590	HA-sp	spinal cord:	n/a	n/a
24	CTCF	chr11:77590260-77590410	AG10803	skin:	n/a	n/a
25	CTCF	chr11:77590420-77590570	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr11:77590500-77590650	GM12873	blood:	n/a	n/a
27	CTCF	chr11:77590316-77590622	K562	blood:	n/a	n/a
28	CTCF	chr11:77590360-77590510	HCM	heart:	n/a	n/a
29	CTCF	chr11:77590280-77590430	GM12864	blood:	n/a	n/a
30	CTCF	chr11:77590380-77590530	GM06990	blood:	n/a	n/a
31	CTCF	chr11:77590460-77590610	GM12878	blood:	n/a	n/a
32	CTCF	chr11:77590400-77590550	GM12868	blood:	n/a	n/a
33	CTCF	chr11:77590500-77590650	Caco-2	colon:	n/a	n/a
34	CTCF	chr11:77590360-77590510	GM12866	blood:	n/a	n/a
35	CTCF	chr11:77590420-77590570	GM12871	blood:	n/a	n/a
36	CTCF	chr11:77590240-77590390	GM12872	blood:	n/a	n/a
37	CTCF	chr11:77590300-77590450	GM12870	blood:	n/a	n/a
38	CTCF	chr11:77590180-77590330	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr11:77590580-77590730	GM12868	blood:	n/a	n/a
40	CTCF	chr11:77590460-77590610	MCF-7	breast:	n/a	n/a
41	CTCF	chr11:77590280-77590430	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr11:77590560-77590710	GM12868	blood:	n/a	n/a
43	CTCF	chr11:77591320-77591470	GM12873	blood:	n/a	n/a
44	CTCF	chr11:77590400-77590550	GM12873	blood:	n/a	n/a
45	CTCF	chr11:77590180-77590330	GM12871	blood:	n/a	n/a
46	CTCF	chr11:77590300-77590450	HMF	breast:	n/a	n/a
47	CTCF	chr11:77590480-77590630	GM12865	blood:	n/a	n/a
48	CTCF	chr11:77590320-77590470	GM12865	blood:	n/a	n/a
49	CTCF	chr11:77590420-77590570	AG04450	lung:	n/a	n/a
50	CTCF	chr11:77590520-77590670	HMF	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:77589972-77590022	GM12878	blood:	n/a
2	chr11:77589972-77590022	PANC-1	pancreas:	n/a
3	chr11:77589972-77590022	NB4	blood:	n/a
4	chr11:77589972-77590022	HCF	heart:	n/a
5	chr11:77589972-77590022	HRCEpiC	kidney:	n/a
6	chr11:77589972-77590022	Hela-S3	cervix:	n/a
7	chr11:77589972-77590022	SK-N-MC	brain:	n/a
8	chr11:77589972-77590022	AG04449	skin:	fetal
9	chr11:77589972-77590022	SKMC	muscle:	n/a
10	chr11:77589972-77590022	AG04450	lung:	fetal
11	chr11:77589972-77590022	Jurkat	blood:	n/a
12	chr11:77589972-77590022	HNPCEpiC	eye:	n/a
13	chr11:77589972-77590022	HCPEpiC	choroid plexus:	n/a
14	chr11:77589972-77590022	RPTEC	kidney:	n/a
15	chr11:77589972-77590022	BJ	skin:	n/a
16	chr11:77589972-77590022	SK-N-SH	brain:	n/a
17	chr11:77589972-77590022	T-47D	breast:	n/a
18	chr11:77589972-77590022	PrEC	prostate:	n/a
19	chr11:77589972-77590022	K562	blood:	n/a
20	chr11:77589972-77590022	AoSMC	blood vessel:	n/a
21	chr11:77589972-77590022	NHBE	bronchial:	n/a
22	chr11:77589972-77590022	GM19239	blood:	n/a
23	chr11:77589972-77590022	ProgFib	skin:	n/a
24	chr11:77589972-77590022	NHDF-neo	bronchial:	n/a
25	chr11:77589972-77590022	MCF-7	breast:	n/a
26	chr11:77589972-77590022	HL-60	blood:	n/a
27	chr11:77589972-77590022	HAEpiC	amniotic membrane:	n/a
28	chr11:77589972-77590022	SK-N-SH_RA	brain:	n/a
29	chr11:77589972-77590022	U87	brain:	n/a
30	chr11:77589972-77590022	HUVEC	blood vessel:	n/a
31	chr11:77589972-77590022	GM12892	blood:	n/a
32	chr11:77589972-77590022	GM06990	blood:	n/a
33	chr11:77589972-77590022	CMK	blood:	n/a
34	chr11:77589972-77590022	Hepatocyte	liver:	n/a
35	chr11:77589972-77590022	MCF10A-Er-Src	breast:	n/a
36	chr11:77589972-77590022	ovcar-3	ovarian:	n/a
37	chr11:77589972-77590022	HEK293	kidney:	embryo
38	chr11:77589972-77590022	HPAEpiC	pulmonary alveolar:	n/a
39	chr11:77589972-77590022	ECC-1	luminal epithelium:	n/a
40	chr11:77589972-77590022	A549	lung:	n/a
41	chr11:77589972-77590022	HRE	kidney:	n/a
42	chr11:77589972-77590022	HRPEpiC	eye:	n/a
43	chr11:77589972-77590022	HIPEpiC	eye:	n/a
44	chr11:77589972-77590022	PFSK-1	brain:	n/a
45	chr11:77589972-77590022	HEEpiC	esophagus:	n/a
46	chr11:77589972-77590022	Caco-2	colon:	n/a
47	chr11:77589972-77590022	AG09309	skin:	n/a
48	chr11:77589972-77590022	NT2-D1	testis:	n/a
49	chr11:77589972-77590022	BE2_C	brain:	n/a
50	chr11:77589972-77590022	GM12891	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:77581791..77584975-chr11:77585313..77588016,3	K562	blood:
2	chr11:77588081..77589729-chr11:77591308..77593403,2	K562	blood:
3	chr11:77578952..77581707-chr11:77586888..77589735,2	K562	blood:
4	chr11:77581791..77584975-chr11:77585313..77588016,3	K562	blood:
5	chr11:77588081..77589729-chr11:77591308..77593403,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-INTS4-2	chr11:77583198-77583308	ENSG00000254459.1

