Variant report

Variant	nsv982991
Chromosome Location	chr11:18424852-18431306
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:372)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:372 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:18427130-18427330	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:18429056-18429644	HepG2	liver:	n/a	n/a
3	BCL3	chr11:18429952-18430937	A549	lung:	n/a	n/a
4	BCL3	chr11:18430222-18430427	K562	blood:	n/a	n/a
5	BCL3	chr11:18428976-18431218	A549	lung:	n/a	n/a
6	BCL3	chr11:18430078-18430741	GM12878	blood:	n/a	n/a
7	BCL3	chr11:18429501-18430863	K562	blood:	n/a	n/a
8	BCLAF1	chr11:18430346-18430780	GM12878	blood:	n/a	n/a
9	BCLAF1	chr11:18430160-18430545	K562	blood:	n/a	n/a
10	CCNT2	chr11:18429733-18430371	K562	blood:	n/a	n/a
11	CEBPB	chr11:18425457-18425688	HepG2	liver:	n/a	chr11:18425533-18425544
12	CEBPB	chr11:18429018-18429652	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr11:18429060-18429676	A549	lung:	n/a	n/a
14	CEBPB	chr11:18429349-18429650	K562	blood:	n/a	n/a
15	CEBPB	chr11:18429308-18429653	HepG2	liver:	n/a	n/a
16	CEBPB	chr11:18425506-18425586	Hela-S3	cervix:	n/a	chr11:18425533-18425544
17	CEBPB	chr11:18429392-18429612	IMR90	lung:	n/a	n/a
18	CEBPB	chr11:18425489-18425627	A549	lung:	n/a	chr11:18425533-18425544
19	CEBPD	chr11:18430049-18430486	HepG2	liver:	n/a	n/a
20	CHD2	chr11:18430353-18430842	K562	blood:	n/a	n/a
21	CHD2	chr11:18430275-18430553	GM12878	blood:	n/a	n/a
22	CHD2	chr11:18430239-18430254	HepG2	liver:	n/a	n/a
23	CREB1	chr11:18430083-18430411	A549	lung:	n/a	n/a
24	CREB1	chr11:18430149-18430585	A549	lung:	n/a	n/a
25	CTCF	chr11:18426965-18427139	T-47D	breast:	n/a	n/a
26	CTCF	chr11:18425173-18425367	T-47D	breast:	n/a	n/a
27	CTCF	chr11:18430200-18430350	GM12878	blood:	n/a	n/a
28	CTCF	chr11:18428660-18429297	T-47D	breast:	n/a	n/a
29	CTCF	chr11:18428659-18428735	GM10266	blood:	n/a	n/a
30	CUX1	chr11:18425225-18425367	GM12878	blood:	n/a	n/a
31	ELF1	chr11:18430248-18430727	A549	lung:	n/a	n/a
32	EP300	chr11:18428641-18429230	T-47D	breast:	n/a	chr11:18428647-18428661
33	EP300	chr11:18425163-18425366	T-47D	breast:	n/a	n/a
34	FOS	chr11:18429013-18429276	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr11:18429022-18429411	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr11:18429025-18429616	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr11:18429021-18429380	MCF10A-Er-Src	breast:	n/a	n/a
38	FOSL2	chr11:18429613-18430944	HepG2	liver:	n/a	n/a
39	FOSL2	chr11:18429011-18429297	A549	lung:	n/a	chr11:18429197-18429208
40	FOSL2	chr11:18428957-18429498	HepG2	liver:	n/a	chr11:18429197-18429208
41	FOSL2	chr11:18428909-18429415	HepG2	liver:	n/a	chr11:18429197-18429208
42	FOSL2	chr11:18428926-18429490	A549	lung:	n/a	chr11:18429197-18429208
43	FOXA1	chr11:18428828-18429382	HepG2	liver:	n/a	n/a
44	FOXA1	chr11:18428973-18429264	HepG2	liver:	n/a	n/a
45	FOXA1	chr11:18428800-18429453	HepG2	liver:	n/a	n/a
46	FOXA1	chr11:18428864-18429228	HepG2	liver:	n/a	n/a
47	FOXA2	chr11:18428853-18429442	A549	lung:	n/a	n/a
48	FOXA2	chr11:18428935-18429265	A549	lung:	n/a	n/a
49	FOXA2	chr11:18428942-18429281	HepG2	liver:	n/a	n/a
50	GABPA	chr11:18429049-18429158	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:18429080-18429130	SAEC	small airway:	n/a
2	chr11:18429080-18429130	BE2_C	brain:	n/a
3	chr11:18429080-18429130	Hela-S3	cervix:	n/a
4	chr11:18429080-18429130	PANC-1	pancreas:	n/a
5	chr11:18429080-18429130	SK-N-MC	brain:	n/a
6	chr11:18429080-18429130	HAEpiC	amniotic membrane:	n/a
7	chr11:18429080-18429130	SK-N-SH	brain:	n/a
8	chr11:18429080-18429130	NHDF-neo	bronchial:	n/a
9	chr11:18429080-18429130	AoSMC	blood vessel:	n/a
10	chr11:18429080-18429130	GM06990	blood:	n/a
11	chr11:18429080-18429130	SKMC	muscle:	n/a
12	chr11:18429080-18429130	ovcar-3	ovarian:	n/a
13	chr11:18429080-18429130	MCF10A-Er-Src	breast:	n/a
14	chr11:18429080-18429130	BJ	skin:	n/a
15	chr11:18429080-18429130	HCT-116	colon:	n/a
16	chr11:18429080-18429130	T-47D	breast:	n/a
17	chr11:18429080-18429130	ProgFib	skin:	n/a
