Variant report

Variant	nsv819964
Chromosome Location	chr11:10537254-10545535
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:52)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:52 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr11:10544507-10544589	IMR90	lung:	n/a	n/a
2	CEBPB	chr11:10544513-10544615	K562	blood:	n/a	n/a
3	CEBPB	chr11:10542194-10542417	HepG2	liver:	n/a	chr11:10542308-10542319
4	CEBPB	chr11:10542156-10542473	IMR90	lung:	n/a	chr11:10542308-10542319
5	CTCF	chr11:10537894-10537916	Spleen_OC	spleen:	n/a	n/a
6	CUX1	chr11:10537995-10538064	K562	blood:	n/a	n/a
7	E2F4	chr11:10540291-10540584	MCF10A-Er-Src	breast:	n/a	n/a
8	E2F4	chr11:10543336-10543404	MCF10A-Er-Src	breast:	n/a	n/a
9	FOS	chr11:10541286-10541529	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr11:10541282-10541418	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr11:10539699-10540127	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr11:10539673-10540134	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr11:10541234-10541434	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr11:10539717-10540101	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr11:10539667-10540085	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr11:10542275-10542395	MCF10A-Er-Src	breast:	n/a	n/a
17	GATA3	chr11:10543809-10543908	SH-SY5Y	brain:	n/a	chr11:10543869-10543886
18	GTF2F1	chr11:10541063-10541140	K562	blood:	n/a	n/a
19	MAFF	chr11:10537035-10537272	K562	blood:	n/a	chr11:10537160-10537178
20	MAFF	chr11:10537039-10537297	HepG2	liver:	n/a	chr11:10537160-10537178
21	MAFF	chr11:10539880-10540025	HepG2	liver:	n/a	chr11:10539940-10539958
22	MAFK	chr11:10539847-10540017	HepG2	liver:	n/a	chr11:10539941-10539956
23	MAFK	chr11:10537046-10537285	HepG2	liver:	n/a	chr11:10537161-10537175
24	MAFK	chr11:10539875-10540038	HepG2	liver:	n/a	chr11:10539941-10539956
25	MAFK	chr11:10537078-10537274	K562	blood:	n/a	chr11:10537161-10537175
26	MAFK	chr11:10537042-10537283	Hela-S3	cervix:	n/a	chr11:10537161-10537175
27	MAFK	chr11:10537027-10537334	HepG2	liver:	n/a	chr11:10537161-10537175
28	POLR2A	chr11:10538105-10538379	K562	blood:	n/a	n/a
29	POLR2A	chr11:10538172-10538257	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr11:10539195-10539230	GM12878	blood:	n/a	n/a
31	POLR2A	chr11:10541938-10542007	ProgFib	skin:	n/a	n/a
32	POLR2A	chr11:10537875-10538371	HL-60	blood:	n/a	n/a
33	POLR2A	chr11:10538382-10538389	K562	blood:	n/a	n/a
34	POLR2A	chr11:10538060-10538240	GM12878	blood:	n/a	n/a
35	POLR2A	chr11:10537879-10538443	GM12892	blood:	n/a	n/a
36	POLR2A	chr11:10535542-10539924	K562	blood:	n/a	n/a
37	POLR2A	chr11:10537848-10538085	GM12891	blood:	n/a	n/a
38	POLR2A	chr11:10537905-10538408	GM12892	blood:	n/a	n/a
39	POLR2A	chr11:10540443-10540752	GM12892	blood:	n/a	n/a
40	POLR2A	chr11:10542013-10542024	ProgFib	skin:	n/a	n/a
41	POLR2A	chr11:10542006-10542080	Gliobla	brain:	n/a	n/a
42	POLR2A	chr11:10537830-10538390	GM12892	blood:	n/a	n/a
43	POLR2A	chr11:10537829-10538379	HCT-116	colon:	n/a	n/a
44	POLR2A	chr11:10538038-10538123	ProgFib	skin:	n/a	n/a
45	POLR2A	chr11:10538125-10538177	ProgFib	skin:	n/a	n/a
46	RFX5	chr11:10540971-10540983	K562	blood:	n/a	n/a
47	STAT3	chr11:10539767-10540039	MCF10A-Er-Src	breast:	n/a	n/a
48	STAT3	chr11:10541236-10541436	MCF10A-Er-Src	breast:	n/a	n/a
49	STAT3	chr11:10539750-10539917	MCF10A-Er-Src	breast:	n/a	n/a
50	STAT3	chr11:10539708-10540043	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:10543456-10543506	HepG2	liver:	n/a
2	chr11:10543456-10543506	AG09309	skin:	n/a
3	chr11:10543456-10543506	HIPEpiC	eye:	n/a
4	chr11:10543456-10543506	HRE	kidney:	n/a
5	chr11:10543456-10543506	BJ	skin:	n/a
6	chr11:10543456-10543506	HNPCEpiC	eye:	n/a
7	chr11:10543456-10543506	AoSMC	blood vessel:	n/a
8	chr11:10543456-10543506	GM06990	blood:	n/a
9	chr11:10543456-10543506	Caco-2	colon:	n/a
10	chr11:10543456-10543506	HRCEpiC	kidney:	n/a
11	chr11:10543456-10543506	ProgFib	skin:	n/a
12	chr11:10543456-10543506	Hela-S3	cervix:	n/a
13	chr11:10543456-10543506	GM12878	blood:	n/a
14	chr11:10543456-10543506	NT2-D1	testis:	n/a
15	chr11:10543456-10543506	HL-60	blood:	n/a
16	chr11:10543456-10543506	NHDF-neo	bronchial:	n/a
17	chr11:10543456-10543506	ovcar-3	ovarian:	n/a
18	chr11:10543456-10543506	MCF10A-Er-Src	breast:	n/a
19	chr11:10543456-10543506	PFSK-1	brain:	n/a
20	chr11:10543456-10543506	SKMC	muscle:	n/a
21	chr11:10543456-10543506	IMR90	lung:	fetal
22	chr11:10543456-10543506	T-47D	breast:	n/a
23	chr11:10543456-10543506	PANC-1	pancreas:	n/a
24	chr11:10543456-10543506	AG04450	lung:	fetal
25	chr11:10543456-10543506	HCF	heart:	n/a
26	chr11:10543456-10543506	H1-hESC	embryonic stem cell:	embryo
27	chr11:10543456-10543506	HPAEpiC	pulmonary alveolar:	n/a
28	chr11:10543456-10543506	LNCaP	prostate:	n/a
29	chr11:10543456-10543506	Jurkat	blood:	n/a
30	chr11:10543456-10543506	K562	blood:	n/a
31	chr11:10543456-10543506	AG04449	skin:	fetal
32	chr11:10543456-10543506	GM12891	blood:	n/a
33	chr11:10543456-10543506	HCM	heart:	n/a
34	chr11:10543456-10543506	PrEC	prostate:	n/a
35	chr11:10543456-10543506	SAEC	small airway:	n/a
36	chr11:10543456-10543506	AG09319	gingival:	n/a
37	chr11:10543456-10543506	RPTEC	kidney:	n/a
38	chr11:10543456-10543506	MCF-7	breast:	n/a
