Variant report

Variant	nsv527368
Chromosome Location	chr6:29709840-29712704
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:9)
CpG islands
(count:794)
Chromatin interactive
region (count:9)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:9 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr6:29709840-29709990	GM12867	blood:	n/a	n/a
2	POLR2A	chr6:29711488-29711540	HepG2	liver:	n/a	n/a
3	POLR2A	chr6:29712419-29712616	GM12878	blood:	n/a	n/a
4	POLR2A	chr6:29708276-29711285	GM12878	blood:	n/a	n/a
5	POLR2A	chr6:29710022-29710239	GM12878	blood:	n/a	n/a
6	POLR2A	chr6:29709365-29709947	GM12878	blood:	n/a	n/a
7	POLR2A	chr6:29711346-29711542	K562	blood:	n/a	n/a
8	POLR2A	chr6:29711561-29711761	GM12878	blood:	n/a	n/a
9	POLR2A	chr6:29712250-29712324	K562	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29711438-29711488	H1-hESC	embryonic stem cell:	embryo
2	chr6:29711438-29711488	H1-hESC	embryonic stem cell:	embryo
3	chr6:29710109-29710159	BJ	skin:	n/a
4	chr6:29710221-29710271	U87	brain:	n/a
5	chr6:29711588-29711638	AG04450	lung:	fetal
6	chr6:29710109-29710159	SK-N-SH_RA	brain:	n/a
7	chr6:29712462-29712512	NHDF-neo	bronchial:	n/a
8	chr6:29712115-29712165	RPTEC	kidney:	n/a
9	chr6:29711438-29711488	IMR90	lung:	fetal
10	chr6:29712115-29712165	BE2_C	brain:	n/a
11	chr6:29711438-29711488	GM19239	blood:	n/a
12	chr6:29710221-29710271	AG10803	skin:	n/a
13	chr6:29711588-29711638	HRPEpiC	eye:	n/a
14	chr6:29710221-29710271	Hepatocyte	liver:	n/a
15	chr6:29712462-29712512	MCF-7	breast:	n/a
16	chr6:29712462-29712512	Jurkat	blood:	n/a
17	chr6:29711249-29711299	H1-hESC	embryonic stem cell:	embryo
18	chr6:29710109-29710159	SAEC	small airway:	n/a
19	chr6:29711975-29712025	ProgFib	skin:	n/a
20	chr6:29712014-29712064	NHBE	bronchial:	n/a
21	chr6:29712115-29712165	HRPEpiC	eye:	n/a
22	chr6:29712115-29712165	Hela-S3	cervix:	n/a
23	chr6:29711249-29711299	K562	blood:	n/a
24	chr6:29712014-29712064	SKMC	muscle:	n/a
25	chr6:29711465-29711515	AoSMC	blood vessel:	n/a
26	chr6:29711975-29712025	GM12878	blood:	n/a
27	chr6:29712541-29712591	GM12878	blood:	n/a
28	chr6:29710830-29710880	CMK	blood:	n/a
29	chr6:29712014-29712064	GM12878	blood:	n/a
30	chr6:29712014-29712064	HMEC	breast:	n/a
31	chr6:29712541-29712591	LNCaP	prostate:	n/a
32	chr6:29711249-29711299	IMR90	lung:	fetal
33	chr6:29710830-29710880	SKMC	muscle:	n/a
34	chr6:29712462-29712512	K562	blood:	n/a
35	chr6:29711465-29711515	HPAEpiC	pulmonary alveolar:	n/a
36	chr6:29711249-29711299	ECC-1	luminal epithelium:	n/a
37	chr6:29712462-29712512	HCF	heart:	n/a
38	chr6:29711975-29712025	RPTEC	kidney:	n/a
39	chr6:29712014-29712064	SAEC	small airway:	n/a
40	chr6:29711249-29711299	SK-N-SH	brain:	n/a
41	chr6:29712462-29712512	PFSK-1	brain:	n/a
42	chr6:29711588-29711638	HCF	heart:	n/a
43	chr6:29712462-29712512	HCT-116	colon:	n/a
44	chr6:29711975-29712025	BJ	skin:	n/a
45	chr6:29711438-29711488	SK-N-SH_RA	brain:	n/a
46	chr6:29711465-29711515	AG09309	skin:	n/a
47	chr6:29712425-29712475	SK-N-MC	brain:	n/a
48	chr6:29712115-29712165	T-47D	breast:	n/a
49	chr6:29711438-29711488	A549	lung:	n/a
50	chr6:29712462-29712512	BJ	skin:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:29710008..29711886-chr6:29712365..29714063,2	K562	blood:
2	chr6:29708611..29711552-chr6:29714400..29717446,4	MCF-7	breast:
3	chr6:29710119..29712623-chr6:29721345..29723379,2	MCF-7	breast:
4	chr6:29710008..29711886-chr6:29712365..29714063,2	K562	blood:
5	chr6:29709930..29711722-chr6:29720449..29722464,2	K562	blood:
6	chr6:29692092..29694262-chr6:29708323..29710900,2	K562	blood:
7	chr6:29710755..29712500-chr6:29714254..29717094,2	K562	blood:
8	chr6:29709817..29712750-chr6:29714477..29716450,2	MCF-7	breast:
9	chr6:29712194..29714049-chr6:29781280..29783856,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP57-7	chr6:29712044-29712321	NONHSAT108548
2	lnc-ZFP57-7	chr6:29711786-29711929	NONHSAT108548

