Variant report

Variant	nsv896950
Chromosome Location	chr11:5740634-5827540
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	CBX3	chr11:5825288-5825535	K562	blood:	n/a	n/a
2	CBX3	chr11:5825224-5825619	K562	blood:	n/a	n/a
3	CEBPB	chr11:5753243-5753353	HepG2	liver:	n/a	n/a
4	CEBPB	chr11:5788174-5788674	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr11:5758474-5758695	K562	blood:	n/a	chr11:5758602-5758613
6	CEBPB	chr11:5818464-5818701	HepG2	liver:	n/a	chr11:5818599-5818608 chr11:5818599-5818608 chr11:5818598-5818609 chr11:5818599-5818608 chr11:5818597-5818608 chr11:5818599-5818608
7	CEBPB	chr11:5775147-5775155	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr11:5741025-5741291	HepG2	liver:	n/a	chr11:5741162-5741173
9	CEBPB	chr11:5758427-5758790	A549	lung:	n/a	chr11:5758602-5758613
10	CEBPB	chr11:5758403-5758769	A549	lung:	n/a	chr11:5758602-5758613
11	CEBPB	chr11:5741115-5741202	H1-hESC	embryonic stem cell:	n/a	chr11:5741162-5741173
12	CEBPB	chr11:5758450-5758768	HepG2	liver:	n/a	chr11:5758602-5758613
13	CEBPB	chr11:5788246-5788520	HepG2	liver:	n/a	n/a
14	CEBPB	chr11:5789182-5789250	A549	lung:	n/a	chr11:5789200-5789211
15	CEBPB	chr11:5758360-5758903	A549	lung:	n/a	chr11:5758602-5758613
16	CEBPB	chr11:5789130-5789308	HepG2	liver:	n/a	chr11:5789200-5789211
17	CEBPB	chr11:5741093-5741225	K562	blood:	n/a	chr11:5741162-5741173
18	CEBPB	chr11:5764267-5764515	IMR90	lung:	n/a	n/a
19	CEBPB	chr11:5818545-5818706	A549	lung:	n/a	chr11:5818599-5818608 chr11:5818599-5818608 chr11:5818598-5818609 chr11:5818599-5818608 chr11:5818597-5818608 chr11:5818599-5818608
20	CEBPB	chr11:5741008-5741306	A549	lung:	n/a	chr11:5741162-5741173
21	CEBPB	chr11:5758427-5758789	IMR90	lung:	n/a	chr11:5758602-5758613
22	CTCF	chr11:5762540-5762690	Caco-2	colon:	n/a	n/a
23	CTCF	chr11:5809320-5809470	GM12866	blood:	n/a	n/a
24	CTCF	chr11:5745860-5746010	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr11:5786760-5786910	GM12864	blood:	n/a	n/a
26	CTCF	chr11:5741528-5741612	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr11:5779380-5779530	AG09319	gingival:	n/a	n/a
28	E2F4	chr11:5800936-5801305	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr11:5771736-5772054	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr11:5783131-5784075	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr11:5782668-5782868	MCF10A-Er-Src	breast:	n/a	n/a
32	EBF1	chr11:5770104-5770416	GM12878	blood:	n/a	chr11:5770256-5770269
33	EBF1	chr11:5770156-5770325	GM12878	blood:	n/a	chr11:5770256-5770269
34	EP300	chr11:5742141-5742210	K562	blood:	n/a	n/a
35	FOS	chr11:5826613-5826885	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr11:5788361-5788464	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr11:5758485-5758597	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr11:5788384-5788549	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr11:5758410-5758734	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr11:5826706-5826801	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr11:5826693-5826790	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr11:5758414-5758737	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr11:5757759-5757937	MCF10A-Er-Src	breast:	n/a	n/a
44	FOSL2	chr11:5758948-5759300	A549	lung:	n/a	chr11:5759254-5759261 chr11:5759254-5759262 chr11:5759254-5759262 chr11:5759253-5759263
45	FOSL2	chr11:5758384-5758702	A549	lung:	n/a	n/a
46	FOXA1	chr11:5777809-5778219	T-47D	breast:	n/a	n/a
47	FOXA1	chr11:5777816-5778159	T-47D	breast:	n/a	n/a
48	GATA3	chr11:5777791-5778192	T-47D	breast:	n/a	n/a
49	GATA3	chr11:5777768-5778219	T-47D	breast:	n/a	n/a
50	GTF2F1	chr11:5767177-5767182	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5801244-5801294	SAEC	small airway:	n/a
2	chr11:5799446-5799496	Caco-2	colon:	n/a
3	chr11:5801244-5801294	HRCEpiC	kidney:	n/a
4	chr11:5758164-5758214	SKMC	muscle:	n/a
5	chr11:5811184-5811234	HEEpiC	esophagus:	n/a
6	chr11:5799446-5799496	K562	blood:	n/a
7	chr11:5758164-5758214	PrEC	prostate:	n/a
8	chr11:5758164-5758214	NB4	blood:	n/a
9	chr11:5811184-5811234	NHDF-neo	bronchial:	n/a
10	chr11:5799446-5799496	Hepatocyte	liver:	n/a
11	chr11:5799446-5799496	BJ	skin:	n/a
12	chr11:5811184-5811234	ECC-1	luminal epithelium:	n/a
13	chr11:5811184-5811234	Hela-S3	cervix:	n/a
14	chr11:5758164-5758214	K562	blood:	n/a
15	chr11:5799446-5799496	HAEpiC	amniotic membrane:	n/a
16	chr11:5811184-5811234	IMR90	lung:	fetal
17	chr11:5800287-5800337	Hela-S3	cervix:	n/a
18	chr11:5758164-5758214	HPAEpiC	pulmonary alveolar:	n/a
19	chr11:5799446-5799496	AG10803	skin:	n/a
20	chr11:5801244-5801294	MCF10A-Er-Src	breast:	n/a
21	chr11:5758164-5758214	IMR90	lung:	fetal
22	chr11:5801244-5801294	HL-60	blood:	n/a
23	chr11:5811184-5811234	NH-A	brain:	n/a
24	chr11:5799446-5799496	NB4	blood:	n/a
25	chr11:5809911-5809961	GM12892	blood:	n/a
26	chr11:5799446-5799496	HepG2	liver:	n/a
27	chr11:5799446-5799496	NHBE	bronchial:	n/a
28	chr11:5758164-5758214	HAEpiC	amniotic membrane:	n/a
29	chr11:5811184-5811234	HRE	kidney:	n/a
30	chr11:5758164-5758214	AG04450	lung:	fetal