39	chr11:10543456-10543506	HEK293	kidney:	embryo
40	chr11:10543456-10543506	HCPEpiC	choroid plexus:	n/a
41	chr11:10543456-10543506	GM12892	blood:	n/a
42	chr11:10543456-10543506	A549	lung:	n/a
43	chr11:10543456-10543506	NH-A	brain:	n/a
44	chr11:10543456-10543506	HEEpiC	esophagus:	n/a
45	chr11:10543456-10543506	AG10803	skin:	n/a
46	chr11:10543456-10543506	SK-N-MC	brain:	n/a
47	chr11:10543456-10543506	CMK	blood:	n/a
48	chr11:10543456-10543506	GM19239	blood:	n/a
49	chr11:10543456-10543506	HRPEpiC	eye:	n/a
50	chr11:10543456-10543506	HCT-116	colon:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:10540875..10544152-chr11:10546119..10548762,4	K562	blood:
2	chr11:10532333..10535020-chr11:10535560..10538529,2	K562	blood:
3	chr11:10541656..10544963-chr11:10560896..10564071,4	K562	blood:
4	chr11:10535540..10537535-chr11:10543160..10545486,2	K562	blood:
5	chr11:10534555..10537040-chr11:10542558..10544660,2	K562	blood:
6	chr11:10534893..10539429-chr11:10540096..10542426,4	K562	blood:
7	chr11:10541835..10545303-chr11:10545348..10548762,4	K562	blood:
8	chr11:10544840..10547633-chr11:10554007..10556925,3	K562	blood:
9	chr11:10541835..10545303-chr11:10545348..10548762,4	K562	blood:
10	chr11:10500501..10502775-chr11:10545214..10548072,2	K562	blood:
11	chr11:10540505..10542590-chr11:10544048..10545735,2	K562	blood:
12	chr11:10544820..10548586-chr11:10548781..10551121,4	K562	blood:
13	chr11:10535540..10537535-chr11:10543160..10545486,2	K562	blood:
14	chr11:10538298..10540845-chr11:10561134..10562717,2	MCF-7	breast:
15	chr11:10540505..10542590-chr11:10544048..10545735,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RNF141	hsa-miR-32-5p	chr11:10540502-10540523
2	RNF141	hsa-miR-124-3p	chr11:10540334-10540353

Variant related genes	Relation type
RNF141	TF binding region
RNF141	CpG island
ENSG00000177112	chromatin interactions
ENSG00000110315	chromatin interactions

Extended variants
information (count: 318 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:318 , 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	rs183401903	chr11:10537258-10537259	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534635929	chr11:10537266-10537267	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs116254462	chr11:10537296-10537297	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186612660	chr11:10537299-10537300	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543629573	chr11:10537303-10537304	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557127562	chr11:10537321-10537322	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs527714189	chr11:10537367-10537368	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs576411267	chr11:10537370-10537371	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545505515	chr11:10537415-10537416	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs565098599	chr11:10537435-10537436	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551559633	chr11:10537465-10537466	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs529254399	chr11:10537474-10537475	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572087784	chr11:10537479-10537480	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541075300	chr11:10537538-10537539	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189935918	chr11:10537549-10537550	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs73411920	chr11:10537581-10537582	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs12789639	chr11:10537610-10537611	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs182553878	chr11:10537680-10537681	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550062788	chr11:10537696-10537697	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs10500725	chr11:10537721-10537722	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs188120679	chr11:10537775-10537776	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554856918	chr11:10537793-10537794	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552235793	chr11:10537811-10537812	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369036739	chr11:10537847-10537848	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs112124363	chr11:10537865-10537866	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534595443	chr11:10537906-10537907	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548245615	chr11:10537907-10537908	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568318785	chr11:10537910-10537911	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs193068526	chr11:10537974-10537975	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556849590	chr11:10537977-10537978	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs576981442	chr11:10537990-10537991	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539289325	chr11:10537993-10537994	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs12225339	chr11:10538036-10538037	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559007235	chr11:10538123-10538124	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185362601	chr11:10538124-10538125	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540987545	chr11:10538136-10538137	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs12290357	