Variant report

Variant	esv2761651
Chromosome Location	chr11:18606832-18621409
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:536)
CpG islands
(count:854)
Chromatin interactive
region (count:30)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:536 , 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	chr11:18610096-18610485	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:18610173-18610356	K562	blood:	n/a	n/a
3	ATF1	chr11:18609453-18609611	K562	blood:	n/a	n/a
4	ATF2	chr11:18610239-18610614	GM12878	blood:	n/a	n/a
5	ATF2	chr11:18609997-18610603	GM12878	blood:	n/a	n/a
6	ATF3	chr11:18610068-18610657	A549	lung:	n/a	n/a
7	ATF3	chr11:18609921-18610632	A549	lung:	n/a	chr11:18610008-18610017
8	ATF3	chr11:18610233-18610481	K562	blood:	n/a	n/a
9	BACH1	chr11:18610312-18610506	K562	blood:	n/a	n/a
10	BACH1	chr11:18610163-18610624	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr11:18610023-18610541	A549	lung:	n/a	n/a
12	BCL3	chr11:18609908-18610716	A549	lung:	n/a	n/a
13	BCLAF1	chr11:18609961-18610673	GM12878	blood:	n/a	n/a
14	BHLHE40	chr11:18610071-18610576	K562	blood:	n/a	n/a
15	BRCA1	chr11:18609896-18610869	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr11:18610046-18610549	K562	blood:	n/a	n/a
17	CBX3	chr11:18609904-18610654	HCT-116	colon:	n/a	n/a
18	CCNT2	chr11:18610049-18610509	K562	blood:	n/a	chr11:18610310-18610319
19	CEBPB	chr11:18610284-18610356	HepG2	liver:	n/a	n/a
20	CEBPB	chr11:18618687-18618996	IMR90	lung:	n/a	chr11:18618851-18618862 chr11:18618850-18618861
21	CEBPB	chr11:18618765-18618995	HepG2	liver:	n/a	chr11:18618851-18618862 chr11:18618850-18618861
22	CEBPB	chr11:18611270-18611543	IMR90	lung:	n/a	n/a
23	CEBPB	chr11:18618717-18619004	A549	lung:	n/a	chr11:18618851-18618862 chr11:18618850-18618861
24	CEBPB	chr11:18617027-18617239	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr11:18609818-18610715	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr11:18609775-18610458	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr11:18618793-18618956	Hela-S3	cervix:	n/a	chr11:18618851-18618862 chr11:18618850-18618861
28	CEBPB	chr11:18618793-18618907	K562	blood:	n/a	chr11:18618851-18618862 chr11:18618850-18618861
29	CEBPB	chr11:18616924-18617324	IMR90	lung:	n/a	n/a
30	CEBPD	chr11:18610138-18610507	HepG2	liver:	n/a	n/a
31	CEBPD	chr11:18610035-18610493	HepG2	liver:	n/a	n/a
32	CHD1	chr11:18609655-18610745	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr11:18610079-18610807	GM12878	blood:	n/a	n/a
34	CHD2	chr11:18609705-18610664	GM12878	blood:	n/a	n/a
35	CHD2	chr11:18616947-18617077	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr11:18609948-18610577	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr11:18610314-18610320	K562	blood:	n/a	n/a
38	CHD2	chr11:18610085-18610539	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr11:18610056-18610461	HepG2	liver:	n/a	n/a
40	CREB1	chr11:18610098-18610469	A549	lung:	n/a	n/a
41	CREB1	chr11:18609965-18610530	A549	lung:	n/a	n/a
42	CTCF	chr11:18610140-18610290	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr11:18609860-18610010	GM12873	blood:	n/a	n/a
44	CTCF	chr11:18617200-18617350	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr11:18610200-18610350	Caco-2	colon:	n/a	n/a
46	CTCF	chr11:18621000-18621150	HAc	cerebellar:	n/a	n/a
47	CTCF	chr11:18610020-18610170	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr11:18610160-18610310	AG04449	skin:	n/a	n/a
49	CTCF	chr11:18608492-18608509	GM13976	blood:	n/a	n/a
50	CTCF	chr11:18610159-18610281	Lung_OC	lung:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:18610448-18610498	ECC-1	luminal epithelium:	n/a
2	chr11:18611549-18611599	Hepatocyte	liver:	n/a
3	chr11:18610297-18610347	K562	blood:	n/a
4	chr11:18610430-18610480	AG04449	skin:	fetal
5	chr11:18618092-18618142	HRCEpiC	kidney:	n/a
6	chr11:18617206-18617256	HCT-116	colon:	n/a
7	chr11:18618092-18618142	SKMC	muscle:	n/a
8	chr11:18618092-18618142	BJ	skin:	n/a
9	chr11:18611549-18611599	HRE	kidney:	n/a
10	chr11:18610448-18610498	MCF10A-Er-Src	breast:	n/a
11	chr11:18610074-18610124	Hepatocyte	liver:	n/a
12	chr11:18610462-18610512	GM12892	blood:	n/a
13	chr11:18610430-18610480	SKMC	muscle:	n/a
14	chr11:18609698-18609748	HCPEpiC	choroid plexus:	n/a
15	chr11:18610430-18610480	HepG2	liver:	n/a
16	chr11:18610462-18610512	SK-N-MC	brain:	n/a
17	chr11:18610440-18610490	Caco-2	colon:	n/a
