Variant report

Variant	esv3341994
Chromosome Location	chr11:67484003-67507176
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:140)
CpG islands
(count:549)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:140 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr11:67502361-67502545	GM12878	blood:	n/a	n/a
2	BRCA1	chr11:67499670-67499817	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr11:67490128-67490285	HepG2	liver:	n/a	chr11:67490201-67490212
4	CEBPB	chr11:67499879-67500141	A549	lung:	n/a	n/a
5	CHD2	chr11:67499726-67499730	H1-hESC	embryonic stem cell:	n/a	n/a
6	CREB1	chr11:67499370-67499887	A549	lung:	n/a	n/a
7	CREB1	chr11:67499595-67499975	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr11:67499728-67499926	GM13977	blood:	n/a	n/a
9	CTCF	chr11:67498880-67500410	SK-N-SH	brain:	n/a	n/a
10	CTCF	chr11:67494880-67495150	GM12870	blood:	n/a	n/a
11	CTCF	chr11:67499702-67499917	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr11:67499698-67500136	MCF-7	breast:	n/a	n/a
13	CTCF	chr11:67494900-67495105	GM20000	blood:	n/a	n/a
14	CTCF	chr11:67499773-67499865	GM12878	blood:	n/a	n/a
15	CTCF	chr11:67499727-67499910	MCF-7	breast:	n/a	n/a
16	CTCF	chr11:67499696-67499964	IMR90	lung:	n/a	n/a
17	CTCF	chr11:67495020-67495170	GM12878	blood:	n/a	n/a
18	CTCF	chr11:67499554-67500093	A549	lung:	n/a	n/a
19	CTCF	chr11:67495041-67495104	GM13977	blood:	n/a	n/a
20	CTCF	chr11:67499709-67499954	K562	blood:	n/a	n/a
21	CTCF	chr11:67499685-67499956	K562	blood:	n/a	n/a
22	CTCF	chr11:67494940-67495090	GM12864	blood:	n/a	n/a
23	CTCF	chr11:67499777-67499872	GM13976	blood:	n/a	n/a
24	CTCF	chr11:67499760-67499910	HEK293	kidney:	n/a	n/a
25	CTCF	chr11:67499744-67499900	GM19239	blood:	n/a	n/a
26	CTCF	chr11:67499700-67499916	GM19238	blood:	n/a	n/a
27	CTCF	chr11:67496440-67496590	GM12873	blood:	n/a	n/a
28	CTCF	chr11:67499752-67499897	GM19240	blood:	n/a	n/a
29	CTCF	chr11:67495080-67495230	GM12873	blood:	n/a	n/a
30	CTCF	chr11:67499727-67500106	LNCaP	prostate:	n/a	n/a
31	CTCF	chr11:67499100-67499168	LNCaP	prostate:	n/a	n/a
32	CTCF	chr11:67494964-67495097	GM19238	blood:	n/a	n/a
33	CTCF	chr11:67495003-67495010	NHEK	skin:	n/a	n/a
34	CTCF	chr11:67499657-67499950	MCF-7	breast:	n/a	n/a
35	CTCF	chr11:67499770-67499869	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr11:67499730-67499921	Gliobla	brain:	n/a	n/a
37	CTCF	chr11:67494960-67495110	GM12873	blood:	n/a	n/a
38	CTCF	chr11:67494998-67495022	MCF-7	breast:	n/a	n/a
39	CTCF	chr11:67499760-67499910	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr11:67494945-67495114	GM12878	blood:	n/a	n/a
41	CTCF	chr11:67499636-67499928	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr11:67499661-67499985	K562	blood:	n/a	n/a
