Variant report

Variant	nsv541029
Chromosome Location	chr11:46442658-46460232
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:209)
CpG islands
(count:244)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:209 , 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	ARID3A	chr11:46443227-46443395	K562	blood:	n/a	n/a
2	ARID3A	chr11:46448994-46449194	K562	blood:	n/a	n/a
3	BACH1	chr11:46448745-46449320	K562	blood:	n/a	n/a
4	BACH1	chr11:46448756-46449380	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr11:46442812-46443109	K562	blood:	n/a	n/a
6	BHLHE40	chr11:46448992-46449140	K562	blood:	n/a	n/a
7	BRCA1	chr11:46444397-46444477	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr11:46448838-46449313	K562	blood:	n/a	n/a
9	CEBPB	chr11:46450045-46450119	K562	blood:	n/a	n/a
10	CTCF	chr11:46455060-46455210	MCF-7	breast:	n/a	n/a
11	CTCF	chr11:46444100-46444250	GM12864	blood:	n/a	n/a
12	CTCF	chr11:46450208-46450455	T-47D	breast:	n/a	n/a
13	CUX1	chr11:46443053-46443232	K562	blood:	n/a	n/a
14	CUX1	chr11:46448985-46449166	K562	blood:	n/a	n/a
15	CUX1	chr11:46459835-46460035	K562	blood:	n/a	n/a
16	E2F6	chr11:46448998-46449154	K562	blood:	n/a	n/a
17	EBF1	chr11:46458754-46459234	GM12878	blood:	n/a	n/a
18	EBF1	chr11:46449094-46449278	GM12878	blood:	n/a	chr11:46449179-46449190 chr11:46449201-46449212
19	EGR1	chr11:46448961-46449317	K562	blood:	n/a	n/a
20	EGR1	chr11:46448960-46449410	K562	blood:	n/a	n/a
21	EP300	chr11:46450160-46450496	T-47D	breast:	n/a	n/a
22	EP300	chr11:46448105-46448438	SK-N-SH_RA	brain:	n/a	n/a
23	EP300	chr11:46448939-46449225	K562	blood:	n/a	n/a
24	EP300	chr11:46448206-46448435	SK-N-SH_RA	brain:	n/a	n/a
25	EP300	chr11:46442819-46443094	K562	blood:	n/a	n/a
26	EP300	chr11:46448217-46448475	K562	blood:	n/a	n/a
27	FOSL2	chr11:46450175-46450475	HepG2	liver:	n/a	n/a
28	FOXA1	chr11:46444118-46444454	T-47D	breast:	n/a	n/a
29	FOXA1	chr11:46444192-46444496	T-47D	breast:	n/a	n/a
30	FOXP2	chr11:46448923-46449274	SK-N-MC	brain:	n/a	chr11:46448945-46448957
31	GATA2	chr11:46448116-46448538	K562	blood:	n/a	n/a
32	GATA2	chr11:46459756-46460229	SH-SY5Y	brain:	n/a	n/a
33	GATA2	chr11:46450062-46450737	K562	blood:	n/a	n/a
34	GATA3	chr11:46444047-46444566	T-47D	breast:	n/a	chr11:46444117-46444127
35	GATA3	chr11:46443929-46444504	MCF-7	breast:	n/a	chr11:46444117-46444127
36	GATA3	chr11:46456752-46457100	SH-SY5Y	brain:	n/a	chr11:46456871-46456881 chr11:46456871-46456878 chr11:46456860-46456877
37	GATA3	chr11:46444051-46444518	T-47D	breast:	n/a	chr11:46444117-46444127
38	GATA3	chr11:46444128-46444546	MCF-7	breast:	n/a	n/a
39	GATA3	chr11:46444200-46444434	MCF-7	breast:	n/a	n/a
40	GATA3	chr11:46444072-46444644	MCF-7	breast:	n/a	chr11:46444117-46444127
41	HDAC2	chr11:46449013-46449280	H1-hESC	embryonic stem cell:	n/a	n/a
42	HEY1	chr11:46450056-46450970	K562	blood:	n/a	n/a
43	HEY1	chr11:46450576-46450975	HepG2	liver:	n/a	n/a
44	HEY1	chr11:46450670-46450940	HepG2	liver:	n/a	n/a
45	HEY1	chr11:46450582-46451013	K562	blood:	n/a	n/a
46	HEY1	chr11:46450222-46450476	HepG2	liver:	n/a	n/a
47	HNF4A	chr11:46442834-46442984	HepG2	liver:	n/a	n/a
48	IKZF1	chr11:46458953-46459180	GM12878	blood:	n/a	n/a
49	IRF1	chr11:46448949-46449262	K562	blood:	n/a	n/a
50	JUND	chr11:46442796-46443103	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:46448921-46448971	NHBE	bronchial:	n/a
2	chr11:46450417-46450467	GM06990	blood:	n/a
3	chr11:46457992-46458042	GM06990	blood:	n/a
4	chr11:46457992-46458042	HRCEpiC	kidney:	n/a
5	chr11:46450417-46450467	SK-N-MC	brain:	n/a
6	chr11:46450256-46450306	K562	blood:	n/a
7	chr11:46457992-46458042	AG04449	skin:	fetal
8	chr11:46450256-46450306	HIPEpiC	eye:	n/a
9	chr11:46448921-46448971	HNPCEpiC	eye:	n/a
10	chr11:46450417-46450467	H1-hESC	embryonic stem cell:	embryo
11	chr11:46448921-46448971	ovcar-3	ovarian:	n/a
12	chr11:46450256-46450306	HCT-116	colon:	n/a
13	chr11:46450417-46450467	BJ	skin:	n/a
14	chr11:46450256-46450306	ECC-1	luminal epithelium:	n/a
15	chr11:46450417-46450467	PANC-1	pancreas:	n/a
16	chr11:46450417-46450467	CMK	blood:	n/a
17	chr11:46450417-46450467	GM12891	blood:	n/a
