Variant report

Variant	nsv511905
Chromosome Location	chr6:88284245-88287678
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	BHLHE40	chr6:88283990-88284319	HepG2	liver:	n/a	n/a
2	BHLHE40	chr6:88283934-88284318	GM12878	blood:	n/a	n/a
3	CEBPB	chr6:88283922-88284369	MCF-7	breast:	n/a	chr6:88284006-88284017
4	CEBPB	chr6:88283984-88284295	HepG2	liver:	n/a	chr6:88284006-88284017
5	EP300	chr6:88284573-88285097	K562	blood:	n/a	n/a
6	EP300	chr6:88283856-88284283	MCF-7	breast:	n/a	n/a
7	ESR1	chr6:88283783-88284304	T-47D	breast:	n/a	chr6:88284053-88284070 chr6:88284052-88284069
8	ESR1	chr6:88283906-88284266	ECC-1	luminal epithelium:	n/a	chr6:88284053-88284070 chr6:88284052-88284069
9	ESR1	chr6:88283837-88284345	T-47D	breast:	n/a	chr6:88284053-88284070 chr6:88284052-88284069
10	ESR1	chr6:88283905-88284274	T-47D	breast:	n/a	chr6:88284053-88284070 chr6:88284052-88284069
11	ESR1	chr6:88283919-88284255	T-47D	breast:	n/a	chr6:88284053-88284070 chr6:88284052-88284069
12	ESR1	chr6:88283801-88284320	ECC-1	luminal epithelium:	n/a	chr6:88284053-88284070 chr6:88284052-88284069
13	ESR1	chr6:88283829-88284315	T-47D	breast:	n/a	chr6:88284053-88284070 chr6:88284052-88284069
14	ESR1	chr6:88283776-88284307	ECC-1	luminal epithelium:	n/a	chr6:88284053-88284070 chr6:88284052-88284069
15	ESR1	chr6:88283839-88284318	T-47D	breast:	n/a	chr6:88284053-88284070 chr6:88284052-88284069
16	FOS	chr6:88284098-88284258	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr6:88284053-88284258	MCF10A-Er-Src	breast:	n/a	n/a
18	FOXA1	chr6:88284018-88284377	HepG2	liver:	n/a	n/a
19	FOXA2	chr6:88283961-88284302	HepG2	liver:	n/a	n/a
20	GATA1	chr6:88284364-88285542	K562	blood:	n/a	n/a
21	GATA1	chr6:88284643-88285113	PBDE	blood:	n/a	n/a
22	GATA3	chr6:88283767-88284434	MCF-7	breast:	n/a	n/a
23	IRF1	chr6:88284807-88285009	K562	blood:	n/a	n/a
24	JUN	chr6:88283997-88284270	HepG2	liver:	n/a	chr6:88284129-88284142
25	JUND	chr6:88284700-88285107	K562	blood:	n/a	n/a
26	MAFK	chr6:88285120-88285179	K562	blood:	n/a	n/a
27	MAFK	chr6:88285336-88285524	HepG2	liver:	n/a	n/a
28	MAX	chr6:88283874-88284426	MCF-7	breast:	n/a	n/a
29	MYC	chr6:88285043-88285114	K562	blood:	n/a	n/a
30	NR2F2	chr6:88283778-88284472	MCF-7	breast:	n/a	n/a
31	POLR2A	chr6:88285250-88285264	HUVEC	blood vessel:	n/a	n/a
32	POLR2A	chr6:88287005-88287016	HepG2	liver:	n/a	n/a
33	POLR2A	chr6:88285234-88285434	HepG2	liver:	n/a	n/a
34	POLR2A	chr6:88287080-88287262	HepG2	liver:	n/a	n/a
35	POLR2A	chr6:88285735-88285886	K562	blood:	n/a	n/a
36	POLR2A	chr6:88284749-88284872	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr6:88285632-88285810	HepG2	liver:	n/a	n/a
38	RCOR1	chr6:88284664-88285111	K562	blood:	n/a	n/a
39	RUNX3	chr6:88283904-88284343	GM12878	blood:	n/a	chr6:88284122-88284131
40	RUNX3	chr6:88283977-88284326	GM12878	blood:	n/a	chr6:88284122-88284131
41	TAL1	chr6:88284735-88285067	K562	blood:	n/a	n/a
42	TBL1XR1	chr6:88284656-88285109	K562	blood:	n/a	n/a
43	TEAD4	chr6:88284581-88285149	K562	blood:	n/a	n/a
44	ZMIZ1	chr6:88284956-88284959	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:88276178..88278517-chr6:88285720..88288387,2	K562	blood:
2	chr6:88276251..88278746-chr6:88282738..88284494,3	MCF-7	breast:
3	chr6:88281663..88283868-chr6:88287306..88289197,2	K562	blood:
4	chr6:88282635..88286754-chr6:88286787..88288868,3	MCF-7	breast:
5	chr6:88287492..88290089-chr6:88410688..88412261,2	MCF-7	breast:
6	chr6:87866903..87868749-chr6:88285297..88287961,2	MCF-7	breast:
7	chr6:88282649..88284478-chr6:88285308..88287961,2	MCF-7	breast:
8	chr6:88182571..88184838-chr6:88283979..88286941,2	MCF-7	breast:
9	chr6:88282635..88286754-chr6:88286787..88288868,3	MCF-7	breast:
10	chr6:88284821..88286391-chr6:88289308..88290910,2	K562	blood:
11	chr6:88268600..88271496-chr6:88285308..88287574,2	MCF-7	breast:
12	chr6:88279883..88284316-chr6:88297696..88301610,6	MCF-7	breast:
13	chr6:88285212..88293434-chr6:88297589..88302538,14	K562	blood:
14	chr6:88285921..88288874-chr6:88289679..88293937,3	MCF-7	breast:
15	chr6:88275961..88278697-chr6:88284157..88285925,2	K562	blood:
16	chr6:88283650..88286214-chr6:88294247..88295894,2	K562	blood:
17	chr6:88282649..88284478-chr6:88285308..88287961,2	MCF-7	breast:

Variant related genes	Relation type
RARS2	TF binding region
ENSG00000135336	chromatin interactions