43	CTCF	chr11:67499810-67499833	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr11:67494924-67495110	GM12892	blood:	n/a	n/a
45	CTCF	chr11:67499701-67499934	MCF-7	breast:	n/a	n/a
46	CTCF	chr11:67499757-67499894	GM10248	blood:	n/a	n/a
47	CTCF	chr11:67499726-67499910	GM12891	blood:	n/a	n/a
48	CTCF	chr11:67500051-67500099	LNCaP	prostate:	n/a	n/a
49	CTCF	chr11:67499760-67499878	ProgFib	skin:	n/a	n/a
50	CTCF	chr11:67499727-67499923	MCF-7	breast:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67499849-67499899	GM06990	blood:	n/a
2	chr11:67494416-67494466	AoSMC	blood vessel:	n/a
3	chr11:67494416-67494466	Hepatocyte	liver:	n/a
4	chr11:67498316-67498366	HRCEpiC	kidney:	n/a
5	chr11:67499849-67499899	AG04450	lung:	fetal
6	chr11:67498995-67499045	HCF	heart:	n/a
7	chr11:67494327-67494377	PrEC	prostate:	n/a
8	chr11:67498995-67499045	HRCEpiC	kidney:	n/a
9	chr11:67498995-67499045	H1-hESC	embryonic stem cell:	embryo
10	chr11:67498271-67498321	HRPEpiC	eye:	n/a
11	chr11:67494416-67494466	NHDF-neo	bronchial:	n/a
12	chr11:67498316-67498366	AG09309	skin:	n/a
13	chr11:67498229-67498279	NHDF-neo	bronchial:	n/a
14	chr11:67498995-67499045	HCM	heart:	n/a
15	chr11:67498995-67499045	HAEpiC	amniotic membrane:	n/a
16	chr11:67498316-67498366	GM12891	blood:	n/a
17	chr11:67494327-67494377	AG04449	skin:	fetal
18	chr11:67498271-67498321	HL-60	blood:	n/a
19	chr11:67494416-67494466	AG09319	gingival:	n/a
20	chr11:67494416-67494466	U87	brain:	n/a
21	chr11:67498229-67498279	GM19239	blood:	n/a
22	chr11:67499525-67499575	NH-A	brain:	n/a
23	chr11:67494327-67494377	PFSK-1	brain:	n/a
24	chr11:67498229-67498279	HEK293	kidney:	embryo
25	chr11:67499849-67499899	PANC-1	pancreas:	n/a
26	chr11:67499431-67499481	AG04449	skin:	fetal
27	chr11:67498229-67498279	HCT-116	colon:	n/a
28	chr11:67499431-67499481	BJ	skin:	n/a
29	chr11:67499525-67499575	LNCaP	prostate:	n/a
30	chr11:67494327-67494377	PANC-1	pancreas:	n/a
31	chr11:67498271-67498321	HUVEC	blood vessel:	n/a
32	chr11:67494416-67494466	HCPEpiC	choroid plexus:	n/a
33	chr11:67498995-67499045	SK-N-SH	brain:	n/a
34	chr11:67499849-67499899	K562	blood:	n/a
35	chr11:67499525-67499575	HL-60	blood:	n/a
36	chr11:67494416-67494466	CMK	blood:	n/a
37	chr11:67494416-67494466	HUVEC	blood vessel:	n/a
38	chr11:67498229-67498279	CMK	blood:	n/a
39	chr11:67499525-67499575	HRE	kidney:	n/a
40	chr11:67498229-67498279	A549	lung:	n/a
41	chr11:67498316-67498366	HRE	kidney:	n/a
42	chr11:67498995-67499045	CMK	blood:	n/a
43	chr11:67498229-67498279	SK-N-SH_RA	brain:	n/a
44	chr11:67498229-67498279	HEEpiC	esophagus:	n/a
45	chr11:67494416-67494466	HEEpiC	esophagus:	n/a
46	chr11:67499525-67499575	GM19239	blood:	n/a
47	chr11:67499849-67499899	NHDF-neo	bronchial:	n/a
48	chr11:67499849-67499899	HL-60	blood:	n/a
49	chr11:67499431-67499481	RPTEC	kidney:	n/a
50	chr11:67494416-67494466	HRPEpiC	eye:	n/a

