Variant report

Variant	nsv983188
Chromosome Location	chr11:73273934-73307064
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:209)
CpG islands
(count:183)
Chromatin interactive
region (count:16)
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	chr11:73290809-73290822	K562	blood:	n/a	n/a
2	ATF1	chr11:73278037-73278488	K562	blood:	n/a	n/a
3	ATF2	chr11:73289691-73290216	GM12878	blood:	n/a	n/a
4	ATF2	chr11:73289783-73290212	GM12878	blood:	n/a	n/a
5	ATF3	chr11:73278163-73278471	K562	blood:	n/a	n/a
6	BATF	chr11:73289721-73290174	GM12878	blood:	n/a	n/a
7	BATF	chr11:73289763-73290084	GM12878	blood:	n/a	n/a
8	BCLAF1	chr11:73289736-73290299	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:73278223-73278280	K562	blood:	n/a	n/a
10	BHLHE40	chr11:73294641-73294830	K562	blood:	n/a	n/a
11	BHLHE40	chr11:73289897-73290217	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:73289862-73290125	HepG2	liver:	n/a	n/a
13	BRCA1	chr11:73306139-73306158	HepG2	liver:	n/a	n/a
14	BRCA1	chr11:73278051-73278541	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr11:73305492-73305757	IMR90	lung:	n/a	chr11:73305640-73305651
16	CEBPB	chr11:73278047-73278630	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr11:73305495-73305691	H1-hESC	embryonic stem cell:	n/a	chr11:73305640-73305651
18	CEBPB	chr11:73305479-73305766	K562	blood:	n/a	chr11:73305640-73305651
19	CEBPB	chr11:73305476-73305702	K562	blood:	n/a	chr11:73305640-73305651
20	CEBPB	chr11:73278096-73278102	K562	blood:	n/a	n/a
21	CEBPB	chr11:73305563-73305685	Hela-S3	cervix:	n/a	chr11:73305640-73305651
22	CEBPB	chr11:73305473-73305766	HepG2	liver:	n/a	chr11:73305640-73305651
23	CEBPB	chr11:73290811-73290972	K562	blood:	n/a	n/a
24	CEBPB	chr11:73290859-73290879	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr11:73305554-73305716	HepG2	liver:	n/a	chr11:73305640-73305651
26	CHD1	chr11:73300779-73300978	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr11:73289951-73290096	GM12878	blood:	n/a	n/a
28	CREB1	chr11:73281436-73281936	ECC-1	luminal epithelium:	n/a	n/a
29	CTCF	chr11:73288440-73288590	HMF	breast:	n/a	n/a
30	CTCF	chr11:73300964-73300981	MCF-7	breast:	n/a	n/a
31	CTCF	chr11:73288522-73288597	GM12878	blood:	n/a	n/a
32	CTCF	chr11:73288500-73288650	AG10803	skin:	n/a	n/a
33	CTCF	chr11:73306260-73306410	A549	lung:	n/a	n/a
34	CTCF	chr11:73282060-73282210	HEK293	kidney:	n/a	n/a
35	CTCF	chr11:73295320-73295343	GM13976	blood:	n/a	n/a
36	CTCF	chr11:73288620-73288770	HFF	foreskin:	n/a	n/a
37	CTCF	chr11:73286980-73287130	HRE	kidney:	n/a	n/a
38	CTCF	chr11:73300960-73301110	AG09319	gingival:	n/a	n/a
39	CTCF	chr11:73288520-73288670	AG09309	skin:	n/a	n/a
40	CTCF	chr11:73300920-73301070	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr11:73295262-73295321	MCF-7	breast:	n/a	n/a
42	CTCF	chr11:73300945-73300981	MCF-7	breast:	n/a	n/a
43	CTCF	chr11:73288480-73288630	HMF	breast:	n/a	n/a
44	CTCF	chr11:73293260-73293376	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr11:73288440-73288590	BJ	skin:	n/a	n/a
46	CUX1	chr11:73289808-73290008	GM12878	blood:	n/a	n/a
47	CUX1	chr11:73277856-73278179	K562	blood:	n/a	n/a
48	E2F4	chr11:73281482-73281969	MCF10A-Er-Src	breast:	n/a	n/a
49	EBF1	chr11:73291909-73292092	GM12878	blood:	n/a	n/a
50	EBF1	chr11:73291781-73292155	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:73306367-73306417	CMK	blood:	n/a
