Variant report

Variant	nsv540908
Chromosome Location	chr11:3685149-3751029
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:571)
CpG islands
(count:1161)
Chromatin interactive
region (count:27)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:571 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:3734293-3734360	K562	blood:	n/a	n/a
2	ATF1	chr11:3706112-3706517	K562	blood:	n/a	n/a
3	CEBPB	chr11:3744204-3744817	A549	lung:	n/a	n/a
4	CEBPB	chr11:3744296-3744686	A549	lung:	n/a	n/a
5	CEBPB	chr11:3710806-3711040	A549	lung:	n/a	chr11:3710926-3710937
6	CEBPB	chr11:3695984-3695993	A549	lung:	n/a	n/a
7	CEBPB	chr11:3710824-3710975	K562	blood:	n/a	chr11:3710926-3710937
8	CEBPB	chr11:3710855-3710974	HepG2	liver:	n/a	chr11:3710926-3710937
9	CEBPB	chr11:3749198-3749438	K562	blood:	n/a	n/a
10	CEBPB	chr11:3749136-3749449	A549	lung:	n/a	n/a
11	CEBPB	chr11:3731225-3731991	ECC-1	luminal epithelium:	n/a	chr11:3731793-3731804 chr11:3731793-3731806 chr11:3731793-3731804
12	CEBPB	chr11:3744196-3744772	IMR90	lung:	n/a	n/a
13	CEBPB	chr11:3710860-3710963	H1-hESC	embryonic stem cell:	n/a	chr11:3710926-3710937
14	CEBPB	chr11:3733518-3733812	HepG2	liver:	n/a	n/a
15	CEBPB	chr11:3749110-3749455	HepG2	liver:	n/a	n/a
16	CEBPB	chr11:3744324-3744648	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr11:3731666-3731948	IMR90	lung:	n/a	chr11:3731793-3731804 chr11:3731793-3731806 chr11:3731793-3731804
18	CEBPB	chr11:3749129-3749443	IMR90	lung:	n/a	n/a
19	CEBPB	chr11:3731189-3731574	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr11:3744281-3744729	A549	lung:	n/a	n/a
21	CEBPB	chr11:3731271-3731962	H1-hESC	embryonic stem cell:	n/a	chr11:3731793-3731804 chr11:3731793-3731806 chr11:3731793-3731804
22	CEBPB	chr11:3749260-3749298	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr11:3710788-3711031	Hela-S3	cervix:	n/a	chr11:3710926-3710937
24	CEBPB	chr11:3749258-3749357	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr11:3744580-3744730	AG10803	skin:	n/a	n/a
26	CTCF	chr11:3704238-3704346	MCF-7	breast:	n/a	n/a
27	CTCF	chr11:3704195-3704350	K562	blood:	n/a	n/a
28	CTCF	chr11:3704160-3704310	HCT-116	colon:	n/a	n/a
29	CTCF	chr11:3704257-3704343	HepG2	liver:	n/a	n/a
30	CTCF	chr11:3704200-3704350	HMF	breast:	n/a	n/a
31	CTCF	chr11:3687100-3687250	K562	blood:	n/a	n/a
32	CTCF	chr11:3704200-3704350	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr11:3704200-3704350	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr11:3705274-3705316	LNCaP	prostate:	n/a	n/a
35	CTCF	chr11:3704080-3704290	NHEK	skin:	n/a	n/a
36	CTCF	chr11:3699420-3699570	GM12874	blood:	n/a	n/a
37	CTCF	chr11:3687019-3687356	K562	blood:	n/a	n/a
38	CTCF	chr11:3704160-3704310	A549	lung:	n/a	n/a
39	CTCF	chr11:3697995-3698044	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr11:3704220-3704370	HEK293	kidney:	n/a	n/a
41	CTCF	chr11:3704140-3704290	RPTEC	kidney:	n/a	n/a
42	CTCF	chr11:3704140-3704290	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr11:3704125-3704416	K562	blood:	n/a	n/a
44	CTCF	chr11:3704249-3704340	MCF-7	breast:	n/a	n/a
45	CTCF	chr11:3704245-3704357	Gliobla	brain:	n/a	n/a
46	CTCF	chr11:3744500-3744650	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr11:3704187-3704353	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr11:3744520-3744670	AG10803	skin:	n/a	n/a
49	CTCF	chr11:3704160-3704310	RPTEC	kidney:	n/a	n/a
50	CTCF	chr11:3704240-3704390	HPAF	blood vessel:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:3706578-3706628	HAEpiC	amniotic membrane:	n/a
2	chr11:3686892-3686942	HRE	kidney:	n/a
3	chr11:3706578-3706628	HAEpiC	amniotic membrane:	n/a
4	chr11:3686892-3686942	HRE	kidney:	n/a
5	chr11:3690320-3690370	HEEpiC	esophagus:	n/a
6	chr11:3723921-3723971	HPAEpiC	pulmonary alveolar:	n/a
7	chr11:3688985-3689035	Hepatocyte	liver:	n/a
8	chr11:3685559-3685609	MCF-7	breast:	n/a
9	chr11:3688722-3688772	AG04450	lung:	fetal
10	chr11:3692562-3692612	NT2-D1	testis:	n/a
11	chr11:3706578-3706628	Jurkat	blood:	n/a
12	chr11:3731649-3731699	SK-N-SH	brain:	n/a
13	chr11:3693157-3693207	PANC-1	pancreas:	n/a
14	chr11:3696925-3696975	HEK293	kidney:	embryo
15	chr11:3693157-3693207	Hela-S3	cervix:	n/a