18	chr11:46457992-46458042	SKMC	muscle:	n/a
19	chr11:46450256-46450306	HCM	heart:	n/a
20	chr11:46457992-46458042	MCF-7	breast:	n/a
21	chr11:46457992-46458042	Hela-S3	cervix:	n/a
22	chr11:46457992-46458042	SK-N-SH_RA	brain:	n/a
23	chr11:46450417-46450467	GM19239	blood:	n/a
24	chr11:46448921-46448971	K562	blood:	n/a
25	chr11:46448921-46448971	SK-N-SH	brain:	n/a
26	chr11:46450256-46450306	AG04450	lung:	fetal
27	chr11:46448921-46448971	HIPEpiC	eye:	n/a
28	chr11:46450256-46450306	AG04449	skin:	fetal
29	chr11:46450417-46450467	AG09309	skin:	n/a
30	chr11:46448921-46448971	NHDF-neo	bronchial:	n/a
31	chr11:46457992-46458042	A549	lung:	n/a
32	chr11:46450417-46450467	HCT-116	colon:	n/a
33	chr11:46450417-46450467	NHBE	bronchial:	n/a
34	chr11:46457992-46458042	MCF10A-Er-Src	breast:	n/a
35	chr11:46457992-46458042	BE2_C	brain:	n/a
36	chr11:46450417-46450467	HRPEpiC	eye:	n/a
37	chr11:46450256-46450306	NHBE	bronchial:	n/a
38	chr11:46457992-46458042	Jurkat	blood:	n/a
39	chr11:46457992-46458042	K562	blood:	n/a
40	chr11:46457992-46458042	AG09309	skin:	n/a
41	chr11:46450256-46450306	NT2-D1	testis:	n/a
42	chr11:46457992-46458042	CMK	blood:	n/a
43	chr11:46450256-46450306	Hela-S3	cervix:	n/a
44	chr11:46457992-46458042	ovcar-3	ovarian:	n/a
45	chr11:46450417-46450467	AG09319	gingival:	n/a
46	chr11:46448921-46448971	AG04450	lung:	fetal
47	chr11:46457992-46458042	RPTEC	kidney:	n/a
48	chr11:46450256-46450306	SK-N-SH_RA	brain:	n/a
49	chr11:46448921-46448971	GM06990	blood:	n/a
50	chr11:46450417-46450467	HL-60	blood:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:46450955..46452945-chr11:46454344..46456750,3	MCF-7	breast:
2	chr11:46437731..46440325-chr11:46455877..46458436,2	K562	blood:
3	chr11:46449218..46452238-chr6:34392341..34394490,5	MCF-7	breast:
4	chr11:46450955..46452945-chr11:46454344..46456750,3	MCF-7	breast:
5	chr11:46450734..46451351-chr6:34393375..34394080,2	Hela-S3	cervix:
6	chr11:46440995..46443504-chr11:46446202..46449083,2	MCF-7	breast:
7	chr11:46440995..46443504-chr11:46446202..46449083,2	MCF-7	breast:
8	chr11:46443696..46446311-chr11:46446481..46448303,2	K562	blood:
9	chr11:46441415..46443647-chr11:46446607..46450426,5	K562	blood:
10	chr11:46448640..46451542-chr11:46454493..46456535,2	K562	blood:
11	chr11:46447241..46449691-chr11:46451827..46453438,2	K562	blood:
12	chr11:46448640..46452068-chr11:46454493..46457739,3	K562	blood:
13	chr11:46449211..46452238-chr6:34390894..34393967,4	K562	blood:
14	chr11:46402325..46406202-chr11:46443344..46445537,3	K562	blood:
15	chr11:46443696..46446311-chr11:46446481..46448303,2	K562	blood:
16	chr11:46448160..46450143-chr11:46548223..46551067,2	MCF-7	breast:
17	chr11:46441415..46443647-chr11:46446607..46450426,5	K562	blood:
18	chr11:46447241..46449691-chr11:46451827..46453438,2	K562	blood:
19	chr11:46443817..46445771-chr11:46447587..46449187,2	K562	blood:
20	chr11:46452244..46454737-chr11:46456753..46459294,3	K562	blood:
21	chr11:46450714..46451218-chr6:34393290..34393849,2	MCF-7	breast:
22	chr11:46452244..46454737-chr11:46456753..46459294,3	K562	blood:
23	chr11:46450716..46451228-chr6:34393228..34393955,2	HCT-116	colon:
24	chr11:46443817..46445771-chr11:46447587..46449187,2	K562	blood:
25	chr11:46423726..46425572-chr11:46451207..46453427,2	MCF-7	breast:
26	chr11:46450213..46450713-chr6:34392822..34393736,2	Hela-S3	cervix:
27	chr11:46450238..46451231-chr6:34393265..34393905,3	MCF-7	breast:
28	chr11:46450731..46452237-chr6:34392318..34394068,7	MCF-7	breast:
29	chr11:46449233..46452238-chr6:34392226..34393967,6	K562	blood:

No data

Variant related genes	Relation type
ENSG00000244313	TF binding region
AMBRA1	TF binding region
ENSG00000244313	CpG island
AMBRA1	CpG island
ENSG00000110497	chromatin interactions
ENSG00000270800	chromatin interactions
ENSG00000244313	chromatin interactions
ENSG00000110492	chromatin interactions
ENSG00000124614	chromatin interactions

Extended variants
