Variant report

Variant	nsv10379
Chromosome Location	chr3:195166939-195170590
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:50)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:195169250-195169466	K562	blood:	n/a	n/a
2	ARID3A	chr3:195167967-195168193	HepG2	liver:	n/a	n/a
3	CEBPB	chr3:195167864-195167870	HepG2	liver:	n/a	n/a
4	CEBPB	chr3:195169232-195169471	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr3:195169210-195169484	K562	blood:	n/a	n/a
6	CEBPB	chr3:195169256-195169496	K562	blood:	n/a	n/a
7	CEBPB	chr3:195169244-195169567	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr3:195169220-195169563	K562	blood:	n/a	n/a
9	CTCF	chr3:195167040-195167190	GM12866	blood:	n/a	n/a
10	CTCF	chr3:195167636-195167762	GM10248	blood:	n/a	n/a
11	E2F6	chr3:195167173-195167519	H1-hESC	embryonic stem cell:	n/a	n/a
12	ELK1	chr3:195170060-195170190	GM12878	blood:	n/a	n/a
13	EP300	chr3:195169092-195169599	K562	blood:	n/a	chr3:195169198-195169212
14	FOSL2	chr3:195167954-195168310	HepG2	liver:	n/a	chr3:195168141-195168152 chr3:195168143-195168154 chr3:195168142-195168150
15	GTF2B	chr3:195166829-195167115	K562	blood:	n/a	n/a
16	GTF2F1	chr3:195166946-195167062	H1-hESC	embryonic stem cell:	n/a	n/a
17	HEY1	chr3:195166406-195167076	K562	blood:	n/a	n/a
18	HEY1	chr3:195166606-195167079	K562	blood:	n/a	n/a
19	JUN	chr3:195168808-195169497	K562	blood:	n/a	chr3:195169009-195169018
20	JUND	chr3:195169126-195169590	K562	blood:	n/a	n/a
21	MAFK	chr3:195166779-195166982	IMR90	lung:	n/a	n/a
22	MAX	chr3:195167142-195167463	H1-hESC	embryonic stem cell:	n/a	chr3:195167311-195167321
23	MAX	chr3:195167106-195167522	H1-hESC	embryonic stem cell:	n/a	chr3:195167311-195167321
24	MAX	chr3:195167189-195167508	H1-hESC	embryonic stem cell:	n/a	chr3:195167311-195167321
25	MAX	chr3:195167146-195167264	HepG2	liver:	n/a	n/a
26	MAX	chr3:195167172-195167408	NB4	blood:	n/a	chr3:195167311-195167321
27	MYC	chr3:195167240-195167327	K562	blood:	n/a	chr3:195167311-195167321
28	MYC	chr3:195169047-195169478	K562	blood:	n/a	n/a
29	PML	chr3:195166484-195167117	K562	blood:	n/a	n/a
30	PML	chr3:195166400-195167049	K562	blood:	n/a	n/a
31	POLR2A	chr3:195166727-195166991	GM12891	blood:	n/a	n/a
32	POLR2A	chr3:195166473-195167089	K562	blood:	n/a	n/a
33	POLR2A	chr3:195166766-195166993	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr3:195166417-195166992	K562	blood:	n/a	n/a
35	POLR2A	chr3:195166611-195167013	GM12891	blood:	n/a	n/a
36	POLR2A	chr3:195168355-195168518	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr3:195166558-195167040	K562	blood:	n/a	n/a
38	POLR2A	chr3:195168347-195168493	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr3:195166757-195166996	H1-hESC	embryonic stem cell:	n/a	n/a
40	RCOR1	chr3:195166815-195166973	K562	blood:	n/a	n/a
41	RCOR1	chr3:195169219-195169598	K562	blood:	n/a	n/a
42	RCOR1	chr3:195169964-195169976	HepG2	liver:	n/a	n/a
43	REST	chr3:195168342-195168505	H1-hESC	embryonic stem cell:	n/a	n/a
44	RXRA	chr3:195168334-195168507	HepG2	liver:	n/a	n/a
45	TAF7	chr3:195166666-195167110	H1-hESC	embryonic stem cell:	n/a	n/a
46	TAF7	chr3:195166666-195167074	K562	blood:	n/a	n/a
47	TBP	chr3:195166902-195167126	K562	blood:	n/a	n/a
48	TEAD4	chr3:195166691-195167174	K562	blood:	n/a	n/a
49	ZBTB33	chr3:195168312-195168607	HepG2	liver:	n/a	n/a
