Variant report

Variant	esv3335996
Chromosome Location	chr11:46818751-46843532
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:318)
CpG islands
(count:61)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:46830444-46830643	K562	blood:	n/a	n/a
2	ARID3A	chr11:46830388-46830678	HepG2	liver:	n/a	n/a
3	BACH1	chr11:46843237-46843607	K562	blood:	n/a	n/a
4	BHLHE40	chr11:46843237-46843607	K562	blood:	n/a	n/a
5	BRCA1	chr11:46843234-46843609	GM12878	blood:	n/a	n/a
6	BRCA1	chr11:46843236-46843602	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr11:46830347-46830714	K562	blood:	n/a	n/a
8	CBX3	chr11:46830281-46830772	HCT-116	colon:	n/a	n/a
9	CEBPB	chr11:46843238-46843613	K562	blood:	n/a	chr11:46843405-46843416
10	CEBPB	chr11:46843401-46843612	HepG2	liver:	n/a	chr11:46843405-46843416
11	CHD2	chr11:46843238-46843605	K562	blood:	n/a	n/a
12	CHD2	chr11:46843238-46843441	HepG2	liver:	n/a	n/a
13	CHD2	chr11:46843235-46843603	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr11:46830500-46830650	AG09309	skin:	n/a	n/a
15	CTCF	chr11:46830480-46830630	AG04449	skin:	n/a	n/a
16	CTCF	chr11:46830480-46830630	HRPEpiC	eye:	n/a	n/a
17	CTCF	chr11:46830500-46830650	NHLF	lung:	n/a	n/a
18	CTCF	chr11:46830480-46830630	Caco-2	colon:	n/a	n/a
19	CTCF	chr11:46830480-46830630	HPAF	blood vessel:	n/a	n/a
20	CTCF	chr11:46843402-46843439	ProgFib	skin:	n/a	n/a
21	CTCF	chr11:46830460-46830610	GM12866	blood:	n/a	n/a
22	CTCF	chr11:46830319-46830688	MCF-7	breast:	n/a	n/a
23	CTCF	chr11:46830400-46830550	GM12873	blood:	n/a	n/a
24	CTCF	chr11:46830520-46830670	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr11:46830440-46830590	HEEpiC	esophagus:	n/a	n/a
26	CTCF	chr11:46830574-46830623	GM19240	blood:	n/a	n/a
27	CTCF	chr11:46830460-46830610	GM12874	blood:	n/a	n/a
28	CTCF	chr11:46830509-46830611	GM20000	blood:	n/a	n/a
29	CTCF	chr11:46830460-46830610	GM12872	blood:	n/a	n/a
30	CTCF	chr11:46830440-46830590	AG10803	skin:	n/a	n/a
31	CTCF	chr11:46830460-46830610	GM12871	blood:	n/a	n/a
32	CTCF	chr11:46830425-46830659	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr11:46830480-46830630	HMF	breast:	n/a	n/a
34	CTCF	chr11:46830380-46830530	NHEK	skin:	n/a	n/a
35	CTCF	chr11:46830480-46830630	GM12873	blood:	n/a	n/a
36	CTCF	chr11:46830366-46830725	GM12878	blood:	n/a	n/a
37	CTCF	chr11:46830460-46830610	HEK293	kidney:	n/a	n/a
38	CTCF	chr11:46830500-46830650	HAc	cerebellar:	n/a	n/a
39	CTCF	chr11:46830480-46830630	NHEK	skin:	n/a	n/a
40	CTCF	chr11:46830559-46830577	MCF-7	breast:	n/a	n/a
41	CTCF	chr11:46830460-46830610	BE2_C	brain:	n/a	n/a
42	CTCF	chr11:46830480-46830630	HRE	kidney:	n/a	n/a
43	CTCF	chr11:46830460-46830610	GM12869	blood:	n/a	n/a
44	CTCF	chr11:46830500-46830650	HA-sp	spinal cord:	n/a	n/a
45	CTCF	chr11:46830540-46830690	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr11:46830460-46830610	Caco-2	colon:	n/a	n/a
47	CTCF	chr11:46830500-46830650	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr11:46830440-46830590	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr11:46830480-46830630	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr11:46830460-46830610	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:46820594-46820644	Caco-2	colon:	n/a
2	chr11:46820594-46820644	NB4	blood:	n/a
3	chr11:46820594-46820644	HCM	heart:	n/a
4	chr11:46820594-46820644	NT2-D1	testis:	n/a
5	chr11:46820594-46820644	Jurkat	blood:	n/a
6	chr11:46820594-46820644	CMK	blood:	n/a
7	chr11:46820594-46820644	HepG2	liver:	n/a
8	chr11:46820594-46820644	LNCaP	prostate:	n/a
9	chr11:46820594-46820644	HIPEpiC	eye:	n/a
10	chr11:46820594-46820644	SK-N-SH_RA	brain:	n/a
11	chr11:46820594-46820644	PrEC	prostate:	n/a
12	chr11:46820594-46820644	SK-N-MC	brain:	n/a
13	chr11:46820594-46820644	PANC-1	pancreas:	n/a
14	chr11:46820594-46820644	HAEpiC	amniotic membrane:	n/a
15	chr11:46820594-46820644	BJ	skin:	n/a
16	chr11:46820594-46820644	HRPEpiC	eye:	n/a
17	chr11:46820594-46820644	RPTEC	kidney:	n/a
18	chr11:46820594-46820644	AoSMC	blood vessel:	n/a
19	chr11:46820594-46820644	Hela-S3	cervix:	n/a
20	chr11:46820594-46820644	HCT-116	colon:	n/a
