Variant report

Variant	nsv469975
Chromosome Location	chr11:85688209-85729372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:286)
CpG islands
(count:0)
Chromatin interactive
region (count:38)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:85717835-85717853	K562	blood:	n/a	n/a
2	ARID3A	chr11:85726451-85726487	K562	blood:	n/a	n/a
3	ATF1	chr11:85719206-85719455	K562	blood:	n/a	n/a
4	BATF	chr11:85699879-85700138	GM12878	blood:	n/a	n/a
5	CEBPB	chr11:85713553-85713792	A549	lung:	n/a	n/a
6	CEBPB	chr11:85700528-85700538	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr11:85713500-85713816	K562	blood:	n/a	n/a
8	CEBPB	chr11:85713624-85713677	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr11:85692541-85692647	K562	blood:	n/a	n/a
10	CEBPB	chr11:85713519-85713841	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr11:85698265-85698327	A549	lung:	n/a	n/a
12	CEBPB	chr11:85726613-85726614	K562	blood:	n/a	n/a
13	CEBPB	chr11:85713540-85713817	IMR90	lung:	n/a	n/a
14	CTCF	chr11:85709897-85709947	MCF-7	breast:	n/a	n/a
15	CTCF	chr11:85709210-85709324	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr11:85709753-85709784	MCF-7	breast:	n/a	n/a
17	CUX1	chr11:85719261-85719341	K562	blood:	n/a	n/a
18	CUX1	chr11:85718055-85718212	K562	blood:	n/a	n/a
19	CUX1	chr11:85727441-85727498	GM12878	blood:	n/a	n/a
20	CUX1	chr11:85726851-85727112	K562	blood:	n/a	chr11:85727024-85727040
21	E2F4	chr11:85689432-85689852	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr11:85725965-85726061	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr11:85699894-85699973	MCF10A-Er-Src	breast:	n/a	n/a
24	EGR1	chr11:85719248-85719461	K562	blood:	n/a	n/a
25	EGR1	chr11:85719195-85719460	K562	blood:	n/a	n/a
26	ELK1	chr11:85716335-85716336	K562	blood:	n/a	n/a
27	EP300	chr11:85719346-85719374	K562	blood:	n/a	n/a
28	FOXA1	chr11:85727564-85727784	T-47D	breast:	n/a	n/a
29	FOXA1	chr11:85727525-85727845	T-47D	breast:	n/a	n/a
30	GATA3	chr11:85701583-85701737	SH-SY5Y	brain:	n/a	n/a
31	HCFC1	chr11:85718954-85718955	K562	blood:	n/a	n/a
32	IRF1	chr11:85723170-85723255	K562	blood:	n/a	n/a
33	IRF1	chr11:85719249-85719352	K562	blood:	n/a	n/a
34	IRF1	chr11:85694480-85694482	K562	blood:	n/a	n/a
35	IRF1	chr11:85714229-85714231	K562	blood:	n/a	n/a
36	JUN	chr11:85718954-85719500	K562	blood:	n/a	n/a
37	JUN	chr11:85688412-85688620	K562	blood:	n/a	n/a
38	JUN	chr11:85696140-85696378	HepG2	liver:	n/a	chr11:85696214-85696226 chr11:85696259-85696268 chr11:85696255-85696268
39	JUN	chr11:85693879-85693977	K562	blood:	n/a	n/a
40	JUND	chr11:85696109-85696433	HepG2	liver:	n/a	chr11:85696214-85696226 chr11:85696259-85696268
41	JUND	chr11:85719162-85719540	K562	blood:	n/a	n/a
42	MAFF	chr11:85702596-85702911	K562	blood:	n/a	chr11:85702737-85702755
43	MAFF	chr11:85729370-85729633	K562	blood:	n/a	n/a
44	MAFF	chr11:85695107-85695289	HepG2	liver:	n/a	n/a
45	MAFF	chr11:85716713-85716874	K562	blood:	n/a	n/a
46	MAFF	chr11:85702589-85702920	HepG2	liver:	n/a	chr11:85702737-85702755
47	MAFF	chr11:85719256-85719404	K562	blood:	n/a	n/a
48	MAFK	chr11:85702605-85702932	IMR90	lung:	n/a	chr11:85702738-85702752 chr11:85702739-85702754 chr11:85702740-85702751 chr11:85702740-85702760 chr11:85702739-85702755 chr11:85702739-85702750 chr11:85702742-85702758 chr11:85702739-85702750
49	MAFK	chr11:85718406-85718524	K562	blood:	n/a	n/a
50	MAFK	chr11:85702585-85702833	K562	blood:	n/a	chr11:85702738-85702752 chr11:85702739-85702754 chr11:85702740-85702751 chr11:85702740-85702760 chr11:85702739-85702755 chr11:85702739-85702750 chr11:85702742-85702758 chr11:85702739-85702750