16	chr11:3689006-3689056	GM19239	blood:	n/a
17	chr11:3689006-3689056	PFSK-1	brain:	n/a
18	chr11:3693172-3693222	HMEC	breast:	n/a
19	chr11:3744085-3744135	NH-A	brain:	n/a
20	chr11:3685559-3685609	NT2-D1	testis:	n/a
21	chr11:3692562-3692612	HCF	heart:	n/a
22	chr11:3696925-3696975	AG09319	gingival:	n/a
23	chr11:3692697-3692747	GM12878	blood:	n/a
24	chr11:3733666-3733716	HPAEpiC	pulmonary alveolar:	n/a
25	chr11:3692562-3692612	HRCEpiC	kidney:	n/a
26	chr11:3692697-3692747	NHBE	bronchial:	n/a
27	chr11:3696925-3696975	SAEC	small airway:	n/a
28	chr11:3688985-3689035	CMK	blood:	n/a
29	chr11:3688722-3688772	AG09309	skin:	n/a
30	chr11:3706578-3706628	CMK	blood:	n/a
31	chr11:3690320-3690370	SK-N-SH_RA	brain:	n/a
32	chr11:3696925-3696975	HCT-116	colon:	n/a
33	chr11:3723921-3723971	ovcar-3	ovarian:	n/a
34	chr11:3731649-3731699	AoSMC	blood vessel:	n/a
35	chr11:3692562-3692612	SKMC	muscle:	n/a
36	chr11:3692187-3692237	RPTEC	kidney:	n/a
37	chr11:3696925-3696975	HRE	kidney:	n/a
38	chr11:3685559-3685609	GM19239	blood:	n/a
39	chr11:3693172-3693222	Hela-S3	cervix:	n/a
40	chr11:3731649-3731699	ProgFib	skin:	n/a
41	chr11:3696925-3696975	AG10803	skin:	n/a
42	chr11:3733666-3733716	NHDF-neo	bronchial:	n/a
43	chr11:3692697-3692747	HCM	heart:	n/a
44	chr11:3693157-3693207	HIPEpiC	eye:	n/a
45	chr11:3692697-3692747	HEK293	kidney:	embryo
46	chr11:3688722-3688772	Caco-2	colon:	n/a
47	chr11:3692697-3692747	IMR90	lung:	fetal
48	chr11:3693172-3693222	H1-hESC	embryonic stem cell:	embryo
49	chr11:3693157-3693207	HUVEC	blood vessel:	n/a
50	chr11:3744085-3744135	BJ	skin:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:3715464..3718270-chr11:3722517..3724123,2	K562	blood:
2	chr11:3692006..3695264-chr11:3695478..3698452,4	K562	blood:
3	chr11:3703030..3704815-chr11:3705964..3708347,2	K562	blood:
4	chr11:3707361..3708925-chr11:3714329..3717007,2	K562	blood:
5	chr11:3728202..3731032-chr11:3737163..3739664,2	MCF-7	breast:
6	chr11:3690214..3692780-chr11:3696076..3698742,2	MCF-7	breast:
7	chr11:3705048..3707585-chr11:4118303..4120939,2	K562	blood:
8	chr11:3732805..3734447-chr11:3756261..3757990,2	K562	blood:
9	chr11:3733596..3735433-chr11:3817089..3819371,2	K562	blood:
10	chr11:3728202..3731032-chr11:3737163..3739664,2	MCF-7	breast:
11	chr11:3732732..3736237-chr11:3737365..3740314,3	K562	blood:
12	chr11:3726751..3729655-chr11:3738609..3740778,2	K562	blood:
13	chr11:3692345..3692867-chr15:44084030..44084743,2	NB4	blood:
14	chr11:3690371..3694787-chr11:3695669..3699766,6	K562	blood:
15	chr11:3715464..3719300-chr11:3722517..3725866,4	K562	blood:
16	chr11:3720373..3721894-chr11:3731559..3733138,2	K562	blood:
17	chr11:3720373..3721894-chr11:3731559..3733138,2	K562	blood:
18	chr11:3690371..3694787-chr11:3695669..3699766,6	K562	blood:
19	chr11:3727085..3729822-chr11:3743744..3745444,2	MCF-7	breast:
20	chr11:3692006..3695264-chr11:3695478..3698452,4	K562	blood:
21	chr11:3690214..3692780-chr11:3696076..3698742,2	MCF-7	breast:
22	chr11:3679748..3681336-chr11:3687439..3689154,2	K562	blood:
23	chr11:3696995..3699038-chr11:3705872..3708869,2	MCF-7	breast:
24	chr11:3715464..3719300-chr11:3722517..3725866,4	K562	blood:
25	chr11:3704347..3707149-chr11:3712744..3714293,2	K562	blood:
26	chr11:3715464..3718270-chr11:3722517..3724123,2	K562	blood:
27	chr11:3703030..3704815-chr11:3705964..3708347,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUP98-1	chr11:3690964-3691117	NONHSAT017612
2	lnc-NUP98-1	chr11:3689730-3690580	NONHSAT017612

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NUP98	hsa-miR-98-5p	chr11:3733411-3733432
2	NUP98	hsa-miR-16-5p	chr11:3733110-3733130
3	NUP98	hsa-miR-98-5p	chr11:3733173-3733167
4	NUP98	hsa-miR-98-5p	chr11:3733167-3733187

Variant related genes	Relation type
ENSG00000201279	TF binding region
CHRNA10	TF binding region
NUP98	TF binding region
ENSG00000238686	TF binding region
RNU6-1143P	TF binding region
ENSG00000200201	TF binding region
ENSG00000201279	CpG island
CHRNA10	CpG island
NUP98	CpG island
ENSG00000238686	CpG island
RNU6-1143P	CpG island
ENSG00000200201	CpG island
ENSG00000251934	chromatin interactions
ENSG00000129749	chromatin interactions
ENSG00000148985	chromatin interactions