chr11:10538170-10538171	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs574766510	chr11:10538172-10538173	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142974980	chr11:10538188-10538189	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs150701030	chr11:10538200-10538201	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs532715464	chr11:10538226-10538227	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189026291	chr11:10538250-10538251	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559479212	chr11:10538287-10538288	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs11042868	chr11:10538328-10538329	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs116601223	chr11:10538365-10538366	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs568082992	chr11:10538402-10538403	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs192346500	chr11:10538404-10538405	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs114047722	chr11:10538408-10538409	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs570704569	chr11:10538416-10538417	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs371034970	chr11:10538423-10538424	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
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
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	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
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Neuroblastoma	18923524	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:399 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:10501600-10550600	Weak transcription	Small Intestine	intestine
2	chr11:10502600-10560800	Weak transcription	Fetal Brain Male	brain
3	chr11:10507800-10544800	Weak transcription	Fetal Kidney	kidney
4	chr11:10512800-10540400	Weak transcription	Fetal Lung	lung
5	chr11:10512800-10548600	Weak transcription	Right Ventricle	heart
6	chr11:10513200-10538000	Weak transcription	Left Ventricle	heart
7	chr11:10515800-10540600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr11:10516000-10544000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr11:10520000-10543400	Weak transcription	Colon Smooth Muscle	Colon
10	chr11:10522200-10541200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr11:10522400-10537800	Weak transcription	Fetal Intestine Large	intestine
12	chr11:10522400-10540600	Weak transcription	Duodenum Mucosa	Duodenum
13	chr11:10522400-10546200	Weak transcription	Rectal Smooth Muscle	rectum
14	chr11:10522400-10560800	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr11:10522800-10540600	Weak transcription	Stomach Smooth Muscle	stomach
16	chr11:10524200-10537800	Weak transcription	Aorta	Aorta
17	chr11:10524600-10540600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr11:10524600-10544800	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr11:10525800-10555600	Strong transcription	Primary B cells from peripheral blood	blood
20	chr11:10526400-10537800	Weak transcription	Pancreas	Pancrea
21	chr11:10526400-10548800	Weak transcription	Spleen	Spleen
22	chr11:10526400-10549000	Weak transcription	Ovary	ovary
23	chr11:10526400-10551800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:10526400-10561600	Weak transcription	Colonic Mucosa	Colon
25	chr11:10526800-10537800	Weak transcription	Fetal Intestine Small	intestine
26	chr11:10526800-10548800	Weak transcription	Psoas Muscle	Psoas
27	chr11:10527200-10537800	Weak transcription	Lung	lung
28	chr11:10527200-10540200	Weak transcription	Liver	Liver
29	chr11:10527200-10540200	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr11:10527200-10540600	Weak transcription	Gastric	stomach
31	chr11:10527600-10542400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr11:10527800-10541000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr11:10528000-10540400	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr11:10528000-10540600	Weak transcription	Fetal Muscle Trunk	muscle
35	chr11:10528000-10540600	Weak transcription	Fetal Muscle Leg	muscle
36	chr11:10528000-10542600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr11:10528200-10538800	Weak transcription	GM12878-XiMat	blood
38	chr11:10528400-10539000	Weak transcription	HMEC	breast
39	chr11:10528400-10540200	Weak transcription	Brain Angular Gyrus	brain
40	chr11:10528400-10548800	Weak transcription	K562	blood
41	chr11:10528400-10550600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr11:10528400-10555800	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr11:10528600-10541000	Weak transcription	Brain Anterior Caudate	brain
44	chr11:10529200-10541000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr11:10531400-10538600	Strong transcription	Primary monocytes fromperipheralblood	blood
46	chr11:10532200-10538200	Strong transcription	Primary T helper cells fromperipheralblood	blood
47	chr11:10532600-10538400	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr11:10532600-10540400	Weak transcription	Placenta	Placenta
49	chr11:10533000-10537800	Weak transcription	Esophagus	oesophagus
50	chr11:10533000-10540200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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