Variant report

Variant	nsv1038294
Chromosome Location	chr11:93918837-93982605
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:517)
CpG islands
(count:245)
Chromatin interactive
region (count:12)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:517 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:93953706-93953959	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:93932567-93932629	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:93934157-93934699	HepG2	liver:	n/a	n/a
4	ATF1	chr11:93971681-93971723	K562	blood:	n/a	n/a
5	BACH1	chr11:93957208-93957365	K562	blood:	n/a	n/a
6	BACH1	chr11:93951679-93951681	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr11:93957221-93957507	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr11:93934100-93934604	A549	lung:	n/a	n/a
9	BCL3	chr11:93934188-93934548	A549	lung:	n/a	n/a
10	BHLHE40	chr11:93930820-93931111	K562	blood:	n/a	n/a
11	BHLHE40	chr11:93930913-93930984	GM12878	blood:	n/a	n/a
12	CBX3	chr11:93952951-93953285	K562	blood:	n/a	n/a
13	CBX3	chr11:93953003-93953298	K562	blood:	n/a	n/a
14	CEBPB	chr11:93934155-93934686	HepG2	liver:	n/a	n/a
15	CEBPB	chr11:93929622-93929969	IMR90	lung:	n/a	n/a
16	CEBPB	chr11:93934435-93934586	HepG2	liver:	n/a	n/a
17	CEBPB	chr11:93933234-93933446	HepG2	liver:	n/a	n/a
18	CEBPB	chr11:93926511-93926824	IMR90	lung:	n/a	n/a
19	CEBPB	chr11:93971210-93971400	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr11:93934226-93934705	A549	lung:	n/a	n/a
21	CEBPB	chr11:93932885-93932991	K562	blood:	n/a	n/a
22	CEBPB	chr11:93944262-93944453	HepG2	liver:	n/a	chr11:93944354-93944365 chr11:93944338-93944349
23	CEBPB	chr11:93928231-93928412	IMR90	lung:	n/a	chr11:93928362-93928375 chr11:93928332-93928345
24	CEBPB	chr11:93934165-93935106	IMR90	lung:	n/a	n/a
25	CEBPB	chr11:93932496-93933771	IMR90	lung:	n/a	n/a
26	CEBPB	chr11:93953690-93953969	HepG2	liver:	n/a	n/a
27	CEBPB	chr11:93933217-93933520	A549	lung:	n/a	n/a
28	CEBPB	chr11:93932490-93932690	HepG2	liver:	n/a	n/a
29	CEBPB	chr11:93934281-93934625	A549	lung:	n/a	n/a
30	CHD1	chr11:93971505-93971702	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr11:93930341-93930658	K562	blood:	n/a	n/a
32	CHD2	chr11:93970730-93971399	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr11:93934444-93934459	HepG2	liver:	n/a	n/a
34	CREB1	chr11:93934001-93934662	HepG2	liver:	n/a	n/a
35	CREB1	chr11:93934136-93934386	A549	lung:	n/a	n/a
36	CTCF	chr11:93970860-93971010	GM12870	blood:	n/a	n/a
37	CTCF	chr11:93954106-93954181	GM20000	blood:	n/a	n/a
38	CTCF	chr11:93970960-93971210	Caco-2	colon:	n/a	n/a
39	CTCF	chr11:93970940-93971090	GM12867	blood:	n/a	n/a
40	CTCF	chr11:93969720-93969870	NB4	blood:	n/a	n/a
41	CTCF	chr11:93970909-93971007	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr11:93971120-93971270	HVMF	connective:	n/a	n/a
43	CTCF	chr11:93971460-93971610	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr11:93970660-93970810	GM12871	blood:	n/a	n/a
45	CTCF	chr11:93971640-93971790	AG10803	skin:	n/a	n/a
46	CTCF	chr11:93971460-93971610	HepG2	liver:	n/a	n/a
47	CTCF	chr11:93971640-93971790	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr11:93970640-93970790	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr11:93969020-93969170	AG10803	skin:	n/a	n/a
50	CTCF	chr11:93970960-93971110	Caco-2	colon:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:93922474-93922524	IMR90	lung:	fetal
2	chr11:93922474-93922524	IMR90	lung:	fetal
3	chr11:93922474-93922524	Hepatocyte	liver:	n/a
4	chr11:93922202-93922252	HNPCEpiC	eye:	n/a