18	chr11:18618452-18618502	HepG2	liver:	n/a
19	chr11:18610448-18610498	MCF-7	breast:	n/a
20	chr11:18610297-18610347	HCPEpiC	choroid plexus:	n/a
21	chr11:18609698-18609748	ovcar-3	ovarian:	n/a
22	chr11:18610422-18610472	HCPEpiC	choroid plexus:	n/a
23	chr11:18618092-18618142	MCF-7	breast:	n/a
24	chr11:18610297-18610347	AG09319	gingival:	n/a
25	chr11:18618452-18618502	NT2-D1	testis:	n/a
26	chr11:18610297-18610347	NHBE	bronchial:	n/a
27	chr11:18610074-18610124	HCF	heart:	n/a
28	chr11:18610271-18610321	AG04450	lung:	fetal
29	chr11:18610422-18610472	BJ	skin:	n/a
30	chr11:18610557-18610607	SK-N-SH	brain:	n/a
31	chr11:18610074-18610124	RPTEC	kidney:	n/a
32	chr11:18610448-18610498	SAEC	small airway:	n/a
33	chr11:18610297-18610347	ovcar-3	ovarian:	n/a
34	chr11:18610440-18610490	HNPCEpiC	eye:	n/a
35	chr11:18610271-18610321	AG09319	gingival:	n/a
36	chr11:18610462-18610512	RPTEC	kidney:	n/a
37	chr11:18618092-18618142	GM12878	blood:	n/a
38	chr11:18610557-18610607	GM12892	blood:	n/a
39	chr11:18618452-18618502	AG04450	lung:	fetal
40	chr11:18617206-18617256	SK-N-SH_RA	brain:	n/a
41	chr11:18618452-18618502	HUVEC	blood vessel:	n/a
42	chr11:18618092-18618142	T-47D	breast:	n/a
43	chr11:18610422-18610472	T-47D	breast:	n/a
44	chr11:18610440-18610490	NT2-D1	testis:	n/a
45	chr11:18610462-18610512	CMK	blood:	n/a
46	chr11:18610448-18610498	K562	blood:	n/a
47	chr11:18610422-18610472	GM12878	blood:	n/a
48	chr11:18610271-18610321	T-47D	breast:	n/a
49	chr11:18617206-18617256	AoSMC	blood vessel:	n/a
50	chr11:18610440-18610490	T-47D	breast:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:18606558..18609018-chr11:18609349..18611794,2	K562	blood:
2	chr1:171454647..171455196-chr11:18610341..18611032,2	Hela-S3	cervix:
3	chr11:18609996..18610733-chr13:28195557..28196494,2	NB4	blood:
4	chr11:18616692..18618721-chr11:18623253..18625857,2	MCF-7	breast:
5	chr11:18613720..18616204-chr11:18617237..18618786,2	K562	blood:
6	chr11:18572038..18574109-chr11:18607520..18610133,2	MCF-7	breast:
7	chr11:18612916..18614635-chr11:18629860..18632297,2	K562	blood:
8	chr11:18608525..18612049-chr11:18615119..18618882,10	MCF-7	breast:
9	chr11:18608525..18612049-chr11:18615119..18618882,10	MCF-7	breast:
10	chr11:18597269..18603847-chr11:18605648..18613112,11	MCF-7	breast:
11	chr11:18547186..18549445-chr11:18607046..18609012,2	K562	blood:
12	chr11:18618133..18619654-chr11:18626232..18627753,2	K562	blood:
13	chr11:18548142..18548670-chr11:18609940..18610633,2	MCF-7	breast:
14	chr11:18546303..18549278-chr11:18609985..18612598,2	K562	blood:
15	chr11:18608086..18610318-chr11:18611041..18613444,3	MCF-7	breast:
16	chr11:18608840..18612225-chr11:18653403..18657833,8	MCF-7	breast:
17	chr11:18547166..18549278-chr11:18610430..18612598,2	K562	blood:
18	chr11:18615620..18618161-chr11:18620162..18622897,2	K562	blood:
19	chr11:18610193..18610780-chr14:20811242..20811842,2	Hela-S3	cervix:
20	chr11:18616067..18617811-chr11:18630289..18631863,2	K562	blood:
21	chr11:18608159..18612115-chr11:18615596..18618860,5	MCF-7	breast:
22	chr11:18615620..18618161-chr11:18620162..18622897,2	K562	blood:
23	chr11:18599363..18605712-chr11:18606522..18612149,6	MCF-7	breast:
24	chr11:18609516..18611215-chr11:18612978..18615321,2	K562	blood:
25	chr11:18606558..18609018-chr11:18609349..18612964,3	K562	blood:
26	chr11:18605180..18608617-chr11:18608689..18610549,5	MCF-7	breast:
27	chr11:18608159..18612115-chr11:18615596..18618860,5	MCF-7	breast:
28	chr11:18546321..18548809-chr11:18607625..18610007,2	K562	blood:
29	chr11:18609259..18612621-chr11:18654534..18657923,6	MCF-7	breast:
30	chr11:18032918..18034516-chr11:18609753..18611706,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UEVLD-3	chr11:18617006-18617196	NONHSAT018301
2	lnc-UEVLD-3	chr11:18617717-18617842	NONHSAT018301
3	lnc-UEVLD-3	chr11:18620978-18621230	NONHSAT018301
4	lnc-UEVLD-1	chr11:18612083-18612500	NONHSAT018300
5	lnc-UEVLD-3	chr11:18617451-18617842	NONHSAT018303
6	lnc-TMEM86A-2	chr11:18621336-18621544	ENSG00000247595
7	lnc-TMEM86A-2	chr11:18621354-18621544	NONHSAT018307
8	lnc-UEVLD-1	chr11:18610405-18611827	NONHSAT018299
9	lnc-UEVLD-1	chr11:18610405-18611832	NONHSAT018300
10	lnc-UEVLD-1	chr11:18612083-18612500	NONHSAT018299
11	lnc-TMEM86A-2	chr11:18610329-18610542	NONHSAT018298
12	lnc-UEVLD-3	chr11:18620978-18621141	NONHSAT018303

No data

Variant related genes	Relation type