No data

Variant related genes	Relation type
HCG9P5	TF binding region
HLA-F-AS1	TF binding region
HCG9P5	CpG island
HLA-F-AS1	CpG island
ENSG00000204642	chromatin interactions
ENSG00000273340	chromatin interactions
ENSG00000214922	chromatin interactions
ENSG00000227758	chromatin interactions

Extended variants
information (count: 126 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:126 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2517938	chr6:29709840-29709841	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs909732	chr6:29709867-29709868	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs540255179	chr6:29709879-29709880	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs553858386	chr6:29709881-29709882	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs577024788	chr6:29709917-29709918	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs885942	chr6:29709949-29709950	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs190826057	chr6:29709993-29709994	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs147991173	chr6:29710026-29710027	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs544541515	chr6:29710073-29710074	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs116097941	chr6:29710102-29710103	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs62391834	chr6:29710208-29710209	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs529995192	chr6:29710221-29710222	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs115176048	chr6:29710222-29710223	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs573205289	chr6:29710241-29710242	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs141673151	chr6:29710251-29710252	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs145895406	chr6:29710310-29710311	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs138744598	chr6:29710335-29710336	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs142784439	chr6:29710352-29710353	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs885941	chr6:29710380-29710381	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs574110206	chr6:29710472-29710473	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs554541047	chr6:29710510-29710511	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs569241748	chr6:29710545-29710546	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs147295559	chr6:29710547-29710548	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs533730384	chr6:29710560-29710561	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs115635977	chr6:29710567-29710568	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs562769539	chr6:29710613-29710614	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs730858	chr6:29710628-29710629	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs538000287	chr6:29710640-29710641	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs111675052	chr6:29710644-29710645	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs374861870	chr6:29710673-29710674	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs368945254	chr6:29710677-29710678	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs544815197	chr6:29710708-29710709	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs4713240	chr6:29710726-29710727	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs117584100	chr6:29710750-29710751	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs1610612	chr6:29710831-29710832	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs2076176	chr6:29710833-29710834	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs538187091	chr6:29710849-29710850	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs549978122	chr6:29710861-29710862	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs181902041	chr6:29710887-29710888	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs1610613	chr6:29710963-29710964	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs147406187	chr6:29711005-29711006	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs139199531	chr6:29711010-29711011	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs563560671	chr6:29711023-29711024	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs9258220	chr6:29711041-29711042	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs9391659	chr6:29711084-29711085	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs2743949	chr6:29711124-29711125	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs376428675	chr6:29711172-29711173	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs576105010	chr6:29711186-29711187	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs374785483	chr6:29711196-29711197	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs544540719	chr6:29711205-29711206	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
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
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	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
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29692200-29715800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr6:29692400-29715800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:29692800-29712000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr6:29693200-29711400	Weak transcription	Pancreas	Pancrea
5	chr6:29693400-29715600	Weak transcription	Esophagus	oesophagus
6	chr6:29693600-29715600	Weak transcription	NHLF	lung
7	chr6:29693800-29715400	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr6:29693800-29716000	Weak transcription	Small Intestine	intestine
9	chr6:29694000-29711200	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr6:29694000-29711400	Weak transcription	Gastric	stomach
11	chr6:29694000-29712200	Weak transcription	Aorta	Aorta
12	chr6:29694000-29715600	Weak transcription	Colon Smooth Muscle	Colon
13	chr6:29696000-29715600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr6:29696000-29715600	Weak transcription	Ovary	ovary
15	chr6:29696200-29711800	Weak transcription	Adipose Nuclei	Adipose
16	chr6:29696200-29715200	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr6:29696200-29715600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr6:29696200-29715600	Weak transcription	Liver	Liver
19	chr6:29696400-29710800	Weak transcription	Lung	lung
20	chr6:29696400-29711400	Weak transcription	Spleen	Spleen
21	chr6:29696400-29711800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr6:29696400-29712000	Weak transcription	Duodenum Mucosa	Duodenum
23	chr6:29696400-29715400	Weak transcription	Stomach Smooth Muscle	stomach
24	chr6:29696600-29715600	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr6:29696800-29714600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr6:29696800-29715800	Weak transcription	Colonic Mucosa	Colon
27	chr6:29699200-29712400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr6:29700000-29715200	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr6:29700600-29711600	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr6:29702000-29711200	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr6:29702000-29711600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr6:29702400-29715400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr6:29702600-29715400	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr6:29702800-29712000	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr6:29702800-29712800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr6:29702800-29713800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr6:29702800-29715400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr6:29702800-29715600	Weak transcription	Primary B cells from peripheral blood	blood
39	chr6:29706000-29712000	Weak transcription	Left Ventricle	heart
40	chr6:29706000-29715400	Weak transcription	Right Atrium	heart
41	chr6:29706000-29715800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr6:29706200-29711200	Weak transcription	Right Ventricle	heart
43	chr6:29706800-29715800	Weak transcription	NHDF-Ad	bronchial
44	chr6:29707400-29713000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr6:29707600-29715400	Weak transcription	NHEK	skin
46	chr6:29708400-29711200	Strong transcription	HMEC	breast
47	chr6:29708600-29710000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr6:29708600-29712600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr6:29708800-29713200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr6:29709800-29710400	Enhancers	H1 Cell Line	embryonic stem cell

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