Variant report

Variant	nsv390
Chromosome Location	chr11:73388188-73432899
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:181)
CpG islands
(count:122)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:181 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:73427211-73427503	K562	blood:	n/a	n/a
2	CEBPB	chr11:73413230-73413278	K562	blood:	n/a	n/a
3	CEBPB	chr11:73413188-73413386	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr11:73413131-73413425	IMR90	lung:	n/a	n/a
5	CEBPB	chr11:73413205-73413385	A549	lung:	n/a	n/a
6	CEBPB	chr11:73413131-73413426	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr11:73428877-73428916	Hela-S3	cervix:	n/a	chr11:73428895-73428908 chr11:73428897-73428908
8	CREB1	chr11:73427127-73427674	GM12878	blood:	n/a	n/a
9	CREB1	chr11:73427102-73427527	GM12878	blood:	n/a	n/a
10	CTCF	chr11:73413245-73413317	GM13976	blood:	n/a	n/a
11	CTCF	chr11:73401502-73401577	LNCaP	prostate:	n/a	n/a
12	CTCF	chr11:73408533-73408579	Medullo	brain:	n/a	n/a
13	CTCF	chr11:73410940-73411090	RPTEC	kidney:	n/a	n/a
14	CTCF	chr11:73428040-73428190	HA-sp	spinal cord:	n/a	n/a
15	CTCF	chr11:73421100-73421135	GM20000	blood:	n/a	n/a
16	CTCF	chr11:73402904-73402987	GM10266	blood:	n/a	n/a
17	E2F4	chr11:73404586-73404673	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr11:73420364-73420500	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr11:73428141-73428328	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr11:73430354-73430446	MCF10A-Er-Src	breast:	n/a	n/a
21	EP300	chr11:73427793-73428252	GM12878	blood:	n/a	chr11:73427870-73427880
22	FOXA1	chr11:73391743-73392206	T-47D	breast:	n/a	chr11:73391952-73391967
23	FOXA1	chr11:73391798-73392121	T-47D	breast:	n/a	chr11:73391952-73391967
24	FOXA1	chr11:73426863-73427486	T-47D	breast:	n/a	chr11:73427070-73427085
25	FOXA2	chr11:73427739-73427941	HepG2	liver:	n/a	chr11:73427912-73427924
26	GABPA	chr11:73427282-73427637	SK-N-SH	brain:	n/a	n/a
27	GATA1	chr11:73418253-73418527	PBDEFetal	blood:	n/a	n/a
28	GATA2	chr11:73427275-73427549	SH-SY5Y	brain:	n/a	n/a
29	GATA2	chr11:73395112-73395528	K562	blood:	n/a	n/a
30	GATA3	chr11:73391723-73392202	T-47D	breast:	n/a	n/a
31	GATA3	chr11:73427014-73427616	T-47D	breast:	n/a	n/a
32	GATA3	chr11:73426867-73427588	T-47D	breast:	n/a	chr11:73426956-73426969 chr11:73426955-73426971 chr11:73426960-73426967 chr11:73426953-73426974 chr11:73426958-73426967
33	GATA3	chr11:73426950-73427805	SK-N-SH	brain:	n/a	chr11:73426956-73426969 chr11:73426955-73426971 chr11:73426960-73426967 chr11:73426953-73426974 chr11:73426958-73426967
34	GATA3	chr11:73391705-73392202	T-47D	breast:	n/a	n/a
35	GATA3	chr11:73426981-73427670	SK-N-SH	brain:	n/a	n/a
36	GATA3	chr11:73426972-73427598	SH-SY5Y	brain:	n/a	n/a
37	JUN	chr11:73412645-73412662	H1-hESC	embryonic stem cell:	n/a	n/a
38	JUN	chr11:73429871-73429899	H1-hESC	embryonic stem cell:	n/a	n/a
39	JUN	chr11:73427281-73427353	HepG2	liver:	n/a	n/a
40	JUND	chr11:73427241-73427513	K562	blood:	n/a	n/a
41	JUND	chr11:73427286-73427403	HepG2	liver:	n/a	n/a
42	JUND	chr11:73426907-73427648	T-47D	breast:	n/a	n/a
43	MAFF	chr11:73427396-73427560	K562	blood:	n/a	n/a
44	MAFF	chr11:73395659-73395781	HepG2	liver:	n/a	chr11:73395733-73395751
45	MAFK	chr11:73395644-73395862	HepG2	liver:	n/a	chr11:73395734-73395749
46	MAFK	chr11:73395624-73395883	HepG2	liver:	n/a	chr11:73395734-73395749
47	MAFK	chr11:73427495-73427656	HepG2	liver:	n/a	chr11:73427572-73427583 chr11:73427572-73427583 chr11:73427573-73427584 chr11:73427571-73427585 chr11:73427568-73427584 chr11:73427573-73427584
48	MAFK	chr11:73427247-73427421	K562	blood:	n/a	n/a
49	MYC	chr11:73394617-73394677	MCF-7	breast:	n/a	n/a
50	MYC	chr11:73422228-73422234	MCF-7	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:73428020-73428070	SKMC	muscle:	n/a
2	chr11:73388802-73388852	HMEC	breast:	n/a
3	chr11:73388802-73388852	SK-N-MC	brain:	n/a
4	chr11:73388802-73388852	NH-A	brain:	n/a
5	chr11:73388802-73388852	NHDF-neo	bronchial:	n/a
6	chr11:73388802-73388852	Jurkat	blood:	n/a
7	chr11:73388802-73388852	RPTEC	kidney:	n/a
8	chr11:73388802-73388852	IMR90	lung:	fetal
9	chr11:73388802-73388852	ECC-1	luminal epithelium:	n/a
10	chr11:73428020-73428070	SK-N-MC	brain:	n/a
11	chr11:73428020-73428070	MCF-7	breast:	n/a
12	chr11:73428020-73428070	HL-60	blood:	n/a
13	chr11:73388802-73388852	HEEpiC	esophagus:	n/a
14	chr11:73388802-73388852	AG04450	lung:	fetal
15	chr11:73388802-73388852	NT2-D1	testis:	n/a
16	chr11:73428020-73428070	AG04449	skin:	fetal
17	chr11:73428020-73428070	ovcar-3	ovarian:	n/a
18	chr11:73388802-73388852	MCF-7	breast:	n/a
19	chr11:73388802-73388852	HNPCEpiC	eye:	n/a
20	chr11:73388802-73388852	HL-60	blood:	n/a
21	chr11:73428020-73428070	GM12891	blood:	n/a
22	chr11:73428020-73428070	Hela-S3	cervix:	n/a
23	chr11:73388802-73388852	T-47D	breast:	n/a
24	chr11:73388802-73388852	HAEpiC	amniotic membrane:	n/a
25	chr11:73428020-73428070	NT2-D1	testis:	n/a
26	chr11:73388802-73388852	HRPEpiC	eye:	n/a
27	chr11:73428020-73428070	HEEpiC	esophagus:	n/a
28	chr11:73428020-73428070	NB4	blood:	n/a
29	chr11:73428020-73428070	AG09319	gingival:	n/a
