Variant report

Variant	nsv5592
Chromosome Location	chr6:166958317-167002951
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:743)
CpG islands
(count:854)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:743 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:167002299-167002766	GM12878	blood:	n/a	n/a
2	ATF2	chr6:167001393-167001971	GM12878	blood:	n/a	n/a
3	ATF3	chr6:167000270-167000513	K562	blood:	n/a	n/a
4	ATF3	chr6:167000246-167000648	GM12878	blood:	n/a	n/a
5	BACH1	chr6:166965198-166965646	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:166960254-166960493	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:166984538-166984622	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr6:166986298-166986452	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr6:166960160-166960446	K562	blood:	n/a	n/a
10	BATF	chr6:167002317-167002739	GM12878	blood:	n/a	chr6:167002529-167002540 chr6:167002530-167002540
11	BATF	chr6:167002365-167002681	GM12878	blood:	n/a	chr6:167002529-167002540 chr6:167002530-167002540
12	BATF	chr6:167002902-167003124	GM12878	blood:	n/a	n/a
13	BCLAF1	chr6:167001220-167001927	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:166982668-166982947	K562	blood:	n/a	chr6:166982816-166982825 chr6:166982815-166982824 chr6:166982814-166982827 chr6:166982810-166982831 chr6:166982816-166982825
15	BHLHE40	chr6:167001637-167001815	GM12878	blood:	n/a	n/a
16	BRCA1	chr6:167002400-167002501	GM12878	blood:	n/a	n/a
17	CBX3	chr6:166970045-166971079	HCT-116	colon:	n/a	n/a
18	CEBPB	chr6:166996726-166996928	K562	blood:	n/a	n/a
19	CEBPB	chr6:166994353-166994587	IMR90	lung:	n/a	n/a
20	CEBPB	chr6:166970161-166970911	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr6:166987131-166987232	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr6:166981890-166982250	K562	blood:	n/a	chr6:166982056-166982067
23	CEBPB	chr6:166981986-166982136	MCF-7	breast:	n/a	chr6:166982056-166982067
24	CEBPB	chr6:166981883-166982162	H1-hESC	embryonic stem cell:	n/a	chr6:166982056-166982067
25	CEBPB	chr6:166985741-166986323	IMR90	lung:	n/a	n/a
26	CEBPB	chr6:166980420-166980981	IMR90	lung:	n/a	chr6:166980822-166980834
27	CEBPB	chr6:166972699-166973031	IMR90	lung:	n/a	n/a
28	CEBPB	chr6:166966953-166967720	IMR90	lung:	n/a	n/a
29	CEBPB	chr6:166981891-166982106	IMR90	lung:	n/a	chr6:166982056-166982067
30	CEBPB	chr6:166981880-166982137	HepG2	liver:	n/a	chr6:166982056-166982067
31	CHD1	chr6:167001325-167001722	GM12878	blood:	n/a	n/a
32	CHD1	chr6:167001924-167002124	GM12878	blood:	n/a	n/a
33	CHD2	chr6:167002247-167002564	GM12878	blood:	n/a	chr6:167002440-167002450
34	CHD2	chr6:167000282-167000605	GM12878	blood:	n/a	n/a
35	CHD2	chr6:167000269-167000599	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr6:167002275-167002388	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr6:167002930-167003130	GM12878	blood:	n/a	n/a
38	CHD2	chr6:167000293-167000620	K562	blood:	n/a	n/a
39	CHD2	chr6:166986159-166986511	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr6:167000296-167000639	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTBP2	chr6:166985986-166986826	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr6:166970341-166970544	NHEK	skin:	n/a	n/a
43	CTCF	chr6:166970300-166970450	HMEC	breast:	n/a	n/a
44	CTCF	chr6:167002880-167003030	GM12865	blood:	n/a	n/a
45	CTCF	chr6:166970600-166970750	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr6:166967480-166967630	AG10803	skin:	n/a	n/a
47	CTCF	chr6:167002900-167003050	AG09319	gingival:	n/a	n/a
48	CTCF	chr6:166999814-166999877	GM10266	blood:	n/a	n/a
49	CTCF	chr6:166970340-166970490	AG04449	skin:	n/a	n/a
50	CTCF	chr6:167002220-167002370	GM12873	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:166984607-166984657	K562	blood:	n/a
2	chr6:166959552-166959602	AG04449	skin:	fetal
3	chr6:166959505-166959555	A549	lung:	n/a
4	chr6:166970727-166970777	A549	lung:	n/a
5	chr6:166959444-166959494	HRCEpiC	kidney:	n/a
6	chr6:166970727-166970777	T-47D	breast:	n/a
7	chr6:166980629-166980679	A549	lung:	n/a
8	chr6:166996837-166996887	A549	lung:	n/a
9	chr6:166984691-166984741	GM12891	blood:	n/a
10	chr6:166959444-166959494	ECC-1	luminal epithelium:	n/a
11	chr6:166970252-166970302	HL-60	blood:	n/a
12	chr6:166967377-166967427	HRE	kidney:	n/a
13	chr6:166984691-166984741	NHDF-neo	bronchial:	n/a
14	chr6:166993541-166993591	SK-N-SH	brain:	n/a
15	chr6:166993541-166993591	HMEC	breast:	n/a
16	chr6:166993541-166993591	ProgFib	skin:	n/a
17	chr6:166984607-166984657	AG04449	skin:	fetal
18	chr6:166959552-166959602	HRE	kidney:	n/a
19	chr6:166970252-166970302	SAEC	small airway:	n/a
20	chr6:166970252-166970302	HMEC	breast:	n/a
21	chr6:166984607-166984657	AG04450	lung:	fetal
22	chr6:166986562-166986612	H1-hESC	embryonic stem cell:	embryo
23	chr6:166970252-166970302	AG09319	gingival:	n/a
24	chr6:166986562-166986612	HEK293	kidney:	embryo
25	chr6:166986562-166986612	ovcar-3	ovarian:	n/a
26	chr6:166970252-166970302	Caco-2	colon:	n/a
27	chr6:166970727-166970777	ovcar-3	ovarian:	n/a
28	chr6:166993541-166993591	AG09309	skin:	n/a
29	chr6:166993541-166993591	AG04449	skin:	fetal
30	chr6:166965512-166965562	HAEpiC	amniotic membrane:	n/a
31	chr6:166970727-166970777	MCF10A-Er-Src	breast:	n/a
32	chr6:166980629-166980679	GM19239	blood:	n/a
33	chr6:166993541-166993591	NT2-D1	testis:	n/a
34	chr6:166970727-166970777	GM06990	blood:	n/a
35	chr6:166959552-166959602	SKMC	muscle:	n/a
36	chr6:166959552-166959602	HEK293	kidney:	embryo