ENSG00000238686	chromatin interactions
ENSG00000140264	chromatin interactions
ENSG00000110713	chromatin interactions

Extended variants
information (count: 2983 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2983 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113897839	chr11:3685163-3685164	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs550718592	chr11:3685166-3685167	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs569346299	chr11:3685174-3685175	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs182049367	chr11:3685175-3685176	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs186271428	chr11:3685188-3685189	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs143630775	chr11:3685193-3685194	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs534958216	chr11:3685210-3685211	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs553300121	chr11:3685241-3685242	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs372338750	chr11:3685274-3685275	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs375470433	chr11:3685281-3685282	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs148115951	chr11:3685299-3685300	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs115159160	chr11:3685301-3685302	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs375438804	chr11:3685319-3685320	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs147582309	chr11:3685325-3685326	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs140449390	chr11:3685335-3685336	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs369600232	chr11:3685348-3685349	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs372804191	chr11:3685374-3685375	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs36041658	chr11:3685380-3685381	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs545567510	chr11:3685381-3685382	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs199801440	chr11:3685396-3685397	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs547934498	chr11:3685419-3685420	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs572751063	chr11:3685420-3685421	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs141913583	chr11:3685423-3685424	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs2271582	chr11:3685443-3685444	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs373087910	chr11:3685463-3685464	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs566327340	chr11:3685475-3685476	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs373315358	chr11:3685504-3685505	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs550781960	chr11:3685508-3685509	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs190792834	chr11:3685549-3685550	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs199992478	chr11:3685566-3685567	Weak transcription Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs201491149	chr11:3685569-3685570	Weak transcription Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs533500779	chr11:3685572-3685573	Weak transcription Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs551573417	chr11:3685582-3685583	Weak transcription Strong transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs72844387	chr11:3685607-3685608	Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs534186662	chr11:3685641-3685642	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs370440270	chr11:3685643-3685644	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs2271583	chr11:3685655-3685656	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs557447373	chr11:3685666-3685667	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs535727091	chr11:3685678-3685679	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs557155912	chr11:3685688-3685689	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs568950540	chr11:3685716-3685717	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs539568562	chr11:3685741-3685742	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs557574016	chr11:3685755-3685756	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs115198556	chr11:3685762-3685763	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs374604357	chr11:3685839-3685840	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs111345474	chr11:3685844-3685845	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs150218717	chr11:3685851-3685852	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs577291588	chr11:3685861-3685862	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs115901897	chr11:3685883-3685884	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs60928568	chr11:3685915-3685916	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	17440070	CNVD