No data

Variant related genes	Relation type
AAMDC	TF binding region
ENSG00000241782	TF binding region
ENSG00000254459	TF binding region
ENSG00000255449	TF binding region
AAMDC	CpG island
ENSG00000241782	CpG island
ENSG00000254459	CpG island
ENSG00000255449	CpG island
ENSG00000255449	chromatin interactions
ENSG00000087884	chromatin interactions
ENSG00000254459	chromatin interactions
ENSG00000241782	chromatin interactions

Extended variants
information (count: 347 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2186564	chr11:77583266-77583267	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs368865821	chr11:77583269-77583270	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
3	rs373537906	chr11:77583280-77583281	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
4	rs146747352	chr11:77583313-77583314	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs200436609	chr11:77583341-77583342	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs588217	chr11:77583376-77583377	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs148604757	chr11:77583379-77583380	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs558708060	chr11:77583473-77583474	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs668701	chr11:77583476-77583477	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs555078639	chr11:77583495-77583496	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs61900171	chr11:77583520-77583521	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs186309835	chr11:77583645-77583646	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs191667202	chr11:77583682-77583683	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs574346700	chr11:77583710-77583711	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs540559247	chr11:77583714-77583715	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs559998076	chr11:77583759-77583760	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs182081010	chr11:77583760-77583761	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs545563761	chr11:77583771-77583772	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs667225	chr11:77583855-77583856	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs186678989	chr11:77583907-77583908	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs550795463	chr11:77583927-77583928	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs377281302	chr11:77583938-77583939	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs576395151	chr11:77584034-77584035	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs530028023	chr11:77584092-77584093	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs547301679	chr11:77584106-77584107	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs567141984	chr11:77584113-77584114	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs611671	chr11:77584138-77584139	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs559153869	chr11:77584162-77584163	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs568975668	chr11:77584185-77584186	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs537991069	chr11:77584197-77584198	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs554357154	chr11:77584207-77584208	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs578007535	chr11:77584226-77584227	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs545279884	chr11:77584231-77584232	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs61900172	chr11:77584302-77584303	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs553669590	chr11:77584332-77584333	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs79304074	chr11:77584338-77584339	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs576689325	chr11:77584356-77584357	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs146683617	chr11:77584365-77584366	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs527521814	chr11:77584367-77584368	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs191572984	chr11:77584427-77584428	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs531399410	chr11:77584493-77584494	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs182514774	chr11:77584501-77584502	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs561206026	chr11:77584530-77584531	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs530130097	chr11:77584567-77584568	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs186663776	chr11:77584609-77584610	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs1783546	chr11:77584647-77584648	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs532807059	chr11:77584679-77584680	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs78863560	chr11:77584703-77584704	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs139309631	chr11:77584752-77584753	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs372210587	chr11:77584820-77584821	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	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