18	chr11:18429080-18429130	AG04450	lung:	fetal
19	chr11:18429080-18429130	HRCEpiC	kidney:	n/a
20	chr11:18429080-18429130	SK-N-SH_RA	brain:	n/a
21	chr11:18429080-18429130	HL-60	blood:	n/a
22	chr11:18429080-18429130	U87	brain:	n/a
23	chr11:18429080-18429130	AG10803	skin:	n/a
24	chr11:18429080-18429130	PFSK-1	brain:	n/a
25	chr11:18429080-18429130	IMR90	lung:	fetal
26	chr11:18429080-18429130	NH-A	brain:	n/a
27	chr11:18429080-18429130	GM12892	blood:	n/a
28	chr11:18429080-18429130	GM19239	blood:	n/a
29	chr11:18429080-18429130	LNCaP	prostate:	n/a
30	chr11:18429080-18429130	GM12891	blood:	n/a
31	chr11:18429080-18429130	ECC-1	luminal epithelium:	n/a
32	chr11:18429080-18429130	HepG2	liver:	n/a
33	chr11:18429080-18429130	A549	lung:	n/a
34	chr11:18429080-18429130	HCPEpiC	choroid plexus:	n/a
35	chr11:18429080-18429130	H1-hESC	embryonic stem cell:	embryo
36	chr11:18429080-18429130	HMEC	breast:	n/a
37	chr11:18429080-18429130	HCM	heart:	n/a
38	chr11:18429080-18429130	HEEpiC	esophagus:	n/a
39	chr11:18429080-18429130	HIPEpiC	eye:	n/a
40	chr11:18429080-18429130	MCF-7	breast:	n/a
41	chr11:18429080-18429130	AG09309	skin:	n/a
42	chr11:18429080-18429130	Caco-2	colon:	n/a
43	chr11:18429080-18429130	GM12878	blood:	n/a
44	chr11:18429080-18429130	HRPEpiC	eye:	n/a
45	chr11:18429080-18429130	AG09319	gingival:	n/a
46	chr11:18429080-18429130	K562	blood:	n/a
47	chr11:18429080-18429130	CMK	blood:	n/a
48	chr11:18429080-18429130	HNPCEpiC	eye:	n/a
49	chr11:18429080-18429130	HUVEC	blood vessel:	n/a
50	chr11:18429080-18429130	RPTEC	kidney:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:18415873..18420206-chr11:18430045..18435036,6	MCF-7	breast:
2	chr11:18430457..18432481-chr11:18456231..18458824,2	K562	blood:
3	chr11:18398568..18400836-chr11:18427462..18430326,2	MCF-7	breast:
4	chr11:18406695..18409198-chr11:18428247..18430111,2	K562	blood:
5	chr11:18415665..18418550-chr11:18429109..18431220,2	MCF-7	breast:
6	chr11:18419996..18422097-chr11:18428785..18430371,2	K562	blood:
7	chr11:18414611..18420404-chr11:18425224..18433817,11	K562	blood:
8	chr11:18423297..18429050-chr11:18429237..18433863,11	K562	blood:
9	chr11:18430626..18432747-chr11:18545645..18547445,2	K562	blood:
10	chr11:18429091..18432597-chr11:18437736..18442022,5	K562	blood:
11	chr11:18428578..18433796-chr11:18433952..18441799,12	K562	blood:
12	chr11:18429708..18432011-chr11:18438993..18440849,2	MCF-7	breast:
13	chr11:18429142..18431296-chr11:18432609..18435165,2	K562	blood:
14	chr11:18430992..18433594-chr11:18671547..18674322,2	K562	blood:
15	chr11:18342292..18344024-chr11:18424254..18426618,2	MCF-7	breast:
16	chr11:18338559..18340815-chr11:18429973..18431538,2	K562	blood:
17	chr11:18415543..18417980-chr11:18429058..18431461,3	K562	blood:
18	chr11:18423297..18429050-chr11:18429237..18433863,11	K562	blood:
19	chr11:18429496..18431588-chr11:18458511..18461417,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LDHC-1	chr11:18428199-18428278	ENSG00000256006.1
2	lnc-LDHC-1	chr11:18427156-18427345	ENSG00000256006.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	LDHA	hsa-miR-34a-5p	chr11:18429085-18429092
2	LDHA	hsa-miR-33a-5p	chr11:18429322-18429340
3	LDHA	hsa-miR-34a-5p	chr11:18429069-18429092
4	LDHA	hsa-miR-33a-5p	chr11:18429333-18429340

Variant related genes	Relation type
ENSG00000256006	TF binding region
LDHC	TF binding region
ENSG00000256006	CpG island
LDHC	CpG island
ENSG00000110756	chromatin interactions
ENSG00000110768	chromatin interactions
ENSG00000166796	chromatin interactions
ENSG00000256006	chromatin interactions
ENSG00000134333	chromatin interactions

Extended variants