information (count: 618 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:618 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527939159	chr11:46442675-46442676	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs547682608	chr11:46442683-46442684	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs547784475	chr11:46442686-46442687	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370609166	chr11:46442689-46442690	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567763571	chr11:46442753-46442754	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs539640926	chr11:46442759-46442760	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs11038892	chr11:46442773-46442774	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs558266848	chr11:46442951-46442952	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs6485680	chr11:46442983-46442984	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs537465334	chr11:46442990-46442991	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs190944962	chr11:46443041-46443042	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs547497820	chr11:46443079-46443080	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs574655466	chr11:46443133-46443134	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs183148382	chr11:46443186-46443187	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs540563352	chr11:46443204-46443205	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs188431671	chr11:46443205-46443206	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs6485681	chr11:46443249-46443250	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs61882701	chr11:46443275-46443276	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs146934022	chr11:46443346-46443347	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs147972448	chr11:46443390-46443391	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs541860901	chr11:46443403-46443404	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs112036748	chr11:46443423-46443424	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs556443000	chr11:46443459-46443460	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs562072590	chr11:46443470-46443471	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs527675436	chr11:46443491-46443492	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs34682193	chr11:46443557-46443558	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs191714193	chr11:46443670-46443671	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141694769	chr11:46443671-46443672	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs183004888	chr11:46443674-46443675	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188090574	chr11:46443742-46443743	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs367782685	chr11:46443777-46443778	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs549935461	chr11:46443785-46443786	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs568615478	chr11:46443826-46443827	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs576814235	chr11:46443872-46443873	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs536203672	chr11:46443884-46443885	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs191478515	chr11:46443934-46443935	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs556083806	chr11:46443974-46443975	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs183566939	chr11:46443978-46443979	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs568096560	chr11:46444016-46444017	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs111542162	chr11:46444032-46444033	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs554140284	chr11:46444114-46444115	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs577172027	chr11:46444130-46444131	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs546040175	chr11:46444168-46444169	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs556344905	chr11:46444184-46444185	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs576468467	chr11:46444224-46444225	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs542349352	chr11:46444226-46444227	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs562038530	chr11:46444260-46444261	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs371266546	chr11:46444261-46444262	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs572430048	chr11:46444266-46444267	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs117962111	chr11:46444301-46444302	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	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
