Variant report

Variant	nsv349384
Chromosome Location	chr6:28075886-28080766
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:15)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:15 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr6:28080485-28080535	GM12878	blood:	n/a	n/a
2	CEBPB	chr6:28076904-28077039	K562	blood:	n/a	chr6:28076969-28076980 chr6:28076942-28076955
3	CHD2	chr6:28077767-28077947	K562	blood:	n/a	n/a
4	POLR2A	chr6:28079334-28079337	GM12878	blood:	n/a	n/a
5	POLR2A	chr6:28079719-28080026	GM12878	blood:	n/a	n/a
6	POLR2A	chr6:28080441-28080481	GM12878	blood:	n/a	n/a
7	POLR2A	chr6:28080368-28080759	K562	blood:	n/a	n/a
8	POLR2A	chr6:28077254-28077381	K562	blood:	n/a	n/a
9	POLR2A	chr6:28080444-28080685	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr6:28080394-28080775	K562	blood:	n/a	n/a
11	POLR2A	chr6:28077969-28082972	K562	blood:	n/a	n/a
12	POLR2A	chr6:28078286-28078351	K562	blood:	n/a	n/a
13	POLR2A	chr6:28080431-28080796	K562	blood:	n/a	n/a
14	POLR2A	chr6:28080483-28080656	GM12878	blood:	n/a	n/a
15	ZNF384	chr6:28080670-28080796	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:28076851-28076901	Hepatocyte	liver:	n/a
2	chr6:28076851-28076901	AG04450	lung:	fetal
3	chr6:28076851-28076901	U87	brain:	n/a
4	chr6:28076851-28076901	NHDF-neo	bronchial:	n/a
5	chr6:28076851-28076901	Hela-S3	cervix:	n/a
6	chr6:28076851-28076901	HCPEpiC	choroid plexus:	n/a
7	chr6:28076851-28076901	NB4	blood:	n/a
8	chr6:28076851-28076901	ovcar-3	ovarian:	n/a
9	chr6:28076851-28076901	Jurkat	blood:	n/a
10	chr6:28076851-28076901	A549	lung:	n/a
11	chr6:28076851-28076901	PrEC	prostate:	n/a
12	chr6:28076851-28076901	ECC-1	luminal epithelium:	n/a
13	chr6:28076851-28076901	NH-A	brain:	n/a
14	chr6:28076851-28076901	PANC-1	pancreas:	n/a
15	chr6:28076851-28076901	HUVEC	blood vessel:	n/a
16	chr6:28076851-28076901	HRPEpiC	eye:	n/a
17	chr6:28076851-28076901	MCF-7	breast:	n/a
18	chr6:28076851-28076901	SKMC	muscle:	n/a
19	chr6:28076851-28076901	AG10803	skin:	n/a
20	chr6:28076851-28076901	HepG2	liver:	n/a
21	chr6:28076851-28076901	SAEC	small airway:	n/a
22	chr6:28076851-28076901	CMK	blood:	n/a
23	chr6:28076851-28076901	GM12891	blood:	n/a
24	chr6:28076851-28076901	AG04449	skin:	fetal
25	chr6:28076851-28076901	RPTEC	kidney:	n/a
26	chr6:28076851-28076901	H1-hESC	embryonic stem cell:	embryo
27	chr6:28076851-28076901	NT2-D1	testis:	n/a
28	chr6:28076851-28076901	IMR90	lung:	fetal
29	chr6:28076851-28076901	LNCaP	prostate:	n/a
30	chr6:28076851-28076901	HIPEpiC	eye:	n/a
31	chr6:28076851-28076901	BE2_C	brain:	n/a
32	chr6:28076851-28076901	HNPCEpiC	eye:	n/a
33	chr6:28076851-28076901	BJ	skin:	n/a
34	chr6:28076851-28076901	SK-N-SH_RA	brain:	n/a
35	chr6:28076851-28076901	HEEpiC	esophagus:	n/a
36	chr6:28076851-28076901	AoSMC	blood vessel:	n/a
37	chr6:28076851-28076901	AG09309	skin:	n/a
38	chr6:28076851-28076901	HPAEpiC	pulmonary alveolar:	n/a
39	chr6:28076851-28076901	PFSK-1	brain:	n/a
40	chr6:28076851-28076901	HRCEpiC	kidney:	n/a
41	chr6:28076851-28076901	T-47D	breast:	n/a
42	chr6:28076851-28076901	HAEpiC	amniotic membrane:	n/a
43	chr6:28076851-28076901	NHBE	bronchial:	n/a
44	chr6:28076851-28076901	HCM	heart:	n/a
45	chr6:28076851-28076901	GM12892	blood:	n/a
46	chr6:28076851-28076901	SK-N-SH	brain:	n/a
47	chr6:28076851-28076901	HMEC	breast:	n/a
48	chr6:28076851-28076901	GM19239	blood:	n/a
49	chr6:28076851-28076901	AG09319	gingival:	n/a
50	chr6:28076851-28076901	MCF10A-Er-Src	breast:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:27858238..27861004-chr6:28077246..28078908,2	K562	blood:
2	chr6:28078804..28081627-chr6:28178928..28180967,2	K562	blood:
3	chr6:27801194..27803769-chr6:28077806..28080000,2	K562	blood:
4	chr6:28078707..28081490-chr6:28095158..28097725,2	K562	blood:
5	chr6:28057160..28060114-chr6:28076848..28078710,3	K562	blood:
6	chr6:28061415..28063110-chr6:28078515..28080517,2	K562	blood:
7	chr6:27775941..27778895-chr6:28077283..28079265,2	K562	blood:
8	chr6:28077736..28080081-chr6:28112119..28113939,2	K562	blood:
9	chr6:28074765..28079544-chr6:28088308..28092763,5	MCF-7	breast:
10	chr6:28071334..28077239-chr6:28089535..28095129,7	MCF-7	breast:
11	chr6:28060510..28063110-chr6:28077574..28080015,2	K562	blood:
12	chr6:28072263..28073986-chr6:28075857..28078538,2	MCF-7	breast:
13	chr6:27855775..27858659-chr6:28079519..28081995,2	MCF-7	breast:
14	chr6:28080238..28082315-chr6:28097763..28099279,2	MCF-7	breast:
15	chr6:28080501..28082072-chr6:28102597..28105100,2	K562	blood:
16	chr6:27863004..27864854-chr6:28080355..28082489,2	MCF-7	breast:
17	chr6:28075060..28076824-chr6:28104395..28106561,2	K562	blood:
18	chr6:28039992..28042846-chr6:28078903..28080587,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000219392	TF binding region
ENSG00000219392	CpG island
ENSG00000233224	chromatin interactions
ENSG00000219891	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000269293	chromatin interactions
ENSG00000261839	chromatin interactions
ENSG00000196812	chromatin interactions
ENSG00000203813	chromatin interactions
ENSG00000220721	chromatin interactions

Extended variants
information (count: 128 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:128 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199850654	chr6:28075886-28075887	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs373918140	chr6:28075890-28075891	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs371348541	chr6:28075910-28075911	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs112615652	chr6:28075911-28075912	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
5	rs1556969	chr6:28075927-28075928	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs563639592	chr6:28075934-28075935	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs369024192	chr6:28075958-28075959	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs189913122	chr6:28075967-28075968	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs147175155	chr6:28075971-28075972	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs368655135	chr6:28076093-28076094	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs181658893	chr6:28076097-28076098	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs571866169	chr6:28076126-28076127	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs536660139	chr6:28076207-28076208	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs35193936	chr6:28076270-28076271	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs547909209	chr6:28076341-28076342	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs374546850	chr6:28076382-28076383	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs140391565	chr6:28076433-28076434	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs114101410	chr6:28076478-28076479	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs185929649	chr6:28076501-28076502	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs558577661	chr6:28076541-28076542	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs575454828	chr6:28076569-28076570	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs544167657	chr6:28076601-28076602	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs556980915	chr6:28076671-28076672	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs368048120	chr6:28076677-28076678	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs573683800	chr6:28076740-28076741	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs542729501	chr6:28076785-28076786	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs559394075	chr6:28076827-28076828	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs528664744	chr6:28076851-28076852	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs368089296	chr6:28076876-28076877	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs203885	chr6:28076886-28076887	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs570953869	chr6:28076906-28076907	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs72851162	chr6:28076960-28076961	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs188436599	chr6:28076967-28076968	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs376845411	chr6:28076968-28076969	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs550561182	chr6:28077048-28077049	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs374784866	chr6:28077128-28077129	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs368576090	chr6:28077312-28077313	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs203884	chr6:28077374-28077375	Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs529678346	chr6:28077557-28077558	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs17711344	chr6:28077602-28077603	Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs551924546	chr6:28077633-28077634	