SPTY2D1-AS1	TF binding region
ENSG00000256282	TF binding region
UEVLD	TF binding region
SPTY2D1-AS1	CpG island
ENSG00000256282	CpG island
UEVLD	CpG island
ENSG00000256282	chromatin interactions
ENSG00000151116	chromatin interactions
ENSG00000129158	chromatin interactions
ENSG00000074319	chromatin interactions
ENSG00000129484	chromatin interactions
ENSG00000179119	chromatin interactions
ENSG00000186184	chromatin interactions
ENSG00000117523	chromatin interactions
ENSG00000259001	chromatin interactions
ENSG00000247595	chromatin interactions

Extended variants
information (count: 541 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551894067	chr11:18606835-18606836	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs548525209	chr11:18606842-18606843	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs560424025	chr11:18606881-18606882	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs192679756	chr11:18606888-18606889	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs570220926	chr11:18606892-18606893	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs551986131	chr11:18606917-18606918	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs138478730	chr11:18606920-18606921	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs35864596	chr11:18606932-18606933	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs556538020	chr11:18606969-18606970	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs373462062	chr11:18606995-18606996	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs537619512	chr11:18607006-18607007	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs549667320	chr11:18607121-18607122	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs112928334	chr11:18607190-18607191	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs200516286	chr11:18607191-18607192	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs116960334	chr11:18607192-18607193	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs200158645	chr11:18607193-18607194	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs75642764	chr11:18607201-18607202	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs75872267	chr11:18607203-18607204	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs553725112	chr11:18607235-18607236	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs71443703	chr11:18607236-18607237	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs184722623	chr11:18607287-18607288	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs112891262	chr11:18607297-18607298	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs143001365	chr11:18607299-18607300	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs557852875	chr11:18607343-18607344	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs577536506	chr11:18607346-18607347	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs544772405	chr11:18607424-18607425	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs375350797	chr11:18607461-18607462	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs563187407	chr11:18607462-18607463	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs575070056	chr11:18607486-18607487	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs541907714	chr11:18607618-18607619	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs143334483	chr11:18607634-18607635	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs527649504	chr11:18607657-18607658	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs545912014	chr11:18607682-18607683	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs564191964	chr11:18607712-18607713	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs11024724	chr11:18607746-18607747	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs78325873	chr11:18607771-18607772	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs533173743	chr11:18607824-18607825	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs549555100	chr11:18607836-18607837	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs12290527	chr11:18607840-18607841	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs554014839	chr11:18607909-18607910	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs563419914	chr11:18607914-18607915	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs566128012	chr11:18607983-18607984	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs529166408	