Variant report

Variant	nsv970372
Chromosome Location	chr6:27695204-27708579
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:180)
CpG islands
(count:183)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:180 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:27705915-27706560	GM12878	blood:	n/a	n/a
2	ATF2	chr6:27706116-27706469	GM12878	blood:	n/a	n/a
3	ATF2	chr6:27698632-27698940	GM12878	blood:	n/a	n/a
4	ATF3	chr6:27706063-27706452	GM12878	blood:	n/a	n/a
5	ATF3	chr6:27706172-27706384	GM12878	blood:	n/a	n/a
6	BATF	chr6:27706091-27706553	GM12878	blood:	n/a	n/a
7	BATF	chr6:27699002-27699284	GM12878	blood:	n/a	n/a
8	BATF	chr6:27706149-27706486	GM12878	blood:	n/a	n/a
9	BCL11A	chr6:27698888-27699197	GM12878	blood:	n/a	n/a
10	BCL3	chr6:27706012-27706456	GM12878	blood:	n/a	n/a
11	BCLAF1	chr6:27705962-27706485	GM12878	blood:	n/a	n/a
12	BCLAF1	chr6:27705966-27706787	GM12878	blood:	n/a	n/a
13	CEBPB	chr6:27702726-27702928	HepG2	liver:	n/a	chr6:27702810-27702821
14	CEBPB	chr6:27702671-27702881	K562	blood:	n/a	chr6:27702810-27702821
15	CEBPB	chr6:27702770-27702926	A549	lung:	n/a	chr6:27702810-27702821
16	CEBPB	chr6:27695221-27695395	A549	lung:	n/a	n/a
17	CHD1	chr6:27706080-27706271	GM12878	blood:	n/a	n/a
18	CREB1	chr6:27706125-27706374	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr6:27705705-27706651	GM12878	blood:	n/a	n/a
20	CREB1	chr6:27706067-27706412	A549	lung:	n/a	n/a
21	CREB1	chr6:27706068-27706481	A549	lung:	n/a	n/a
22	CREB1	chr6:27705824-27706610	GM12878	blood:	n/a	n/a
23	CTCF	chr6:27703782-27703801	LNCaP	prostate:	n/a	n/a
24	CTCF	chr6:27706254-27706285	GM12878	blood:	n/a	n/a
25	CTCF	chr6:27706139-27706184	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr6:27706270-27706337	Fibrobl	skin:	n/a	n/a
27	E2F4	chr6:27706153-27706462	MCF10A-Er-Src	breast:	n/a	chr6:27706309-27706321
28	E2F4	chr6:27706164-27706486	GM12878	blood:	n/a	chr6:27706309-27706321
29	E2F6	chr6:27706110-27706389	A549	lung:	n/a	chr6:27706309-27706321
30	E2F6	chr6:27705966-27706580	A549	lung:	n/a	chr6:27706309-27706321
31	EBF1	chr6:27706032-27706221	GM12878	blood:	n/a	n/a
32	EBF1	chr6:27698652-27698899	GM12878	blood:	n/a	n/a
33	EGR1	chr6:27706117-27706442	GM12878	blood:	n/a	n/a
34	EGR1	chr6:27706106-27706390	GM12878	blood:	n/a	n/a
35	EGR1	chr6:27706109-27706451	MCF-7	breast:	n/a	n/a
36	EGR1	chr6:27696972-27697226	K562	blood:	n/a	n/a
37	ELF1	chr6:27706036-27706419	GM12878	blood:	n/a	n/a
38	ELF1	chr6:27706035-27706738	GM12878	blood:	n/a	n/a
39	ETS1	chr6:27706023-27706418	GM12878	blood:	n/a	n/a
40	FOS	chr6:27697695-27697812	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr6:27697694-27697899	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr6:27697655-27697841	MCF10A-Er-Src	breast:	n/a	n/a
43	FOXM1	chr6:27706053-27706527	GM12878	blood:	n/a	n/a
44	FOXP2	chr6:27706092-27706352	PFSK-1	brain:	n/a	n/a
45	IRF4	chr6:27706036-27706558	GM12878	blood:	n/a	n/a
46	IRF4	chr6:27705999-27706569	GM12878	blood:	n/a	n/a
47	MAFF	chr6:27704492-27704826	HepG2	liver:	n/a	chr6:27704660-27704678
48	MAFF	chr6:27705848-27705912	K562	blood:	n/a	n/a
49	MAFF	chr6:27704526-27704799	K562	blood:	n/a	chr6:27704660-27704678
50	MAFK	chr6:27704495-27704834	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:27706340-27706390	BE2_C	brain:	n/a
2	chr6:27706179-27706229	HEEpiC	esophagus:	n/a
3	chr6:27706275-27706325	HepG2	liver:	n/a
4	chr6:27706275-27706325	SK-N-SH_RA	brain:	n/a
5	chr6:27706275-27706325	HUVEC	blood vessel:	n/a
6	chr6:27706179-27706229	PANC-1	pancreas:	n/a
7	chr6:27706179-27706229	HMEC	breast:	n/a
8	chr6:27706179-27706229	AG09309	skin:	n/a
9	chr6:27706275-27706325	K562	blood:	n/a
10	chr6:27706179-27706229	AoSMC	blood vessel:	n/a
11	chr6:27706179-27706229	HRCEpiC	kidney:	n/a
12	chr6:27706275-27706325	HAEpiC	amniotic membrane:	n/a
13	chr6:27706340-27706390	SK-N-SH	brain:	n/a
14	chr6:27706275-27706325	HIPEpiC	eye:	n/a
15	chr6:27706340-27706390	Hepatocyte	liver:	n/a
16	chr6:27706275-27706325	NHDF-neo	bronchial:	n/a
17	chr6:27706340-27706390	MCF-7	breast:	n/a
18	chr6:27706179-27706229	Hela-S3	cervix:	n/a
19	chr6:27706275-27706325	MCF-7	breast:	n/a
20	chr6:27706275-27706325	HPAEpiC	pulmonary alveolar:	n/a
21	chr6:27706340-27706390	NB4	blood:	n/a
22	chr6:27706179-27706229	HAEpiC	amniotic membrane:	n/a
23	chr6:27706340-27706390	HCM	heart:	n/a
24	chr6:27706179-27706229	NT2-D1	testis:	n/a
25	chr6:27706275-27706325	HL-60	blood:	n/a
26	chr6:27706179-27706229	RPTEC	kidney:	n/a
27	chr6:27706340-27706390	MCF10A-Er-Src	breast:	n/a
28	chr6:27706179-27706229	GM19239	blood:	n/a
29	chr6:27706340-27706390	Caco-2	colon:	n/a
30	chr6:27706340-27706390	K562	blood:	n/a
31	chr6:27706275-27706325	AG04450	lung:	fetal
32	chr6:27706179-27706229	MCF10A-Er-Src	breast:	n/a
33	chr6:27706340-27706390	HMEC	breast:	n/a
