Variant report

Variant	nsv884732
Chromosome Location	chr6:32311459-32345283
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:162)
CpG islands
(count:1962)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:162 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:32341778-32342105	HepG2	liver:	n/a	n/a
2	BATF	chr6:32313528-32313764	GM12878	blood:	n/a	chr6:32313546-32313555
3	BRCA1	chr6:32337516-32337917	Hela-S3	cervix:	n/a	n/a
4	CBX3	chr6:32337349-32337928	HCT-116	colon:	n/a	n/a
5	CBX3	chr6:32341732-32342198	HCT-116	colon:	n/a	n/a
6	CEBPB	chr6:32338273-32338693	A549	lung:	n/a	chr6:32338479-32338490
7	CEBPB	chr6:32338366-32338566	HepG2	liver:	n/a	chr6:32338479-32338490
8	CEBPB	chr6:32337397-32337887	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr6:32334419-32334604	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr6:32338339-32338640	A549	lung:	n/a	chr6:32338479-32338490
11	CEBPB	chr6:32341733-32341934	A549	lung:	n/a	n/a
12	CEBPB	chr6:32321136-32321610	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr6:32334428-32334621	K562	blood:	n/a	n/a
14	CEBPB	chr6:32337490-32337785	IMR90	lung:	n/a	n/a
15	CEBPB	chr6:32338237-32338741	Hela-S3	cervix:	n/a	chr6:32338479-32338490
16	CHD1	chr6:32337451-32338056	IMR90	lung:	n/a	n/a
17	CHD2	chr6:32337443-32337845	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr6:32341860-32342010	GM12864	blood:	n/a	n/a
19	CTCF	chr6:32317340-32317490	Caco-2	colon:	n/a	n/a
20	CTCF	chr6:32333160-32333310	HFF-Myc	foreskin:	n/a	n/a
21	E2F4	chr6:32311658-32311738	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr6:32337560-32337756	MCF10A-Er-Src	breast:	n/a	n/a
23	EBF1	chr6:32344047-32344247	GM12878	blood:	n/a	chr6:32344133-32344144
24	ELK1	chr6:32337477-32337817	Hela-S3	cervix:	n/a	n/a
25	EP300	chr6:32321139-32321500	Hela-S3	cervix:	n/a	n/a
26	EP300	chr6:32341731-32342181	A549	lung:	n/a	n/a
27	EP300	chr6:32338263-32338802	Hela-S3	cervix:	n/a	chr6:32338504-32338511
28	EP300	chr6:32337414-32337932	Hela-S3	cervix:	n/a	n/a
29	FAM48A	chr6:32344986-32345116	GM12878	blood:	n/a	n/a
30	FOS	chr6:32337382-32337953	MCF10A-Er-Src	breast:	n/a	chr6:32337653-32337664
31	FOS	chr6:32321184-32321501	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr6:32313504-32313882	MCF10A-Er-Src	breast:	n/a	chr6:32313731-32313742 chr6:32313530-32313539
33	FOS	chr6:32338246-32338672	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr6:32314098-32314129	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr6:32337460-32337846	MCF10A-Er-Src	breast:	n/a	chr6:32337653-32337664
36	FOS	chr6:32338259-32338662	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr6:32321122-32321561	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr6:32337452-32337994	MCF10A-Er-Src	breast:	n/a	chr6:32337653-32337664
39	FOS	chr6:32321115-32321505	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr6:32338376-32338636	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr6:32317556-32317801	MCF10A-Er-Src	breast:	n/a	chr6:32317643-32317652
42	FOS	chr6:32337477-32337880	Hela-S3	cervix:	n/a	chr6:32337653-32337664
43	FOS	chr6:32321132-32321502	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr6:32337393-32337942	MCF10A-Er-Src	breast:	n/a	chr6:32337653-32337664
45	FOS	chr6:32313505-32313875	HUVEC	blood vessel:	n/a	chr6:32313731-32313742 chr6:32313530-32313539
46	FOS	chr6:32313531-32313873	MCF10A-Er-Src	breast:	n/a	chr6:32313731-32313742
47	FOS	chr6:32337437-32338092	HUVEC	blood vessel:	n/a	chr6:32337653-32337664
48	FOS	chr6:32317500-32317812	MCF10A-Er-Src	breast:	n/a	chr6:32317643-32317652
49	FOS	chr6:32317508-32317764	MCF10A-Er-Src	breast:	n/a	chr6:32317643-32317652
50	FOS	chr6:32313508-32313881	MCF10A-Er-Src	breast:	n/a	chr6:32313731-32313742 chr6:32313530-32313539