information (count: 312 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:312 , 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	rs144496208	chr11:18424882-18424883	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs542603354	chr11:18424908-18424909	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs544501453	chr11:18424922-18424923	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs16935413	chr11:18424939-18424940	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs547674559	chr11:18424978-18424979	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs1881716	chr11:18425018-18425019	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs533687086	chr11:18425029-18425030	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs552140004	chr11:18425064-18425065	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs538352453	chr11:18425088-18425089	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs377663876	chr11:18425101-18425102	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs143728814	chr11:18425138-18425139	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs377156358	chr11:18425187-18425188	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs200096279	chr11:18425205-18425206	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs200998448	chr11:18425228-18425229	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs112255990	chr11:18425239-18425240	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs373534867	chr11:18425242-18425243	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs34305721	chr11:18425256-18425257	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs370781767	chr11:18425258-18425259	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs199918200	chr11:18425320-18425321	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs141158742	chr11:18425344-18425345	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs150740870	chr11:18425352-18425353	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs182873744	chr11:18425367-18425368	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs200198118	chr11:18425372-18425373	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs376918699	chr11:18425374-18425375	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs11024643	chr11:18425461-18425462	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs538423002	chr11:18425474-18425475	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs556882708	chr11:18425534-18425535	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs111461382	chr11:18425558-18425559	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs200031803	chr11:18425565-18425566	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs575178047	chr11:18425571-18425572	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs187467694	chr11:18425580-18425581	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs560891872	chr11:18425588-18425589	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs572870525	chr11:18425614-18425615	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs192351379	chr11:18425635-18425636	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs373308408	chr11:18425639-18425640	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs564960172	chr11:18425671-18425672	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs56261949	chr11:18425687-18425688	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs397724785	chr11:18425697-18425698	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs542162368	chr11:18425805-18425806	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs552003093	chr11:18425845-18425846	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs61884347	chr11:18425864-18425865	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs145662285	chr11:18425904-18425905	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs550823219	chr11:18425971-18425972	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs549112311	chr11:18425980-18425981	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs112627800	chr11:18426022-18426023	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs527770925	chr11:18426054-18426055	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs373733667	chr11:18426091-18426092	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs187464585	chr11:18426121-18426122	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs7947664	chr11:18426138-18426139	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs551535785	chr11:18426171-18426172	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
