Variant report

Variant	nsv917318
Chromosome Location	chr6:109885195-109982375
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:349)
CpG islands
(count:244)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:349 , 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	chr6:109947743-109947775	HepG2	liver:	n/a	n/a
2	BATF	chr6:109900613-109900853	GM12878	blood:	n/a	chr6:109900728-109900739
3	BATF	chr6:109900545-109900857	GM12878	blood:	n/a	chr6:109900728-109900739
4	BATF	chr6:109953633-109953962	GM12878	blood:	n/a	n/a
5	BCL11A	chr6:109900625-109900865	GM12878	blood:	n/a	n/a
6	BCL11A	chr6:109900625-109900952	GM12878	blood:	n/a	n/a
7	BHLHE40	chr6:109901915-109901921	K562	blood:	n/a	n/a
8	CEBPB	chr6:109957648-109957810	K562	blood:	n/a	n/a
9	CEBPB	chr6:109957671-109957789	A549	lung:	n/a	n/a
10	CEBPB	chr6:109947555-109947885	HepG2	liver:	n/a	n/a
11	CEBPB	chr6:109952640-109952967	IMR90	lung:	n/a	chr6:109952785-109952796
12	CEBPB	chr6:109952623-109952968	HepG2	liver:	n/a	chr6:109952785-109952796
13	CEBPB	chr6:109952735-109952897	K562	blood:	n/a	chr6:109952785-109952796
14	CEBPB	chr6:109952629-109952933	A549	lung:	n/a	chr6:109952785-109952796
15	CTCF	chr6:109886672-109886724	Lung_OC	lung:	n/a	n/a
16	CTCF	chr6:109917195-109917429	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr6:109926971-109926998	Lung_OC	lung:	n/a	n/a
18	CTCF	chr6:109957220-109957370	HAc	cerebellar:	n/a	n/a
19	CTCF	chr6:109917280-109917430	HRE	kidney:	n/a	n/a
20	CTCF	chr6:109917200-109917350	NHLF	lung:	n/a	n/a
21	CTCF	chr6:109917240-109917390	GM12873	blood:	n/a	n/a
22	CTCF	chr6:109916983-109917494	HCT-116	colon:	n/a	n/a
23	CTCF	chr6:109917180-109917330	HAc	cerebellar:	n/a	n/a
24	CTCF	chr6:109917220-109917370	AG09309	skin:	n/a	n/a
25	CTCF	chr6:109917260-109917410	GM12874	blood:	n/a	n/a
26	CTCF	chr6:109917256-109917405	MCF-7	breast:	n/a	n/a
27	CTCF	chr6:109917224-109917494	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr6:109917215-109917423	NHEK	skin:	n/a	n/a
29	CTCF	chr6:109917200-109917350	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr6:109966599-109966677	GM10248	blood:	n/a	n/a
31	CTCF	chr6:109917220-109917370	HMEC	breast:	n/a	n/a
32	CTCF	chr6:109917234-109917430	GM19240	blood:	n/a	n/a
33	CTCF	chr6:109917260-109917410	AG09309	skin:	n/a	n/a
34	CTCF	chr6:109917201-109917417	LNCaP	prostate:	n/a	n/a
35	CTCF	chr6:109917200-109917350	GM12870	blood:	n/a	n/a
36	CTCF	chr6:109917240-109917390	AG09319	gingival:	n/a	n/a
37	CTCF	chr6:109978084-109978136	GM10248	blood:	n/a	n/a
38	CTCF	chr6:109917203-109917387	K562	blood:	n/a	n/a
39	CTCF	chr6:109917240-109917390	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr6:109917220-109917370	GM12873	blood:	n/a	n/a
41	CTCF	chr6:109917240-109917390	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr6:109917220-109917370	HCFaa	heart:	n/a	n/a
43	CTCF	chr6:109917240-109917390	HMF	breast:	n/a	n/a
44	CTCF	chr6:109917240-109917390	GM12866	blood:	n/a	n/a
45	CTCF	chr6:109974237-109974272	GM10266	blood:	n/a	n/a
46	CTCF	chr6:109917222-109917396	GM13977	blood:	n/a	n/a
47	CTCF	chr6:109917240-109917390	GM12864	blood:	n/a	n/a
48	CTCF	chr6:109917300-109917450	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:109966408-109966468	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:109949380-109949530	GM12868	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:109960018-109960068	HIPEpiC	eye:	n/a
2	chr6:109941310-109941360	BE2_C	brain:	n/a
3	chr6:109940408-109940458	A549	lung:	n/a
4	chr6:109941310-109941360	HUVEC	blood vessel:	n/a
5	chr6:109940408-109940458	HCPEpiC	choroid plexus:	n/a
6	chr6:109953157-109953207	HCPEpiC	choroid plexus:	n/a
7	chr6:109953157-109953207	A549	lung:	n/a
8	chr6:109941310-109941360	MCF-7	breast:	n/a
9	chr6:109941310-109941360	K562	blood:	n/a
10	chr6:109941310-109941360	IMR90	lung:	fetal
11	chr6:109940408-109940458	AG09309	skin:	n/a
12	chr6:109960018-109960068	AG04449	skin:	fetal
13	chr6:109941310-109941360	CMK	blood:	n/a
14	chr6:109941310-109941360	HEEpiC	esophagus:	n/a
15	chr6:109941310-109941360	ECC-1	luminal epithelium:	n/a
16	chr6:109953157-109953207	T-47D	breast:	n/a
17	chr6:109960018-109960068	HRPEpiC	eye:	n/a
18	chr6:109960018-109960068	A549	lung:	n/a
19	chr6:109941310-109941360	HCF	heart:	n/a
20	chr6:109960018-109960068	HCT-116	colon:	n/a
21	chr6:109960018-109960068	GM12878	blood:	n/a
22	chr6:109953157-109953207	HL-60	blood:	n/a
23	chr6:109960018-109960068	HCF	heart:	n/a
24	chr6:109940408-109940458	MCF-7	breast:	n/a
25	chr6:109960018-109960068	HMEC	breast:	n/a
26	chr6:109953157-109953207	GM19239	blood:	n/a
27	chr6:109941310-109941360	LNCaP	prostate:	n/a
28	chr6:109953157-109953207	AG09319	gingival:	n/a
29	chr6:109953157-109953207	PANC-1	pancreas:	n/a
30	chr6:109960018-109960068	Hela-S3	cervix:	n/a
31	chr6:109953157-109953207	AoSMC	blood vessel:	n/a
32	chr6:109953157-109953207	NT2-D1	testis:	n/a
33	chr6:109941310-109941360	NT2-D1	testis:	n/a
34	chr6:109953157-109953207	SK-N-MC	brain:	n/a
35	chr6:109940408-109940458	SK-N-MC	brain:	n/a
36	chr6:109960018-109960068	NT2-D1	testis:	n/a
37	chr6:109960018-109960068	AoSMC	blood vessel:	n/a
38	chr6:109940408-109940458	Hepatocyte	liver:	n/a