50	ZMIZ1	chr3:195166773-195166975	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195167302-195167352	HRE	kidney:	n/a
2	chr3:195167302-195167352	Hela-S3	cervix:	n/a
3	chr3:195167302-195167352	AG09319	gingival:	n/a
4	chr3:195167302-195167352	ProgFib	skin:	n/a
5	chr3:195167302-195167352	SAEC	small airway:	n/a
6	chr3:195167302-195167352	MCF10A-Er-Src	breast:	n/a
7	chr3:195167302-195167352	HEEpiC	esophagus:	n/a
8	chr3:195167302-195167352	ECC-1	luminal epithelium:	n/a
9	chr3:195167302-195167352	AG04449	skin:	fetal
10	chr3:195167302-195167352	AG09309	skin:	n/a
11	chr3:195167302-195167352	HNPCEpiC	eye:	n/a
12	chr3:195167302-195167352	GM12878	blood:	n/a
13	chr3:195167302-195167352	GM19239	blood:	n/a
14	chr3:195167302-195167352	HMEC	breast:	n/a
15	chr3:195167302-195167352	Caco-2	colon:	n/a
16	chr3:195167302-195167352	SK-N-MC	brain:	n/a
17	chr3:195167302-195167352	GM12892	blood:	n/a
18	chr3:195167302-195167352	NB4	blood:	n/a
19	chr3:195167302-195167352	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:195167302-195167352	Jurkat	blood:	n/a
21	chr3:195167302-195167352	ovcar-3	ovarian:	n/a
22	chr3:195167302-195167352	HCT-116	colon:	n/a
23	chr3:195167302-195167352	HAEpiC	amniotic membrane:	n/a
24	chr3:195167302-195167352	Hepatocyte	liver:	n/a
25	chr3:195167302-195167352	A549	lung:	n/a
26	chr3:195167302-195167352	AG10803	skin:	n/a
27	chr3:195167302-195167352	K562	blood:	n/a
28	chr3:195167302-195167352	AoSMC	blood vessel:	n/a
29	chr3:195167302-195167352	LNCaP	prostate:	n/a
30	chr3:195167302-195167352	HEK293	kidney:	embryo
31	chr3:195167302-195167352	SK-N-SH	brain:	n/a
32	chr3:195167302-195167352	NT2-D1	testis:	n/a
33	chr3:195167302-195167352	GM12891	blood:	n/a
34	chr3:195167302-195167352	IMR90	lung:	fetal
35	chr3:195167302-195167352	HIPEpiC	eye:	n/a
36	chr3:195167302-195167352	HCF	heart:	n/a
37	chr3:195167302-195167352	NH-A	brain:	n/a
38	chr3:195167302-195167352	HRPEpiC	eye:	n/a
39	chr3:195167302-195167352	PrEC	prostate:	n/a
40	chr3:195167302-195167352	PANC-1	pancreas:	n/a
41	chr3:195167302-195167352	HCPEpiC	choroid plexus:	n/a
42	chr3:195167302-195167352	H1-hESC	embryonic stem cell:	embryo
43	chr3:195167302-195167352	U87	brain:	n/a
44	chr3:195167302-195167352	SKMC	muscle:	n/a
45	chr3:195167302-195167352	RPTEC	kidney:	n/a
46	chr3:195167302-195167352	PFSK-1	brain:	n/a
47	chr3:195167302-195167352	HCM	heart:	n/a
48	chr3:195167302-195167352	HUVEC	blood vessel:	n/a
49	chr3:195167302-195167352	MCF-7	breast:	n/a
50	chr3:195167302-195167352	BJ	skin:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:195167880..195169802-chr3:195171668..195174752,4	K562	blood:
2	chr3:195164614..195167496-chr3:195169106..195172382,4	K562	blood:
3	chr3:195164614..195167496-chr3:195169106..195172382,4	K562	blood:
4	chr3:195162020..195165766-chr3:195166533..195172631,9	MCF-7	breast:
5	chr3:195162962..195165336-chr3:195165436..195167180,2	MCF-7	breast:
6	chr3:195167880..195169802-chr3:195172457..195174752,3	K562	blood:
7	chr3:195167466..195170078-chr3:195181038..195183808,2	MCF-7	breast:
8	chr3:195164614..195167502-chr3:195169044..195171295,4	K562	blood:
9	chr3:195161410..195164177-chr3:195169867..195173510,4	K562	blood:
10	chr3:195163742..195165509-chr3:195165685..195167332,2	K562	blood:
11	chr3:195164614..195167502-chr3:195169044..195171295,4	K562	blood:
12	chr3:194980181..194984046-chr3:195161738..195167079,6	K562	blood:

