Variant report

Variant	nsv819291
Chromosome Location	chr6:30003841-30009815
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:189)
CpG islands
(count:611)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:189 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:30009660-30009874	K562	blood:	n/a	chr6:30009839-30009856
2	CEBPB	chr6:30004917-30005184	HepG2	liver:	n/a	chr6:30005018-30005029
3	CEBPB	chr6:30009686-30009886	Hela-S3	cervix:	n/a	chr6:30009839-30009856
4	CEBPB	chr6:30009617-30009908	IMR90	lung:	n/a	chr6:30009839-30009856
5	CEBPB	chr6:30009594-30009921	HepG2	liver:	n/a	chr6:30009839-30009856
6	CTCF	chr6:30005111-30005252	GM13976	blood:	n/a	n/a
7	CTCF	chr6:30005020-30005170	RPTEC	kidney:	n/a	n/a
8	CTCF	chr6:30005100-30005250	GM12874	blood:	n/a	n/a
9	CTCF	chr6:30004817-30005406	HCT-116	colon:	n/a	n/a
10	CTCF	chr6:30005036-30005281	Medullo	brain:	n/a	n/a
11	CTCF	chr6:30004925-30005280	K562	blood:	n/a	n/a
12	CTCF	chr6:30005046-30005285	MCF-7	breast:	n/a	n/a
13	CTCF	chr6:30005080-30005230	HBMEC	blood vessel:	n/a	n/a
14	CTCF	chr6:30005080-30005230	GM12870	blood:	n/a	n/a
15	CTCF	chr6:30004934-30005415	MCF-7	breast:	n/a	n/a
16	CTCF	chr6:30005060-30005210	GM12866	blood:	n/a	n/a
17	CTCF	chr6:30005120-30005270	HFF-Myc	foreskin:	n/a	n/a
18	CTCF	chr6:30005080-30005230	GM12878	blood:	n/a	n/a
19	CTCF	chr6:30005060-30005210	HCM	heart:	n/a	n/a
20	CTCF	chr6:30005088-30005246	A549	lung:	n/a	n/a
21	CTCF	chr6:30005005-30005315	A549	lung:	n/a	n/a
22	CTCF	chr6:30005020-30005170	HEK293	kidney:	n/a	n/a
23	CTCF	chr6:30005140-30005290	GM12866	blood:	n/a	n/a
24	CTCF	chr6:30004958-30005292	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr6:30005033-30005257	Lung_OC	lung:	n/a	n/a
26	CTCF	chr6:30005060-30005210	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr6:30005080-30005230	HPF	lung:	n/a	n/a
28	CTCF	chr6:30005080-30005230	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr6:30004973-30005349	K562	blood:	n/a	n/a
30	CTCF	chr6:30005080-30005230	GM12801	blood:	n/a	n/a
31	CTCF	chr6:30005078-30005254	Fibrobl	skin:	n/a	n/a
32	CTCF	chr6:30005080-30005230	K562	blood:	n/a	n/a
33	CTCF	chr6:30004960-30005110	WI-38	lung:	n/a	n/a
34	CTCF	chr6:30005120-30005270	HAc	cerebellar:	n/a	n/a
35	CTCF	chr6:30005004-30005280	K562	blood:	n/a	n/a
36	CTCF	chr6:30005080-30005230	NB4	blood:	n/a	n/a
37	CTCF	chr6:30005100-30005250	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr6:30005083-30005244	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr6:30005135-30005137	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:30005100-30005250	GM12875	blood:	n/a	n/a
41	CTCF	chr6:30005060-30005210	GM12871	blood:	n/a	n/a
42	CTCF	chr6:30005100-30005250	GM12871	blood:	n/a	n/a
43	CTCF	chr6:30005020-30005170	GM12870	blood:	n/a	n/a
44	CTCF	chr6:30005064-30005285	LNCaP	prostate:	n/a	n/a
45	CTCF	chr6:30005080-30005230	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr6:30005074-30005273	GM10248	blood:	n/a	n/a
47	CTCF	chr6:30003880-30004030	GM06990	blood:	n/a	n/a
48	CTCF	chr6:30005060-30005210	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:30004983-30005292	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr6:30005436-30005475	GM10248	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:30003910-30003960	HMEC	breast:	n/a