34	chr6:27706340-27706390	HL-60	blood:	n/a
35	chr6:27706275-27706325	MCF10A-Er-Src	breast:	n/a
36	chr6:27706179-27706229	HRE	kidney:	n/a
37	chr6:27706179-27706229	K562	blood:	n/a
38	chr6:27706340-27706390	HIPEpiC	eye:	n/a
39	chr6:27706275-27706325	AoSMC	blood vessel:	n/a
40	chr6:27706340-27706390	HPAEpiC	pulmonary alveolar:	n/a
41	chr6:27706275-27706325	HCF	heart:	n/a
42	chr6:27706179-27706229	SAEC	small airway:	n/a
43	chr6:27706179-27706229	HCPEpiC	choroid plexus:	n/a
44	chr6:27706275-27706325	RPTEC	kidney:	n/a
45	chr6:27706179-27706229	H1-hESC	embryonic stem cell:	embryo
46	chr6:27706340-27706390	GM12891	blood:	n/a
47	chr6:27706275-27706325	IMR90	lung:	fetal
48	chr6:27706179-27706229	BE2_C	brain:	n/a
49	chr6:27706340-27706390	Jurkat	blood:	n/a
50	chr6:27706340-27706390	ovcar-3	ovarian:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:27687163..27689366-chr6:27693364..27696456,4	K562	blood:
2	chr6:27697073..27699346-chr6:27703837..27706008,2	K562	blood:
3	chr6:27655233..27657099-chr6:27693355..27695720,2	K562	blood:
4	chr6:27669358..27671049-chr6:27700076..27702911,2	K562	blood:
5	chr6:27251230..27254173-chr6:27693136..27695463,2	K562	blood:
6	chr6:27694961..27696569-chr6:27720410..27723324,2	K562	blood:
7	chr6:27692126..27696307-chr6:27696693..27700869,4	K562	blood:
8	chr6:27692126..27696307-chr6:27696693..27700869,4	K562	blood:
9	chr6:27690338..27692656-chr6:27698623..27701642,3	K562	blood:
10	chr6:27694126..27696434-chr6:27711146..27712696,2	K562	blood:
11	chr6:27697073..27699346-chr6:27703837..27706008,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000216915	TF binding region
ENSG00000216915	CpG island

Extended variants
information (count: 299 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549176309	chr6:27695245-27695246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138650425	chr6:27695246-27695247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191596160	chr6:27695249-27695250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112722188	chr6:27695267-27695268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149312326	chr6:27695273-27695274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577302314	chr6:27695284-27695285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs74868707	chr6:27695317-27695318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs9348775	chr6:27695329-27695330	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs183879999	chr6:27695330-27695331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188609635	chr6:27695396-27695397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558273049	chr6:27695399-27695400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs180680265	chr6:27695407-27695408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373781285	chr6:27695454-27695455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146990219	chr6:27695467-27695468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541315026	chr6:27695485-27695486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138082334	chr6:27695511-27695512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143563826	chr6:27695557-27695558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs202055599	chr6:27695562-27695563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549387244	chr6:27695723-27695724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375495468	chr6:27695752-27695753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563203606	chr6:27695767-27695768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576938625	chr6:27695770-27695771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548834713	chr6:27695771-27695772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565865503	chr6:27695780-27695781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534851550	chr6:27695838-27695839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74695368	chr6:27695882-27695883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs70983903	chr6:27695883-27695884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs398001072	chr6:27695898-27695899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531194456	chr6:27695988-27695989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184669710	chr6:27696019-27696020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549720189	chr6:27696054-27696055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571570867	chr6:27696073-27696074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553922580	chr6:27696089-27696090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552907058	chr6:27696106-27696107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190343534	chr6:27696136-27696137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147160164	