No data

Variant related genes	Relation type
ACAP2	TF binding region
ACAP2	CpG island
ENSG00000114331	chromatin interactions
ENSG00000173950	chromatin interactions

Extended variants
information (count: 154 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:154 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114457345	chr3:195166950-195166951	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs577534217	chr3:195166951-195166952	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs138929994	chr3:195166955-195166956	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs545987879	chr3:195166961-195166962	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs543125020	chr3:195166994-195166995	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs375792288	chr3:195167012-195167013	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs143294453	chr3:195167066-195167067	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs542793934	chr3:195167073-195167074	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs147466459	chr3:195167075-195167076	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs12630162	chr3:195167114-195167115	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs540653106	chr3:195167188-195167189	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs78575501	chr3:195167235-195167236	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs532887282	chr3:195167288-195167289	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs111412828	chr3:195167323-195167324	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs184079701	chr3:195167350-195167351	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs115446492	chr3:195167381-195167382	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs186888456	chr3:195167456-195167457	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs548448307	chr3:195167507-195167508	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs112119943	chr3:195167525-195167526	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs567379292	chr3:195167542-195167543	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs534388865	chr3:195167546-195167547	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs191625583	chr3:195167576-195167577	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs570888356	chr3:195167634-195167635	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs538595682	chr3:195167651-195167652	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs145497759	chr3:195167720-195167721	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs550156830	chr3:195167774-195167775	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs201676633	chr3:195167776-195167777	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs367873549	chr3:195167785-195167786	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs573301720	chr3:195167825-195167826	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs540712660	chr3:195167856-195167857	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs565304146	chr3:195167968-195167969	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs540888376	chr3:195167985-195167986	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs185272695	chr3:195168094-195168095	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs565137239	chr3:195168120-195168121	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs6785964	chr3:195168140-195168141	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs530302990	chr3:195168146-195168147	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs148457720	chr3:195168162-195168163	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs560506842	chr3:195168185-195168186	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs190220618	chr3:195168188-195168189	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs377170054	chr3:195168195-195168196	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs570951653	chr3:195168233-195168234	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs538257307	chr3:195168244-195168245	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs550112874	chr3:195168281-195168282	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs142597612	chr3:195168285-195168286	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs536122622	chr3:195168286-195168287	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs554781819	chr3:195168290-195168291	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs541978944	chr3:195168322-195168323	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs151015432	chr3:195168358-195168359	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs35283136	chr3:195168438-195168439	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs182273066	chr3:195168454-195168455	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195164600-195167200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr3:195164600-195170800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr3:195164600-195171000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr3:195164600-195171200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:195164800-195167000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr3:195164800-195167000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr3:195164800-195167000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr3:195164800-195167000	Weak transcription	Stomach Mucosa	stomach
9	chr3:195164800-195167200	Weak transcription	Fetal Intestine Large	intestine
10	chr3:195164800-195167400	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr3:195164800-195167800	Weak transcription	Fetal Intestine Small	intestine
12	chr3:195165000-195167200	Enhancers	Primary T cells from cord blood	blood
13	chr3:195165200-195167000	Weak transcription	K562	blood
14	chr3:195166400-195167400	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr3:195166400-195167400	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr3:195166400-195167400	Enhancers	GM12878-XiMat	blood
17	chr3:195166600-195167000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr3:195166600-195167200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr3:195166600-195167200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr3:195166600-195167200	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr3:195166600-195167400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr3:195166600-195167600	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr3:195166600-195172600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr3:195166800-195167000	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr3:195166800-195167000	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr3:195166800-195167000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr3:195166800-195167200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr3:195166800-195167200	Enhancers	Primary T cells fromperipheralblood	blood
29	chr3:195166800-195167200	Enhancers	Primary T helper naive cells from peripheral blood	blood
30	chr3:195166800-195167200	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr3:195166800-195167200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
32	chr3:195166800-195167400	Enhancers	H1 Cell Line	embryonic stem cell
33	chr3:195166800-195167400	Enhancers	Primary B cells from cord blood	blood
34	chr3:195166800-195167400	Enhancers	Fetal Thymus	thymus
35	chr3:195166800-195167400	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr3:195166800-195167800	Enhancers	Duodenum Mucosa	Duodenum
37	chr3:195166800-195168200	Enhancers	HepG2	liver
38	chr3:195167000-195167200	Enhancers	Stomach Mucosa	stomach
39	chr3:195167000-195167400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr3:195167000-195167400	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr3:195167000-195167400	Enhancers	K562	blood
42	chr3:195167000-195168000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr3:195167200-195167400	Enhancers	H9 Cell Line	embryonic stem cell
44	chr3:195167200-195167400	Weak transcription	Stomach Mucosa	stomach
45	chr3:195167200-195168400	Enhancers	Fetal Intestine Large	intestine
46	chr3:195167200-195171600	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr3:195167400-195167800	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr3:195167400-195169000	Weak transcription	K562	blood
49	chr3:195167400-195170400	Weak transcription	Primary monocytes fromperipheralblood	blood
50	chr3:195167400-195171000	Weak transcription	Primary neutrophils fromperipheralblood	blood

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