21	chr11:46820594-46820644	MCF10A-Er-Src	breast:	n/a
22	chr11:46820594-46820644	HMEC	breast:	n/a
23	chr11:46820594-46820644	GM06990	blood:	n/a
24	chr11:46820594-46820644	NHBE	bronchial:	n/a
25	chr11:46820594-46820644	H1-hESC	embryonic stem cell:	embryo
26	chr11:46820594-46820644	U87	brain:	n/a
27	chr11:46820594-46820644	HEEpiC	esophagus:	n/a
28	chr11:46820594-46820644	IMR90	lung:	fetal
29	chr11:46820594-46820644	A549	lung:	n/a
30	chr11:46820594-46820644	HRE	kidney:	n/a
31	chr11:46820594-46820644	SKMC	muscle:	n/a
32	chr11:46820594-46820644	NH-A	brain:	n/a
33	chr11:46820594-46820644	AG04449	skin:	fetal
34	chr11:46820594-46820644	SK-N-SH	brain:	n/a
35	chr11:46820594-46820644	HCPEpiC	choroid plexus:	n/a
36	chr11:46820594-46820644	GM12891	blood:	n/a
37	chr11:46820594-46820644	HPAEpiC	pulmonary alveolar:	n/a
38	chr11:46820594-46820644	HL-60	blood:	n/a
39	chr11:46820594-46820644	ovcar-3	ovarian:	n/a
40	chr11:46820594-46820644	GM12892	blood:	n/a
41	chr11:46820594-46820644	HNPCEpiC	eye:	n/a
42	chr11:46820594-46820644	Hepatocyte	liver:	n/a
43	chr11:46820594-46820644	BE2_C	brain:	n/a
44	chr11:46820594-46820644	AG09319	gingival:	n/a
45	chr11:46820594-46820644	MCF-7	breast:	n/a
46	chr11:46820594-46820644	T-47D	breast:	n/a
47	chr11:46820594-46820644	GM12878	blood:	n/a
48	chr11:46820594-46820644	ProgFib	skin:	n/a
49	chr11:46820594-46820644	AG04450	lung:	fetal
50	chr11:46820594-46820644	PFSK-1	brain:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:46830314..46832517-chr11:47174781..47176798,2	K562	blood:
2	chr11:46824423..46826594-chr11:46829282..46831781,2	MCF-7	breast:
3	chr1:145012787..145014315-chr11:46834339..46836400,2	MCF-7	breast:
4	chr11:46835200..46837262-chr11:46837857..46839815,2	K562	blood:
5	chr11:46842194..46844369-chr11:46847198..46849731,2	K562	blood:
6	chr11:46839608..46842454-chr11:46847155..46850058,2	MCF-7	breast:
7	chr11:46824600..46826880-chr11:46829114..46830702,3	K562	blood:
8	chr11:46842912..46843429-chr14:88237081..88237681,2	MCF-7	breast:
9	chr11:46829226..46831857-chr11:46836190..46837895,2	K562	blood:
10	chr11:46839503..46842068-chr11:46852399..46855233,2	K562	blood:
11	chr11:46812144..46815531-chr11:46816972..46819757,4	K562	blood:
12	chr11:46824600..46826880-chr11:46829114..46830702,3	K562	blood:
13	chr11:46839791..46842440-chr11:46844022..46846821,2	MCF-7	breast:
14	chr11:46787403..46789216-chr11:46830914..46832486,2	K562	blood:
15	chr11:46835868..46836380-chr11:47182883..47183547,2	MCF-7	breast:
16	chr11:46829226..46831857-chr11:46836190..46837895,2	K562	blood:
17	chr11:46829027..46831966-chr11:46832483..46835445,2	K562	blood:
18	chr11:46828781..46830541-chr11:46867184..46869388,2	MCF-7	breast:
19	chr11:46812144..46813760-chr11:46816972..46819757,2	K562	blood:
20	chr11:46830883..46837323-chr11:46838185..46842346,7	K562	blood:
21	chr11:46815521..46817270-chr11:46825873..46827721,2	K562	blood:
22	chr11:46830883..46837323-chr11:46838185..46842346,7	K562	blood:
23	chr11:46835200..46837262-chr11:46837857..46839815,2	K562	blood:
24	chr11:46829027..46831966-chr11:46832483..46835445,2	K562	blood:
25	chr11:46828755..46831301-chr11:46844947..46847653,2	K562	blood:
26	chr11:46824423..46826594-chr11:46829282..46831781,2	MCF-7	breast:
27	chr11:46821601..46822104-chr3:11267250..11268208,2	Hela-S3	cervix:
28	chr11:46842194..46845139-chr11:46848231..46850202,2	K562	blood:
29	chr11:46774424..46776540-chr11:46824127..46827022,2	MCF-7	breast:
30	chr11:46838312..46841025-chr11:46845017..46847859,4	K562	blood:
31	chr11:46840513..46842114-chr11:46846709..46848551,2	K562	blood:

No data

Variant related genes	Relation type
CKAP5	TF binding region
CKAP5	CpG island
ENSG00000175216	chromatin interactions
ENSG00000247675	chromatin interactions
ENSG00000196639	chromatin interactions
ENSG00000149179	chromatin interactions
ENSG00000263540	chromatin interactions

Extended variants
