Variant report

Variant	nsv966647
Chromosome Location	chr6:82469158-82472452
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:82470524-82470653	HepG2	liver:	n/a	n/a
2	CTCF	chr6:82471980-82472130	AoAF	blood vessel:	n/a	chr6:82472086-82472094
3	CTCF	chr6:82472000-82472150	AG04449	skin:	n/a	chr6:82472086-82472094
4	CTCF	chr6:82472000-82472150	NHDF-neo	bronchial:	n/a	chr6:82472086-82472094
5	CTCF	chr6:82472040-82472190	NHDF-neo	bronchial:	n/a	chr6:82472086-82472094
6	CTCF	chr6:82472000-82472150	AG04450	lung:	n/a	chr6:82472086-82472094
7	CTCF	chr6:82472000-82472150	SK-N-SH_RA	brain:	n/a	chr6:82472086-82472094
8	CTCF	chr6:82472020-82472170	HBMEC	blood vessel:	n/a	chr6:82472086-82472094
9	CTCF	chr6:82471980-82472130	SK-N-SH_RA	brain:	n/a	chr6:82472086-82472094
10	CTCF	chr6:82472040-82472190	HCFaa	heart:	n/a	chr6:82472086-82472094
11	CTCF	chr6:82471980-82472130	HPF	lung:	n/a	chr6:82472086-82472094
12	CTCF	chr6:82472040-82472190	HPAF	blood vessel:	n/a	chr6:82472086-82472094
13	CTCF	chr6:82471960-82472110	HMF	breast:	n/a	chr6:82472086-82472094
14	CTCF	chr6:82472040-82472190	AG09319	gingival:	n/a	chr6:82472086-82472094
15	CTCF	chr6:82471920-82472070	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr6:82472020-82472170	BJ	skin:	n/a	chr6:82472086-82472094
17	CTCF	chr6:82471940-82472090	AG10803	skin:	n/a	n/a
18	CTCF	chr6:82472000-82472150	HMF	breast:	n/a	chr6:82472086-82472094
19	CTCF	chr6:82471960-82472110	AG10803	skin:	n/a	chr6:82472086-82472094
20	CTCF	chr6:82472000-82472150	HCPEpiC	choroid plexus:	n/a	chr6:82472086-82472094
21	CTCF	chr6:82471980-82472130	BE2_C	brain:	n/a	chr6:82472086-82472094
22	CTCF	chr6:82471920-82472070	BE2_C	brain:	n/a	n/a
23	CTCF	chr6:82472020-82472170	AoAF	blood vessel:	n/a	chr6:82472086-82472094
24	CTCF	chr6:82472000-82472150	AG09319	gingival:	n/a	chr6:82472086-82472094
25	CTCF	chr6:82471980-82472130	AG04449	skin:	n/a	chr6:82472086-82472094
26	EP300	chr6:82471015-82471404	SK-N-SH_RA	brain:	n/a	chr6:82471094-82471103
27	EP300	chr6:82471747-82472299	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr6:82470756-82471511	SK-N-SH	brain:	n/a	chr6:82470823-82470837 chr6:82471094-82471103
29	EP300	chr6:82471781-82472251	SK-N-SH_RA	brain:	n/a	n/a
30	EP300	chr6:82470455-82472858	SK-N-SH	brain:	n/a	chr6:82470823-82470837 chr6:82472760-82472774 chr6:82471094-82471103
31	EP300	chr6:82469637-82469883	GM12878	blood:	n/a	n/a
32	EP300	chr6:82469513-82469943	GM12878	blood:	n/a	n/a
33	EP300	chr6:82470881-82471430	SK-N-SH	brain:	n/a	chr6:82471094-82471103
34	EP300	chr6:82470163-82470426	SK-N-SH_RA	brain:	n/a	n/a
35	EP300	chr6:82470877-82471332	SK-N-SH_RA	brain:	n/a	chr6:82471094-82471103
36	FOS	chr6:82469554-82469937	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr6:82470904-82471285	MCF10A-Er-Src	breast:	n/a	chr6:82471093-82471102 chr6:82471093-82471103 chr6:82471094-82471101 chr6:82471094-82471103 chr6:82471092-82471104 chr6:82471093-82471103 chr6:82471092-82471103
38	FOS	chr6:82469484-82469984	MCF10A-Er-Src	breast:	n/a	chr6:82469947-82469956
39	FOS	chr6:82469554-82469934	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr6:82470865-82471360	MCF10A-Er-Src	breast:	n/a	chr6:82471093-82471102 chr6:82471093-82471103 chr6:82471094-82471101 chr6:82471094-82471103 chr6:82471092-82471104 chr6:82471093-82471103 chr6:82471092-82471103
41	FOS	chr6:82470912-82471287	MCF10A-Er-Src	breast:	n/a	chr6:82471093-82471102 chr6:82471093-82471103 chr6:82471094-82471101 chr6:82471094-82471103 chr6:82471092-82471104 chr6:82471093-82471103 chr6:82471092-82471103
42	FOS	chr6:82469486-82469949	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr6:82470870-82471378	MCF10A-Er-Src	breast:	n/a	chr6:82471093-82471102 chr6:82471093-82471103 chr6:82471094-82471101 chr6:82471094-82471103 chr6:82471092-82471104 chr6:82471093-82471103 chr6:82471092-82471103
44	FOS	chr6:82470844-82471326	HUVEC	blood vessel:	n/a	chr6:82471093-82471102 chr6:82471093-82471103 chr6:82471094-82471101 chr6:82471094-82471103 chr6:82471092-82471104 chr6:82471093-82471103 chr6:82471092-82471103
45	FOSL1	chr6:82470859-82471258	HCT-116	colon:	n/a	chr6:82471093-82471102 chr6:82471093-82471103 chr6:82471094-82471101 chr6:82471094-82471103 chr6:82471092-82471104 chr6:82471093-82471103
46	FOSL2	chr6:82470892-82471445	SK-N-SH	brain:	n/a	chr6:82471093-82471102 chr6:82471093-82471103 chr6:82471094-82471101 chr6:82471094-82471103 chr6:82471092-82471104 chr6:82471093-82471103
47	FOSL2	chr6:82470986-82471339	SK-N-SH	brain:	n/a	chr6:82471093-82471102 chr6:82471093-82471103 chr6:82471094-82471101 chr6:82471094-82471103 chr6:82471092-82471104 chr6:82471093-82471103
