Variant report

Variant	nsv518163
Chromosome Location	chr11:71142350-71155153
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:281)
CpG islands
(count:977)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71144739-71144757	HepG2	liver:	n/a	n/a
2	BHLHE40	chr11:71144741-71144795	K562	blood:	n/a	n/a
3	CCNT2	chr11:71146414-71146869	K562	blood:	n/a	n/a
4	CCNT2	chr11:71148913-71149171	K562	blood:	n/a	n/a
5	CEBPB	chr11:71144553-71145157	Hela-S3	cervix:	n/a	chr11:71144774-71144787
6	CEBPB	chr11:71144611-71145026	MCF-7	breast:	n/a	chr11:71144774-71144787
7	CEBPB	chr11:71144601-71144955	IMR90	lung:	n/a	chr11:71144774-71144787
8	CEBPB	chr11:71144510-71145069	MCF-7	breast:	n/a	chr11:71144774-71144787
9	CEBPB	chr11:71144527-71145038	K562	blood:	n/a	chr11:71144774-71144787
10	CEBPB	chr11:71144655-71144852	H1-hESC	embryonic stem cell:	n/a	chr11:71144774-71144787
11	CEBPB	chr11:71144587-71145212	HepG2	liver:	n/a	chr11:71144774-71144787
12	CEBPB	chr11:71144607-71144916	K562	blood:	n/a	chr11:71144774-71144787
13	CEBPB	chr11:71144540-71144894	HepG2	liver:	n/a	chr11:71144774-71144787
14	CEBPB	chr11:71144587-71145099	HepG2	liver:	n/a	chr11:71144774-71144787
15	CEBPB	chr11:71144663-71144902	HepG2	liver:	n/a	chr11:71144774-71144787
16	CEBPB	chr11:71144658-71144926	K562	blood:	n/a	chr11:71144774-71144787
17	CEBPB	chr11:71144580-71144925	A549	lung:	n/a	chr11:71144774-71144787
18	CEBPD	chr11:71144641-71144912	HepG2	liver:	n/a	n/a
19	CEBPD	chr11:71144556-71144951	HepG2	liver:	n/a	n/a
20	CHD2	chr11:71144642-71144860	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr11:71144521-71144710	K562	blood:	n/a	n/a
22	CHD2	chr11:71144418-71144712	HepG2	liver:	n/a	n/a
23	CHD2	chr11:71144938-71145024	K562	blood:	n/a	n/a
24	CTCF	chr11:71148977-71149196	GM19238	blood:	n/a	n/a
25	CTCF	chr11:71149005-71149144	GM13977	blood:	n/a	n/a
26	CTCF	chr11:71148980-71149130	Caco-2	colon:	n/a	n/a
27	CTCF	chr11:71149140-71149290	MCF-7	breast:	n/a	n/a
28	CTCF	chr11:71149037-71149153	MCF-7	breast:	n/a	n/a
29	CTCF	chr11:71142942-71142975	Lung_OC	lung:	n/a	n/a
30	CTCF	chr11:71149069-71149097	GM10248	blood:	n/a	n/a
31	CTCF	chr11:71148970-71149196	GM12891	blood:	n/a	n/a
32	CTCF	chr11:71142541-71142555	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr11:71148980-71149130	GM06990	blood:	n/a	n/a
34	CTCF	chr11:71142400-71142550	HepG2	liver:	n/a	n/a
35	CTCF	chr11:71142904-71142993	GM13976	blood:	n/a	n/a
36	CTCF	chr11:71148980-71149130	HL-60	blood:	n/a	n/a
37	CTCF	chr11:71149000-71149150	K562	blood:	n/a	n/a
38	CTCF	chr11:71149005-71149103	GM13976	blood:	n/a	n/a
39	CTCF	chr11:71142380-71142530	GM12873	blood:	n/a	n/a
40	CTCF	chr11:71148991-71149173	GM12892	blood:	n/a	n/a
41	CTCF	chr11:71149009-71149160	GM19240	blood:	n/a	n/a
42	CTCF	chr11:71149052-71149142	K562	blood:	n/a	n/a
43	CTCF	chr11:71149018-71149134	GM19239	blood:	n/a	n/a
44	CTCF	chr11:71149037-71149117	MCF-7	breast:	n/a	n/a
45	CTCF	chr11:71149080-71149230	GM06990	blood:	n/a	n/a
46	CTCF	chr11:71144493-71144522	Lung_OC	lung:	n/a	n/a
47	CTCF	chr11:71149071-71149111	Gliobla	brain:	n/a	n/a
48	CTCF	chr11:71149020-71149170	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr11:71149059-71149141	K562	blood:	n/a	n/a
50	CTCF	chr11:71149005-71149167	GM12878	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71146831-71146881	IMR90	lung:	fetal
2	chr11:71146831-71146881	IMR90	lung:	fetal
3	chr11:71150020-71150070	GM12892	blood:	n/a
4	chr11:71147213-71147263	NHDF-neo	bronchial:	n/a
5	chr11:71144007-71144057	HCT-116	colon:	n/a
6	chr11:71146764-71146814	HepG2	liver:	n/a
7	chr11:71150247-71150297	NHDF-neo	bronchial:	n/a
8	chr11:71147213-71147263	HIPEpiC	eye:	n/a
9	chr11:71146831-71146881	HIPEpiC	eye:	n/a
10	chr11:71146096-71146146	HMEC	breast:	n/a
11	chr11:71149985-71150035	NH-A	brain:	n/a
12	chr11:71150315-71150365	Hepatocyte	liver:	n/a
13	chr11:71146456-71146506	AG04449	skin:	fetal
14	chr11:71146211-71146261	GM19239	blood:	n/a
15	chr11:71147213-71147263	HCM	heart:	n/a
16	chr11:71146456-71146506	AG09309	skin:	n/a
17	chr11:71145665-71145715	Hepatocyte	liver:	n/a
18	chr11:71146831-71146881	HCF	heart:	n/a
19	chr11:71149985-71150035	HL-60	blood:	n/a
20	chr11:71149985-71150035	K562	blood:	n/a
21	chr11:71146831-71146881	AG04450	lung:	fetal
22	chr11:71150020-71150070	T-47D	breast:	n/a
23	chr11:71144007-71144057	HCM	heart:	n/a
24	chr11:71146658-71146708	H1-hESC	embryonic stem cell:	embryo
25	chr11:71155081-71155131	GM12891	blood:	n/a
26	chr11:71150247-71150297	K562	blood:	n/a
27	chr11:71146456-71146506	AG10803	skin:	n/a
28	chr11:71150200-71150250	HCF	heart:	n/a
29	chr11:71150247-71150297	Caco-2	colon:	n/a
30	chr11:71146211-71146261	IMR90	lung:	fetal
31	chr11:71146456-71146506	SKMC	muscle:	n/a
32	chr11:71155081-71155131	ovcar-3	ovarian:	n/a
33	chr11:71145665-71145715	MCF-7	breast:	n/a
34	chr11:71146096-71146146	RPTEC	kidney:	n/a
35	chr11:71146658-71146708	HEK293	kidney:	embryo
36	chr11:71145665-71145715	AG04449	skin:	fetal
37	chr11:71145904-71145954	AG04450	lung:	fetal
38	chr11:71150315-71150365	PFSK-1	brain:	n/a
39	chr11:71146764-71146814	LNCaP	prostate:	n/a