5	chr11:93922474-93922524	NH-A	brain:	n/a
6	chr11:93922202-93922252	CMK	blood:	n/a
7	chr11:93920113-93920163	HEEpiC	esophagus:	n/a
8	chr11:93920113-93920163	NHDF-neo	bronchial:	n/a
9	chr11:93920113-93920163	MCF10A-Er-Src	breast:	n/a
10	chr11:93922202-93922252	GM12892	blood:	n/a
11	chr11:93920113-93920163	BE2_C	brain:	n/a
12	chr11:93922202-93922252	BJ	skin:	n/a
13	chr11:93922202-93922252	HPAEpiC	pulmonary alveolar:	n/a
14	chr11:93922202-93922252	HUVEC	blood vessel:	n/a
15	chr11:93927425-93927475	HL-60	blood:	n/a
16	chr11:93927425-93927475	HPAEpiC	pulmonary alveolar:	n/a
17	chr11:93922474-93922524	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:93927425-93927475	AG04449	skin:	fetal
19	chr11:93927425-93927475	AG10803	skin:	n/a
20	chr11:93920113-93920163	HCT-116	colon:	n/a
21	chr11:93922202-93922252	U87	brain:	n/a
22	chr11:93927425-93927475	HEEpiC	esophagus:	n/a
23	chr11:93922202-93922252	AG09319	gingival:	n/a
24	chr11:93922474-93922524	HEEpiC	esophagus:	n/a
25	chr11:93927425-93927475	GM19239	blood:	n/a
26	chr11:93927425-93927475	HEK293	kidney:	embryo
27	chr11:93920113-93920163	GM12892	blood:	n/a
28	chr11:93920113-93920163	HepG2	liver:	n/a
29	chr11:93922474-93922524	HIPEpiC	eye:	n/a
30	chr11:93922202-93922252	NHBE	bronchial:	n/a
31	chr11:93922202-93922252	SAEC	small airway:	n/a
32	chr11:93922474-93922524	H1-hESC	embryonic stem cell:	embryo
33	chr11:93922202-93922252	HEEpiC	esophagus:	n/a
34	chr11:93920113-93920163	T-47D	breast:	n/a
35	chr11:93922474-93922524	MCF-7	breast:	n/a
36	chr11:93922474-93922524	NT2-D1	testis:	n/a
37	chr11:93927425-93927475	AoSMC	blood vessel:	n/a
38	chr11:93922474-93922524	A549	lung:	n/a
39	chr11:93922202-93922252	HMEC	breast:	n/a
40	chr11:93927425-93927475	HCM	heart:	n/a
41	chr11:93922202-93922252	HCPEpiC	choroid plexus:	n/a
42	chr11:93927425-93927475	Caco-2	colon:	n/a
43	chr11:93922474-93922524	HepG2	liver:	n/a
44	chr11:93922474-93922524	ECC-1	luminal epithelium:	n/a
45	chr11:93922202-93922252	HL-60	blood:	n/a
46	chr11:93922202-93922252	MCF10A-Er-Src	breast:	n/a
47	chr11:93927425-93927475	GM12878	blood:	n/a
48	chr11:93922202-93922252	NH-A	brain:	n/a
49	chr11:93922202-93922252	HEK293	kidney:	embryo
50	chr11:93920113-93920163	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:93917086..93919356-chr11:93920990..93923600,2	K562	blood:
2	chr11:93937398..93939250-chr11:93947688..93950358,2	K562	blood:
3	chr11:93928773..93931046-chr11:93935026..93936548,2	MCF-7	breast:
4	chr11:93929115..93931956-chr11:94225381..94228826,3	K562	blood:
5	chr11:93946184..93948199-chr11:93950840..93953246,2	K562	blood:
6	chr11:93945976..93948199-chr11:93951746..93953756,2	K562	blood:
7	chr11:93945976..93948199-chr11:93951746..93953756,2	K562	blood:
8	chr11:93932886..93934765-chr11:93936534..93938531,2	K562	blood:
9	chr11:93946184..93948199-chr11:93950840..93953246,2	K562	blood:
10	chr11:93932886..93934765-chr11:93936534..93938531,2	K562	blood:
11	chr11:93937398..93939250-chr11:93947688..93950358,2	K562	blood:
12	chr11:93928773..93931046-chr11:93935026..93936548,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PANX1-1	chr11:93935412-93935672	NONHSAT023711
2	lnc-GPR83-2	chr11:93932428-93932509	NONHSAT023709
3	lnc-FOLR4-1	chr11:93971316-93971443	ENSG00000250519
4	lnc-GPR83-2	chr11:93932661-93932887	NONHSAT023709
5	lnc-GPR83-2	chr11:93932429-93932509	XLOC_009524
6	lnc-GPR83-2	chr11:93932662-93932887	XLOC_009524
7	lnc-FOLR4-1	chr11:93971316-93971443	ENSG00000250519
8	lnc-GPR83-5	chr11:93921615-93922163	NONHSAT023708

