Variant report

Variant	nsv1016940
Chromosome Location	chr6:167222633-167289747
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:628)
CpG islands
(count:2018)
Chromatin interactive
region (count:25)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:628 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167264235-167264605	K562	blood:	n/a	n/a
2	ATF1	chr6:167260351-167260433	K562	blood:	n/a	n/a
3	ATF1	chr6:167264121-167264564	K562	blood:	n/a	n/a
4	ATF1	chr6:167255068-167255231	K562	blood:	n/a	n/a
5	ATF1	chr6:167287376-167287880	K562	blood:	n/a	n/a
6	ATF1	chr6:167240077-167240150	K562	blood:	n/a	n/a
7	ATF1	chr6:167238143-167238339	K562	blood:	n/a	n/a
8	ATF2	chr6:167243498-167244485	GM12878	blood:	n/a	n/a
9	ATF2	chr6:167247492-167247983	GM12878	blood:	n/a	n/a
10	ATF2	chr6:167243583-167244420	GM12878	blood:	n/a	n/a
11	ATF2	chr6:167263194-167263607	GM12878	blood:	n/a	n/a
12	ATF2	chr6:167247521-167247974	GM12878	blood:	n/a	n/a
13	BACH1	chr6:167276270-167276880	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr6:167243631-167244353	GM12878	blood:	n/a	n/a
15	BATF	chr6:167263166-167263351	GM12878	blood:	n/a	n/a
16	BATF	chr6:167263100-167263391	GM12878	blood:	n/a	n/a
17	BATF	chr6:167247528-167247858	GM12878	blood:	n/a	n/a
18	BATF	chr6:167247594-167247848	GM12878	blood:	n/a	n/a
19	BATF	chr6:167243652-167243968	GM12878	blood:	n/a	n/a
20	BCL11A	chr6:167244064-167244380	GM12878	blood:	n/a	n/a
21	BCL11A	chr6:167243593-167243973	GM12878	blood:	n/a	n/a
22	BCL11A	chr6:167243668-167243958	GM12878	blood:	n/a	n/a
23	BCL11A	chr6:167244040-167244445	GM12878	blood:	n/a	n/a
24	BCLAF1	chr6:167243535-167244464	GM12878	blood:	n/a	n/a
25	BCLAF1	chr6:167243590-167244485	GM12878	blood:	n/a	n/a
26	BCLAF1	chr6:167247514-167247888	GM12878	blood:	n/a	n/a
27	BHLHE40	chr6:167256306-167256412	K562	blood:	n/a	n/a
28	BHLHE40	chr6:167247873-167248126	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:167263347-167263548	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:167276161-167276327	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:167264030-167264513	K562	blood:	n/a	n/a
32	CBX3	chr6:167264115-167264437	K562	blood:	n/a	n/a
33	CCNT2	chr6:167254977-167255146	K562	blood:	n/a	n/a
34	CCNT2	chr6:167264000-167264442	K562	blood:	n/a	chr6:167264339-167264359
35	CEBPB	chr6:167269110-167269239	A549	lung:	n/a	n/a
36	CEBPB	chr6:167246565-167246688	A549	lung:	n/a	n/a
37	CEBPB	chr6:167269019-167269228	K562	blood:	n/a	n/a
38	CEBPB	chr6:167248017-167248058	A549	lung:	n/a	n/a
39	CEBPB	chr6:167269010-167269276	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:167240813-167241002	HepG2	liver:	n/a	chr6:167240916-167240927 chr6:167240904-167240915
41	CEBPD	chr6:167245206-167245696	K562	blood:	n/a	n/a
42	CHD1	chr6:167275559-167276071	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr6:167272213-167272327	GM12878	blood:	n/a	n/a
44	CHD2	chr6:167275963-167276282	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr6:167243660-167244855	GM12878	blood:	n/a	chr6:167244383-167244393
46	CHD2	chr6:167276445-167276497	GM12878	blood:	n/a	n/a
47	CTCF	chr6:167276226-167276350	SK-N-SH_RA	brain:	n/a	chr6:167276287-167276300
48	CTCF	chr6:167223220-167223370	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr6:167266318-167266466	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr6:167276260-167276410	GM06990	blood:	n/a	chr6:167276287-167276300

(count:2018 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167271883-167271933	NH-A	brain:	n/a
2	chr6:167275395-167275445	ovcar-3	ovarian:	n/a
3	chr6:167284542-167284592	U87	brain:	n/a
4	chr6:167275999-167276049	ProgFib	skin:	n/a
5	chr6:167276567-167276617	GM12892	blood:	n/a
6	chr6:167271883-167271933	NH-A	brain:	n/a
7	chr6:167275395-167275445	ovcar-3	ovarian:	n/a
8	chr6:167284542-167284592	U87	brain:	n/a
9	chr6:167275999-167276049	ProgFib	skin:	n/a
10	chr6:167276567-167276617	GM12892	blood:	n/a
11	chr6:167275834-167275884	HUVEC	blood vessel:	n/a
12	chr6:167250513-167250563	T-47D	breast:	n/a
13	chr6:167279026-167279076	HEK293	kidney:	embryo
14	chr6:167284353-167284403	K562	blood:	n/a
