Variant report

Variant	nsv969374
Chromosome Location	chr6:29992833-30001543
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:35)
CpG islands
(count:1039)
Chromatin interactive
region (count:3)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:35 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:30001182-30001561	HepG2	liver:	n/a	chr6:30001416-30001427 chr6:30001275-30001288 chr6:30001416-30001427
2	CEBPB	chr6:29995168-29995360	K562	blood:	n/a	n/a
3	CEBPB	chr6:30001216-30001547	A549	lung:	n/a	chr6:30001416-30001427 chr6:30001275-30001288 chr6:30001416-30001427
4	CEBPB	chr6:30001302-30001520	Hela-S3	cervix:	n/a	chr6:30001416-30001427 chr6:30001416-30001427
5	CEBPB	chr6:30001177-30001584	IMR90	lung:	n/a	chr6:30001416-30001427 chr6:30001275-30001288 chr6:30001416-30001427
6	CTCF	chr6:29994335-29994371	GM13976	blood:	n/a	n/a
7	E2F4	chr6:30001355-30001410	MCF10A-Er-Src	breast:	n/a	n/a
8	FOS	chr6:30001326-30001526	MCF10A-Er-Src	breast:	n/a	chr6:30001430-30001438
9	FOS	chr6:30001312-30001598	MCF10A-Er-Src	breast:	n/a	chr6:30001430-30001438
10	FOS	chr6:30001209-30001539	MCF10A-Er-Src	breast:	n/a	chr6:30001430-30001438
11	FOS	chr6:30001216-30001539	MCF10A-Er-Src	breast:	n/a	chr6:30001430-30001438
12	FOSL2	chr6:30001203-30001607	HepG2	liver:	n/a	chr6:30001429-30001440 chr6:30001430-30001438
13	FOSL2	chr6:30001224-30001566	HepG2	liver:	n/a	chr6:30001429-30001440 chr6:30001430-30001438
14	FOXA1	chr6:30001287-30001680	HepG2	liver:	n/a	n/a
15	FOXA2	chr6:30001346-30001587	A549	lung:	n/a	n/a
16	FOXA2	chr6:30001334-30001561	HepG2	liver:	n/a	n/a
17	FOXA2	chr6:30001359-30001623	A549	lung:	n/a	n/a
18	GATA3	chr6:29996016-29996219	SH-SY5Y	brain:	n/a	n/a
19	JUND	chr6:30001346-30001512	HepG2	liver:	n/a	chr6:30001430-30001438
20	JUND	chr6:30001279-30001576	HepG2	liver:	n/a	chr6:30001430-30001438
21	MYC	chr6:30001340-30001528	NB4	blood:	n/a	chr6:30001430-30001439
22	MYC	chr6:30001221-30001408	MCF10A-Er-Src	breast:	n/a	n/a
23	POLR2A	chr6:30000880-30000909	Gliobla	brain:	n/a	n/a
24	POLR2A	chr6:30000779-30000850	Gliobla	brain:	n/a	n/a
25	POLR2A	chr6:30000928-30000980	Gliobla	brain:	n/a	n/a
26	POLR2A	chr6:29998698-29998712	MCF10A-Er-Src	breast:	n/a	n/a
27	POLR2A	chr6:30001307-30001605	GM12878	blood:	n/a	n/a
28	SPI1	chr6:29997356-29997760	HL-60	blood:	n/a	n/a
29	SPI1	chr6:29997387-29997680	HL-60	blood:	n/a	n/a
30	SPI1	chr6:29997441-29997658	GM12891	blood:	n/a	n/a
31	SPI1	chr6:29997429-29997654	GM12878	blood:	n/a	n/a
32	SPI1	chr6:29997463-29997726	GM12891	blood:	n/a	n/a
33	SPI1	chr6:29997431-29997637	K562	blood:	n/a	n/a
34	SPI1	chr6:29997449-29997636	K562	blood:	n/a	n/a