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
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18418200-18425600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:18418200-18433800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:18418400-18430600	Strong transcription	Fetal Muscle Trunk	muscle
4	chr11:18418400-18430800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr11:18418400-18430800	Strong transcription	Left Ventricle	heart
6	chr11:18418400-18433200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr11:18418600-18427800	Strong transcription	Liver	Liver
8	chr11:18418600-18428600	Strong transcription	Fetal Intestine Large	intestine
9	chr11:18418600-18429400	Strong transcription	Primary T killer memory cells from peripheral blood	blood
10	chr11:18418600-18429800	Strong transcription	H1 Cell Line	embryonic stem cell
11	chr11:18418600-18430400	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr11:18418600-18430400	Strong transcription	Primary B cells from peripheral blood	blood
13	chr11:18418600-18430400	Strong transcription	Placenta	Placenta
14	chr11:18418600-18430400	Strong transcription	Rectal Mucosa Donor 31	rectum
15	chr11:18418600-18430400	Strong transcription	Skeletal Muscle Male	skeletal muscle
16	chr11:18418600-18430600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr11:18418600-18430600	Strong transcription	Placenta Amnion	Placenta Amnion
18	chr11:18418600-18430600	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr11:18418600-18430800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr11:18418600-18430800	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr11:18418600-18430800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr11:18418600-18430800	Strong transcription	Duodenum Smooth Muscle	Duodenum
23	chr11:18418600-18430800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr11:18418600-18430800	Strong transcription	Fetal Muscle Leg	muscle
25	chr11:18418600-18430800	Strong transcription	Fetal Stomach	stomach
26	chr11:18418600-18430800	Strong transcription	Fetal Thymus	thymus
27	chr11:18418600-18430800	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr11:18418600-18430800	Strong transcription	Right Ventricle	heart
29	chr11:18418800-18427400	Strong transcription	Primary hematopoietic stem cells	blood
30	chr11:18418800-18427600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr11:18418800-18430400	Strong transcription	HUES48 Cell Line	embryonic stem cell
32	chr11:18418800-18430600	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr11:18418800-18430600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
34	chr11:18418800-18430600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr11:18418800-18430600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr11:18418800-18430800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr11:18418800-18430800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr11:18418800-18430800	Strong transcription	Adipose Nuclei	Adipose
39	chr11:18418800-18430800	Strong transcription	Osteobl	bone
40	chr11:18418800-18431000	Strong transcription	Primary neutrophils fromperipheralblood	blood
41	chr11:18419000-18426800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr11:18419000-18428000	Strong transcription	Colonic Mucosa	Colon
43	chr11:18419000-18429200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr11:18419000-18430000	Strong transcription	Primary T helper naive cells from peripheral blood	blood
45	chr11:18419000-18430400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr11:18419000-18430600	Strong transcription	Duodenum Mucosa	Duodenum
47	chr11:18419000-18430800	Strong transcription	Brain Anterior Caudate	brain
48	chr11:18419000-18430800	Strong transcription	Fetal Intestine Small	intestine
49	chr11:18419000-18431400	Strong transcription	HSMM	muscle
50	chr11:18419200-18428400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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