39	chr6:109953157-109953207	AG04450	lung:	fetal
40	chr6:109941310-109941360	Jurkat	blood:	n/a
41	chr6:109941310-109941360	HNPCEpiC	eye:	n/a
42	chr6:109941310-109941360	A549	lung:	n/a
43	chr6:109953157-109953207	CMK	blood:	n/a
44	chr6:109960018-109960068	GM12892	blood:	n/a
45	chr6:109953157-109953207	Hepatocyte	liver:	n/a
46	chr6:109941310-109941360	AoSMC	blood vessel:	n/a
47	chr6:109940408-109940458	IMR90	lung:	fetal
48	chr6:109940408-109940458	K562	blood:	n/a
49	chr6:109953157-109953207	NH-A	brain:	n/a
50	chr6:109960018-109960068	HNPCEpiC	eye:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:109927783..109929912-chr6:109931522..109933858,2	K562	blood:
2	chr6:109916966..109917798-chr6:110016397..110017380,5	MCF-7	breast:
3	chr6:109916901..109917812-chr6:110016606..110017379,4	MCF-7	breast:
4	chr6:109926146..109927722-chr6:109932421..109934095,2	MCF-7	breast:
5	chr6:109917095..109917599-chr6:110026112..110027051,2	MCF-7	breast:
6	chr6:109926146..109927722-chr6:109932421..109934095,2	MCF-7	breast:
7	chr6:109963602..109966014-chr6:110009596..110012309,2	MCF-7	breast:
8	chr6:109932824..109934658-chr6:109936171..109939061,2	K562	blood:
9	chr6:109927783..109929912-chr6:109931522..109933858,2	K562	blood:
10	chr6:109932824..109934658-chr6:109936171..109939061,2	K562	blood:

No data

Variant related genes	Relation type
AK9	TF binding region
AK9	CpG island
ENSG00000155085	chromatin interactions

Extended variants
information (count: 3674 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:3674 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544786986	chr6:109885247-109885248	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543828088	chr6:109885292-109885293	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560777833	chr6:109885363-109885364	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs117513176	chr6:109885396-109885397	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201166033	chr6:109885417-109885418	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371990680	chr6:109885431-109885432	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559897810	chr6:109885434-109885435	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528722340	chr6:109885439-109885440	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375094114	chr6:109885466-109885467	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10499052	chr6:109885475-109885476	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs7753224	chr6:109885479-109885480	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs530896454	chr6:109885535-109885536	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550954664	chr6:109885595-109885596	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs11752791	chr6:109885646-109885647	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs536741499	chr6:109885654-109885655	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145534037	chr6:109885735-109885736	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566643957	chr6:109885759-109885760	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143388371	chr6:109885780-109885781	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs367615932	chr6:109885781-109885782	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs562415466	chr6:109885790-109885791	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558404376	chr6:109885869-109885870	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544580452	chr6:109885915-109885916	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562360385	chr6:109885937-109885938	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376701100	chr6:109885942-109885943	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568816940	chr6:109885979-109885980	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114500582	chr6:109886001-109886002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7757895	chr6:109886005-109886006	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs574398909	chr6:109886018-109886019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540299423	chr6:109886034-109886035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553617036	chr6:109886064-109886065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148865857	chr6:109886118-109886119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs10872047	chr6:109886159-109886160	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs374145517	chr6:109886190-109886191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184408323	chr6:109886194-109886195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531239301	chr6:109886210-109886211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189558069	chr6:109886216-109886217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114184417	chr6:109886217-109886218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530073674	chr6:109886298-109886299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547037693	chr6:109886331-109886332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573016356	chr6:109886358-109886359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181781741	