Variant report

Variant	nsv518499
Chromosome Location	chr11:36466814-36479789
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:219)
CpG islands
(count:367)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:219 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:36475482-36475750	K562	blood:	n/a	n/a
2	BHLHE40	chr11:36475658-36475791	K562	blood:	n/a	n/a
3	CEBPB	chr11:36469158-36469438	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr11:36469111-36469552	ECC-1	luminal epithelium:	n/a	n/a
5	CEBPB	chr11:36469155-36469983	MCF-7	breast:	n/a	n/a
6	CEBPB	chr11:36469173-36469496	IMR90	lung:	n/a	n/a
7	CEBPB	chr11:36477254-36477823	IMR90	lung:	n/a	n/a
8	CEBPB	chr11:36477347-36477628	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr11:36469142-36469495	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr11:36469115-36469527	ECC-1	luminal epithelium:	n/a	n/a
11	CHD2	chr11:36477379-36477664	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr11:36476635-36476752	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr11:36477420-36477570	AoAF	blood vessel:	n/a	n/a
14	CTCF	chr11:36474020-36474170	HCPEpiC	choroid plexus:	n/a	chr11:36474039-36474052
15	CTCF	chr11:36477520-36477670	AG10803	skin:	n/a	n/a
16	CTCF	chr11:36479520-36479670	GM12871	blood:	n/a	n/a
17	CTCF	chr11:36477580-36477730	NHDF-neo	bronchial:	n/a	n/a
18	CTCF	chr11:36477820-36477970	AG10803	skin:	n/a	n/a
19	CTCF	chr11:36477500-36477650	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr11:36477520-36477670	BJ	skin:	n/a	n/a
21	CTCF	chr11:36477580-36477730	HAc	cerebellar:	n/a	n/a
22	CTCF	chr11:36477440-36477590	HEK293	kidney:	n/a	n/a
23	CTCF	chr11:36477440-36477590	AG09319	gingival:	n/a	n/a
24	CTCF	chr11:36477500-36477650	AG09309	skin:	n/a	n/a
25	CTCF	chr11:36477600-36477750	HCM	heart:	n/a	n/a
26	CTCF	chr11:36477440-36477590	NHDF-neo	bronchial:	n/a	n/a
27	CTCF	chr11:36477640-36477790	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr11:36477382-36477775	IMR90	lung:	n/a	n/a
29	CTCF	chr11:36477480-36477630	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr11:36471820-36471970	GM12864	blood:	n/a	n/a
31	CTCF	chr11:36477440-36477590	AG04449	skin:	n/a	n/a
32	CTCF	chr11:36477480-36477630	BJ	skin:	n/a	n/a
33	CTCF	chr11:36477440-36477590	HMEC	breast:	n/a	n/a
34	CTCF	chr11:36477640-36477790	HFF	foreskin:	n/a	n/a
35	CTCF	chr11:36477540-36477690	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr11:36471769-36471813	Pancreas_OC	pancreas:	n/a	n/a
37	CTCF	chr11:36477500-36477650	HVMF	connective:	n/a	n/a
38	CTCF	chr11:36479562-36479877	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr11:36477640-36477790	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr11:36477440-36477590	HPF	lung:	n/a	n/a
41	CTCF	chr11:36477300-36477450	HCM	heart:	n/a	n/a
42	CTCF	chr11:36477580-36477730	HMF	breast:	n/a	n/a
43	CTCF	chr11:36477420-36477570	AG10803	skin:	n/a	n/a
44	CTCF	chr11:36477840-36477990	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr11:36477580-36477730	NHEK	skin:	n/a	n/a
46	CTCF	chr11:36471540-36471690	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr11:36477500-36477650	AG09319	gingival:	n/a	n/a
48	CTCF	chr11:36477460-36477610	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr11:36477460-36477610	RPTEC	kidney:	n/a	n/a