information (count: 853 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:853 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535810503	chr11:46818764-46818765	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189503527	chr11:46818777-46818778	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74429725	chr11:46818779-46818780	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs7109707	chr11:46818814-46818815	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs180695866	chr11:46818838-46818839	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs11038994	chr11:46818870-46818871	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs527952174	chr11:46818916-46818917	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576066429	chr11:46818928-46818929	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534730562	chr11:46818932-46818933	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372888394	chr11:46818939-46818940	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112909367	chr11:46818940-46818941	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs60301522	chr11:46818941-46818942	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs60748677	chr11:46818942-46818943	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs72228365	chr11:46818943-46818944	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545590293	chr11:46818946-46818947	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs397970883	chr11:46818953-46818954	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185907986	chr11:46818960-46818961	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562569984	chr11:46818966-46818967	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187569776	chr11:46818973-46818974	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs540263769	chr11:46819016-46819017	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376527732	chr11:46819017-46819018	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143732785	chr11:46819022-46819023	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562002863	chr11:46819036-46819037	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs527579405	chr11:46819070-46819071	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs117183893	chr11:46819165-46819166	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570667761	chr11:46819247-46819248	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370502114	chr11:46819319-46819320	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533113903	chr11:46819364-46819365	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368069494	chr11:46819413-46819414	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs142946079	chr11:46819451-46819452	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550025952	chr11:46819513-46819514	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374185425	chr11:46819537-46819538	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375526938	chr11:46819552-46819553	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552776296	chr11:46819580-46819581	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs377624650	chr11:46819594-46819595	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113937457	chr11:46819596-46819597	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201848818	chr11:46819644-46819645	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374699226	chr11:46819694-46819695	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555335700	chr11:46819710-46819711	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566080226	chr11:46819713-46819714	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374968931	chr11:46819768-46819769	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111906597	chr11:46819788-46819789	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7950923	chr11:46819815-46819816	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534990598	chr11:46819824-46819825	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76939761	chr11:46819832-46819833	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78632754	chr11:46819833-46819834	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7936100	chr11:46819847-46819848	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557990784	chr11:46819975-46819976	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs578122264	chr11:46819981-46819982	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140336784	chr11:46820044-46820045	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:805 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46761400-46840000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr11:46761400-46845200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:46761600-46824600	Strong transcription	Fetal Thymus	thymus