No data

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:85721705..85724500-chr11:85725494..85727078,2	MCF-7	breast:
2	chr11:85685544..85689773-chr11:85693823..85697719,5	K562	blood:
3	chr11:85702541..85705321-chr11:85738673..85740319,2	K562	blood:
4	chr11:85706920..85709532-chr11:85710356..85714188,3	K562	blood:
5	chr11:85708264..85711014-chr11:85715226..85717341,2	MCF-7	breast:
6	chr11:85722163..85724146-chr11:85731929..85734605,2	K562	blood:
7	chr11:85685544..85689773-chr11:85693823..85697719,5	K562	blood:
8	chr11:85707326..85709532-chr11:85711313..85714188,2	K562	blood:
9	chr11:85708264..85711014-chr11:85715226..85717341,2	MCF-7	breast:
10	chr11:85723939..85728998-chr11:85730873..85735840,5	K562	blood:
11	chr11:85697805..85699832-chr11:85707374..85708928,2	K562	blood:
12	chr11:85726928..85728602-chr11:85729875..85731910,2	K562	blood:
13	chr11:85720851..85723422-chr11:85723803..85726700,2	K562	blood:
14	chr11:85706920..85709532-chr11:85710356..85714188,3	K562	blood:
15	chr11:85690766..85693169-chr11:85693529..85695523,2	K562	blood:
16	chr11:85704658..85706834-chr11:85708165..85710507,4	K562	blood:
17	chr11:85705046..85706635-chr11:85716420..85718688,2	K562	blood:
18	chr11:85720851..85723422-chr11:85723803..85726700,2	K562	blood:
19	chr11:85710067..85712653-chr11:85717011..85721337,4	K562	blood:
20	chr11:85704658..85706834-chr11:85708165..85710507,4	K562	blood:
21	chr11:85693271..85695512-chr11:85698266..85700653,2	K562	blood:
22	chr11:85566679..85569060-chr11:85698600..85700675,2	K562	blood:
23	chr11:85707326..85709532-chr11:85711313..85714188,2	K562	blood:
24	chr11:85712516..85716003-chr11:85725889..85728737,3	K562	blood:
25	chr11:85700649..85702593-chr11:85712728..85715089,2	K562	blood:
26	chr11:85705296..85706834-chr11:85708464..85710286,2	K562	blood:
27	chr11:85705046..85706635-chr11:85716420..85718688,2	K562	blood:
28	chr11:85711253..85714931-chr11:85726869..85728797,3	K562	blood:
29	chr11:85721705..85724500-chr11:85725494..85727078,2	MCF-7	breast:
30	chr11:85705296..85706834-chr11:85708464..85710286,2	K562	blood:
31	chr11:85565205..85567430-chr11:85698598..85700468,2	MCF-7	breast:
32	chr11:85687169..85689223-chr11:85690219..85693440,3	K562	blood:
33	chr11:85690198..85692699-chr11:85699878..85701452,2	K562	blood:
34	chr11:85687169..85689223-chr11:85690219..85693440,3	K562	blood:
35	chr11:85689777..85692184-chr11:85694082..85696432,2	K562	blood:
36	chr11:85700649..85702593-chr11:85712728..85715089,2	K562	blood:
37	chr11:85685478..85688187-chr11:85691942..85693675,2	K562	blood:
38	chr11:85725973..85728229-chr11:85733987..85735840,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC83-1	chr11:85723166-85725382	ENSG00000247103
2	lnc-CCDC83-1	chr11:85718321-85719570	ENSG00000247103

No data

Variant related genes	Relation type
PICALM	TF binding region
ENSG00000150676	chromatin interactions
ENSG00000073921	chromatin interactions
ENSG00000215504	chromatin interactions
LIN28B	miRNA target sites