No data

Variant related genes	Relation type
ENSG00000250519	TF binding region
ENSG00000256745	TF binding region
ENSG00000250519	CpG island
ENSG00000256745	CpG island
ENSG00000020922	chromatin interactions
ENSG00000256745	chromatin interactions
ENSG00000168876	chromatin interactions

Extended variants
information (count: 1308 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1308 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3020004	chr11:93918837-93918838	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs61905104	chr11:93918840-93918841	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs558466119	chr11:93918842-93918843	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs141069581	chr11:93918880-93918881	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150233135	chr11:93918912-93918913	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs555955561	chr11:93918959-93918960	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs574487845	chr11:93918970-93918971	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs140581156	chr11:93919007-93919008	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs72972568	chr11:93919034-93919035	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs555392468	chr11:93919037-93919038	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs527935282	chr11:93919039-93919040	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs529974381	chr11:93919056-93919057	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs202074402	chr11:93919057-93919058	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs138294015	chr11:93919058-93919059	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs371335651	chr11:93919060-93919061	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs185793012	chr11:93919062-93919063	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs67946813	chr11:93919098-93919099	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs544106613	chr11:93919148-93919149	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs550164566	chr11:93919223-93919224	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs145651568	chr11:93919232-93919233	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs572325129	chr11:93919278-93919279	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs529351728	chr11:93919289-93919290	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs548060294	chr11:93919348-93919349	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs566323201	chr11:93919466-93919467	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs533773823	chr11:93919468-93919469	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs144189575	chr11:93919478-93919479	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs371740158	chr11:93919534-93919535	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs556616637	chr11:93919553-93919554	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs537406266	chr11:93919572-93919573	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs535029139	chr11:93919575-93919576	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs1540177	chr11:93919628-93919629	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs545527820	chr11:93919631-93919632	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs141262363	chr11:93919635-93919636	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150762169	chr11:93919695-93919696	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553948487	chr11:93919715-93919716	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191051600	chr11:93919716-93919717	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369013413	chr11:93919735-93919736	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs546442023	chr11:93919750-93919751	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564591927	chr11:93919781-93919782	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576683058	chr11:93919788-93919789	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117463752	chr11:93919821-93919822	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562113329	chr11:93919845-93919846	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs72972571	chr11:93919864-93919865	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574901298	chr11:93919866-93919867	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547472577	chr11:93919873-93919874	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559447233	chr11:93919897-93919898	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs16920011	chr11:93919901-93919902	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs11601530	chr11:93919917-93919918	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs577014816	chr11:93920004-93920005	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372365971	chr11:93920038-93920039	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	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	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	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
Myelofibrosis	22110671	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Cancer	21499728	CNVD
Breast cancer	19181860	CNVD
Breast cancer	17603634	CNVD
Mantle cell lymphoma	19029149	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	18852474	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93897800-93920000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:93901400-93921200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr11:93904800-93920000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:93905400-93919600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr11:93907200-93919600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr11:93910400-93919000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr11:93910600-93919200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:93912200-93921000	Weak transcription	Brain Anterior Caudate	brain
9	chr11:93913600-93919200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr11:93913600-93929400	Weak transcription	Gastric	stomach
11	chr11:93913800-93921400	Weak transcription	Fetal Brain Male	brain
12	chr11:93914400-93920400	Weak transcription	Primary B cells from cord blood	blood
13	chr11:93914800-93919800	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr11:93914800-93920400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr11:93914800-93920600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr11:93914800-93921000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr11:93914800-93921600	Weak transcription	Thymus	Thymus
18	chr11:93914800-93926200	Weak transcription	Esophagus	oesophagus
19	chr11:93914800-93926200	Weak transcription	Spleen	Spleen
20	chr11:93915000-93921000	Weak transcription	Right Ventricle	heart
21	chr11:93915400-93919000	Weak transcription	Fetal Brain Female	brain
22	chr11:93915600-93920400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr11:93915600-93929400	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr11:93915800-93919000	Enhancers	Fetal Kidney	kidney
25	chr11:93916200-93920800	Weak transcription	Primary hematopoietic stem cells	blood
26	chr11:93916200-93921200	Weak transcription	Primary T cells from cord blood	blood
27	chr11:93916400-93922000	Weak transcription	Brain Germinal Matrix	brain
28	chr11:93916800-93920200	Weak transcription	Fetal Muscle Trunk	muscle
29	chr11:93916800-93920200	Enhancers	NHLF	lung
30	chr11:93916800-93920600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr11:93916800-93926200	Weak transcription	HMEC	breast
32	chr11:93917000-93919400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr11:93917000-93919400	Enhancers	HSMMtube	muscle
34	chr11:93917000-93919600	Enhancers	HSMM	muscle
35	chr11:93917000-93920800	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr11:93917200-93919800	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr11:93917200-93919800	Weak transcription	A549	lung
38	chr11:93917200-93920200	Weak transcription	Dnd41	blood
39	chr11:93917200-93926200	Weak transcription	NHEK	skin
40	chr11:93917400-93919000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr11:93917400-93919000	Weak transcription	Stomach Smooth Muscle	stomach
42	chr11:93917400-93919200	Enhancers	Fetal Lung	lung
43	chr11:93917400-93919400	Strong transcription	H1 Cell Line	embryonic stem cell
44	chr11:93917400-93919400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr11:93917400-93919400	Enhancers	Muscle Satellite Cultured Cells	--
46	chr11:93917400-93920000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr11:93917400-93921000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr11:93917400-93921200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr11:93917400-93922000	Weak transcription	Lung	lung
50	chr11:93917600-93919200	Weak transcription	Fetal Intestine Large	intestine

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