37	chr6:166973498-166973548	MCF10A-Er-Src	breast:	n/a
38	chr6:166980629-166980679	Hepatocyte	liver:	n/a
39	chr6:166984691-166984741	NH-A	brain:	n/a
40	chr6:166967377-166967427	HUVEC	blood vessel:	n/a
41	chr6:166959505-166959555	ProgFib	skin:	n/a
42	chr6:166984607-166984657	Hepatocyte	liver:	n/a
43	chr6:166959444-166959494	SK-N-SH_RA	brain:	n/a
44	chr6:166970252-166970302	HAEpiC	amniotic membrane:	n/a
45	chr6:166996837-166996887	SK-N-SH	brain:	n/a
46	chr6:166959444-166959494	U87	brain:	n/a
47	chr6:166959444-166959494	PrEC	prostate:	n/a
48	chr6:166959444-166959494	AG04450	lung:	fetal
49	chr6:166967377-166967427	GM06990	blood:	n/a
50	chr6:166967377-166967427	HCPEpiC	choroid plexus:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:166982541..166984779-chr6:166986370..166988271,2	K562	blood:
2	chr6:166950092..166951979-chr6:166959386..166961071,2	K562	blood:
3	chr6:166970917..166973753-chr6:166974346..166977201,2	K562	blood:
4	chr6:166959907..166962150-chr6:166966800..166968664,2	K562	blood:
5	chr15:91415474..91417592-chr6:166982215..166983716,2	K562	blood:
6	chr6:166964236..166966556-chr6:166978667..166980857,2	K562	blood:
7	chr6:166982541..166984779-chr6:166986370..166988271,2	K562	blood:
8	chr6:166974194..166976909-chr6:166977553..166980494,3	K562	blood:
9	chr6:166959907..166962150-chr6:166966800..166968664,2	K562	blood:
10	chr6:166974194..166976909-chr6:166977553..166980494,3	K562	blood:
11	chr6:166970917..166973753-chr6:166974346..166977201,2	K562	blood:
12	chr6:166987161..166988700-chr6:166996130..166998368,2	K562	blood:
13	chr6:166975267..166978295-chr6:166978843..166980508,3	K562	blood:
14	chr6:166969437..166971704-chr6:167039008..167042376,3	MCF-7	breast:
15	chr6:166975267..166978295-chr6:166978843..166980508,3	K562	blood:
16	chr6:166964236..166966556-chr6:166978667..166980857,2	K562	blood:
17	chr6:166987161..166988700-chr6:166996130..166998368,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BRP44L-3	chr6:166999612-166999965	NONHSAT116053

No data

Variant related genes	Relation type
RPS6KA2	TF binding region
FAM103A2P	TF binding region
RPS6KA2	CpG island
FAM103A2P	CpG island
ENSG00000140564	chromatin interactions
ENSG00000071242	chromatin interactions

Extended variants
information (count: 1991 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1991 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561581665	chr6:166958320-166958321	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs556738665	chr6:166958340-166958341	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs371864400	chr6:166958344-166958345	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149927512	chr6:166958355-166958356	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565155675	chr6:166958364-166958365	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs3799632	chr6:166958388-166958389	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs144963489	chr6:166958395-166958396	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs140878609	chr6:166958404-166958405	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143172362	chr6:166958528-166958529	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190975436	chr6:166958540-166958541	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182266629	chr6:166958545-166958546	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537767115	chr6:166958553-166958554	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs3778408	chr6:166958556-166958557	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs3778407	chr6:166958562-166958563	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs547360128	chr6:166958569-166958570	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146650027	chr6:166958583-166958584	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192358270	chr6:166958698-166958699	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572173866	chr6:166958714-166958715	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543202329	chr6:166958730-166958731	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184620033	chr6:166958740-166958741	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs576645161	chr6:166958749-166958750	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs117918795	chr6:166958850-166958851	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565604478	chr6:166958923-166958924	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs532785190	chr6:166958926-166958927	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140231572	chr6:166958939-166958940	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371224207	chr6:166958940-166958941	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs78098725	chr6:166958943-166958944	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs79910407	chr6:166958987-166958988	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79236912	chr6:166959006-166959007	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs374982054	chr6:166959053-166959054	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs537156470	chr6:166959055-166959056	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs370812966	chr6:166959063-166959064	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs143839232	chr6:166959210-166959211	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs35494279	chr6:166959214-166959215	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs117079031	chr6:166959226-166959227	