Variant report

Variant	esv3376653
Chromosome Location	chr6:166783590-166798116
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	ARID3A	chr6:166795144-166795477	K562	blood:	n/a	n/a
2	ARID3A	chr6:166796328-166797478	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:166796573-166796755	K562	blood:	n/a	n/a
4	ARID3A	chr6:166795192-166795590	HepG2	liver:	n/a	n/a
5	ATF2	chr6:166796376-166796843	GM12878	blood:	n/a	n/a
6	ATF2	chr6:166795205-166795713	GM12878	blood:	n/a	n/a
7	ATF2	chr6:166796996-166797487	GM12878	blood:	n/a	n/a
8	ATF3	chr6:166796334-166796977	HepG2	liver:	n/a	chr6:166796817-166796825 chr6:166796479-166796499 chr6:166796616-166796625
9	ATF3	chr6:166796333-166796743	H1-hESC	embryonic stem cell:	n/a	chr6:166796479-166796499 chr6:166796616-166796625
10	ATF3	chr6:166796271-166797080	K562	blood:	n/a	chr6:166796817-166796825 chr6:166796479-166796499 chr6:166796616-166796625
11	ATF3	chr6:166796274-166796847	GM12878	blood:	n/a	chr6:166796817-166796825 chr6:166796479-166796499 chr6:166796616-166796625
12	ATF3	chr6:166795332-166795630	K562	blood:	n/a	chr6:166795452-166795461
13	BACH1	chr6:166796971-166797154	K562	blood:	n/a	n/a
14	BACH1	chr6:166795411-166795584	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr6:166796586-166797268	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr6:166796390-166797220	GM12878	blood:	n/a	chr6:166796612-166796625 chr6:166796995-166797008 chr6:166796621-166796634
17	BCLAF1	chr6:166796980-166797517	GM12878	blood:	n/a	chr6:166796995-166797008
18	BCLAF1	chr6:166795172-166795686	GM12878	blood:	n/a	chr6:166795474-166795487
19	BCLAF1	chr6:166796099-166796903	GM12878	blood:	n/a	chr6:166796612-166796625 chr6:166796621-166796634
20	BCLAF1	chr6:166795168-166795681	GM12878	blood:	n/a	chr6:166795474-166795487
21	BHLHE40	chr6:166795294-166795735	HepG2	liver:	n/a	n/a
22	BHLHE40	chr6:166795239-166795687	GM12878	blood:	n/a	n/a
23	BHLHE40	chr6:166796185-166797343	HepG2	liver:	n/a	chr6:166796445-166796461 chr6:166796987-166797003 chr6:166796619-166796635
24	BHLHE40	chr6:166795026-166795846	K562	blood:	n/a	n/a
25	BHLHE40	chr6:166796246-166797436	GM12878	blood:	n/a	chr6:166796445-166796461 chr6:166796987-166797003 chr6:166796619-166796635
26	BHLHE40	chr6:166796078-166797514	K562	blood:	n/a	chr6:166796445-166796461 chr6:166796987-166797003 chr6:166796619-166796635
27	BRCA1	chr6:166795395-166795778	HepG2	liver:	n/a	n/a
28	BRCA1	chr6:166796652-166796762	HepG2	liver:	n/a	n/a
29	BRCA1	chr6:166796261-166796416	HepG2	liver:	n/a	n/a
30	CBX3	chr6:166795182-166795715	K562	blood:	n/a	n/a
31	CBX3	chr6:166796163-166797683	K562	blood:	n/a	n/a
32	CCNT2	chr6:166795256-166797209	K562	blood:	n/a	chr6:166796616-166796625 chr6:166795492-166795501
33	CEBPB	chr6:166797513-166797711	IMR90	lung:	n/a	chr6:166797642-166797653
34	CEBPB	chr6:166797474-166797819	K562	blood:	n/a	chr6:166797642-166797653
35	CEBPB	chr6:166797188-166797727	Hela-S3	cervix:	n/a	chr6:166797642-166797653
36	CEBPB	chr6:166797504-166797721	K562	blood:	n/a	chr6:166797642-166797653
37	CEBPB	chr6:166796543-166796821	HepG2	liver:	n/a	n/a
38	CEBPB	chr6:166796251-166796923	Hela-S3	cervix:	n/a	chr6:166796419-166796427
39	CEBPB	chr6:166795361-166795561	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:166797516-166797728	HepG2	liver:	n/a	chr6:166797642-166797653
41	CEBPB	chr6:166797481-166797711	H1-hESC	embryonic stem cell:	n/a	chr6:166797642-166797653
42	CEBPB	chr6:166785292-166785497	HepG2	liver:	n/a	chr6:166785372-166785383 chr6:166785484-166785497
43	CEBPB	chr6:166796347-166796891	K562	blood:	n/a	chr6:166796419-166796427
44	CEBPB	chr6:166788603-166788854	K562	blood:	n/a	n/a
45	CEBPB	chr6:166788583-166788876	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr6:166797528-166797658	A549	lung:	n/a	chr6:166797642-166797653
47	CEBPB	chr6:166794880-166795644	GM12878	blood:	n/a	n/a
48	CEBPB	chr6:166797499-166797808	HepG2	liver:	n/a	chr6:166797642-166797653
49	CEBPB	chr6:166797537-166797739	HepG2	liver:	n/a	chr6:166797642-166797653
50	CEBPD	chr6:166796204-166796905	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:166797125-166797175	K562	blood:	n/a