(count:1962 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:32317528-32317578	MCF-7	breast:	n/a
2	chr6:32317028-32317078	IMR90	lung:	fetal
3	chr6:32320708-32320758	CMK	blood:	n/a
4	chr6:32335123-32335173	SKMC	muscle:	n/a
5	chr6:32336160-32336210	GM06990	blood:	n/a
6	chr6:32314182-32314232	IMR90	lung:	fetal
7	chr6:32336160-32336210	SKMC	muscle:	n/a
8	chr6:32326581-32326631	HL-60	blood:	n/a
9	chr6:32317429-32317479	PFSK-1	brain:	n/a
10	chr6:32340354-32340404	LNCaP	prostate:	n/a
11	chr6:32317528-32317578	MCF-7	breast:	n/a
12	chr6:32317028-32317078	IMR90	lung:	fetal
13	chr6:32320708-32320758	CMK	blood:	n/a
14	chr6:32335123-32335173	SKMC	muscle:	n/a
15	chr6:32336160-32336210	GM06990	blood:	n/a
16	chr6:32314182-32314232	IMR90	lung:	fetal
17	chr6:32336160-32336210	SKMC	muscle:	n/a
18	chr6:32326581-32326631	HL-60	blood:	n/a
19	chr6:32317429-32317479	PFSK-1	brain:	n/a
20	chr6:32340354-32340404	LNCaP	prostate:	n/a
21	chr6:32315253-32315303	Hela-S3	cervix:	n/a
22	chr6:32317429-32317479	GM12878	blood:	n/a
23	chr6:32317528-32317578	K562	blood:	n/a
24	chr6:32311517-32311567	PFSK-1	brain:	n/a
25	chr6:32335060-32335110	MCF-7	breast:	n/a
26	chr6:32335123-32335173	MCF-7	breast:	n/a
27	chr6:32326581-32326631	PANC-1	pancreas:	n/a
28	chr6:32335060-32335110	NT2-D1	testis:	n/a
29	chr6:32339554-32339604	ovcar-3	ovarian:	n/a
30	chr6:32330188-32330238	SAEC	small airway:	n/a
31	chr6:32339208-32339258	AG09309	skin:	n/a
32	chr6:32320708-32320758	SKMC	muscle:	n/a
33	chr6:32337970-32338020	HIPEpiC	eye:	n/a
34	chr6:32339511-32339561	Jurkat	blood:	n/a
35	chr6:32339208-32339258	HPAEpiC	pulmonary alveolar:	n/a
36	chr6:32312351-32312401	HRE	kidney:	n/a
37	chr6:32311517-32311567	Hela-S3	cervix:	n/a
38	chr6:32335123-32335173	Hela-S3	cervix:	n/a
39	chr6:32337930-32337980	U87	brain:	n/a
40	chr6:32336160-32336210	HCPEpiC	choroid plexus:	n/a
41	chr6:32339511-32339561	HPAEpiC	pulmonary alveolar:	n/a
42	chr6:32320708-32320758	Jurkat	blood:	n/a
43	chr6:32337906-32337956	MCF10A-Er-Src	breast:	n/a
44	chr6:32336160-32336210	SK-N-SH_RA	brain:	n/a
45	chr6:32340354-32340404	SK-N-SH	brain:	n/a
46	chr6:32339208-32339258	RPTEC	kidney:	n/a
47	chr6:32313583-32313633	AG09319	gingival:	n/a
48	chr6:32313583-32313633	CMK	blood:	n/a
49	chr6:32315772-32315822	SK-N-SH_RA	brain:	n/a
50	chr6:32313583-32313633	HPAEpiC	pulmonary alveolar:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:32310954..32313823-chr6:32318938..32321332,2	K562	blood:
2	chr6:32312156..32313758-chr6:32316689..32318846,2	MCF-7	breast:
3	chr6:32338535..32340842-chr6:32342130..32344081,2	K562	blood:
4	chr6:32312156..32313758-chr6:32316689..32318846,2	MCF-7	breast:
5	chr6:32340623..32343267-chr6:32371760..32373920,2	K562	blood:
6	chr6:32341767..32343740-chr6:32372075..32373920,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HLA-DRA-6	chr6:32317289-32317601	NONHSAT108900

No data

Variant related genes	Relation type
RNU6-603P	TF binding region
C6orf10	TF binding region
RNU6-603P	CpG island
C6orf10	CpG island
ENSG00000204296	chromatin interactions
ENSG00000223335	chromatin interactions