35	STAT3	chr6:30001342-30001375	MCF10A-Er-Src	breast:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29999730-29999780	T-47D	breast:	n/a
2	chr6:29996229-29996279	HRE	kidney:	n/a
3	chr6:29999730-29999780	T-47D	breast:	n/a
4	chr6:29996229-29996279	HRE	kidney:	n/a
5	chr6:30000621-30000671	HCPEpiC	choroid plexus:	n/a
6	chr6:30001368-30001418	HepG2	liver:	n/a
7	chr6:30000200-30000250	Jurkat	blood:	n/a
8	chr6:30000566-30000616	GM12891	blood:	n/a
9	chr6:30000621-30000671	U87	brain:	n/a
10	chr6:29995826-29995876	SK-N-SH	brain:	n/a
11	chr6:30001368-30001418	AoSMC	blood vessel:	n/a
12	chr6:29999708-29999758	GM12892	blood:	n/a
13	chr6:29999730-29999780	NB4	blood:	n/a
14	chr6:29996229-29996279	SK-N-SH_RA	brain:	n/a
15	chr6:29996229-29996279	HPAEpiC	pulmonary alveolar:	n/a
16	chr6:30000566-30000616	AG09309	skin:	n/a
17	chr6:29999730-29999780	SKMC	muscle:	n/a
18	chr6:29995441-29995491	HepG2	liver:	n/a
19	chr6:29999887-29999937	HepG2	liver:	n/a
20	chr6:29999708-29999758	NHBE	bronchial:	n/a
21	chr6:29996229-29996279	HCF	heart:	n/a
22	chr6:29995826-29995876	AoSMC	blood vessel:	n/a
23	chr6:30001368-30001418	AG10803	skin:	n/a
24	chr6:29999852-29999902	SK-N-MC	brain:	n/a
25	chr6:29999852-29999902	HCT-116	colon:	n/a
26	chr6:30000786-30000836	HMEC	breast:	n/a
27	chr6:29995826-29995876	NT2-D1	testis:	n/a
28	chr6:29999887-29999937	HCT-116	colon:	n/a
29	chr6:29995441-29995491	PFSK-1	brain:	n/a
30	chr6:29999908-29999958	SK-N-SH	brain:	n/a
31	chr6:30000621-30000671	GM12891	blood:	n/a
32	chr6:29999852-29999902	SK-N-SH	brain:	n/a
33	chr6:29999730-29999780	NH-A	brain:	n/a
34	chr6:30000797-30000847	HL-60	blood:	n/a
35	chr6:29999615-29999665	GM06990	blood:	n/a
36	chr6:29995826-29995876	GM19239	blood:	n/a
37	chr6:30000786-30000836	MCF10A-Er-Src	breast:	n/a
38	chr6:29999908-29999958	NHBE	bronchial:	n/a
39	chr6:29995441-29995491	SAEC	small airway:	n/a
40	chr6:30000566-30000616	HL-60	blood:	n/a
41	chr6:29995441-29995491	AG09319	gingival:	n/a
42	chr6:29996229-29996279	NB4	blood:	n/a
43	chr6:29996229-29996279	MCF-7	breast:	n/a
44	chr6:30000786-30000836	HUVEC	blood vessel:	n/a
45	chr6:30000786-30000836	NHDF-neo	bronchial:	n/a
46	chr6:29995441-29995491	HPAEpiC	pulmonary alveolar:	n/a
47	chr6:29999852-29999902	NHDF-neo	bronchial:	n/a
48	chr6:30000187-30000237	HCF	heart:	n/a
49	chr6:29999852-29999902	BJ	skin:	n/a
50	chr6:29999730-29999780	HL-60	blood:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:29991364..29993183-chr6:30027943..30031048,3	K562	blood:
2	chr6:29992994..29995481-chr6:29997109..29999804,2	K562	blood:
3	chr6:29999651..30002590-chr6:30017205..30019223,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNRD1-3	chr6:29999490-29999925	NONHSAT108589
2	lnc-ZNRD1-3	chr6:30000233-30000780	NONHSAT108589