15	chr6:167276275-167276325	HCM	heart:	n/a
16	chr6:167279026-167279076	NH-A	brain:	n/a
17	chr6:167287812-167287862	ECC-1	luminal epithelium:	n/a
18	chr6:167275832-167275882	IMR90	lung:	fetal
19	chr6:167250541-167250591	PFSK-1	brain:	n/a
20	chr6:167275834-167275884	PFSK-1	brain:	n/a
21	chr6:167263454-167263504	AG04449	skin:	fetal
22	chr6:167275834-167275884	GM12878	blood:	n/a
23	chr6:167275684-167275734	Jurkat	blood:	n/a
24	chr6:167276567-167276617	HPAEpiC	pulmonary alveolar:	n/a
25	chr6:167250429-167250479	NB4	blood:	n/a
26	chr6:167276650-167276700	AoSMC	blood vessel:	n/a
27	chr6:167275755-167275805	RPTEC	kidney:	n/a
28	chr6:167283835-167283885	HEK293	kidney:	embryo
29	chr6:167276275-167276325	ECC-1	luminal epithelium:	n/a
30	chr6:167284542-167284592	Hepatocyte	liver:	n/a
31	chr6:167284353-167284403	HIPEpiC	eye:	n/a
32	chr6:167263401-167263451	HEK293	kidney:	embryo
33	chr6:167284542-167284592	NHDF-neo	bronchial:	n/a
34	chr6:167275778-167275828	AG04449	skin:	fetal
35	chr6:167250513-167250563	AoSMC	blood vessel:	n/a
36	chr6:167287812-167287862	HMEC	breast:	n/a
37	chr6:167276359-167276409	PrEC	prostate:	n/a
38	chr6:167275999-167276049	HEK293	kidney:	embryo
39	chr6:167275755-167275805	MCF-7	breast:	n/a
40	chr6:167280873-167280923	A549	lung:	n/a
41	chr6:167279026-167279076	HRPEpiC	eye:	n/a
42	chr6:167276650-167276700	HAEpiC	amniotic membrane:	n/a
43	chr6:167284542-167284592	Caco-2	colon:	n/a
44	chr6:167275781-167275831	H1-hESC	embryonic stem cell:	embryo
45	chr6:167275832-167275882	K562	blood:	n/a
46	chr6:167283835-167283885	PrEC	prostate:	n/a
47	chr6:167275832-167275882	HCT-116	colon:	n/a
48	chr6:167280873-167280923	ovcar-3	ovarian:	n/a
49	chr6:167276650-167276700	HRE	kidney:	n/a
50	chr6:167275395-167275445	GM19239	blood:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167285809..167288027-chr6:167289441..167291420,2	K562	blood:
2	chr6:167268417..167269941-chr6:167289089..167292061,2	K562	blood:
3	chr6:167244459..167246952-chr6:167353805..167356355,2	K562	blood:
4	chr6:167287783..167290388-chr6:167293843..167295742,3	K562	blood:
5	chr6:167234510..167236019-chr6:167237889..167239702,2	MCF-7	breast:
6	chr6:167244883..167247077-chr6:167250402..167252258,2	K562	blood:
7	chr6:167280811..167283547-chr6:167284862..167287593,2	K562	blood:
8	chr6:167234151..167235885-chr6:167241479..167243381,2	K562	blood:
9	chr6:167232177..167234702-chr6:167235338..167237852,2	K562	blood:
10	chr6:167234510..167236019-chr6:167237889..167239702,2	MCF-7	breast:
11	chr6:167244883..167247077-chr6:167250402..167252258,2	K562	blood:
12	chr6:167221917..167225316-chr6:167226153..167228902,3	K562	blood:
13	chr6:167263153..167265718-chr6:167272365..167274771,2	K562	blood:
14	chr6:167274608..167276505-chr6:167368344..167370567,2	MCF-7	breast:
15	chr6:167232177..167234702-chr6:167235338..167237852,2	K562	blood:
16	chr6:167268417..167269941-chr6:167289089..167292061,2	K562	blood:
17	chr6:167221917..167225316-chr6:167226153..167228902,3	K562	blood:
18	chr6:167280811..167283547-chr6:167284862..167287593,2	K562	blood:
19	chr6:167287783..167289646-chr6:167293843..167295409,2	K562	blood:
20	chr6:167234151..167235885-chr6:167241479..167243381,2	K562	blood:
21	chr6:167285809..167288027-chr6:167289441..167291420,2	K562	blood:
22	chr6:167218838..167220495-chr6:167220755..167222846,2	K562	blood:
23	chr6:167263153..167265718-chr6:167272365..167274771,2	K562	blood:
24	chr6:166870182..166872414-chr6:167234943..167236564,2	K562	blood:
25	chr6:167266120..167268418-chr6:167368019..167370456,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGFR1OP-10	chr6:167254947-167255400	l_3320_chr6:167242351-167255400_testes
2	lnc-FGFR1OP-10	chr6:167242352-167242576	l_3320_chr6:167242351-167255400_testes
3	lnc-FGFR1OP-11	chr6:167237778-167238313	NONHSAT116055
4	lnc-FGFR1OP-11	chr6:167237176-167237266	NONHSAT116055

No data

Variant related genes	Relation type
RPS6KA2	TF binding region
RPS6KA2	CpG island
ENSG00000026297	chromatin interactions
ENSG00000249141	chromatin interactions

Extended variants