ENSG00000135334	chromatin interactions
ENSG00000146282	chromatin interactions
ENSG00000164414	chromatin interactions

Extended variants
information (count: 142 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:142 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189534144	chr6:88284273-88284274	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs368305497	chr6:88284291-88284292	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs78086984	chr6:88284309-88284310	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs7738268	chr6:88284363-88284364	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs374918621	chr6:88284382-88284383	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs562987482	chr6:88284394-88284395	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs533391865	chr6:88284416-88284417	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs551559569	chr6:88284426-88284427	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538640911	chr6:88284587-88284588	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs566680943	chr6:88284625-88284626	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs144768773	chr6:88284634-88284635	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs373936066	chr6:88284638-88284639	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs140903411	chr6:88284668-88284669	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs142052734	chr6:88284680-88284681	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs549621981	chr6:88284690-88284691	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs3934838	chr6:88284699-88284700	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs200254173	chr6:88284743-88284744	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs145906460	chr6:88284766-88284767	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs112069154	chr6:88284790-88284791	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs35422712	chr6:88284791-88284792	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs369439064	chr6:88284792-88284793	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs370135151	chr6:88284794-88284795	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs397814540	chr6:88284795-88284796	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs201045044	chr6:88284798-88284799	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs537274805	chr6:88284848-88284849	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs148240809	chr6:88284884-88284885	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs577808740	chr6:88284937-88284938	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs137938502	chr6:88284943-88284944	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs200726488	chr6:88284944-88284945	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs557871074	chr6:88284947-88284948	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs201110631	chr6:88284987-88284988	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs375949359	chr6:88284989-88284990	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs181840830	chr6:88284995-88284996	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs58168335	chr6:88284996-88284997	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs557143445	chr6:88285068-88285069	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs554019777	chr6:88285070-88285071	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs140315063	chr6:88285137-88285138	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs574089014	chr6:88285172-88285173	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs114612130	chr6:88285173-88285174	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs573986403	chr6:88285244-88285245	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs544587068	chr6:88285313-88285314	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs530630111	chr6:88285365-88285366	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs562692122	chr6:88285436-88285437	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs187289330	chr6:88285437-88285438	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs150369013	chr6:88285454-88285455	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs527862459	chr6:88285535-88285536	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs549444849	chr6:88285538-88285539	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs79375827	chr6:88285550-88285551	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs542666083	chr6:88285586-88285587	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs190934098	chr6:88285612-88285613	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	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