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs151111891	chr6:166959249-166959250	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs573401840	chr6:166959265-166959266	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs566968176	chr6:166959267-166959268	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs188510318	chr6:166959321-166959322	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs193065230	chr6:166959327-166959328	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs553811662	chr6:166959348-166959349	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs184956101	chr6:166959364-166959365	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs552882085	chr6:166959404-166959405	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs35553191	chr6:166959408-166959409	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs189804049	chr6:166959441-166959442	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554675183	chr6:166959447-166959448	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs576543247	chr6:166959457-166959458	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs112362427	chr6:166959487-166959488	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs577492506	chr6:166959506-166959507	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs141058531	chr6:166959542-166959543	Weak transcription Strong transcription Genic enhancers Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
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
Melanoma	18172304	CNVD
Cancer	21637783	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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	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	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1420 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166935400-166966400	Weak transcription	NH-A	brain
2	chr6:166944600-166958600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:166947400-166969400	Weak transcription	Aorta	Aorta
4	chr6:166949800-166964800	Weak transcription	Fetal Intestine Small	intestine
5	chr6:166950200-166960600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr6:166950800-166958600	Weak transcription	NHDF-Ad	bronchial
7	chr6:166951800-166959000	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr6:166952400-166969000	Weak transcription	Psoas Muscle	Psoas
9	chr6:166953000-166959000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr6:166953400-166964600	Weak transcription	Primary T cells from cord blood	blood
11	chr6:166953400-166967400	Weak transcription	Fetal Lung	lung
12	chr6:166954000-166959000	Enhancers	Fetal Muscle Leg	muscle
13	chr6:166954200-166965000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:166954400-166958800	Weak transcription	Fetal Brain Female	brain
15	chr6:166954400-166962000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:166954600-166958400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:166954600-166959000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr6:166954600-166959600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr6:166954800-166965000	Weak transcription	Brain Cingulate Gyrus	brain
20	chr6:166955000-166959200	Weak transcription	Brain Angular Gyrus	brain
21	chr6:166955000-166959400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr6:166955000-166967000	Weak transcription	Brain Substantia Nigra	brain
23	chr6:166955200-166962400	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr6:166955200-166970600	Weak transcription	Pancreas	Pancrea
25	chr6:166955200-166970600	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr6:166955400-166958400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr6:166955800-166959200	Weak transcription	Brain Germinal Matrix	brain
28	chr6:166956000-166960200	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr6:166956000-166962400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr6:166956000-166964000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr6:166956000-166966400	Weak transcription	Adipose Nuclei	Adipose
32	chr6:166956000-166966600	Weak transcription	Stomach Smooth Muscle	stomach
33	chr6:166956000-166967800	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr6:166956000-166969000	Weak transcription	Gastric	stomach
35	chr6:166956200-166967400	Weak transcription	Ovary	ovary
36	chr6:166956400-166959600	Weak transcription	Osteobl	bone
37	chr6:166956400-166966400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr6:166956600-166966400	Weak transcription	HMEC	breast
39	chr6:166956800-166966200	Weak transcription	HSMM	muscle
40	chr6:166956800-166966600	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr6:166957000-166958400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr6:166957000-166959800	Strong transcription	Muscle Satellite Cultured Cells	--
43	chr6:166957000-166962400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr6:166957000-166967200	Weak transcription	HUVEC	blood vessel
45	chr6:166957000-166967400	Weak transcription	Right Atrium	heart
46	chr6:166957200-166959800	Enhancers	Fetal Brain Male	brain
47	chr6:166957200-166961400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr6:166957200-166968000	Weak transcription	Spleen	Spleen
49	chr6:166957400-166959200	Strong transcription	Lung	lung
50	chr6:166957400-166961200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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