Variant report

Variant	esv20896
Chromosome Location	chr11:73306779-73309297
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	ARID3A	chr11:73309122-73309835	HepG2	liver:	n/a	n/a
2	ATF1	chr11:73309097-73309836	K562	blood:	n/a	n/a
3	ATF2	chr11:73309195-73309895	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr11:73309078-73309990	GM12878	blood:	n/a	n/a
5	ATF2	chr11:73309041-73309861	GM12878	blood:	n/a	n/a
6	ATF3	chr11:73309119-73309475	K562	blood:	n/a	chr11:73309367-73309376 chr11:73309251-73309260
7	BACH1	chr11:73309126-73309896	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr11:73309134-73310174	A549	lung:	n/a	chr11:73309760-73309769 chr11:73309338-73309351 chr11:73309175-73309188
9	BCL3	chr11:73309153-73310056	A549	lung:	n/a	chr11:73309760-73309769 chr11:73309338-73309351 chr11:73309175-73309188
10	BCLAF1	chr11:73308818-73309902	GM12878	blood:	n/a	chr11:73308993-73309002 chr11:73309760-73309769 chr11:73308995-73309008 chr11:73309338-73309351 chr11:73309175-73309188 chr11:73308996-73309005 chr11:73308992-73309005 chr11:73308991-73309004
11	BCLAF1	chr11:73308865-73309957	GM12878	blood:	n/a	chr11:73308993-73309002 chr11:73309760-73309769 chr11:73308995-73309008 chr11:73309338-73309351 chr11:73309175-73309188 chr11:73308996-73309005 chr11:73308992-73309005 chr11:73308991-73309004
12	BHLHE40	chr11:73308999-73309937	K562	blood:	n/a	chr11:73309170-73309186 chr11:73309347-73309363
13	BHLHE40	chr11:73309011-73310163	GM12878	blood:	n/a	chr11:73309170-73309186 chr11:73309347-73309363
14	BRCA1	chr11:73309205-73309714	GM12878	blood:	n/a	n/a
15	BRCA1	chr11:73309147-73309874	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr11:73308970-73309975	K562	blood:	n/a	chr11:73309415-73309426
17	CCNT2	chr11:73308917-73309919	K562	blood:	n/a	chr11:73309163-73309172 chr11:73309526-73309535
18	CEBPB	chr11:73309031-73309829	Hela-S3	cervix:	n/a	chr11:73309816-73309824
19	CEBPD	chr11:73308983-73309242	HepG2	liver:	n/a	n/a
20	CEBPD	chr11:73308858-73309311	HepG2	liver:	n/a	n/a
21	CHD1	chr11:73309288-73310003	GM12878	blood:	n/a	chr11:73309338-73309348 chr11:73309526-73309536
22	CHD2	chr11:73308915-73309949	K562	blood:	n/a	chr11:73309338-73309348 chr11:73309526-73309536 chr11:73309162-73309172
23	CHD2	chr11:73308810-73309908	Hela-S3	cervix:	n/a	chr11:73309338-73309348 chr11:73308857-73308867 chr11:73309526-73309536 chr11:73309162-73309172
24	CHD2	chr11:73308869-73310146	GM12878	blood:	n/a	chr11:73309338-73309348 chr11:73309526-73309536 chr11:73309162-73309172
25	CHD2	chr11:73308399-73308599	GM12878	blood:	n/a	n/a
26	CHD2	chr11:73308835-73310111	H1-hESC	embryonic stem cell:	n/a	chr11:73309338-73309348 chr11:73308857-73308867 chr11:73309526-73309536 chr11:73309162-73309172
27	CHD2	chr11:73308969-73309901	HepG2	liver:	n/a	chr11:73309338-73309348 chr11:73309526-73309536 chr11:73309162-73309172
28	CREB1	chr11:73308682-73310183	HepG2	liver:	n/a	n/a
29	CREB1	chr11:73308833-73309968	K562	blood:	n/a	n/a
30	CREB1	chr11:73308824-73310153	GM12878	blood:	n/a	n/a
31	CREB1	chr11:73308787-73309920	A549	lung:	n/a	n/a
32	CREB1	chr11:73309049-73309227	A549	lung:	n/a	n/a
33	CREB1	chr11:73308807-73309987	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr11:73308916-73309981	HepG2	liver:	n/a	n/a
35	CREB1	chr11:73309149-73309990	ECC-1	luminal epithelium:	n/a	n/a
36	CREB1	chr11:73308916-73309927	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTBP2	chr11:73308930-73309867	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr11:73309020-73309170	HCT-116	colon:	n/a	n/a
