Variant report

Variant	nsv516461
Chromosome Location	chr11:93231476-93240847
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr11:93237330-93237592	GM12878	blood:	n/a	chr11:93237530-93237538
2	CEBPB	chr11:93240707-93240979	HepG2	liver:	n/a	chr11:93240850-93240861
3	CEBPB	chr11:93240738-93240900	K562	blood:	n/a	chr11:93240850-93240861
4	CHD2	chr11:93231526-93231603	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr11:93236881-93236904	ProgFib	skin:	n/a	n/a
6	EP300	chr11:93231640-93232250	ECC-1	luminal epithelium:	n/a	n/a
7	FAM48A	chr11:93235377-93235555	GM12878	blood:	n/a	n/a
8	FOS	chr11:93231847-93232066	MCF10A-Er-Src	breast:	n/a	n/a
9	FOS	chr11:93231966-93232016	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr11:93231866-93232049	MCF10A-Er-Src	breast:	n/a	n/a
11	FOSL2	chr11:93231773-93232143	A549	lung:	n/a	n/a
12	GATA2	chr11:93232164-93232472	SH-SY5Y	brain:	n/a	n/a
13	GATA2	chr11:93234877-93235408	SH-SY5Y	brain:	n/a	n/a
14	GATA3	chr11:93235235-93235299	SH-SY5Y	brain:	n/a	n/a
15	HNF4A	chr11:93235017-93235359	HepG2	liver:	n/a	chr11:93235198-93235210 chr11:93235198-93235210 chr11:93235198-93235210 chr11:93235197-93235210 chr11:93235195-93235213 chr11:93235197-93235212 chr11:93235197-93235212 chr11:93235197-93235211 chr11:93235198-93235210 chr11:93235197-93235212 chr11:93235196-93235211 chr11:93235198-93235211
16	HNF4A	chr11:93235035-93235375	HepG2	liver:	n/a	chr11:93235198-93235210 chr11:93235198-93235210 chr11:93235198-93235210 chr11:93235197-93235210 chr11:93235195-93235213 chr11:93235197-93235212 chr11:93235197-93235212 chr11:93235197-93235211 chr11:93235198-93235210 chr11:93235197-93235212 chr11:93235196-93235211 chr11:93235198-93235211
17	JUN	chr11:93231849-93232129	H1-hESC	embryonic stem cell:	n/a	n/a
18	JUND	chr11:93231520-93232171	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr11:93232682-93232757	A549	lung:	n/a	n/a
20	POLR2A	chr11:93232695-93232696	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr11:93235073-93235129	HepG2	liver:	n/a	n/a
22	RAD21	chr11:93231571-93231643	H1-hESC	embryonic stem cell:	n/a	n/a
23	SIN3A	chr11:93231452-93231642	H1-hESC	embryonic stem cell:	n/a	n/a
24	STAT3	chr11:93233249-93233330	MCF10A-Er-Src	breast:	n/a	chr11:93233249-93233257
25	TBP	chr11:93231502-93231618	H1-hESC	embryonic stem cell:	n/a	n/a
26	TEAD4	chr11:93231472-93232242	ECC-1	luminal epithelium:	n/a	n/a
27	TEAD4	chr11:93231560-93232300	ECC-1	luminal epithelium:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:93231842-93231892	PANC-1	pancreas:	n/a
2	chr11:93231842-93231892	HCT-116	colon:	n/a
3	chr11:93231842-93231892	HIPEpiC	eye:	n/a
4	chr11:93231842-93231892	GM19239	blood:	n/a
5	chr11:93231842-93231892	BJ	skin:	n/a
6	chr11:93231842-93231892	SK-N-SH_RA	brain:	n/a
7	chr11:93231842-93231892	HNPCEpiC	eye:	n/a
8	chr11:93231842-93231892	SK-N-MC	brain:	n/a
9	chr11:93231842-93231892	HEEpiC	esophagus:	n/a
10	chr11:93231842-93231892	SKMC	muscle:	n/a
11	chr11:93231842-93231892	IMR90	lung:	fetal
12	chr11:93231842-93231892	RPTEC	kidney:	n/a
13	chr11:93231842-93231892	HRE	kidney:	n/a
14	chr11:93231842-93231892	HMEC	breast:	n/a
15	chr11:93231842-93231892	HEK293	kidney:	embryo
16	chr11:93231842-93231892	GM12878	blood:	n/a
17	chr11:93231842-93231892	GM12891	blood:	n/a
18	chr11:93231842-93231892	Hepatocyte	liver:	n/a
19	chr11:93231842-93231892	HRCEpiC	kidney:	n/a
20	chr11:93231842-93231892	HAEpiC	amniotic membrane:	n/a
21	chr11:93231842-93231892	BE2_C	brain:	n/a
22	chr11:93231842-93231892	Hela-S3	cervix:	n/a
23	chr11:93231842-93231892	AG04449	skin:	fetal
24	chr11:93231842-93231892	PFSK-1	brain:	n/a
25	chr11:93231842-93231892	HCM	heart:	n/a
26	chr11:93231842-93231892	Caco-2	colon:	n/a
27	chr11:93231842-93231892	Jurkat	blood:	n/a
28	chr11:93231842-93231892	AG04450	lung:	fetal
29	chr11:93231842-93231892	NHBE	bronchial:	n/a
30	chr11:93231842-93231892	AG09309	skin:	n/a
31	chr11:93231842-93231892	SK-N-SH	brain:	n/a
32	chr11:93231842-93231892	ECC-1	luminal epithelium:	n/a
33	chr11:93231842-93231892	NT2-D1	testis:	n/a
34	chr11:93231842-93231892	NH-A	brain:	n/a
35	chr11:93231842-93231892	AG09319	gingival:	n/a
36	chr11:93231842-93231892	HepG2	liver:	n/a
37	chr11:93231842-93231892	NHDF-neo	bronchial:	n/a
38	chr11:93231842-93231892	CMK	blood:	n/a
39	chr11:93231842-93231892	T-47D	breast:	n/a
40	chr11:93231842-93231892	ovcar-3	ovarian:	n/a
41	chr11:93231842-93231892	HUVEC	blood vessel:	n/a
42	chr11:93231842-93231892	MCF-7	breast:	n/a