information (count: 2880 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2880 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527676239	chr6:167222641-167222642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs549545530	chr6:167222677-167222678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79737752	chr6:167222796-167222797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146480562	chr6:167222802-167222803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556845097	chr6:167222871-167222872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569156132	chr6:167222915-167222916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183930086	chr6:167222982-167222983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557344416	chr6:167223018-167223019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572546990	chr6:167223038-167223039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539841762	chr6:167223045-167223046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115872854	chr6:167223066-167223067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573618566	chr6:167223080-167223081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs845670	chr6:167223099-167223100	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs61194672	chr6:167223110-167223111	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs533686886	chr6:167223126-167223127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545756532	chr6:167223141-167223142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537159077	chr6:167223186-167223187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188267100	chr6:167223226-167223227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs192521881	chr6:167223228-167223229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs845671	chr6:167223262-167223263	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs113295724	chr6:167223293-167223294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534319187	chr6:167223301-167223302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140944045	chr6:167223312-167223313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs16899505	chr6:167223329-167223330	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs539614712	chr6:167223332-167223333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553271766	chr6:167223339-167223340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551311564	chr6:167223385-167223386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566410510	chr6:167223390-167223391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533556202	chr6:167223429-167223430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185521509	chr6:167223587-167223588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs74915786	chr6:167223605-167223606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537500160	chr6:167223651-167223652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556214154	chr6:167223667-167223668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370373775	chr6:167223706-167223707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs845672	chr6:167223716-167223717	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs545595209	chr6:167223722-167223723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs845673	chr6:167223774-167223775	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs34516969	chr6:167223782-167223783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142097806	chr6:167223797-167223798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371600878	chr6:167223830-167223831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs543066185	chr6:167223841-167223842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs845674	chr6:167223842-167223843	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs845675	chr6:167223849-167223850	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs73266902	chr6:167223878-167223879	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs565377238	chr6:167223883-167223884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190044669	