48	FOSL2	chr6:82470855-82471290	A549	lung:	n/a	chr6:82471093-82471102 chr6:82471093-82471103 chr6:82471094-82471101 chr6:82471094-82471103 chr6:82471092-82471104 chr6:82471093-82471103
49	FOXA2	chr6:82470479-82470688	HepG2	liver:	n/a	n/a
50	FOXA2	chr6:82469536-82469854	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:82462433..82465260-chr6:82471408..82474584,3	K562	blood:
2	chr6:82457043..82462432-chr6:82464909..82471112,8	MCF-7	breast:
3	chr6:82469013..82471227-chr6:82473397..82475724,2	MCF-7	breast:
4	chr6:82460615..82464438-chr6:82472382..82478506,11	MCF-7	breast:

Variant related genes	Relation type
ENSG00000219702	TF binding region
ENSG00000206886	TF binding region
ENSG00000112773	chromatin interactions
ENSG00000206886	chromatin interactions
ENSG00000219702	chromatin interactions

Extended variants
information (count: 91 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:91 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537984219	chr6:82469159-82469160	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs149810812	chr6:82469190-82469191	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs12215262	chr6:82469255-82469256	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs114420809	chr6:82469279-82469280	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs77797919	chr6:82469290-82469291	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs192851616	chr6:82469312-82469313	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs528062623	chr6:82469325-82469326	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs551698677	chr6:82469327-82469328	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs576976580	chr6:82469361-82469362	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs145749801	chr6:82469400-82469401	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs184399212	chr6:82469565-82469566	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs530254083	chr6:82469578-82469579	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs548282259	chr6:82469579-82469580	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs202223160	chr6:82469591-82469592	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs149094360	chr6:82469662-82469663	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs142173888	chr6:82469694-82469695	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs549490401	chr6:82469710-82469711	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs199884910	chr6:82469732-82469733	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs566127980	chr6:82469745-82469746	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs534665679	chr6:82469816-82469817	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs367779451	chr6:82469955-82469956	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs187712181	chr6:82469961-82469962	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs548065901	chr6:82470004-82470005	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs193100223	chr6:82470013-82470014	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs147816251	chr6:82470109-82470110	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs185867766	chr6:82470111-82470112	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs61465428	chr6:82470138-82470139	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs573877574	chr6:82470168-82470169	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs189283281	chr6:82470170-82470171	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs567775255	chr6:82470200-82470201	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs11270317	chr6:82470201-82470202	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs34009609	chr6:82470202-82470203	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs5013253	chr6:82470203-82470204	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs550373045	chr6:82470215-82470216	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs551694574	chr6:82470216-82470217	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs375341726	chr6:82470217-82470218	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs112830368	chr6:82470233-82470234	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs544645954	chr6:82470293-82470294	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs568803409	chr6:82470440-82470441	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs565208392	chr6:82470472-82470473	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs7749739	