43	chr11:93231842-93231892	HL-60	blood:	n/a
44	chr11:93231842-93231892	HCF	heart:	n/a
45	chr11:93231842-93231892	HRPEpiC	eye:	n/a
46	chr11:93231842-93231892	AG10803	skin:	n/a
47	chr11:93231842-93231892	LNCaP	prostate:	n/a
48	chr11:93231842-93231892	PrEC	prostate:	n/a
49	chr11:93231842-93231892	K562	blood:	n/a
50	chr11:93231842-93231892	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:93239503..93241482-chr11:93273372..93276296,2	K562	blood:
2	chr11:93239199..93241218-chr11:93245473..93247114,2	K562	blood:

Variant related genes	Relation type
SMCO4	TF binding region
SMCO4	CpG island

Extended variants
information (count: 388 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2658765	chr11:93231476-93231477	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539713751	chr11:93231500-93231501	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs571551804	chr11:93231512-93231513	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs189436248	chr11:93231525-93231526	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs143456005	chr11:93231528-93231529	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs547715611	chr11:93231568-93231569	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs374659028	chr11:93231578-93231579	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs34028949	chr11:93231586-93231587	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs549362319	chr11:93231636-93231637	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79356655	chr11:93231640-93231641	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113557225	chr11:93231650-93231651	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546761688	chr11:93231651-93231652	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114865721	chr11:93231659-93231660	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556559065	chr11:93231676-93231677	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs58656683	chr11:93231684-93231685	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs58336329	chr11:93231774-93231775	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs181028654	chr11:93231801-93231802	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187212369	chr11:93231821-93231822	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs190892847	chr11:93231874-93231875	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368207641	chr11:93231900-93231901	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2605613	chr11:93231903-93231904	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs541313757	chr11:93231914-93231915	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7124358	chr11:93231929-93231930	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs181440417	chr11:93231930-93231931	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113949000	chr11:93231944-93231945	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545237740	chr11:93231947-93231948	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557557621	chr11:93231977-93231978	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563586278	chr11:93231985-93231986	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531044027	chr11:93232007-93232008	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542620340	chr11:93232013-93232014	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs75549718	chr11:93232014-93232015	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528494315	chr11:93232016-93232017	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546872383	chr11:93232083-93232084	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571646748	chr11:93232097-93232098	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532562918	chr11:93232121-93232122	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75302266	chr11:93232143-93232144	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537174762	chr11:93232144-93232145	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs60912147	chr11:93232149-93232150	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs567257347	chr11:93232161-93232162	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574904014	chr11:93232181-93232182	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143324822	chr11:93232222-93232223	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185925521	chr11:93232223-93232224	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2658766	chr11:93232229-93232230	