Chromatin state (count:1680 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:3671000-3686800	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr11:3673000-3687200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr11:3676800-3685400	Weak transcription	Right Ventricle	heart
4	chr11:3680200-3689400	Strong transcription	Skeletal Muscle Female	skeletal muscle
5	chr11:3681000-3685600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr11:3681000-3687800	Weak transcription	A549	lung
7	chr11:3681400-3685400	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr11:3681400-3685400	Weak transcription	Spleen	Spleen
9	chr11:3681400-3686400	Weak transcription	Pancreas	Pancrea
10	chr11:3681400-3691200	Strong transcription	Skeletal Muscle Male	skeletal muscle
11	chr11:3681600-3686000	Weak transcription	Fetal Brain Female	brain
12	chr11:3681800-3685200	Weak transcription	Fetal Intestine Small	intestine
13	chr11:3681800-3685200	Weak transcription	Fetal Stomach	stomach
14	chr11:3681800-3685400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr11:3681800-3685800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr11:3681800-3693200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr11:3682000-3685200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr11:3682000-3685200	Weak transcription	Brain Germinal Matrix	brain
19	chr11:3682000-3686600	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr11:3682200-3685200	Weak transcription	Brain Cingulate Gyrus	brain
21	chr11:3682200-3685400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr11:3682200-3685400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr11:3682400-3685200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr11:3682400-3685400	Weak transcription	Fetal Intestine Large	intestine
25	chr11:3682400-3685400	Weak transcription	Fetal Muscle Trunk	muscle
26	chr11:3682400-3685800	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr11:3682400-3697200	Weak transcription	Fetal Brain Male	brain
28	chr11:3682600-3685200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr11:3682600-3685200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr11:3682600-3685400	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr11:3682600-3685400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr11:3682600-3685400	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr11:3682600-3685400	Weak transcription	NHLF	lung
34	chr11:3682600-3685800	Weak transcription	Primary B cells from peripheral blood	blood
35	chr11:3682600-3685800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr11:3682800-3685400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr11:3682800-3685400	Weak transcription	Brain Hippocampus Middle	brain
38	chr11:3682800-3685400	Weak transcription	NHEK	skin
39	chr11:3682800-3685600	Weak transcription	Primary T cells from cord blood	blood
40	chr11:3682800-3686400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr11:3682800-3688400	Weak transcription	Small Intestine	intestine
42	chr11:3683000-3685200	Weak transcription	Lung	lung
43	chr11:3683000-3685400	Weak transcription	Osteobl	bone
44	chr11:3683000-3685600	Weak transcription	Adipose Nuclei	Adipose
45	chr11:3683000-3685800	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr11:3683000-3686600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr11:3683000-3686600	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr11:3683000-3686600	Weak transcription	HMEC	breast
49	chr11:3683000-3696600	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr11:3683200-3685200	Weak transcription	Thymus	Thymus

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