4	chr11:46762600-46826000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:46762600-46841400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr11:46762800-46835600	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr11:46762800-46842400	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr11:46763400-46839600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr11:46778800-46841200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr11:46779400-46824600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr11:46782600-46847400	Weak transcription	Stomach Mucosa	stomach
12	chr11:46787000-46828200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr11:46787800-46824600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
14	chr11:46788000-46826200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr11:46788200-46825800	Strong transcription	HUES6 Cell Line	embryonic stem cell
16	chr11:46788200-46841400	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr11:46788600-46824200	Strong transcription	Fetal Muscle Trunk	muscle
18	chr11:46788600-46840600	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr11:46788800-46824000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
20	chr11:46795200-46820400	Strong transcription	Primary T helper cells PMA-I stimulated	--
21	chr11:46796400-46821400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr11:46796400-46824600	Strong transcription	Primary T helper cells fromperipheralblood	blood
23	chr11:46796600-46825800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr11:46796800-46819600	Strong transcription	Skeletal Muscle Female	skeletal muscle
25	chr11:46796800-46820600	Strong transcription	Fetal Brain Female	brain
26	chr11:46796800-46820800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr11:46796800-46823800	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr11:46796800-46824000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr11:46796800-46824200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr11:46796800-46824200	Strong transcription	Duodenum Mucosa	Duodenum
31	chr11:46796800-46824400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr11:46796800-46824400	Strong transcription	Brain Germinal Matrix	brain
33	chr11:46796800-46824600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr11:46797000-46821600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr11:46797000-46824200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr11:46797000-46825200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr11:46797200-46824200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr11:46797200-46824400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr11:46797200-46826000	Strong transcription	Dnd41	blood
40	chr11:46797400-46823800	Strong transcription	Osteobl	bone
41	chr11:46797400-46824400	Strong transcription	Placenta	Placenta
42	chr11:46801400-46822800	Strong transcription	Primary B cells from cord blood	blood
43	chr11:46803600-46820800	Strong transcription	Fetal Lung	lung
44	chr11:46803800-46825000	Strong transcription	Adipose Nuclei	Adipose
45	chr11:46804000-46820400	Strong transcription	Duodenum Smooth Muscle	Duodenum
46	chr11:46804000-46824000	Strong transcription	Primary T cells from cord blood	blood
47	chr11:46804000-46826000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr11:46804200-46822200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr11:46804200-46824600	Strong transcription	Fetal Intestine Large	intestine
50	chr11:46804200-46825400	Strong transcription	Fetal Muscle Leg	muscle

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