31	chr11:5809911-5809961	AG10803	skin:	n/a
32	chr11:5799446-5799496	H1-hESC	embryonic stem cell:	embryo
33	chr11:5811184-5811234	SK-N-MC	brain:	n/a
34	chr11:5801244-5801294	PrEC	prostate:	n/a
35	chr11:5801244-5801294	GM12892	blood:	n/a
36	chr11:5809911-5809961	HAEpiC	amniotic membrane:	n/a
37	chr11:5811184-5811234	AG09309	skin:	n/a
38	chr11:5811184-5811234	HCT-116	colon:	n/a
39	chr11:5811184-5811234	HCF	heart:	n/a
40	chr11:5809911-5809961	NH-A	brain:	n/a
41	chr11:5811184-5811234	HMEC	breast:	n/a
42	chr11:5758164-5758214	H1-hESC	embryonic stem cell:	embryo
43	chr11:5800287-5800337	LNCaP	prostate:	n/a
44	chr11:5801244-5801294	SK-N-SH_RA	brain:	n/a
45	chr11:5758164-5758214	Caco-2	colon:	n/a
46	chr11:5801244-5801294	K562	blood:	n/a
47	chr11:5809911-5809961	HCM	heart:	n/a
48	chr11:5800287-5800337	GM19239	blood:	n/a
49	chr11:5811184-5811234	Jurkat	blood:	n/a
50	chr11:5809911-5809961	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:5811775..5813823-chr11:5815438..5817025,2	K562	blood:
2	11:5076469-5081549..11:5767550-5775401	K562	blood:
3	chr11:5757074..5759023-chr11:5763300..5765136,2	K562	blood:
4	chr11:5705116..5707493-chr11:5742282..5744602,2	K562	blood:
5	chr11:5811775..5813823-chr11:5815438..5817025,2	K562	blood:
6	11:5616559-5618985..11:5754988-5756879	K562	blood:
7	chr11:5823269..5825988-chr11:5829238..5831177,2	K562	blood:
8	chr11:5628897..5631737-chr11:5750557..5752492,2	K562	blood:
9	11:4778081-4789138..11:5740069-5747001	K562	blood:

Variant related genes	Relation type
OR52N1	TF binding region
OR56B1	TF binding region
OR56B2P	TF binding region
OR52N5	TF binding region
OR52N4	TF binding region
OR52P1P	TF binding region
OR52N3P	TF binding region
OR52N1	CpG island
OR56B1	CpG island
OR56B2P	CpG island
OR52N5	CpG island
OR52N4	CpG island
OR52P1P	CpG island
OR52N3P	CpG island
ENSG00000132256	chromatin interactions
ENSG00000176787	chromatin interactions
ENSG00000121236	chromatin interactions
ENSG00000258588	chromatin interactions
ENSG00000181023	chromatin interactions
ENSG00000167346	chromatin interactions

Extended variants
information (count: 1721 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1721 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12285602	chr11:5740634-5740635	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs138909708	chr11:5740661-5740662	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs571307652	chr11:5740682-5740683	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs73404276	chr11:5740683-5740684	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs530990533	chr11:5740686-5740687	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs189846274	chr11:5740699-5740700	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs570803386	chr11:5740709-5740710	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs551559417	chr11:5740717-5740718	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs182107855	chr11:5740720-5740721	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs141931700	chr11:5740738-5740739	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs185358816	chr11:5740762-5740763	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs190899896	chr11:5740878-5740879	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs557461014	chr11:5740905-5740906	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575536825	chr11:5740917-5740918	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs546003555	chr11:5740923-5740924	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs34289607	chr11:5740971-5740972	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs558125185	chr11:5740973-5740974	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs573171312	chr11:5740981-5740982	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs184148696	chr11:5741087-5741088	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs12281165	chr11:5741102-5741103	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs35378018	chr11:5741117-5741118	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs544324112	chr11:5741137-5741138	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs566886139	chr11:5741144-5741145	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs10769200	chr11:5741151-5741152	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs531051710	chr11:5741172-5741173	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs34279421	chr11:5741204-5741205	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs570278945	chr11:5741284-5741285	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs570668191	chr11:5741314-5741315	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs528789207	chr11:5741332-5741333	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188291712	chr11:5741393-5741394	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs568461844	chr11:5741451-5741452	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs145390812	chr11:5741453-5741454	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs75310397	chr11:5741477-5741478	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs78313893	