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:792 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46417000-46444400	Strong transcription	Fetal Stomach	stomach
2	chr11:46417800-46463400	Weak transcription	Fetal Brain Male	brain
3	chr11:46421000-46444800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr11:46421000-46447000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr11:46423400-46444600	Strong transcription	Stomach Smooth Muscle	stomach
6	chr11:46426800-46468800	Weak transcription	Psoas Muscle	Psoas
7	chr11:46427000-46442800	Weak transcription	Right Atrium	heart
8	chr11:46427000-46444600	Strong transcription	Lung	lung
9	chr11:46428000-46443800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr11:46429200-46446400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
11	chr11:46430200-46450600	Weak transcription	HUVEC	blood vessel
12	chr11:46430200-46456000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr11:46430600-46451600	Weak transcription	NHDF-Ad	bronchial
14	chr11:46430600-46455000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr11:46433000-46443200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr11:46433200-46449200	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr11:46433600-46444200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr11:46433600-46466400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr11:46434200-46444800	Strong transcription	Primary B cells from cord blood	blood
20	chr11:46434600-46444200	Strong transcription	Sigmoid Colon	Sigmoid Colon
21	chr11:46435000-46446400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr11:46436400-46450600	Weak transcription	Osteobl	bone
23	chr11:46436400-46454400	Weak transcription	A549	lung
24	chr11:46436600-46443200	Weak transcription	Small Intestine	intestine
25	chr11:46436600-46448600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr11:46436600-46466400	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr11:46436800-46442800	Strong transcription	Fetal Intestine Large	intestine
28	chr11:46437000-46452000	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr11:46437200-46449200	Strong transcription	Primary T helper cells PMA-I stimulated	--
30	chr11:46437200-46452600	Weak transcription	HMEC	breast
31	chr11:46437400-46444600	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr11:46437400-46455000	Weak transcription	Stomach Mucosa	stomach
33	chr11:46437600-46452600	Weak transcription	NH-A	brain
34	chr11:46437800-46443600	Weak transcription	Primary hematopoietic stem cells	blood
35	chr11:46437800-46450600	Weak transcription	HSMM	muscle
36	chr11:46437800-46452400	Weak transcription	Fetal Kidney	kidney
37	chr11:46438000-46444200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr11:46438000-46461400	Strong transcription	Primary T cells from cord blood	blood
39	chr11:46438200-46442800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr11:46438400-46442800	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr11:46438400-46447800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr11:46438400-46448600	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr11:46438400-46451800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr11:46438400-46454400	Weak transcription	Brain Angular Gyrus	brain
45	chr11:46438400-46457200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr11:46438400-46459600	Strong transcription	Dnd41	blood
47	chr11:46438600-46442800	Weak transcription	Aorta	Aorta
48	chr11:46438600-46442800	Weak transcription	Gastric	stomach
49	chr11:46438600-46443000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr11:46439000-46452200	Weak transcription	Rectal Smooth Muscle	rectum

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