40	chr11:71147213-71147263	RPTEC	kidney:	n/a
41	chr11:71146658-71146708	NH-A	brain:	n/a
42	chr11:71147213-71147263	H1-hESC	embryonic stem cell:	embryo
43	chr11:71147213-71147263	CMK	blood:	n/a
44	chr11:71146658-71146708	GM12878	blood:	n/a
45	chr11:71146211-71146261	HAEpiC	amniotic membrane:	n/a
46	chr11:71146764-71146814	HEEpiC	esophagus:	n/a
47	chr11:71155081-71155131	AoSMC	blood vessel:	n/a
48	chr11:71150020-71150070	HL-60	blood:	n/a
49	chr11:71150315-71150365	HMEC	breast:	n/a
50	chr11:71150315-71150365	ProgFib	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:71150692..71153685-chr11:71157371..71159231,2	K562	blood:
2	chr11:71144398..71146962-chr11:71155881..71158329,2	K562	blood:
3	chr11:71138911..71140880-chr11:71154532..71157322,2	K562	blood:
4	chr11:71145861..71148478-chr11:71150680..71152334,2	K562	blood:
5	chr11:71142709..71145080-chr11:71152155..71155719,3	K562	blood:
6	chr11:71144482..71146798-chr11:71158407..71160975,3	K562	blood:
7	chr11:71146059..71148297-chr11:71153188..71155860,2	K562	blood:
8	chr11:71139536..71142433-chr11:71147657..71149469,2	K562	blood:
9	chr11:71145861..71148478-chr11:71150680..71152334,2	K562	blood:
10	chr11:70982645..70985292-chr11:71142311..71143975,2	MCF-7	breast:
11	chr11:71138540..71142714-chr11:71144455..71147360,4	K562	blood:
12	chr11:71139168..71142453-chr11:71148977..71152491,3	K562	blood:
13	chr11:71139536..71142433-chr11:71147657..71149469,2	K562	blood:
14	chr11:71154436..71156970-chr11:71198755..71201662,2	MCF-7	breast:
15	chr11:71146059..71148297-chr11:71153188..71155860,2	K562	blood:
16	chr11:71138540..71142714-chr11:71144455..71147360,4	K562	blood:
17	chr11:71141203..71142816-chr11:71167410..71170126,2	K562	blood:
18	chr11:71140807..71143299-chr11:71274419..71277304,2	MCF-7	breast:
19	chr11:71137647..71140040-chr11:71141812..71145984,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000254682	TF binding region
DHCR7	TF binding region
ENSG00000254682	CpG island
DHCR7	CpG island
ENSG00000254682	chromatin interactions
ENSG00000204572	chromatin interactions
ENSG00000172893	chromatin interactions

Extended variants
information (count: 678 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:678 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1790349	chr11:71142350-71142351	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536510715	chr11:71142380-71142381	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs557378990	chr11:71142414-71142415	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs145563108	chr11:71142423-71142424	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs566675037	chr11:71142424-71142425	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs142261483	chr11:71142466-71142467	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs186217864	chr11:71142472-71142473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs78363005	chr11:71142477-71142478	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs191138596	chr11:71142479-71142480	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs544173063	chr11:71142497-71142498	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs556167730	chr11:71142513-71142514	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs1792272	chr11:71142518-71142519	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs558370762	chr11:71142546-71142547	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs148884139	chr11:71142570-71142571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs527470477	chr11:71142577-71142578	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs540415707	chr11:71142590-71142591	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs143489302	chr11:71142595-71142596	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs117291152	chr11:71142606-71142607	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs183444024	chr11:71142608-71142609	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs568868496	chr11:71142635-71142636	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs530339113	chr11:71142652-71142653	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs548465826	chr11:71142659-71142660	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs577464068	chr11:71142716-71142717	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs1792271	chr11:71142744-71142745	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs534382734	chr11:71142781-71142782	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs558403930	chr11:71142798-71142799	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs570543511	chr11:71142846-71142847	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs147998267	chr11:71142938-71142939	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs556198217	chr11:71142959-71142960	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs574444590	chr11:71142970-71142971	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs143545632	chr11:71143020-71143021	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs558998125	chr11:71143054-71143055	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs371489347	