chr11:5741561-5741562	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs12287413	chr11:5741594-5741595	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs11038845	chr11:5741628-5741629	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs557986106	chr11:5741634-5741635	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs79317917	chr11:5741646-5741647	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs541049320	chr11:5741655-5741656	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs139181412	chr11:5741675-5741676	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs193189320	chr11:5741706-5741707	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs376543624	chr11:5741764-5741765	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs12287535	chr11:5741845-5741846	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs573618697	chr11:5741884-5741885	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs34241724	chr11:5741920-5741921	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs375794575	chr11:5741921-5741922	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs397849327	chr11:5741934-5741935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs543530688	chr11:5741972-5741973	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs563230420	chr11:5742105-5742106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs540702131	chr11:5742149-5742150	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
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
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	23613489	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ollier disease	21235737	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5713600-5745800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr11:5731000-5741000	Weak transcription	HSMMtube	muscle
3	chr11:5731000-5743800	Weak transcription	Liver	Liver
4	chr11:5731200-5741000	Weak transcription	Osteobl	bone
5	chr11:5731200-5748000	Weak transcription	Spleen	Spleen
6	chr11:5731200-5748200	Weak transcription	Placenta	Placenta
7	chr11:5731200-5749200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr11:5731800-5742400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr11:5732400-5742000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr11:5732400-5742200	Weak transcription	Ovary	ovary
11	chr11:5732400-5743000	Weak transcription	Primary T cells from cord blood	blood
12	chr11:5732400-5750000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr11:5732600-5742000	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr11:5732600-5743000	Weak transcription	Primary B cells from peripheral blood	blood
15	chr11:5732800-5740800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr11:5732800-5741800	Weak transcription	HSMM	muscle
17	chr11:5733000-5741000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr11:5734400-5740800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr11:5735400-5740800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr11:5735400-5741000	Weak transcription	Lung	lung
21	chr11:5735400-5742200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr11:5740600-5741000	ZNF genes & repeats	Adipose Nuclei	Adipose
23	chr11:5740600-5741200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr11:5740600-5741600	Strong transcription	Primary B cells from cord blood	blood
25	chr11:5740800-5741200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr11:5740800-5741800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr11:5740800-5742000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr11:5740800-5742000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr11:5741000-5741200	Enhancers	Lung	lung
30	chr11:5741000-5741800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr11:5741000-5741800	Enhancers	Osteobl	bone
32	chr11:5741000-5742200	Enhancers	HSMMtube	muscle
33	chr11:5741200-5748000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr11:5741600-5744200	Weak transcription	Primary B cells from cord blood	blood
35	chr11:5741800-5742000	Enhancers	HSMM	muscle
36	chr11:5741800-5743600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr11:5743800-5744000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr11:5743800-5744000	Enhancers	Liver	Liver
39	chr11:5743800-5744400	Enhancers	HepG2	liver
40	chr11:5745800-5746200	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr11:5747400-5762400	Weak transcription	Left Ventricle	heart
42	chr11:5747800-5748000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr11:5747800-5748200	Enhancers	Gastric	stomach
44	chr11:5748000-5748200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr11:5748000-5748200	ZNF genes & repeats	Pancreas	Pancrea
46	chr11:5748000-5748200	Active TSS	Spleen	Spleen
47	chr11:5748200-5748400	Enhancers	Pancreas	Pancrea
48	chr11:5748200-5748800	Enhancers	Placenta	Placenta
49	chr11:5748200-5749400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr11:5754400-5754600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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