39	CTCF	chr11:73308960-73309110	GM12865	blood:	n/a	n/a
40	CTCF	chr11:73308966-73309100	GM13977	blood:	n/a	n/a
41	CTCF	chr11:73309000-73309150	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr11:73309020-73309170	AG10803	skin:	n/a	n/a
43	CTCF	chr11:73309080-73309230	AG09309	skin:	n/a	n/a
44	CTCF	chr11:73309040-73309190	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr11:73308980-73309130	GM12874	blood:	n/a	n/a
46	CTCF	chr11:73308960-73309110	GM12875	blood:	n/a	n/a
47	CTCF	chr11:73309040-73309190	Caco-2	colon:	n/a	n/a
48	CTCF	chr11:73309007-73309187	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr11:73308960-73309110	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr11:73308980-73309130	GM12875	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:73308991-73309041	BE2_C	brain:	n/a
2	chr11:73308991-73309041	BE2_C	brain:	n/a
3	chr11:73309287-73309337	NH-A	brain:	n/a
4	chr11:73308991-73309041	NHBE	bronchial:	n/a
5	chr11:73309262-73309312	PANC-1	pancreas:	n/a
6	chr11:73309264-73309314	HCPEpiC	choroid plexus:	n/a
7	chr11:73309256-73309306	PFSK-1	brain:	n/a
8	chr11:73309287-73309337	MCF10A-Er-Src	breast:	n/a
9	chr11:73308997-73309047	AG04450	lung:	fetal
10	chr11:73308756-73308806	A549	lung:	n/a
11	chr11:73308756-73308806	AG04450	lung:	fetal
12	chr11:73308756-73308806	HCF	heart:	n/a
13	chr11:73309287-73309337	HUVEC	blood vessel:	n/a
14	chr11:73308997-73309047	HMEC	breast:	n/a
15	chr11:73309269-73309319	HPAEpiC	pulmonary alveolar:	n/a
16	chr11:73309287-73309337	SK-N-SH_RA	brain:	n/a
17	chr11:73308756-73308806	GM12878	blood:	n/a
18	chr11:73308997-73309047	HEEpiC	esophagus:	n/a
19	chr11:73309262-73309312	Caco-2	colon:	n/a
20	chr11:73309256-73309306	GM12891	blood:	n/a
21	chr11:73308997-73309047	BE2_C	brain:	n/a
22	chr11:73308756-73308806	Caco-2	colon:	n/a
23	chr11:73309262-73309312	NHBE	bronchial:	n/a
24	chr11:73309269-73309319	HEK293	kidney:	embryo
25	chr11:73309262-73309312	GM12892	blood:	n/a
26	chr11:73308991-73309041	LNCaP	prostate:	n/a
27	chr11:73308997-73309047	BJ	skin:	n/a
28	chr11:73308997-73309047	SAEC	small airway:	n/a
29	chr11:73309287-73309337	HL-60	blood:	n/a
30	chr11:73308991-73309041	GM19239	blood:	n/a
31	chr11:73309264-73309314	HNPCEpiC	eye:	n/a
32	chr11:73309262-73309312	MCF10A-Er-Src	breast:	n/a
33	chr11:73309269-73309319	HRPEpiC	eye:	n/a
34	chr11:73309262-73309312	HRE	kidney:	n/a
35	chr11:73309287-73309337	HEK293	kidney:	embryo
36	chr11:73309287-73309337	AG10803	skin:	n/a
37	chr11:73309287-73309337	ProgFib	skin:	n/a
38	chr11:73309269-73309319	HUVEC	blood vessel:	n/a
39	chr11:73309256-73309306	AoSMC	blood vessel:	n/a
40	chr11:73308997-73309047	MCF-7	breast:	n/a
41	chr11:73309264-73309314	HMEC	breast:	n/a
42	chr11:73309256-73309306	PrEC	prostate:	n/a
43	chr11:73309256-73309306	MCF-7	breast:	n/a
44	chr11:73309256-73309306	HCPEpiC	choroid plexus:	n/a
45	chr11:73308991-73309041	IMR90	lung:	fetal
46	chr11:73309264-73309314	Hepatocyte	liver:	n/a
47	chr11:73309264-73309314	GM06990	blood:	n/a
48	chr11:73308997-73309047	CMK	blood:	n/a
49	chr11:73309264-73309314	NH-A	brain:	n/a
50	chr11:73309269-73309319	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:73307696..73311155-chr11:73356118..73358808,4	MCF-7	breast:
2	chr11:73289699..73292318-chr11:73308150..73310462,2	K562	blood:
3	chr11:73309145..73309670-chr8:143484529..143485324,2	HCT-116	colon:
4	chr11:73308527..73310864-chr11:73370877..73373752,3	MCF-7	breast:
5	chr11:73309124..73309770-chr12:89746078..89746676,2	NB4	blood:

Variant related genes	Relation type
FAM168A	TF binding region
FAM168A	CpG island
ENSG00000139318	chromatin interactions
ENSG00000231726	chromatin interactions
ENSG00000171045	chromatin interactions
ENSG00000021300	chromatin interactions
ENSG00000261693	chromatin interactions

Extended variants
information (count: 79 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:79 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376357605	chr11:73306780-73306781	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs547700918	chr11:73306781-73306782	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs185474469	chr11:73306813-73306814	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs539818218	chr11:73306848-73306849	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs188472059	chr11:73306866-73306867	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs555300140	chr11:73307031-73307032	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs576851150	chr11:73307102-73307103	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs191392795	chr11:73307104-73307105	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs535675194	chr11:73307107-73307108	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs555974706	chr11:73307124-73307125	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs572288352	chr11:73307182-73307183	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs183637352	chr11:73307194-73307195	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs558939533	chr11:73307263-73307264	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs564410773	chr11:73307291-73307292	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs576445441	chr11:73307294-73307295	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs368008904	chr11:73307328-73307329	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs76665245	chr11:73307341-73307342	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs35666404	chr11:73307387-73307388	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs373561959	chr11:73307403-73307404	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs117840456	chr11:73307421-73307422	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs188700641	chr11:73307431-73307432	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs181187497	chr11:73307432-73307433	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs76170427	chr11:73307506-73307507	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs561954655	chr11:73307520-73307521	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs187037486	chr11:73307552-73307553	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs74930174	chr11:73307554-73307555	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs570107330	chr11:73307563-73307564	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs189933547	chr11:73307630-73307631	Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541482445	chr11:73307727-73307728	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs550105019	chr11:73307744-73307745	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs11606281	chr11:73307762-73307763	Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs675832	chr11:73307833-73307834	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs138238758	chr11:73307852-73307853	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs182585002	chr11:73307954-73307955	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs34509251	chr11:73307955-73307956	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs149583102	chr11:73307970-73307971	Flanking Active TSS Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs534852367	chr11:73308021-73308022	Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs558039834	chr11:73308034-73308035	Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs542982759	chr11:73308037-73308038	Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs72973625	chr11:73308091-73308092	Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs543755531	chr11:73308117-73308118	Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs113200503	chr11:73308161-73308162	Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs556163207	chr11:73308172-73308173	Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs575933792	chr11:73308202-73308203	Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs541937482	chr11:73308221-73308222	Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs186211070	chr11:73308238-73308239	Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs527497776	chr11:73308269-73308270	Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs541190110	chr11:73308300-73308301	Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs542459164	chr11:73308312-73308313	Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs533313909	chr11:73308330-73308331	Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung cancer	21203850	CNVD

Chromatin state (count:464 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73250000-73307800	Weak transcription	Stomach Smooth Muscle	stomach
2	chr11:73253800-73307000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr11:73266600-73307800	Weak transcription	Fetal Intestine Small	intestine
4	chr11:73272200-73307600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:73275400-73307000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr11:73276400-73307000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr11:73277400-73307800	Weak transcription	Fetal Intestine Large	intestine
8	chr11:73279400-73307000	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr11:73281600-73307800	Weak transcription	Hela-S3	cervix
10	chr11:73286800-73307600	Weak transcription	Lung	lung
11	chr11:73288400-73307800	Weak transcription	Aorta	Aorta
12	chr11:73288800-73307600	Weak transcription	Fetal Kidney	kidney
13	chr11:73289400-73307000	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr11:73289600-73306800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr11:73290000-73308000	Weak transcription	Primary B cells from cord blood	blood
16	chr11:73290200-73307000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr11:73290200-73307000	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr11:73290200-73307000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr11:73290400-73308000	Weak transcription	Primary hematopoietic stem cells	blood
20	chr11:73291400-73307600	Weak transcription	Pancreas	Pancrea
21	chr11:73294200-73307800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr11:73297400-73307600	Weak transcription	Osteobl	bone
23	chr11:73297600-73307000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr11:73297800-73307200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr11:73297800-73307400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr11:73297800-73307600	Weak transcription	HMEC	breast
27	chr11:73298000-73307000	Weak transcription	Small Intestine	intestine
28	chr11:73298000-73307600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr11:73299800-73307600	Weak transcription	Fetal Stomach	stomach
30	chr11:73300000-73307600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr11:73300600-73307000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr11:73302600-73307000	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr11:73303200-73307600	Weak transcription	Fetal Heart	heart
34	chr11:73303400-73307600	Weak transcription	Primary B cells from peripheral blood	blood
35	chr11:73303800-73307600	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr11:73303800-73307600	Weak transcription	Right Atrium	heart
37	chr11:73304000-73307000	Weak transcription	Fetal Thymus	thymus
38	chr11:73304000-73307600	Weak transcription	Left Ventricle	heart
39	chr11:73304600-73307000	Enhancers	Brain Anterior Caudate	brain
40	chr11:73304600-73307000	Enhancers	Fetal Brain Male	brain
41	chr11:73304600-73307400	Enhancers	HepG2	liver
42	chr11:73304600-73307800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr11:73304600-73307800	Enhancers	Brain Substantia Nigra	brain
44	chr11:73304800-73307000	Enhancers	K562	blood
45	chr11:73304800-73307600	Weak transcription	NHLF	lung
46	chr11:73305000-73307600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr11:73305000-73307600	Weak transcription	Thymus	Thymus
48	chr11:73305200-73307000	Weak transcription	Colon Smooth Muscle	Colon
49	chr11:73305200-73307000	Weak transcription	Fetal Lung	lung
50	chr11:73305200-73307800	Weak transcription	Duodenum Mucosa	Duodenum

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