chr6:82470510-82470511	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs550880565	chr6:82470528-82470529	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs141439856	chr6:82470559-82470560	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs74973662	chr6:82470623-82470624	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs168952	chr6:82470706-82470707	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs549502970	chr6:82470721-82470722	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs566001343	chr6:82470725-82470726	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs194618	chr6:82470820-82470821	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs572560443	chr6:82470834-82470835	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs188607671	chr6:82470945-82470946	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	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
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Ductal carcinoma	22052326	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82463800-82476000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:82463800-82477000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr6:82464000-82469200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr6:82464000-82469600	Weak transcription	A549	lung
5	chr6:82464000-82477000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:82464200-82469200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr6:82464200-82469200	Weak transcription	HMEC	breast
8	chr6:82464200-82469600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr6:82464200-82469600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr6:82464200-82469600	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr6:82464200-82469600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr6:82464200-82469600	Weak transcription	Osteobl	bone
13	chr6:82464200-82469800	Weak transcription	NHLF	lung
14	chr6:82464200-82470600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr6:82464200-82472800	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr6:82464400-82475800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr6:82464600-82469200	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr6:82464600-82471800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr6:82464800-82469200	Weak transcription	Fetal Intestine Small	intestine
20	chr6:82464800-82469400	Weak transcription	Fetal Intestine Large	intestine
21	chr6:82465200-82469200	Weak transcription	Stomach Mucosa	stomach
22	chr6:82465200-82472000	Weak transcription	Primary hematopoietic stem cells	blood
23	chr6:82465600-82470600	Weak transcription	Fetal Stomach	stomach
24	chr6:82465600-82470600	Weak transcription	NHDF-Ad	bronchial
25	chr6:82467200-82469200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr6:82467200-82474000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr6:82467400-82477000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr6:82467800-82476200	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr6:82468000-82469200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr6:82468000-82476000	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr6:82468400-82471800	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr6:82468800-82472000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:82468800-82472000	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr6:82468800-82472200	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr6:82469000-82469800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr6:82469000-82471000	Enhancers	HepG2	liver
37	chr6:82469000-82472200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr6:82469000-82472200	Enhancers	NHEK	skin
39	chr6:82469200-82469400	Enhancers	Small Intestine	intestine
40	chr6:82469200-82469800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr6:82469200-82469800	Enhancers	Fetal Intestine Small	intestine
42	chr6:82469200-82469800	Enhancers	Stomach Mucosa	stomach
43	chr6:82469200-82469800	Enhancers	HSMM	muscle
44	chr6:82469200-82470000	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr6:82469200-82472400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr6:82469200-82472600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr6:82469200-82472600	Enhancers	HMEC	breast
48	chr6:82469200-82473200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:82469400-82470600	Weak transcription	Small Intestine	intestine
50	chr6:82469400-82470800	Enhancers	Fetal Intestine Large	intestine

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