30	chr11:73428020-73428070	HIPEpiC	eye:	n/a
31	chr11:73428020-73428070	T-47D	breast:	n/a
32	chr11:73428020-73428070	HCPEpiC	choroid plexus:	n/a
33	chr11:73388802-73388852	HRCEpiC	kidney:	n/a
34	chr11:73388802-73388852	HepG2	liver:	n/a
35	chr11:73428020-73428070	NHBE	bronchial:	n/a
36	chr11:73428020-73428070	HPAEpiC	pulmonary alveolar:	n/a
37	chr11:73388802-73388852	HEK293	kidney:	embryo
38	chr11:73428020-73428070	U87	brain:	n/a
39	chr11:73428020-73428070	MCF10A-Er-Src	breast:	n/a
40	chr11:73388802-73388852	SKMC	muscle:	n/a
41	chr11:73428020-73428070	A549	lung:	n/a
42	chr11:73428020-73428070	SK-N-SH	brain:	n/a
43	chr11:73388802-73388852	A549	lung:	n/a
44	chr11:73388802-73388852	SAEC	small airway:	n/a
45	chr11:73428020-73428070	LNCaP	prostate:	n/a
46	chr11:73428020-73428070	PANC-1	pancreas:	n/a
47	chr11:73428020-73428070	AG10803	skin:	n/a
48	chr11:73388802-73388852	ovcar-3	ovarian:	n/a
49	chr11:73388802-73388852	K562	blood:	n/a
50	chr11:73428020-73428070	AG04450	lung:	fetal

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:73426792..73429606-chr11:73433522..73435254,2	MCF-7	breast:
2	chr11:73375007..73377512-chr11:73395012..73396634,2	MCF-7	breast:
3	chr11:73421710..73424009-chr11:73461398..73464221,2	K562	blood:
4	chr1:10002595..10003396-chr11:73419578..73420422,2	NB4	blood:
5	chr11:73418211..73420499-chr11:73425095..73426709,2	MCF-7	breast:
6	chr11:72478740..72480809-chr11:73389809..73392340,2	MCF-7	breast:
7	chr11:73418211..73420499-chr11:73425095..73426709,2	MCF-7	breast:
8	chr11:73415553..73417778-chr11:73420155..73422839,2	MCF-7	breast:
9	chr11:73415553..73417778-chr11:73420155..73422839,2	MCF-7	breast:
10	chr11:73385994..73387956-chr11:73388947..73391693,2	K562	blood:
11	chr11:73422546..73424731-chr11:73470843..73472960,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000255928	TF binding region
ENSG00000255928	CpG island
ENSG00000175582	chromatin interactions
ENSG00000252732	chromatin interactions
ENSG00000256034	chromatin interactions
ENSG00000228150	chromatin interactions
ENSG00000162441	chromatin interactions

Extended variants
information (count: 1728 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1728 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562861184	chr11:73388211-73388212	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs571109512	chr11:73388259-73388260	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114530588	chr11:73388297-73388298	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538869111	chr11:73388343-73388344	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs10898931	chr11:73388363-73388364	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs562295978	chr11:73388450-73388451	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572334888	chr11:73388465-73388466	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375650535	chr11:73388479-73388480	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192854935	chr11:73388488-73388489	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs548120907	chr11:73388493-73388494	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11235851	chr11:73388499-73388500	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs148313469	chr11:73388517-73388518	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374803619	chr11:73388518-73388519	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554571591	chr11:73388524-73388525	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs35511174	chr11:73388538-73388539	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs10898932	chr11:73388589-73388590	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs552116992	chr11:73388590-73388591	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs568747205	chr11:73388591-73388592	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537976584	chr11:73388673-73388674	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185274837	chr11:73388693-73388694	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs3182808	chr11:73388716-73388717	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs3182807	chr11:73388726-73388727	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs3182803	chr11:73388760-73388761	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs3182802	chr11:73388770-73388771	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182003499	chr11:73388771-73388772	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs3182801	chr11:73388781-73388782	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138418818	chr11:73388789-73388790	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577036954	chr11:73388802-73388803	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs539462213	chr11:73388803-73388804	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556554278	chr11:73388811-73388812	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs3182799	chr11:73388830-73388831	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576335933	chr11:73388832-73388833	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs3182798	chr11:73388840-73388841	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs200630973	