2	chr6:166797258-166797308	MCF10A-Er-Src	breast:	n/a
3	chr6:166796744-166796794	SAEC	small airway:	n/a
4	chr6:166797125-166797175	K562	blood:	n/a
5	chr6:166797258-166797308	MCF10A-Er-Src	breast:	n/a
6	chr6:166796744-166796794	SAEC	small airway:	n/a
7	chr6:166796744-166796794	HCT-116	colon:	n/a
8	chr6:166796579-166796629	BE2_C	brain:	n/a
9	chr6:166797178-166797228	U87	brain:	n/a
10	chr6:166797125-166797175	HEK293	kidney:	embryo
11	chr6:166796588-166796638	AG04450	lung:	fetal
12	chr6:166797128-166797178	MCF-7	breast:	n/a
13	chr6:166796458-166796508	NB4	blood:	n/a
14	chr6:166796284-166796334	HRPEpiC	eye:	n/a
15	chr6:166796700-166796750	K562	blood:	n/a
16	chr6:166793890-166793940	Jurkat	blood:	n/a
17	chr6:166797367-166797417	HUVEC	blood vessel:	n/a
18	chr6:166796759-166796809	K562	blood:	n/a
19	chr6:166796284-166796334	A549	lung:	n/a
20	chr6:166796752-166796802	U87	brain:	n/a
21	chr6:166796752-166796802	GM12878	blood:	n/a
22	chr6:166793890-166793940	HepG2	liver:	n/a
23	chr6:166796752-166796802	GM19239	blood:	n/a
24	chr6:166796756-166796806	PrEC	prostate:	n/a
25	chr6:166796284-166796334	HEK293	kidney:	embryo
26	chr6:166797224-166797274	HCT-116	colon:	n/a
27	chr6:166797267-166797317	HPAEpiC	pulmonary alveolar:	n/a
28	chr6:166796984-166797034	HCPEpiC	choroid plexus:	n/a
29	chr6:166797417-166797467	HCT-116	colon:	n/a
30	chr6:166796744-166796794	HCF	heart:	n/a
31	chr6:166797125-166797175	MCF10A-Er-Src	breast:	n/a
32	chr6:166797224-166797274	HMEC	breast:	n/a
33	chr6:166795816-166795866	Hela-S3	cervix:	n/a
34	chr6:166797367-166797417	Caco-2	colon:	n/a
35	chr6:166796756-166796806	K562	blood:	n/a
36	chr6:166797738-166797788	HepG2	liver:	n/a
37	chr6:166796579-166796629	MCF-7	breast:	n/a
38	chr6:166797128-166797178	HUVEC	blood vessel:	n/a
39	chr6:166796588-166796638	IMR90	lung:	fetal
40	chr6:166796588-166796638	AG09319	gingival:	n/a
41	chr6:166797417-166797467	GM12878	blood:	n/a
42	chr6:166797125-166797175	Hepatocyte	liver:	n/a
43	chr6:166797260-166797310	BJ	skin:	n/a
44	chr6:166796706-166796756	HRE	kidney:	n/a
45	chr6:166797367-166797417	HRE	kidney:	n/a
46	chr6:166796759-166796809	HepG2	liver:	n/a
47	chr6:166797120-166797170	HAEpiC	amniotic membrane:	n/a
48	chr6:166797120-166797170	SKMC	muscle:	n/a
49	chr6:166796984-166797034	Hepatocyte	liver:	n/a
50	chr6:166791393-166791443	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:166745010..166748939-chr6:166789384..166792180,3	K562	blood:
2	chr6:166755930..166757619-chr6:166781019..166784045,3	MCF-7	breast:
3	chr6:166751804..166757558-chr6:166793969..166799153,5	K562	blood:
4	chr6:166796680..166799689-chr6:166808021..166810118,3	K562	blood:
5	chr6:166744561..166747704-chr6:166784212..166786864,3	K562	blood:
6	chr6:166383156..166385383-chr6:166793262..166795662,2	K562	blood:
7	chr6:166743853..166744743-chr6:166794927..166795865,3	K562	blood:
8	chr6:166744077..166744772-chr6:166795075..166795860,2	MCF-7	breast:
9	chr6:166726357..166727438-chr6:166794885..166795636,3	K562	blood:
10	chr6:166740985..166743870-chr6:166796738..166798607,2	MCF-7	breast:
11	chr6:166743072..166748840-chr6:166793771..166798653,8	K562	blood:
12	chr6:166755781..166758045-chr6:166792453..166794502,3	K562	blood:
13	chr6:166754173..166757774-chr6:166795355..166798060,3	MCF-7	breast:
14	chr6:166750705..166753304-chr6:166793796..166795469,2	K562	blood:
15	chr6:166747123..166748829-chr6:166792076..166793890,2	K562	blood:
16	chr6:166689127..166689809-chr6:166795241..166795961,2	K562	blood:
17	chr6:166726860..166727411-chr6:166795185..166795905,2	MCF-7	breast:
18	chr6:166786321..166788886-chr6:166835816..166837569,2	K562	blood:
19	chr6:166753320..166757958-chr6:166794622..166799153,8	K562	blood:
20	chr6:166722651..166724604-chr6:166784233..166785851,2	K562	blood:
21	chr6:166746293..166747904-chr6:166796894..166799021,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGFR1OP-2	chr6:166796677-166798312	ENSG00000261420.1
2	lnc-FGFR1OP-2	chr6:166796964-166802453	NONHSAT116046

Variant related genes	Relation type
ENSG00000261420	TF binding region
MPC1	TF binding region
ENSG00000261420	CpG island
MPC1	CpG island
ENSG00000071242	chromatin interactions
ENSG00000198818	chromatin interactions