No data

Variant related genes	Relation type
ETF1P1	TF binding region
ETF1P1	CpG island
ENSG00000232757	chromatin interactions
ENSG00000204623	chromatin interactions
ENSG00000066379	chromatin interactions

Extended variants
information (count: 347 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549445875	chr6:29992880-29992881	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs372017344	chr6:29992952-29992953	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs9261158	chr6:29992953-29992954	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs9261159	chr6:29992973-29992974	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs371514932	chr6:29992978-29992979	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs548519923	chr6:29992989-29992990	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs376520380	chr6:29993023-29993024	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs368920931	chr6:29993042-29993043	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs539227200	chr6:29993069-29993070	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs147424450	chr6:29993070-29993071	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs9261160	chr6:29993086-29993087	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs542245595	chr6:29993128-29993129	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs377465368	chr6:29993200-29993201	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs188012048	chr6:29993270-29993271	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs369621867	chr6:29993361-29993362	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs139785223	chr6:29993375-29993376	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs62388750	chr6:29993421-29993422	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs543354293	chr6:29993484-29993485	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs369743578	chr6:29993519-29993520	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs1245503	chr6:29993530-29993531	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs563299952	chr6:29993562-29993563	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs529192215	chr6:29993649-29993650	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs191251697	chr6:29993742-29993743	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs377442316	chr6:29993801-29993802	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs144249387	chr6:29993850-29993851	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs369793118	chr6:29993970-29993971	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs3121596	chr6:29994021-29994022	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs530480547	chr6:29994042-29994043	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs575456404	chr6:29994045-29994046	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs200739722	chr6:29994051-29994052	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs202183038	chr6:29994065-29994066	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs550351505	chr6:29994071-29994072	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs4644107	chr6:29994092-29994093	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs184878516	chr6:29994116-29994117	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs9261162	chr6:29994134-29994135	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs189154064	chr6:29994169-29994170	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs35763150	chr6:29994171-29994172	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs150853727	chr6:29994190-29994191	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
39	rs139653663	chr6:29994193-29994194	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs376523016	chr6:29994261-29994262	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs9261163	chr6:29994273-29994274	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs374328953	chr6:29994274-29994275	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs557143587	chr6:29994292-29994293	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs201172145	chr6:29994294-29994295	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs9280850	chr6:29994302-29994303	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs368644728	chr6:29994305-29994306	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs542942621	chr6:29994336-29994337	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs4422656	chr6:29994338-29994339	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs77541578	chr6:29994381-29994382	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs114489154	chr6:29994419-29994420	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

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	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29974800-30002400	Weak transcription	Dnd41	blood
2	chr6:29975200-30027800	Weak transcription	Aorta	Aorta
3	chr6:29975600-30027800	Weak transcription	Right Ventricle	heart
4	chr6:29975800-30027800	Weak transcription	Gastric	stomach
5	chr6:29976200-30001800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:29976600-30023000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr6:29976800-30000800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr6:29977000-30002000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr6:29977000-30002000	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr6:29977200-30000400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr6:29977200-30003800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr6:29977200-30024600	Weak transcription	Brain Anterior Caudate	brain
13	chr6:29977200-30027600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr6:29977200-30027800	Weak transcription	Fetal Intestine Small	intestine
15	chr6:29979000-30027600	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr6:29979400-30024600	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr6:29979600-30022800	Weak transcription	Ovary	ovary
18	chr6:29979800-30027800	Weak transcription	Pancreas	Pancrea
19	chr6:29980200-30012000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr6:29981200-30023000	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr6:29981800-30010600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr6:29982800-30009800	Weak transcription	Psoas Muscle	Psoas
23	chr6:29982800-30022800	Weak transcription	Fetal Muscle Leg	muscle
24	chr6:29983400-30012400	Weak transcription	NHEK	skin
25	chr6:29984600-30023400	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr6:29985000-30024600	Weak transcription	Brain Angular Gyrus	brain
27	chr6:29985400-30008200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr6:29987400-30001600	Weak transcription	Primary B cells from cord blood	blood
29	chr6:29987800-29996000	Weak transcription	Lung	lung
30	chr6:29987800-30010600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr6:29987800-30024800	Weak transcription	Fetal Intestine Large	intestine
32	chr6:29988000-30010400	Weak transcription	Fetal Muscle Trunk	muscle
33	chr6:29988200-30000600	Weak transcription	Brain Substantia Nigra	brain
34	chr6:29988200-30000800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr6:29988200-30009800	Weak transcription	HepG2	liver
36	chr6:29988200-30022800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr6:29988200-30027800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr6:29988200-30027800	Weak transcription	Esophagus	oesophagus
39	chr6:29988400-30001200	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr6:29988400-30006200	Weak transcription	Brain Cingulate Gyrus	brain
41	chr6:29988400-30021600	Weak transcription	Primary hematopoietic stem cells	blood
42	chr6:29988400-30023400	Weak transcription	Adipose Nuclei	Adipose
43	chr6:29988400-30027800	Weak transcription	Thymus	Thymus
44	chr6:29988600-30003800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr6:29988600-30009800	Weak transcription	Left Ventricle	heart
46	chr6:29988600-30022200	Weak transcription	Stomach Smooth Muscle	stomach
47	chr6:29988600-30027400	Weak transcription	Duodenum Mucosa	Duodenum
48	chr6:29988800-29997600	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr6:29988800-30001800	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr6:29988800-30001800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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