chr11:73388856-73388857	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs3741142	chr11:73388874-73388875	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs75464956	chr11:73388875-73388876	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572682513	chr11:73388883-73388884	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541610538	chr11:73388896-73388897	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs199692881	chr11:73388897-73388898	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs201030643	chr11:73388950-73388951	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs3182792	chr11:73388955-73388956	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs41298115	chr11:73388956-73388957	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs3182790	chr11:73388958-73388959	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs3182789	chr11:73388964-73388965	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs370888337	chr11:73388967-73388968	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374282553	chr11:73388992-73388993	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147274444	chr11:73388994-73388995	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs375679902	chr11:73389015-73389016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201274283	chr11:73389024-73389025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs377432274	chr11:73389027-73389028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1448 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73372400-73388200	Weak transcription	HSMMtube	muscle
2	chr11:73372400-73395400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr11:73372600-73388200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr11:73372600-73388200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr11:73372600-73388400	Weak transcription	Dnd41	blood
6	chr11:73372600-73394800	Weak transcription	Brain Germinal Matrix	brain
7	chr11:73372800-73388400	Weak transcription	NHLF	lung
8	chr11:73372800-73390600	Weak transcription	HUVEC	blood vessel
9	chr11:73373400-73388200	Weak transcription	Fetal Thymus	thymus
10	chr11:73374200-73391800	Weak transcription	Hela-S3	cervix
11	chr11:73374400-73427200	Weak transcription	A549	lung
12	chr11:73374800-73388800	Weak transcription	GM12878-XiMat	blood
13	chr11:73375200-73388400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr11:73375200-73388400	Weak transcription	Fetal Lung	lung
15	chr11:73375200-73388800	Weak transcription	Brain Hippocampus Middle	brain
16	chr11:73375200-73404400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr11:73375400-73388200	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr11:73375400-73388200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr11:73375400-73388200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr11:73375400-73388400	Weak transcription	Brain Angular Gyrus	brain
21	chr11:73375800-73388200	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr11:73375800-73388400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr11:73375800-73400000	Weak transcription	Lung	lung
24	chr11:73375800-73416200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr11:73376000-73388200	Weak transcription	Brain Substantia Nigra	brain
26	chr11:73376000-73388400	Weak transcription	HepG2	liver
27	chr11:73376200-73388400	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr11:73376200-73390400	Weak transcription	Brain Anterior Caudate	brain
29	chr11:73376200-73395600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr11:73376200-73398400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr11:73376400-73388200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr11:73376600-73399200	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr11:73376600-73400000	Weak transcription	Spleen	Spleen
34	chr11:73376800-73388800	Weak transcription	Fetal Kidney	kidney
35	chr11:73377000-73400000	Weak transcription	Psoas Muscle	Psoas
36	chr11:73377200-73388200	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr11:73377200-73388600	Weak transcription	Brain Cingulate Gyrus	brain
38	chr11:73379400-73388600	Weak transcription	K562	blood
39	chr11:73381400-73389000	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr11:73381800-73400000	Weak transcription	Rectal Smooth Muscle	rectum
41	chr11:73382200-73399000	Weak transcription	Primary hematopoietic stem cells	blood
42	chr11:73382200-73436000	Weak transcription	Small Intestine	intestine
43	chr11:73382200-73441200	Weak transcription	Stomach Mucosa	stomach
44	chr11:73382400-73388800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr11:73382400-73421600	Weak transcription	Gastric	stomach
46	chr11:73382600-73388400	Weak transcription	Fetal Brain Female	brain
47	chr11:73382800-73388800	Weak transcription	Fetal Stomach	stomach
48	chr11:73382800-73400400	Weak transcription	Pancreas	Pancrea
49	chr11:73383000-73388200	Weak transcription	Primary B cells from cord blood	blood
50	chr11:73383000-73388200	Weak transcription	Colon Smooth Muscle	Colon

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