ENSG00000233231	chromatin interactions

Extended variants
information (count: 530 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543032256	chr6:166783599-166783600	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs115309123	chr6:166783636-166783637	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs376361823	chr6:166783670-166783671	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs138551064	chr6:166783707-166783708	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs199844593	chr6:166783729-166783730	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs369678367	chr6:166783730-166783731	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs565185010	chr6:166783738-166783739	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs375114109	chr6:166783763-166783764	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs369476309	chr6:166783777-166783778	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs149266533	chr6:166783833-166783834	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs188329884	chr6:166783836-166783837	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs527374466	chr6:166783854-166783855	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs548997671	chr6:166783872-166783873	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs77687797	chr6:166783880-166783881	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs542321228	chr6:166783919-166783920	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs550101499	chr6:166784014-166784015	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs115994102	chr6:166784015-166784016	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs538854169	chr6:166784080-166784081	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561141962	chr6:166784091-166784092	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6928141	chr6:166784136-166784137	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs139064675	chr6:166784146-166784147	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554989055	chr6:166784148-166784149	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs111238246	chr6:166784152-166784153	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs115513136	chr6:166784162-166784163	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs543366775	chr6:166784163-166784164	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs531586940	chr6:166784217-166784218	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs558834637	chr6:166784324-166784325	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs542846477	chr6:166784373-166784374	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs543635275	chr6:166784400-166784401	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs541637912	chr6:166784454-166784455	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs75107282	chr6:166784460-166784461	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs77577192	chr6:166784461-166784462	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs192925112	chr6:166784510-166784511	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559675396	chr6:166784511-166784512	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs6905635	chr6:166784543-166784544	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs114807663	chr6:166784550-166784551	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs560988228	chr6:166784571-166784572	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs531339525	chr6:166784580-166784581	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs549761677	chr6:166784597-166784598	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs143076360	chr6:166784639-166784640	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs532428122	chr6:166784678-166784679	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs12110519	chr6:166784856-166784857	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs184644463	chr6:166784862-166784863	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs536800044	chr6:166784919-166784920	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs548396491	chr6:166785085-166785086	