Extended variants
information (count: 1779 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1779 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs713346	chr11:85688209-85688210	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143057595	chr11:85688226-85688227	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs190867316	chr11:85688272-85688273	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs114285285	chr11:85688289-85688290	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs369686430	chr11:85688319-85688320	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs557278657	chr11:85688338-85688339	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs373835103	chr11:85688360-85688361	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs183687456	chr11:85688384-85688385	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs188554649	chr11:85688399-85688400	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs546271045	chr11:85688427-85688428	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs375910402	chr11:85688517-85688518	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs562616290	chr11:85688538-85688539	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs557865776	chr11:85688547-85688548	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs572681022	chr11:85688551-85688552	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs544711196	chr11:85688580-85688581	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs540010904	chr11:85688619-85688620	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs560108110	chr11:85688647-85688648	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs527264446	chr11:85688660-85688661	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs547273911	chr11:85688682-85688683	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs562204078	chr11:85688683-85688684	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs529491103	chr11:85688806-85688807	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs10898428	chr11:85688893-85688894	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs569045361	chr11:85688915-85688916	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs533268146	chr11:85688916-85688917	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs575994638	chr11:85688917-85688918	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs566864027	chr11:85689050-85689051	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs200457806	chr11:85689068-85689069	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs371402533	chr11:85689093-85689094	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs193085915	chr11:85689103-85689104	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs372053430	chr11:85689113-85689114	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs141993999	chr11:85689131-85689132	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs375351370	chr11:85689171-85689172	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs369526946	chr11:85689172-85689173	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs199558359	chr11:85689175-85689176	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs138593326	chr11:85689180-85689181	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs183128872	chr11:85689214-85689215	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs370802160	chr11:85689218-85689219	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs35715728	chr11:85689230-85689231	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs577876060	chr11:85689248-85689249	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs111447339	chr11:85689250-85689251	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs529145948	chr11:85689290-85689291	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs553539230	chr11:85689296-85689297	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs572016034	chr11:85689299-85689300	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs377457728	chr11:85689309-85689310	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs186913869	chr11:85689379-85689380	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs562073702	chr11:85689391-85689392	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs618639	chr11:85689428-85689429	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs544181592	chr11:85689434-85689435	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs618629	chr11:85689435-85689436	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs569294673	chr11:85689436-85689437	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
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
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	21364760	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ductal carcinoma	22052326	CNVD
Obesity	20622171	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Attention deficit hyperactivity disorder	22241247	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1204 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85659400-85745800	Weak transcription	Stomach Mucosa	stomach
2	chr11:85663400-85692000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr11:85663800-85740200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr11:85664400-85693600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr11:85664400-85699800	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr11:85664400-85726800	Strong transcription	Liver	Liver
7	chr11:85664400-85729000	Strong transcription	Placenta	Placenta
8	chr11:85664600-85693200	Strong transcription	Fetal Thymus	thymus
9	chr11:85664600-85730800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:85664800-85689400	Strong transcription	Primary B cells from cord blood	blood
11	chr11:85664800-85733000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr11:85665200-85742600	Strong transcription	Primary T helper cells fromperipheralblood	blood
13	chr11:85665200-85743000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr11:85665400-85699800	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr11:85665800-85699600	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr11:85665800-85701200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr11:85665800-85711400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:85666000-85735800	Strong transcription	Primary T helper cells PMA-I stimulated	--
19	chr11:85666400-85693600	Strong transcription	Primary hematopoietic stem cells	blood
20	chr11:85667800-85701800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr11:85667800-85712000	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr11:85668000-85691400	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr11:85670000-85715800	Weak transcription	Colonic Mucosa	Colon
24	chr11:85671800-85710600	Weak transcription	Psoas Muscle	Psoas
25	chr11:85673200-85702800	Weak transcription	Small Intestine	intestine
26	chr11:85674000-85695200	Strong transcription	HSMM	muscle
27	chr11:85674000-85708600	Strong transcription	K562	blood
28	chr11:85674200-85715400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr11:85675000-85693200	Strong transcription	Rectal Mucosa Donor 31	rectum
30	chr11:85675000-85742600	Strong transcription	Primary B cells from peripheral blood	blood
31	chr11:85675200-85700000	Strong transcription	GM12878-XiMat	blood
32	chr11:85675400-85693200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr11:85675600-85693000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr11:85677800-85709600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr11:85678000-85690200	Weak transcription	Pancreas	Pancrea
36	chr11:85679400-85688600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr11:85679800-85697000	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr11:85680000-85693600	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr11:85680600-85731600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr11:85680800-85708400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr11:85680800-85714400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:85680800-85725600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:85681000-85693400	Strong transcription	HUES6 Cell Line	embryonic stem cell
44	chr11:85681000-85694600	Strong transcription	NHDF-Ad	bronchial
45	chr11:85681000-85701800	Strong transcription	Duodenum Mucosa	Duodenum
46	chr11:85681000-85725800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr11:85681000-85729400	Strong transcription	NH-A	brain
48	chr11:85681200-85693000	Strong transcription	Left Ventricle	heart
49	chr11:85681200-85693200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr11:85681200-85696200	Strong transcription	Rectal Mucosa Donor 29	rectum

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