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs566524032	chr6:28077656-28077657	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs369937566	chr6:28077688-28077689	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs538464709	chr6:28077690-28077691	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs558757370	chr6:28077738-28077739	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs151143940	chr6:28077758-28077759	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs373157033	chr6:28077759-28077760	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs534491332	chr6:28077783-28077784	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs140058532	chr6:28077785-28077786	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs373123196	chr6:28077808-28077809	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:28073000-28083800	Weak transcription	Aorta	Aorta
2	chr6:28073200-28081600	Weak transcription	Primary T cells from cord blood	blood
3	chr6:28073200-28081600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr6:28073200-28082200	Weak transcription	HSMM	muscle
5	chr6:28073200-28082400	Weak transcription	Fetal Stomach	stomach
6	chr6:28073200-28083000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr6:28073200-28083400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr6:28073200-28091400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr6:28073200-28091800	Weak transcription	Right Ventricle	heart
10	chr6:28073400-28076000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:28073400-28080200	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr6:28073400-28081200	Weak transcription	Adipose Nuclei	Adipose
13	chr6:28073400-28081600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr6:28073400-28081600	Weak transcription	Fetal Muscle Trunk	muscle
15	chr6:28073400-28081600	Weak transcription	HSMMtube	muscle
16	chr6:28073400-28081600	Weak transcription	NH-A	brain
17	chr6:28073400-28081800	Weak transcription	Primary B cells from cord blood	blood
18	chr6:28073400-28082000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr6:28073400-28082000	Weak transcription	Fetal Thymus	thymus
20	chr6:28073400-28082200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr6:28073400-28082200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr6:28073400-28082200	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr6:28073400-28082200	Weak transcription	GM12878-XiMat	blood
24	chr6:28073400-28082400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr6:28073400-28082400	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr6:28073400-28082400	Weak transcription	Fetal Muscle Leg	muscle
27	chr6:28073400-28082400	Weak transcription	Stomach Smooth Muscle	stomach
28	chr6:28073400-28082600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr6:28073400-28082600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr6:28073400-28082600	Weak transcription	Placenta	Placenta
31	chr6:28073400-28082800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr6:28073400-28082800	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr6:28073400-28083000	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr6:28073400-28083000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr6:28073400-28083000	Weak transcription	Fetal Lung	lung
36	chr6:28073400-28083000	Weak transcription	Thymus	Thymus
37	chr6:28073400-28083000	Weak transcription	Spleen	Spleen
38	chr6:28073400-28083200	Weak transcription	Brain Angular Gyrus	brain
39	chr6:28073400-28083400	Weak transcription	A549	lung
40	chr6:28073400-28083600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr6:28073400-28083600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr6:28073400-28083600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
43	chr6:28073400-28083600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr6:28073400-28083600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr6:28073400-28083600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr6:28073400-28083600	Weak transcription	Fetal Kidney	kidney
47	chr6:28073400-28083800	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr6:28073400-28083800	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr6:28073400-28088000	Weak transcription	NHLF	lung
50	chr6:28073400-28091200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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