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
Lung adenocarcinoma	21935476	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
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
Myelodysplastic syndrome	18508791	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	21364760	CNVD
Developmental delay	19490664	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:88217800-88295800	Weak transcription	Fetal Brain Male	brain
2	chr6:88227800-88298800	Weak transcription	Esophagus	oesophagus
3	chr6:88228400-88298400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:88228600-88285200	Weak transcription	Spleen	Spleen
5	chr6:88229600-88289000	Weak transcription	Lung	lung
6	chr6:88251000-88291400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:88251200-88284800	Weak transcription	Stomach Mucosa	stomach
8	chr6:88256200-88297600	Weak transcription	Right Ventricle	heart
9	chr6:88256400-88295800	Weak transcription	Gastric	stomach
10	chr6:88263400-88291400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr6:88264600-88291000	Weak transcription	Brain Angular Gyrus	brain
12	chr6:88269600-88291400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr6:88271400-88288200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr6:88271600-88288800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr6:88271600-88288800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr6:88272200-88297000	Weak transcription	Brain Germinal Matrix	brain
17	chr6:88272400-88284800	Weak transcription	Pancreas	Pancrea
18	chr6:88272400-88289200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr6:88272400-88291000	Weak transcription	Fetal Brain Female	brain
20	chr6:88272400-88296000	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr6:88272400-88297400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr6:88272400-88297400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr6:88272600-88291200	Weak transcription	HSMMtube	muscle
24	chr6:88272600-88292000	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr6:88272800-88289800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr6:88272800-88291000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr6:88273000-88292000	Weak transcription	Colonic Mucosa	Colon
28	chr6:88273000-88296000	Weak transcription	Brain Substantia Nigra	brain
29	chr6:88273400-88290200	Weak transcription	HMEC	breast
30	chr6:88273600-88292400	Weak transcription	Hela-S3	cervix
31	chr6:88273600-88298200	Weak transcription	Fetal Kidney	kidney
32	chr6:88274000-88288800	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr6:88274000-88288800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr6:88274000-88290800	Weak transcription	Stomach Smooth Muscle	stomach
35	chr6:88274200-88284600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr6:88274200-88288800	Weak transcription	NHDF-Ad	bronchial
37	chr6:88274200-88295000	Weak transcription	NHLF	lung
38	chr6:88274400-88284400	Weak transcription	Dnd41	blood
39	chr6:88274400-88289000	Weak transcription	Fetal Muscle Leg	muscle
40	chr6:88274400-88292200	Weak transcription	Fetal Lung	lung
41	chr6:88274600-88284800	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr6:88274800-88298800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr6:88276400-88288800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr6:88278200-88286800	Weak transcription	Fetal Stomach	stomach
45	chr6:88278400-88285000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr6:88278600-88289600	Weak transcription	Fetal Muscle Trunk	muscle
47	chr6:88278800-88290200	Weak transcription	Primary B cells from cord blood	blood
48	chr6:88278800-88290600	Weak transcription	HSMM	muscle
49	chr6:88278800-88297400	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr6:88279200-88288800	Weak transcription	Primary monocytes fromperipheralblood	blood

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