2	chr6:30003910-30003960	HMEC	breast:	n/a
3	chr6:30009242-30009292	HRE	kidney:	n/a
4	chr6:30005173-30005223	SK-N-MC	brain:	n/a
5	chr6:30008143-30008193	HCM	heart:	n/a
6	chr6:30005372-30005422	BE2_C	brain:	n/a
7	chr6:30009745-30009795	HNPCEpiC	eye:	n/a
8	chr6:30008143-30008193	SK-N-SH_RA	brain:	n/a
9	chr6:30009242-30009292	ProgFib	skin:	n/a
10	chr6:30003910-30003960	HRE	kidney:	n/a
11	chr6:30009180-30009230	GM12878	blood:	n/a
12	chr6:30009751-30009801	CMK	blood:	n/a
13	chr6:30005372-30005422	GM12891	blood:	n/a
14	chr6:30005372-30005422	ovcar-3	ovarian:	n/a
15	chr6:30009745-30009795	GM12892	blood:	n/a
16	chr6:30009751-30009801	BJ	skin:	n/a
17	chr6:30008143-30008193	ProgFib	skin:	n/a
18	chr6:30008094-30008144	NHDF-neo	bronchial:	n/a
19	chr6:30009751-30009801	HIPEpiC	eye:	n/a
20	chr6:30009242-30009292	SKMC	muscle:	n/a
21	chr6:30005173-30005223	BJ	skin:	n/a
22	chr6:30003910-30003960	NHBE	bronchial:	n/a
23	chr6:30009751-30009801	GM12878	blood:	n/a
24	chr6:30003910-30003960	ovcar-3	ovarian:	n/a
25	chr6:30008143-30008193	HRPEpiC	eye:	n/a
26	chr6:30003910-30003960	HIPEpiC	eye:	n/a
27	chr6:30008094-30008144	SK-N-MC	brain:	n/a
28	chr6:30009745-30009795	U87	brain:	n/a
29	chr6:30005372-30005422	GM12892	blood:	n/a
30	chr6:30008143-30008193	HMEC	breast:	n/a
31	chr6:30009751-30009801	BE2_C	brain:	n/a
32	chr6:30005173-30005223	HUVEC	blood vessel:	n/a
33	chr6:30003910-30003960	A549	lung:	n/a
34	chr6:30008143-30008193	HRCEpiC	kidney:	n/a
35	chr6:30009751-30009801	PrEC	prostate:	n/a
36	chr6:30008094-30008144	CMK	blood:	n/a
37	chr6:30009242-30009292	PrEC	prostate:	n/a
38	chr6:30005372-30005422	HNPCEpiC	eye:	n/a
39	chr6:30007709-30007759	PFSK-1	brain:	n/a
40	chr6:30007709-30007759	K562	blood:	n/a
41	chr6:30005173-30005223	SKMC	muscle:	n/a
42	chr6:30009180-30009230	Jurkat	blood:	n/a
43	chr6:30009242-30009292	AG09319	gingival:	n/a
44	chr6:30005372-30005422	BJ	skin:	n/a
45	chr6:30009180-30009230	ProgFib	skin:	n/a
46	chr6:30009745-30009795	Jurkat	blood:	n/a
47	chr6:30005372-30005422	HepG2	liver:	n/a
48	chr6:30009180-30009230	HIPEpiC	eye:	n/a
49	chr6:30005372-30005422	SK-N-SH_RA	brain:	n/a
50	chr6:30007709-30007759	HCT-116	colon:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:30001672..30004034-chr6:30026395..30027961,2	K562	blood:
2	chr6:30006360..30008334-chr6:30017621..30020296,2	MCF-7	breast:
3	chr6:30005064..30005630-chr6:30098498..30099274,2	K562	blood:
4	chr6:30004933..30007814-chr6:30068168..30069816,2	MCF-7	breast:
5	chr6:29815545..29816511-chr6:30004700..30005650,3	MCF-7	breast:
6	chr6:30003872..30007108-chr6:30008649..30012245,4	K562	blood:
7	chr6:30004722..30005615-chr6:30098646..30099168,2	MCF-7	breast:
8	chr6:30006757..30011718-chr6:30026888..30030646,5	K562	blood:
9	chr6:30002424..30006428-chr6:30027567..30030890,5	MCF-7	breast:
10	chr6:30003872..30007108-chr6:30008649..30012245,4	K562	blood:
11	chr6:30002740..30005205-chr6:30029200..30030838,2	MCF-7	breast:
12	chr6:30009359..30013727-chr6:30026247..30028970,3	K562	blood:
13	chr6:30006290..30008332-chr6:30012073..30013953,2	K562	blood:
14	chr6:29815601..29816421-chr6:30004834..30005555,3	MCF-7	breast:

No data

Variant related genes	Relation type
ZNRD1-AS1	TF binding region
ZNRD1-AS1	CpG island
ENSG00000204623	chromatin interactions
ENSG00000066379	chromatin interactions

Extended variants
information (count: 239 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:239 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529394653	chr6:30003857-30003858	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs544465545	chr6:30003864-30003865	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs41272559	chr6:30003911-30003912	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs368106522	chr6:30003918-30003919	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs148909949	chr6:30003938-30003939	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs371832131	chr6:30003957-30003958	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs58278649	chr6:30003974-30003975	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs184207849	chr6:30004010-30004011	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs545985325	chr6:30004013-30004014	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs562648526	chr6:30004043-30004044	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs550552890	chr6:30004048-30004049	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs371665641	chr6:30004049-30004050	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs3869068	chr6:30004052-30004053	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs41272563	chr6:30004053-30004054	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs568092714	chr6:30004116-30004117	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs527280970	chr6:30004121-30004122	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs539826861	chr6:30004166-30004167	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs372754235	chr6:30004191-30004192	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs559120994	chr6:30004237-30004238	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs567171984	chr6:30004239-30004240	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs143653387	chr6:30004253-30004254	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs9261201	chr6:30004259-30004260	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs554837890	chr6:30004331-30004332	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs574531503	chr6:30004340-30004341	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs561617335	chr6:30004363-30004364	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs259931	chr6:30004371-30004372	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs553836560	chr6:30004372-30004373	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs375015932	chr6:30004383-30004384	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs113909693	chr6:30004386-30004387	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs372667607	chr6:30004411-30004412	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376749712	chr6:30004443-30004444	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs138256588	chr6:30004450-30004451	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs545945783	chr6:30004457-30004458	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs573769453	chr6:30004473-30004474	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs369141230	chr6:30004480-30004481	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs562707886	chr6:30004507-30004508	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs373891618	chr6:30004508-30004509	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs373978090	chr6:30004515-30004516	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs58980848	chr6:30004528-30004529	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs529376727	chr6:30004532-30004533	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs527544656	chr6:30004533-30004534	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs188756985	chr6:30004544-30004545	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs371353535	chr6:30004545-30004546	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs386698687	chr6:30004548-30004549	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs9261202	chr6:30004549-30004550	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
46	rs200232262	chr6:30004553-30004554	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs577537779	chr6:30004555-30004556	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs564836354	chr6:30004564-30004565	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs373795363	chr6:30004582-30004583	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs569153221	chr6:30004583-30004584	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:117)

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
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
Ovarian cancer	21781307	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
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	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	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	21293372	CNVD
Myelofibrosis	22110671	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
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Rett syndrome	21593744	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29975200-30027800	Weak transcription	Aorta	Aorta
2	chr6:29975600-30027800	Weak transcription	Right Ventricle	heart
3	chr6:29975800-30027800	Weak transcription	Gastric	stomach
4	chr6:29976600-30023000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr6:29977200-30024600	Weak transcription	Brain Anterior Caudate	brain
6	chr6:29977200-30027600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr6:29977200-30027800	Weak transcription	Fetal Intestine Small	intestine
8	chr6:29979000-30027600	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr6:29979400-30024600	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr6:29979600-30022800	Weak transcription	Ovary	ovary
11	chr6:29979800-30027800	Weak transcription	Pancreas	Pancrea
12	chr6:29980200-30012000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr6:29981200-30023000	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr6:29981800-30010600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr6:29982800-30009800	Weak transcription	Psoas Muscle	Psoas
16	chr6:29982800-30022800	Weak transcription	Fetal Muscle Leg	muscle
17	chr6:29983400-30012400	Weak transcription	NHEK	skin
18	chr6:29984600-30023400	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr6:29985000-30024600	Weak transcription	Brain Angular Gyrus	brain
20	chr6:29985400-30008200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr6:29987800-30010600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr6:29987800-30024800	Weak transcription	Fetal Intestine Large	intestine
23	chr6:29988000-30010400	Weak transcription	Fetal Muscle Trunk	muscle
24	chr6:29988200-30009800	Weak transcription	HepG2	liver
25	chr6:29988200-30022800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr6:29988200-30027800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr6:29988200-30027800	Weak transcription	Esophagus	oesophagus
28	chr6:29988400-30006200	Weak transcription	Brain Cingulate Gyrus	brain
29	chr6:29988400-30021600	Weak transcription	Primary hematopoietic stem cells	blood
30	chr6:29988400-30023400	Weak transcription	Adipose Nuclei	Adipose
31	chr6:29988400-30027800	Weak transcription	Thymus	Thymus
32	chr6:29988600-30009800	Weak transcription	Left Ventricle	heart
33	chr6:29988600-30022200	Weak transcription	Stomach Smooth Muscle	stomach
34	chr6:29988600-30027400	Weak transcription	Duodenum Mucosa	Duodenum
35	chr6:29988800-30022800	Weak transcription	Brain Hippocampus Middle	brain
36	chr6:29989000-30009800	Weak transcription	GM12878-XiMat	blood
37	chr6:29989000-30023000	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr6:29989400-30021400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr6:29996600-30012200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr6:29998000-30027600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr6:29998400-30012200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr6:29998400-30012200	Weak transcription	HMEC	breast
43	chr6:29999200-30027200	Weak transcription	Fetal Heart	heart
44	chr6:29999800-30012400	Weak transcription	Hela-S3	cervix
45	chr6:29999800-30022200	Weak transcription	Primary B cells from peripheral blood	blood
46	chr6:30000000-30027400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr6:30001200-30025000	Weak transcription	Fetal Lung	lung
48	chr6:30001200-30027800	Weak transcription	Fetal Kidney	kidney
49	chr6:30001400-30004200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr6:30001400-30012000	Weak transcription	HSMM	muscle

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