50	CTCF	chr11:36477480-36477630	HVMF	connective:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:36477229-36477279	K562	blood:	n/a
2	chr11:36477229-36477279	K562	blood:	n/a
3	chr11:36474744-36474794	HEEpiC	esophagus:	n/a
4	chr11:36477229-36477279	PrEC	prostate:	n/a
5	chr11:36476232-36476282	HNPCEpiC	eye:	n/a
6	chr11:36469878-36469928	LNCaP	prostate:	n/a
7	chr11:36476319-36476369	SKMC	muscle:	n/a
8	chr11:36474744-36474794	GM19239	blood:	n/a
9	chr11:36476232-36476282	SK-N-SH_RA	brain:	n/a
10	chr11:36476272-36476322	HRE	kidney:	n/a
11	chr11:36474744-36474794	ovcar-3	ovarian:	n/a
12	chr11:36474744-36474794	Hela-S3	cervix:	n/a
13	chr11:36476232-36476282	AG09319	gingival:	n/a
14	chr11:36469878-36469928	GM12878	blood:	n/a
15	chr11:36476272-36476322	T-47D	breast:	n/a
16	chr11:36476272-36476322	BE2_C	brain:	n/a
17	chr11:36476272-36476322	HUVEC	blood vessel:	n/a
18	chr11:36476319-36476369	SAEC	small airway:	n/a
19	chr11:36476272-36476322	PrEC	prostate:	n/a
20	chr11:36476272-36476322	NT2-D1	testis:	n/a
21	chr11:36474744-36474794	HNPCEpiC	eye:	n/a
22	chr11:36474744-36474794	AoSMC	blood vessel:	n/a
23	chr11:36477229-36477279	H1-hESC	embryonic stem cell:	embryo
24	chr11:36476232-36476282	Hepatocyte	liver:	n/a
25	chr11:36476319-36476369	HPAEpiC	pulmonary alveolar:	n/a
26	chr11:36476272-36476322	GM12878	blood:	n/a
27	chr11:36469878-36469928	CMK	blood:	n/a
28	chr11:36476319-36476369	AG09309	skin:	n/a
29	chr11:36477229-36477279	Caco-2	colon:	n/a
30	chr11:36474744-36474794	GM12892	blood:	n/a
31	chr11:36477229-36477279	HNPCEpiC	eye:	n/a
32	chr11:36474744-36474794	ECC-1	luminal epithelium:	n/a
33	chr11:36476319-36476369	HAEpiC	amniotic membrane:	n/a
34	chr11:36469878-36469928	GM06990	blood:	n/a
35	chr11:36476232-36476282	PrEC	prostate:	n/a
36	chr11:36474744-36474794	IMR90	lung:	fetal
37	chr11:36476272-36476322	SK-N-MC	brain:	n/a
38	chr11:36469878-36469928	T-47D	breast:	n/a
39	chr11:36476319-36476369	HEEpiC	esophagus:	n/a
40	chr11:36477229-36477279	SK-N-MC	brain:	n/a
41	chr11:36477229-36477279	AoSMC	blood vessel:	n/a
42	chr11:36476232-36476282	HPAEpiC	pulmonary alveolar:	n/a
43	chr11:36469878-36469928	AG09319	gingival:	n/a
44	chr11:36474744-36474794	RPTEC	kidney:	n/a
45	chr11:36476272-36476322	MCF10A-Er-Src	breast:	n/a
46	chr11:36476272-36476322	SK-N-SH	brain:	n/a
47	chr11:36477229-36477279	AG09309	skin:	n/a
48	chr11:36476319-36476369	U87	brain:	n/a
49	chr11:36476272-36476322	HMEC	breast:	n/a
50	chr11:36477229-36477279	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:36469566..36471413-chr11:36472825..36475082,2	MCF-7	breast:
2	chr11:36472788..36474841-chr11:36478990..36481077,2	MCF-7	breast:
3	chr11:36477306..36479015-chr11:36479369..36482198,2	K562	blood:
4	chr11:36477306..36479015-chr11:36479369..36482198,2	K562	blood:
5	chr11:36471715..36474622-chr11:36475747..36477445,2	MCF-7	breast:
6	chr11:36472925..36474426-chr3:25827190..25829497,2	K562	blood:
7	chr11:36469765..36471992-chr11:36474085..36476889,3	K562	blood:
8	chr11:36469765..36471660-chr11:36474085..36476889,2	K562	blood:
9	chr11:36477011..36480828-chr11:36482519..36484281,3	MCF-7	breast:
10	chr11:36469566..36471413-chr11:36472825..36475082,2	MCF-7	breast:
11	chr11:36478697..36481136-chr11:36486249..36488109,2	K562	blood:
12	chr11:36472788..36474841-chr11:36478990..36481077,2	MCF-7	breast:

No data

Variant related genes	Relation type
PRR5L	TF binding region
PRR5L	CpG island
ENSG00000135362	chromatin interactions

Extended variants
information (count: 552 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4756322	chr11:36466814-36466815	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562130753	chr11:36466834-36466835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191080949	chr11:36466853-36466854	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550671007	chr11:36466894-36466895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569503529	chr11:36466992-36466993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182446397	chr11:36467031-36467032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567216889	chr11:36467049-36467050	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528067033	chr11:36467069-36467070	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs537829738	chr11:36467135-36467136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs510479	chr11:36467231-36467232	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs510428	chr11:36467248-36467249	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs141022784	chr11:36467278-36467279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555675108	chr11:36467282-36467283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566356595	chr11:36467296-36467297	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538073136	chr11:36467399-36467400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560893315	chr11:36467412-36467413	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs557007553	chr11:36467421-36467422	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576933718	chr11:36467435-36467436	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545745745	chr11:36467466-36467467	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112006106	chr11:36467486-36467487	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs41461648	chr11:36467501-36467502	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs186689106	chr11:36467512-36467513	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145586755	chr11:36467560-36467561	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562431981	chr11:36467627-36467628	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192617313	chr11:36467632-36467633	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs551209882	chr11:36467669-36467670	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113514839	chr11:36467709-36467710	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147956871	chr11:36467713-36467714	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs546766337	chr11:36467736-36467737	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566337180	chr11:36467773-36467774	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs112588084	chr11:36467789-36467790	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs368035456	chr11:36467794-36467795	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548986203	chr11:36467823-36467824	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141172360	chr11:36467824-36467825	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537603402	chr11:36467827-36467828	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs142114791	chr11:36467854-36467855	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs150115424	chr11:36467900-36467901	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs138250255	chr11:36467918-36467919	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372300904	chr11:36467945-36467946	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149619272	chr11:36467949-36467950	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375583647	chr11:36467960-36467961	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200287266	chr11:36467964-36467965	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183333097	chr11:36468000-36468001	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs146924663	chr11:36468012-36468013	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs376119167	chr11:36468035-36468036	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs368735959	chr11:36468064-36468065	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372414322	chr11:36468071-36468072	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs187672992	chr11:36468099-36468100	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147017495	chr11:36468102-36468103	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372629808	chr11:36468110-36468111	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
WAGR syndrome	19222835	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	21829676	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	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
Lung cancer	21911935	CNVD

Chromatin state (count:821 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:36400200-36475400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr11:36413000-36471000	Weak transcription	Aorta	Aorta
3	chr11:36414800-36475600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr11:36432000-36467800	Weak transcription	Esophagus	oesophagus
5	chr11:36433800-36471400	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr11:36444000-36471400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr11:36444200-36471400	Weak transcription	Small Intestine	intestine
8	chr11:36447600-36471000	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr11:36448400-36470600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr11:36448600-36470600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr11:36448600-36471000	Weak transcription	Fetal Thymus	thymus
12	chr11:36448600-36471000	Strong transcription	Rectal Mucosa Donor 29	rectum
13	chr11:36448800-36471400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr11:36449200-36467800	Weak transcription	Ovary	ovary
15	chr11:36449200-36469200	Weak transcription	Placenta	Placenta
16	chr11:36449200-36471400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr11:36449400-36471200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr11:36449400-36471200	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr11:36449600-36467600	Weak transcription	Rectal Smooth Muscle	rectum
20	chr11:36449600-36469000	Weak transcription	Fetal Muscle Trunk	muscle
21	chr11:36449600-36474000	Weak transcription	Right Ventricle	heart
22	chr11:36450000-36468400	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr11:36452400-36470600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr11:36452800-36473800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr11:36453400-36471200	Strong transcription	Sigmoid Colon	Sigmoid Colon
26	chr11:36453600-36471200	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr11:36454200-36467400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr11:36454200-36468000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr11:36454200-36468400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr11:36454200-36468600	Weak transcription	HMEC	breast
31	chr11:36454200-36468800	Weak transcription	Osteobl	bone
32	chr11:36454800-36473600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr11:36455800-36473800	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr11:36456600-36470800	Strong transcription	Fetal Intestine Large	intestine
35	chr11:36457400-36471400	Weak transcription	Stomach Mucosa	stomach
36	chr11:36459600-36468400	Weak transcription	Fetal Lung	lung
37	chr11:36460200-36467800	Weak transcription	Duodenum Mucosa	Duodenum
38	chr11:36461000-36467800	Weak transcription	Pancreas	Pancrea
39	chr11:36461200-36467800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr11:36461600-36472600	Weak transcription	NH-A	brain
41	chr11:36462000-36471400	Weak transcription	Liver	Liver
42	chr11:36462400-36467800	Weak transcription	Adipose Nuclei	Adipose
43	chr11:36462600-36468000	Weak transcription	NHEK	skin
44	chr11:36462800-36467800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr11:36463000-36467600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr11:36463000-36474000	Weak transcription	Fetal Kidney	kidney
47	chr11:36463200-36468600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr11:36463400-36467600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr11:36463400-36468000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr11:36463400-36469000	Weak transcription	HSMMtube	muscle

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