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
Ovarian cancer	21720365	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:77566000-77592600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr11:77566200-77589000	Weak transcription	NHLF	lung
3	chr11:77566200-77589600	Weak transcription	Esophagus	oesophagus
4	chr11:77566200-77594600	Weak transcription	Colon Smooth Muscle	Colon
5	chr11:77566800-77587800	Weak transcription	A549	lung
6	chr11:77567000-77586600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr11:77567600-77589600	Weak transcription	HepG2	liver
8	chr11:77567800-77589400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr11:77567800-77594800	Weak transcription	Brain Angular Gyrus	brain
10	chr11:77568000-77586800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr11:77568000-77587000	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr11:77568200-77589400	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr11:77568200-77590400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr11:77568200-77594600	Weak transcription	Fetal Kidney	kidney
15	chr11:77569000-77597600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr11:77574600-77593200	Weak transcription	Gastric	stomach
17	chr11:77576200-77586800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr11:77577200-77583800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr11:77577400-77588800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr11:77577400-77589400	Strong transcription	Fetal Muscle Leg	muscle
21	chr11:77577400-77630800	Weak transcription	Fetal Heart	heart
22	chr11:77578000-77585800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr11:77578200-77589600	Strong transcription	Adipose Nuclei	Adipose
24	chr11:77578400-77586600	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr11:77578400-77589400	Weak transcription	NHDF-Ad	bronchial
26	chr11:77578600-77591400	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr11:77578600-77597400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr11:77578800-77590600	Weak transcription	Hela-S3	cervix
29	chr11:77578800-77601400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr11:77579000-77593200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr11:77579200-77625000	Weak transcription	HMEC	breast
32	chr11:77579400-77589400	Weak transcription	NHEK	skin
33	chr11:77579600-77583400	Strong transcription	Left Ventricle	heart
34	chr11:77579600-77589800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr11:77579800-77583400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr11:77579800-77583400	Strong transcription	Thymus	Thymus
37	chr11:77579800-77583600	Strong transcription	Fetal Muscle Trunk	muscle
38	chr11:77579800-77583600	Strong transcription	Skeletal Muscle Male	skeletal muscle
39	chr11:77579800-77583800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr11:77579800-77583800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr11:77579800-77584400	Strong transcription	Fetal Intestine Large	intestine
42	chr11:77579800-77585200	Strong transcription	Fetal Lung	lung
43	chr11:77579800-77589000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr11:77579800-77589000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr11:77579800-77597800	Strong transcription	Skeletal Muscle Female	skeletal muscle
46	chr11:77580000-77583600	Strong transcription	Primary T cells fromperipheralblood	blood
47	chr11:77580000-77583800	Strong transcription	Duodenum Smooth Muscle	Duodenum
48	chr11:77580000-77584000	Strong transcription	Liver	Liver
49	chr11:77580000-77597800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr11:77580200-77597400	Strong transcription	Monocytes-CD14+_RO01746	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links