chr6:167223884-167223885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530940262	chr6:167223907-167223908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4710106	chr6:167223962-167223963	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs140048095	chr6:167223963-167223964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554277610	chr6:167224017-167224018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Autism	22549408	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:608 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167221800-167244400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:167234800-167235000	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:167235000-167235600	Enhancers	Brain Anterior Caudate	brain
4	chr6:167235200-167235600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:167235400-167235800	Bivalent Enhancer	Fetal Muscle Leg	muscle
6	chr6:167235400-167236400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:167235600-167239000	Weak transcription	Brain Anterior Caudate	brain
8	chr6:167238000-167238400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr6:167238000-167238400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
10	chr6:167238200-167238400	Bivalent/Poised TSS	Fetal Brain Male	brain
11	chr6:167238400-167244400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:167238600-167240000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
13	chr6:167239000-167239400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr6:167239000-167239400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr6:167239000-167239400	Enhancers	Ovary	ovary
16	chr6:167239000-167239800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr6:167239000-167241800	Enhancers	Brain Anterior Caudate	brain
18	chr6:167239200-167239400	Enhancers	Brain Cingulate Gyrus	brain
19	chr6:167239200-167240000	Enhancers	Left Ventricle	heart
20	chr6:167239200-167240000	Enhancers	NH-A	brain
21	chr6:167239400-167240000	Enhancers	HSMMtube	muscle
22	chr6:167240000-167240200	Enhancers	Brain Cingulate Gyrus	brain
23	chr6:167241600-167241800	Enhancers	Spleen	Spleen
24	chr6:167241600-167242000	ZNF genes & repeats	GM12878-XiMat	blood
25	chr6:167241800-167244200	Weak transcription	Brain Anterior Caudate	brain
26	chr6:167241800-167244600	Weak transcription	Spleen	Spleen
27	chr6:167242000-167242400	Weak transcription	GM12878-XiMat	blood
28	chr6:167242400-167244000	Enhancers	GM12878-XiMat	blood
29	chr6:167242600-167244800	Enhancers	Primary B cells from peripheral blood	blood
30	chr6:167243200-167243400	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr6:167243200-167245200	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr6:167243200-167245200	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr6:167243400-167244400	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr6:167243400-167244600	Enhancers	Primary B cells from cord blood	blood
35	chr6:167244000-167244400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr6:167244000-167244400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
37	chr6:167244000-167244800	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr6:167244000-167245200	Flanking Active TSS	GM12878-XiMat	blood
39	chr6:167244200-167244600	Enhancers	Brain Anterior Caudate	brain
40	chr6:167244200-167244800	Enhancers	Fetal Thymus	thymus
41	chr6:167244200-167245200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr6:167244400-167244800	Enhancers	Brain Hippocampus Middle	brain
43	chr6:167244400-167244800	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr6:167244400-167244800	Enhancers	Lung	lung
45	chr6:167244400-167245000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr6:167244400-167245000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr6:167244400-167253800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr6:167244600-167244800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
49	chr6:167244600-167245000	Enhancers	Spleen	Spleen
50	chr6:167244800-167253600	Weak transcription	Primary B cells from peripheral blood	blood

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