chr6:109886434-109886435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532129812	chr6:109886478-109886479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372195910	chr6:109886483-109886484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551963934	chr6:109886487-109886488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549449929	chr6:109886516-109886517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368465671	chr6:109886517-109886518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568753899	chr6:109886523-109886524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533883530	chr6:109886594-109886595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538142654	chr6:109886663-109886664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549829741	chr6:109886676-109886677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	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
Ependymoma	16718352	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
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Autism	17483303	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
abnormal development	18461090	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Intellectual disability	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:470 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:109867000-109885800	Weak transcription	Ovary	ovary
2	chr6:109878400-109886200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr6:109878800-109894000	Weak transcription	Pancreas	Pancrea
4	chr6:109878800-109903600	Weak transcription	Psoas Muscle	Psoas
5	chr6:109879000-109903800	Weak transcription	Thymus	Thymus
6	chr6:109879000-109906000	Weak transcription	Left Ventricle	heart
7	chr6:109879000-109917400	Weak transcription	Aorta	Aorta
8	chr6:109879400-109893400	Weak transcription	Primary T cells from cord blood	blood
9	chr6:109879600-109886400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr6:109879800-109900600	Weak transcription	Primary hematopoietic stem cells	blood
11	chr6:109880800-109900000	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr6:109881000-109900000	Weak transcription	Adipose Nuclei	Adipose
13	chr6:109881200-109902400	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr6:109883400-109886200	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr6:109884000-109885200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr6:109884000-109885600	Strong transcription	Primary T helper cells PMA-I stimulated	--
17	chr6:109884000-109886200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr6:109885000-109886000	Strong transcription	Primary B cells from cord blood	blood
19	chr6:109885000-109886600	Weak transcription	Primary B cells from peripheral blood	blood
20	chr6:109885000-109902400	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr6:109885200-109900200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr6:109885600-109887800	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr6:109886000-109910600	Weak transcription	Primary B cells from cord blood	blood
24	chr6:109893400-109894800	Strong transcription	Primary T cells from cord blood	blood
25	chr6:109894000-109894800	Strong transcription	Pancreas	Pancrea
26	chr6:109894800-109896400	Weak transcription	Pancreas	Pancrea
27	chr6:109894800-109899800	Weak transcription	Primary T cells from cord blood	blood
28	chr6:109899200-109901800	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr6:109899600-109901600	Weak transcription	Lung	lung
30	chr6:109899800-109901000	Strong transcription	Primary T cells from cord blood	blood
31	chr6:109900000-109900600	Strong transcription	Adipose Nuclei	Adipose
32	chr6:109900000-109900600	Strong transcription	Skeletal Muscle Female	skeletal muscle
33	chr6:109900200-109900800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr6:109900200-109900800	Enhancers	GM12878-XiMat	blood
35	chr6:109900400-109900800	Enhancers	NHEK	skin
36	chr6:109900400-109901200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr6:109900600-109902400	Weak transcription	Adipose Nuclei	Adipose
38	chr6:109900600-109902400	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr6:109900800-109906000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr6:109901000-109901600	Weak transcription	Primary T cells from cord blood	blood
41	chr6:109901200-109901600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr6:109901400-109902200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr6:109901600-109902000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:109901600-109902200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr6:109901600-109902400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr6:109901600-109902400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr6:109901600-109902400	Strong transcription	Primary T cells from cord blood	blood
48	chr6:109901800-109902200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr6:109901800-109902200	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr6:109901800-109902400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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