chr11:71143122-71143123	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs554103315	chr11:71143123-71143124	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs572172876	chr11:71143127-71143128	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs145716474	chr11:71143152-71143153	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs564089673	chr11:71143222-71143223	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs12797951	chr11:71143266-71143267	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs34359608	chr11:71143327-71143328	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs12271661	chr11:71143383-71143384	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs562585112	chr11:71143384-71143385	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs75906111	chr11:71143395-71143396	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs187179745	chr11:71143445-71143446	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs35649052	chr11:71143469-71143470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs560824595	chr11:71143510-71143511	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs541771844	chr11:71143515-71143516	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs190467337	chr11:71143561-71143562	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs77328506	chr11:71143570-71143571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs1790348	chr11:71143580-71143581	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs76105291	chr11:71143622-71143623	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71132600-71144000	Weak transcription	Spleen	Spleen
2	chr11:71135000-71150600	Weak transcription	NH-A	brain
3	chr11:71135400-71145000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr11:71137000-71144800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:71137200-71144000	Weak transcription	Hela-S3	cervix
6	chr11:71137200-71145000	Weak transcription	Brain Germinal Matrix	brain
7	chr11:71137200-71149600	Weak transcription	Primary B cells from peripheral blood	blood
8	chr11:71137600-71146000	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr11:71138000-71144800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:71138000-71145200	Weak transcription	HMEC	breast
11	chr11:71139200-71145000	Weak transcription	GM12878-XiMat	blood
12	chr11:71139200-71145800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr11:71139400-71145000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr11:71139600-71145200	Enhancers	Ovary	ovary
15	chr11:71139800-71142800	Enhancers	HepG2	liver
16	chr11:71140000-71144000	Weak transcription	Fetal Brain Female	brain
17	chr11:71140400-71142600	Weak transcription	Fetal Intestine Small	intestine
18	chr11:71140400-71145000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr11:71140600-71143000	Weak transcription	Brain Anterior Caudate	brain
20	chr11:71140600-71143200	Weak transcription	Brain Cingulate Gyrus	brain
21	chr11:71140600-71144000	Weak transcription	Left Ventricle	heart
22	chr11:71140600-71144000	Weak transcription	Lung	lung
23	chr11:71140600-71144600	Weak transcription	Right Ventricle	heart
24	chr11:71140600-71158200	Weak transcription	Fetal Brain Male	brain
25	chr11:71140800-71143200	Weak transcription	Brain Angular Gyrus	brain
26	chr11:71140800-71143200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr11:71140800-71144000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr11:71140800-71144000	Weak transcription	Gastric	stomach
29	chr11:71140800-71144800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr11:71140800-71145800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr11:71140800-71154000	Weak transcription	Fetal Lung	lung
32	chr11:71140800-71154000	Weak transcription	HSMM	muscle
33	chr11:71141000-71142400	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr11:71141000-71143800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr11:71141000-71145800	Weak transcription	HSMMtube	muscle
36	chr11:71141200-71142400	Weak transcription	Right Atrium	heart
37	chr11:71141200-71143800	Weak transcription	Stomach Mucosa	stomach
38	chr11:71141200-71148200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr11:71141600-71142400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr11:71141600-71142800	Enhancers	Placenta	Placenta
41	chr11:71141600-71143000	Weak transcription	Adipose Nuclei	Adipose
42	chr11:71141600-71144600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr11:71141600-71144800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr11:71141600-71145000	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr11:71141600-71145200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr11:71141800-71144400	Weak transcription	Primary T cells from cord blood	blood
47	chr11:71141800-71144800	Weak transcription	Fetal Stomach	stomach
48	chr11:71141800-71145800	Enhancers	Liver	Liver
49	chr11:71142000-71144800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr11:71142200-71144200	Weak transcription	Skeletal Muscle Male	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links