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs146140837	chr6:166785103-166785104	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs537063216	chr6:166785111-166785112	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs565214171	chr6:166785163-166785164	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs577150973	chr6:166785209-166785210	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs534996996	chr6:166785210-166785211	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:599 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166773200-166794600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr6:166773400-166790000	Weak transcription	Fetal Brain Male	brain
3	chr6:166774400-166790600	Weak transcription	Psoas Muscle	Psoas
4	chr6:166774800-166784000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr6:166774800-166787200	Weak transcription	Esophagus	oesophagus
6	chr6:166774800-166795000	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr6:166775000-166793800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr6:166775200-166788400	Weak transcription	HMEC	breast
9	chr6:166775400-166785400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr6:166775400-166787000	Weak transcription	Fetal Kidney	kidney
11	chr6:166775800-166794800	Weak transcription	Primary hematopoietic stem cells	blood
12	chr6:166776200-166784600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
13	chr6:166777400-166795400	Weak transcription	Gastric	stomach
14	chr6:166777800-166788400	Weak transcription	NHEK	skin
15	chr6:166778200-166790600	Weak transcription	Right Ventricle	heart
16	chr6:166778200-166790800	Weak transcription	Fetal Brain Female	brain
17	chr6:166778200-166792800	Weak transcription	Aorta	Aorta
18	chr6:166778200-166794600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr6:166778200-166795000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr6:166778400-166784000	Weak transcription	Spleen	Spleen
21	chr6:166778400-166786600	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr6:166778400-166790600	Weak transcription	Pancreas	Pancrea
23	chr6:166778400-166792600	Weak transcription	Lung	lung
24	chr6:166778400-166794600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr6:166778400-166794600	Weak transcription	Fetal Intestine Small	intestine
26	chr6:166778400-166794600	Weak transcription	Stomach Smooth Muscle	stomach
27	chr6:166778400-166794800	Weak transcription	Fetal Stomach	stomach
28	chr6:166778400-166795000	Weak transcription	Colonic Mucosa	Colon
29	chr6:166778600-166794600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr6:166778600-166794600	Weak transcription	Colon Smooth Muscle	Colon
31	chr6:166778800-166785000	Weak transcription	Placenta	Placenta
32	chr6:166779200-166788400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr6:166779200-166793400	Weak transcription	K562	blood
34	chr6:166779400-166794600	Weak transcription	HSMM	muscle
35	chr6:166779400-166794800	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr6:166779600-166785400	Weak transcription	Fetal Muscle Leg	muscle
37	chr6:166779600-166785800	Weak transcription	Primary B cells from cord blood	blood
38	chr6:166779600-166789200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr6:166779600-166790600	Weak transcription	Left Ventricle	heart
40	chr6:166779600-166791400	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr6:166779600-166791800	Weak transcription	Brain Germinal Matrix	brain
42	chr6:166779600-166792800	Weak transcription	Ovary	ovary
43	chr6:166779600-166794600	Weak transcription	Brain Angular Gyrus	brain
44	chr6:166779600-166794600	Weak transcription	Brain Cingulate Gyrus	brain
45	chr6:166779600-166794600	Weak transcription	Brain Substantia Nigra	brain
46	chr6:166779600-166794600	Weak transcription	Thymus	Thymus
47	chr6:166779600-166794800	Weak transcription	Fetal Intestine Large	intestine
48	chr6:166779800-166786000	Weak transcription	Fetal Muscle Trunk	muscle
49	chr6:166779800-166793200	Weak transcription	Brain Anterior Caudate	brain
50	chr6:166779800-166794400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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