Extended variants
information (count: 1161 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3132954	chr6:32311459-32311460	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561793076	chr6:32311503-32311504	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs190098425	chr6:32311515-32311516	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565800826	chr6:32311549-32311550	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs72843221	chr6:32311571-32311572	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs377040282	chr6:32311693-32311694	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs550660547	chr6:32311707-32311708	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs568874417	chr6:32311751-32311752	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs181874256	chr6:32311790-32311791	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs551427329	chr6:32311798-32311799	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs566755711	chr6:32311828-32311829	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs74223626	chr6:32311834-32311835	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs376632664	chr6:32311846-32311847	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs2395145	chr6:32311871-32311872	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs2395146	chr6:32311875-32311876	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs184969618	chr6:32311949-32311950	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
17	rs28732194	chr6:32311957-32311958	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs9279585	chr6:32312042-32312043	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs145758755	chr6:32312046-32312047	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs186333702	chr6:32312049-32312050	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs77607556	chr6:32312052-32312053	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs141539469	chr6:32312055-32312056	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs6904320	chr6:32312082-32312083	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs188166009	chr6:32312120-32312121	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs371447500	chr6:32312132-32312133	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs146714775	chr6:32312133-32312134	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs180885148	chr6:32312152-32312153	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs118163679	chr6:32312155-32312156	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs112891419	chr6:32312171-32312172	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs554756891	chr6:32312242-32312243	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs114539073	chr6:32312274-32312275	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543760628	chr6:32312334-32312335	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs386699287	chr6:32312351-32312352	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs112052317	chr6:32312352-32312353	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs7383144	chr6:32312353-32312354	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs532835934	chr6:32312418-32312419	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs186179246	chr6:32312438-32312439	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs191374361	chr6:32312453-32312454	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs117705671	chr6:32312458-32312459	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs9268267	chr6:32312495-32312496	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs373291925	chr6:32312510-32312511	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs548839373	chr6:32312521-32312522	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs9268268	chr6:32312610-32312611	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs181397799	chr6:32312622-32312623	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs556277164	chr6:32312623-32312624	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs571707977	chr6:32312636-32312637	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs386699289	chr6:32312637-32312638	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs9268270	chr6:32312638-32312639	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs4576281	chr6:32312650-32312651	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs555263137	chr6:32312651-32312652	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:126)

Disease	PMID	Source
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
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	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
Ovarian cancer	21781307	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	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
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	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	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:32310000-32311600	Enhancers	Primary B cells from peripheral blood	blood
2	chr6:32311200-32311800	Enhancers	GM12878-XiMat	blood
3	chr6:32312200-32312600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:32312600-32315200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:32315000-32315600	Enhancers	Brain Cingulate Gyrus	brain
6	chr6:32315000-32315800	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr6:32315200-32315600	Enhancers	Brain Hippocampus Middle	brain
8	chr6:32315200-32316000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr6:32315200-32316000	Enhancers	Brain Substantia Nigra	brain
10	chr6:32315400-32316000	Enhancers	Brain Angular Gyrus	brain
11	chr6:32317400-32317800	Enhancers	Hela-S3	cervix
12	chr6:32317800-32320800	Weak transcription	Hela-S3	cervix
13	chr6:32320800-32321800	Enhancers	Hela-S3	cervix
14	chr6:32320800-32322000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr6:32321800-32323000	Weak transcription	Hela-S3	cervix
16	chr6:32322000-32323200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:32322800-32323600	Enhancers	HUVEC	blood vessel
18	chr6:32323000-32323400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr6:32323000-32324200	Enhancers	Hela-S3	cervix
20	chr6:32323200-32324000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:32324200-32324600	Weak transcription	Hela-S3	cervix
22	chr6:32324600-32325600	Enhancers	Hela-S3	cervix
23	chr6:32325600-32332600	Weak transcription	Hela-S3	cervix
24	chr6:32332600-32332800	Enhancers	Hela-S3	cervix
25	chr6:32332800-32335800	Weak transcription	Hela-S3	cervix
26	chr6:32335800-32337800	Enhancers	Hela-S3	cervix
27	chr6:32336000-32339200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr6:32337200-32339000	Enhancers	HUVEC	blood vessel
29	chr6:32337400-32337800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr6:32337400-32338000	Enhancers	Osteobl	bone
31	chr6:32337400-32338200	Enhancers	A549	lung
32	chr6:32337400-32338200	Enhancers	NH-A	brain
33	chr6:32337400-32338800	Enhancers	NHDF-Ad	bronchial
34	chr6:32337400-32339000	Enhancers	HMEC	breast
35	chr6:32337400-32339400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr6:32337400-32339600	Enhancers	NHEK	skin
37	chr6:32337600-32337800	Enhancers	Small Intestine	intestine
38	chr6:32337600-32338400	Enhancers	Muscle Satellite Cultured Cells	--
39	chr6:32337800-32338200	Flanking Active TSS	Hela-S3	cervix
40	chr6:32337800-32338800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr6:32337800-32342000	Weak transcription	Small Intestine	intestine
42	chr6:32338200-32338600	Weak transcription	A549	lung
43	chr6:32338200-32338600	Weak transcription	NH-A	brain
44	chr6:32338200-32339800	Enhancers	Hela-S3	cervix
45	chr6:32338400-32338800	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr6:32338600-32339400	Enhancers	A549	lung
47	chr6:32338600-32339600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr6:32338600-32339600	Enhancers	NH-A	brain
49	chr6:32338800-32339200	Enhancers	Muscle Satellite Cultured Cells	--
50	chr6:32339000-32339200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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