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs557135351	chr11:93232247-93232248	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575621141	chr11:93232252-93232253	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190630202	chr11:93232338-93232339	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs58731812	chr11:93232345-93232346	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573997907	chr11:93232375-93232376	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183179434	chr11:93232417-93232418	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs540276038	chr11:93232446-93232447	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Cancer	21499728	CNVD
Breast cancer	19181860	CNVD
Breast cancer	17603634	CNVD
Mantle cell lymphoma	19029149	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:204 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93207000-93239000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr11:93209000-93235200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr11:93210600-93231600	Weak transcription	A549	lung
4	chr11:93211000-93253400	Weak transcription	Primary T cells from cord blood	blood
5	chr11:93211600-93243800	Weak transcription	Fetal Thymus	thymus
6	chr11:93212200-93234800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr11:93214800-93234400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr11:93218600-93254400	Weak transcription	Hela-S3	cervix
9	chr11:93218800-93231800	Weak transcription	Ovary	ovary
10	chr11:93218800-93238200	Weak transcription	Esophagus	oesophagus
11	chr11:93218800-93245800	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr11:93220600-93232000	Weak transcription	Left Ventricle	heart
13	chr11:93220800-93235400	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr11:93222000-93231600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr11:93222200-93232000	Weak transcription	Spleen	Spleen
16	chr11:93222400-93238000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr11:93222800-93231800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr11:93222800-93236000	Weak transcription	Fetal Muscle Trunk	muscle
19	chr11:93223000-93242800	Weak transcription	Adipose Nuclei	Adipose
20	chr11:93225400-93242800	Weak transcription	GM12878-XiMat	blood
21	chr11:93225600-93231800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr11:93225600-93248800	Weak transcription	Fetal Muscle Leg	muscle
23	chr11:93225800-93232800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr11:93226000-93235000	Weak transcription	Small Intestine	intestine
25	chr11:93226400-93257400	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr11:93226600-93238000	Weak transcription	Fetal Lung	lung
27	chr11:93226800-93233600	Weak transcription	Stomach Mucosa	stomach
28	chr11:93227000-93231600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr11:93227000-93234600	Weak transcription	Gastric	stomach
30	chr11:93227000-93243800	Weak transcription	Lung	lung
31	chr11:93227200-93231600	Weak transcription	Aorta	Aorta
32	chr11:93227200-93257600	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr11:93227400-93239800	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr11:93227600-93232800	Strong transcription	Fetal Stomach	stomach
35	chr11:93227800-93231600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr11:93227800-93235000	Weak transcription	Pancreas	Pancrea
37	chr11:93228200-93234000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr11:93228200-93243400	Weak transcription	Right Ventricle	heart
39	chr11:93228200-93248200	Weak transcription	Brain Hippocampus Middle	brain
40	chr11:93228400-93231600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr11:93228400-93231600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr11:93228400-93231600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr11:93228400-93231600	Weak transcription	HSMMtube	muscle
44	chr11:93228400-93235000	Weak transcription	HepG2	liver
45	chr11:93228400-93237800	Weak transcription	Osteobl	bone
46	chr11:93228600-93231600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr11:93229200-93232600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr11:93229800-93235000	Weak transcription	Duodenum Mucosa	Duodenum
49	chr11:93230000-93232800	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr11:93230400-93231600	Enhancers	HUES64 Cell Line	embryonic stem cell

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