chr6:27696147-27696148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182523572	chr6:27696151-27696152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148623698	chr6:27696160-27696161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534598866	chr6:27696169-27696170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572263776	chr6:27696291-27696292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77293346	chr6:27696332-27696333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12662916	chr6:27696333-27696334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186000120	chr6:27696334-27696335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190520016	chr6:27696338-27696339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368756620	chr6:27696341-27696342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181637908	chr6:27696354-27696355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs16867942	chr6:27696359-27696360	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs185534953	chr6:27696360-27696361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs9468210	chr6:27696362-27696363	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs543930092	chr6:27696370-27696371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:164 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27694400-27697600	Weak transcription	A549	lung
2	chr6:27697600-27697800	Enhancers	A549	lung
3	chr6:27698800-27699000	Enhancers	GM12878-XiMat	blood
4	chr6:27702200-27706000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr6:27702800-27703000	ZNF genes & repeats	Gastric	stomach
6	chr6:27704800-27705600	Enhancers	K562	blood
7	chr6:27705000-27705400	Enhancers	A549	lung
8	chr6:27705000-27705400	ZNF genes & repeats	GM12878-XiMat	blood
9	chr6:27705400-27705600	Flanking Active TSS	GM12878-XiMat	blood
10	chr6:27705400-27707400	Active TSS	A549	lung
11	chr6:27705600-27705800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
12	chr6:27705600-27705800	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr6:27705600-27705800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
14	chr6:27705600-27705800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr6:27705600-27705800	Enhancers	Adipose Nuclei	Adipose
16	chr6:27705600-27705800	Bivalent Enhancer	HepG2	liver
17	chr6:27705600-27705800	Enhancers	NHEK	skin
18	chr6:27705600-27706000	Enhancers	Primary B cells from peripheral blood	blood
19	chr6:27705600-27706000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
20	chr6:27705600-27706000	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr6:27705600-27706600	Active TSS	Stomach Smooth Muscle	stomach
22	chr6:27705600-27707000	Active TSS	Duodenum Mucosa	Duodenum
23	chr6:27705600-27707000	Active TSS	GM12878-XiMat	blood
24	chr6:27705600-27710400	Weak transcription	K562	blood
25	chr6:27705800-27706000	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr6:27705800-27706000	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr6:27705800-27706000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
28	chr6:27705800-27706000	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr6:27705800-27706000	Flanking Active TSS	Adipose Nuclei	Adipose
30	chr6:27705800-27706000	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
31	chr6:27705800-27706000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
32	chr6:27705800-27706000	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
33	chr6:27705800-27706000	Enhancers	Fetal Intestine Small	intestine
34	chr6:27705800-27706000	ZNF genes & repeats	Fetal Kidney	kidney
35	chr6:27705800-27706000	Flanking Active TSS	NHEK	skin
36	chr6:27705800-27706200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
37	chr6:27705800-27706200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr6:27705800-27706200	Bivalent/Poised TSS	Fetal Heart	heart
39	chr6:27705800-27706400	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr6:27705800-27706400	Enhancers	HepG2	liver
41	chr6:27705800-27706600	Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr6:27705800-27706600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
43	chr6:27705800-27706600	Active TSS	Liver	Liver
44	chr6:27705800-27706600	Active TSS	Colon Smooth Muscle	Colon
45	chr6:27705800-27706600	Active TSS	HMEC	breast
46	chr6:27705800-27706600	Active TSS	NHDF-Ad	bronchial
47	chr6:27705800-27706800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr6:27705800-27706800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:27705800-27706800	Active TSS	Primary B cells from cord blood	blood
50	chr6:27705800-27706800	Active TSS	Primary T helper naive cells from peripheral blood	blood

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