No data

Variant related genes	Relation type
OR7E11P	TF binding region
UNC93B5	TF binding region
ENSG00000266451	TF binding region
ENSG00000254883	TF binding region
ENSG00000235855	TF binding region
OR7E11P	CpG island
UNC93B5	CpG island
ENSG00000266451	CpG island
ENSG00000254883	CpG island
ENSG00000235855	CpG island

Extended variants
information (count: 1576 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1576 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116913057	chr11:67484004-67484005	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs555904458	chr11:67484006-67484007	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs574347858	chr11:67484013-67484014	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs541950250	chr11:67484023-67484024	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs560250213	chr11:67484040-67484041	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs187170407	chr11:67484049-67484050	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs191882656	chr11:67484052-67484053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564432269	chr11:67484060-67484061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531490917	chr11:67484064-67484065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181498444	chr11:67484084-67484085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561959356	chr11:67484086-67484087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566000561	chr11:67484100-67484101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547492936	chr11:67484104-67484105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186615591	chr11:67484107-67484108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs11227895	chr11:67484113-67484114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142403521	chr11:67484116-67484117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190124532	chr11:67484119-67484120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377086731	chr11:67484144-67484145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574495368	chr11:67484161-67484162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535434136	chr11:67484170-67484171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530553496	chr11:67484174-67484175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370564058	chr11:67484183-67484184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570084621	chr11:67484195-67484196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182586051	chr11:67484217-67484218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186914420	chr11:67484220-67484221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs57487233	chr11:67484222-67484223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11227896	chr11:67484227-67484228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs11227897	chr11:67484228-67484229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529285286	chr11:67484232-67484233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184070062	chr11:67484233-67484234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559457510	chr11:67484240-67484241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs188622734	chr11:67484241-67484242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574810720	chr11:67484246-67484247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7933342	chr11:67484248-67484249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs10750802	chr11:67484257-67484258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs531434149	chr11:67484266-67484267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537612324	chr11:67484270-67484271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549453066	chr11:67484273-67484274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567957077	chr11:67484278-67484279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535470816	chr11:67484279-67484280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs71480235	chr11:67484280-67484281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs572035026	chr11:67484282-67484283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs187297690	chr11:67484283-67484284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191828636	chr11:67484284-67484285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs55720623	chr11:67484290-67484291	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs543591991	chr11:67484297-67484298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs561692019	chr11:67484299-67484300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573585954	chr11:67484307-67484308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540895483	chr11:67484308-67484309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs57028729	chr11:67484324-67484325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	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
Acute myeloid leukemia	21251322	CNVD
Lung cancer	19153074	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:201 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67481200-67485200	Enhancers	Primary B cells from peripheral blood	blood
2	chr11:67481200-67499400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:67481800-67484800	Enhancers	Primary B cells from cord blood	blood
4	chr11:67485000-67485200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:67486200-67486400	Enhancers	H1 Cell Line	embryonic stem cell
6	chr11:67489000-67490200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr11:67489200-67490600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr11:67490000-67490200	Enhancers	H1 Cell Line	embryonic stem cell
9	chr11:67490000-67490600	Enhancers	H9 Cell Line	embryonic stem cell
10	chr11:67490000-67495200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr11:67490200-67494400	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr11:67490200-67495000	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr11:67494000-67495600	Enhancers	Pancreas	Pancrea
14	chr11:67494400-67495400	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr11:67494400-67495800	Enhancers	H1 Cell Line	embryonic stem cell
16	chr11:67494400-67496400	Enhancers	Placenta	Placenta
17	chr11:67494400-67496800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr11:67494400-67497000	Enhancers	Stomach Mucosa	stomach
19	chr11:67494400-67499200	Weak transcription	Right Atrium	heart
20	chr11:67494800-67495600	Enhancers	Gastric	stomach
21	chr11:67495000-67495400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr11:67495000-67495400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr11:67495000-67495400	Enhancers	Duodenum Mucosa	Duodenum
24	chr11:67495000-67495800	Enhancers	Placenta Amnion	Placenta Amnion
25	chr11:67495000-67496800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr11:67495000-67498400	Enhancers	Fetal Intestine Large	intestine
27	chr11:67495000-67498600	Enhancers	Fetal Intestine Small	intestine
28	chr11:67495200-67495400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr11:67495200-67495400	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr11:67495200-67495400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr11:67495200-67495400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr11:67495200-67495600	Enhancers	Esophagus	oesophagus
33	chr11:67495200-67495800	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr11:67495200-67496200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr11:67495200-67497000	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr11:67495200-67497200	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr11:67495200-67497200	Enhancers	HepG2	liver
38	chr11:67495200-67498200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr11:67495400-67496200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr11:67495400-67496400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr11:67495400-67497200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:67495400-67499200	Weak transcription	Duodenum Mucosa	Duodenum
43	chr11:67495400-67499400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr11:67495600-67499600	Weak transcription	Pancreas	Pancrea
45	chr11:67495600-67499800	Weak transcription	Gastric	stomach
46	chr11:67495800-67496200	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr11:67495800-67499200	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr11:67495800-67499200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr11:67496200-67496400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr11:67496200-67496400	Enhancers	Placenta Amnion	Placenta Amnion

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