2	chr11:73278053-73278103	GM19239	blood:	n/a
3	chr11:73278053-73278103	AG04449	skin:	fetal
4	chr11:73306367-73306417	MCF10A-Er-Src	breast:	n/a
5	chr11:73278053-73278103	BE2_C	brain:	n/a
6	chr11:73278053-73278103	SAEC	small airway:	n/a
7	chr11:73306367-73306417	GM12878	blood:	n/a
8	chr11:73278053-73278103	SK-N-SH_RA	brain:	n/a
9	chr11:73289224-73289274	HNPCEpiC	eye:	n/a
10	chr11:73278053-73278103	HNPCEpiC	eye:	n/a
11	chr11:73289224-73289274	NB4	blood:	n/a
12	chr11:73278053-73278103	HepG2	liver:	n/a
13	chr11:73278053-73278103	PFSK-1	brain:	n/a
14	chr11:73278053-73278103	HCM	heart:	n/a
15	chr11:73306367-73306417	HUVEC	blood vessel:	n/a
16	chr11:73289224-73289274	U87	brain:	n/a
17	chr11:73289224-73289274	HCM	heart:	n/a
18	chr11:73306367-73306417	U87	brain:	n/a
19	chr11:73306367-73306417	HNPCEpiC	eye:	n/a
20	chr11:73306367-73306417	AG09319	gingival:	n/a
21	chr11:73306367-73306417	HAEpiC	amniotic membrane:	n/a
22	chr11:73289224-73289274	HRCEpiC	kidney:	n/a
23	chr11:73278053-73278103	Jurkat	blood:	n/a
24	chr11:73289224-73289274	CMK	blood:	n/a
25	chr11:73278053-73278103	MCF10A-Er-Src	breast:	n/a
26	chr11:73278053-73278103	Caco-2	colon:	n/a
27	chr11:73278053-73278103	IMR90	lung:	fetal
28	chr11:73289224-73289274	ProgFib	skin:	n/a
29	chr11:73289224-73289274	AG04449	skin:	fetal
30	chr11:73289224-73289274	PANC-1	pancreas:	n/a
31	chr11:73289224-73289274	A549	lung:	n/a
32	chr11:73278053-73278103	A549	lung:	n/a
33	chr11:73278053-73278103	PrEC	prostate:	n/a
34	chr11:73306367-73306417	AG04450	lung:	fetal
35	chr11:73289224-73289274	AG10803	skin:	n/a
36	chr11:73289224-73289274	GM06990	blood:	n/a
37	chr11:73306367-73306417	BJ	skin:	n/a
38	chr11:73278053-73278103	HCF	heart:	n/a
39	chr11:73278053-73278103	SK-N-MC	brain:	n/a
40	chr11:73278053-73278103	GM06990	blood:	n/a
41	chr11:73278053-73278103	U87	brain:	n/a
42	chr11:73289224-73289274	HIPEpiC	eye:	n/a
43	chr11:73289224-73289274	AG04450	lung:	fetal
44	chr11:73306367-73306417	HRCEpiC	kidney:	n/a
45	chr11:73306367-73306417	HepG2	liver:	n/a
46	chr11:73306367-73306417	SK-N-SH	brain:	n/a
47	chr11:73278053-73278103	HEEpiC	esophagus:	n/a
48	chr11:73306367-73306417	HL-60	blood:	n/a
49	chr11:73289224-73289274	HAEpiC	amniotic membrane:	n/a
50	chr11:73306367-73306417	AoSMC	blood vessel:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:73296523..73298839-chr11:73307777..73311638,3	MCF-7	breast:
2	chr11:73304467..73306612-chr11:73307479..73309635,2	K562	blood:
3	chr11:73287022..73288650-chr11:73298158..73299719,2	MCF-7	breast:
4	chr11:73277014..73278822-chr11:73613258..73614797,2	K562	blood:
5	chr11:73303459..73306739-chr11:73310819..73313013,3	K562	blood:
6	chr11:73304614..73306739-chr11:73310819..73312531,2	K562	blood:
7	chr11:73287100..73289867-chr11:73302120..73304102,3	K562	blood:
8	chr11:73275181..73277869-chr11:73279088..73282119,3	MCF-7	breast:
9	chr11:73289699..73292318-chr11:73308150..73310462,2	K562	blood:
10	chr11:73275181..73277869-chr11:73279088..73282119,3	MCF-7	breast:
11	chr11:73265451..73268306-chr11:73275988..73278927,2	K562	blood:
12	chr11:73287100..73289867-chr11:73302120..73304102,3	K562	blood:
13	chr11:73300001..73301643-chr11:73308590..73310552,2	MCF-7	breast:
14	chr11:73286935..73287612-chr3:95303237..95304152,2	MCF-7	breast:
15	chr11:73297071..73299471-chr11:73307672..73310016,3	MCF-7	breast:
16	chr11:73287022..73288650-chr11:73298158..73299719,2	MCF-7	breast:

No data

Variant related genes	Relation type
HMGN2P38	TF binding region
HMGN2P38	CpG island
ENSG00000054965	chromatin interactions

Extended variants
information (count: 1160 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553862242	chr11:73273946-73273947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs530591269	chr11:73273956-73273957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550763761	chr11:73273960-73273961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567303571	chr11:73273978-73273979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572535878	chr11:73273987-73273988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186157871	chr11:73274035-73274036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546622134	chr11:73274045-73274046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566743961	chr11:73274086-73274087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538676207	chr11:73274151-73274152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558501620	chr11:73274196-73274197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543250106	chr11:73274238-73274239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569027049	chr11:73274243-73274244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537907521	chr11:73274330-73274331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555146492	chr11:73274331-73274332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574980127	chr11:73274356-73274357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540812566	chr11:73274426-73274427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs77867073	chr11:73274460-73274461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs117101179	chr11:73274470-73274471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs151337700	chr11:73274508-73274509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs56021202	chr11:73274536-73274537	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs190723021	chr11:73274553-73274554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544025757	chr11:73274559-73274560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs200931159	chr11:73274611-73274612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140597747	chr11:73274714-73274715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183382025	chr11:73274720-73274721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs546752505	chr11:73274722-73274723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576816172	chr11:73274734-73274735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566451771	chr11:73274738-73274739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186340597	chr11:73274816-73274817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs61018857	chr11:73274832-73274833	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs17310374	chr11:73274874-73274875	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs145589995	chr11:73274919-73274920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371540657	chr11:73274934-73274935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554804627	chr11:73274936-73274937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs369274577	chr11:73274943-73274944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs115236808	chr11:73274975-73274976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550867172	chr11:73274981-73274982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532578332	chr11:73274999-73275000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534154766	chr11:73275083-73275084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554311527	chr11:73275156-73275157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190802371	chr11:73275162-73275163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546476801	chr11:73275169-73275170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs78218270	chr11:73275176-73275177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575353457	chr11:73275222-73275223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544183216	chr11:73275237-73275238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112754849	chr11:73275248-73275249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560847994	chr11:73275296-73275297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529768113	chr11:73275313-73275314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540071300	chr11:73275344-73275345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547895302	chr11:73275396-73275397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
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
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
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung cancer	18438408	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
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung cancer	21203850	CNVD

Chromatin state (count:702 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73243400-73279600	Weak transcription	Fetal Stomach	stomach
2	chr11:73249600-73276000	Weak transcription	Fetal Muscle Leg	muscle
3	chr11:73250000-73307800	Weak transcription	Stomach Smooth Muscle	stomach
4	chr11:73250200-73278800	Weak transcription	Primary hematopoietic stem cells	blood
5	chr11:73250800-73282800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr11:73251000-73288800	Weak transcription	Thymus	Thymus
7	chr11:73253800-73307000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr11:73258800-73278000	Weak transcription	Primary B cells from cord blood	blood
9	chr11:73262200-73281000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr11:73262600-73276800	Weak transcription	Brain Germinal Matrix	brain
11	chr11:73263200-73276000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr11:73263200-73306000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr11:73263800-73288800	Weak transcription	Colon Smooth Muscle	Colon
14	chr11:73264200-73276800	Weak transcription	Hela-S3	cervix
15	chr11:73264600-73287000	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr11:73264800-73276000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr11:73265400-73287200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr11:73266400-73274400	Weak transcription	Brain Substantia Nigra	brain
19	chr11:73266400-73280000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:73266600-73275000	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr11:73266600-73307800	Weak transcription	Fetal Intestine Small	intestine
22	chr11:73266800-73275000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr11:73267000-73275000	Weak transcription	Brain Anterior Caudate	brain
24	chr11:73267200-73277000	Weak transcription	Primary T cells from cord blood	blood
25	chr11:73267400-73275000	Weak transcription	Psoas Muscle	Psoas
26	chr11:73267400-73281400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr11:73267400-73284800	Weak transcription	Right Atrium	heart
28	chr11:73268400-73281000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr11:73269800-73279600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr11:73270600-73288000	Weak transcription	NHLF	lung
31	chr11:73271400-73277400	Weak transcription	Left Ventricle	heart
32	chr11:73271400-73277600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr11:73272000-73277800	Weak transcription	Esophagus	oesophagus
34	chr11:73272200-73307600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr11:73274400-73274600	Enhancers	Brain Cingulate Gyrus	brain
36	chr11:73274400-73274600	Enhancers	Brain Substantia Nigra	brain
37	chr11:73274400-73275400	Enhancers	GM12878-XiMat	blood
38	chr11:73274600-73287000	Weak transcription	Brain Cingulate Gyrus	brain
39	chr11:73274600-73287000	Weak transcription	Brain Substantia Nigra	brain
40	chr11:73274800-73275000	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr11:73274800-73275200	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr11:73274800-73290800	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr11:73275000-73275200	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr11:73275000-73275200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr11:73275000-73275200	Enhancers	Brain Anterior Caudate	brain
46	chr11:73275000-73275200	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr11:73275000-73275400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr11:73275000-73275400	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr11:73275000-73275600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr11:73275000-73275600	Enhancers	Psoas Muscle	Psoas

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