chr11:18607996-18607997	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs539836563	chr11:18608053-18608054	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs141669133	chr11:18608062-18608063	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs565685282	chr11:18608099-18608100	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs539412718	chr11:18608118-18608119	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs376522548	chr11:18608200-18608201	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs557891963	chr11:18608221-18608222	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs541193502	chr11:18608278-18608279	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:967 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18549600-18608600	Weak transcription	Fetal Heart	heart
2	chr11:18549600-18609000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr11:18549600-18609000	Weak transcription	Fetal Brain Male	brain
4	chr11:18563800-18608800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr11:18565200-18609400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr11:18574400-18609400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:18575000-18609200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr11:18575200-18609200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr11:18578000-18608800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr11:18578000-18609000	Weak transcription	Right Ventricle	heart
11	chr11:18578200-18609000	Weak transcription	Primary T cells from cord blood	blood
12	chr11:18578400-18609000	Weak transcription	Primary hematopoietic stem cells	blood
13	chr11:18578600-18608400	Weak transcription	Psoas Muscle	Psoas
14	chr11:18580000-18608600	Weak transcription	Hela-S3	cervix
15	chr11:18580200-18608600	Weak transcription	Brain Cingulate Gyrus	brain
16	chr11:18581000-18609000	Weak transcription	Pancreas	Pancrea
17	chr11:18583000-18608200	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr11:18583000-18609400	Weak transcription	Esophagus	oesophagus
19	chr11:18584200-18608000	Weak transcription	Small Intestine	intestine
20	chr11:18584400-18609800	Weak transcription	Spleen	Spleen
21	chr11:18585800-18608600	Weak transcription	Fetal Brain Female	brain
22	chr11:18586400-18609000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr11:18588200-18608800	Weak transcription	Fetal Kidney	kidney
24	chr11:18591800-18608800	Weak transcription	NHEK	skin
25	chr11:18592200-18609000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr11:18592200-18609400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr11:18593000-18608200	Weak transcription	Brain Germinal Matrix	brain
28	chr11:18593400-18608600	Weak transcription	Dnd41	blood
29	chr11:18593600-18609400	Weak transcription	Aorta	Aorta
30	chr11:18594800-18608800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr11:18594800-18609000	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr11:18595000-18608600	Weak transcription	Brain Angular Gyrus	brain
33	chr11:18595000-18609000	Weak transcription	Primary B cells from cord blood	blood
34	chr11:18595200-18609200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr11:18595800-18608800	Weak transcription	NHLF	lung
36	chr11:18596400-18608400	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr11:18597200-18608000	Weak transcription	Brain Hippocampus Middle	brain
38	chr11:18597200-18608800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr11:18597200-18609000	Weak transcription	Fetal Thymus	thymus
40	chr11:18597400-18608400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr11:18597400-18608600	Weak transcription	HMEC	breast
42	chr11:18597600-18608600	Weak transcription	Brain Anterior Caudate	brain
43	chr11:18597600-18608800	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr11:18597600-18608800	Weak transcription	Brain Substantia Nigra	brain
45	chr11:18597600-18608800	Weak transcription	HUVEC	blood vessel
46	chr11:18598400-18608800	Weak transcription	Thymus	Thymus
47	chr11:18598800-18608400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr11:18599000-18608800	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr11:18599000-18608800	Weak transcription	Fetal Lung	lung
50	chr11:18599200-18607800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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