Variant report

Variant	nsv508303
Chromosome Location	chr4:110579305-110604452
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:192)
CpG islands
(count:244)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:192 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr4:110592185-110592862	K562	blood:	n/a	n/a
2	CBX3	chr4:110599998-110600212	K562	blood:	n/a	n/a
3	CEBPB	chr4:110584057-110584199	H1-hESC	embryonic stem cell:	n/a	chr4:110584087-110584098
4	CTCF	chr4:110598180-110598330	BJ	skin:	n/a	n/a
5	CTCF	chr4:110598180-110598330	AG09309	skin:	n/a	n/a
6	CTCF	chr4:110598180-110598330	HEEpiC	esophagus:	n/a	n/a
7	CTCF	chr4:110580108-110580354	IMR90	lung:	n/a	n/a
8	CTCF	chr4:110598174-110598228	GM12891	blood:	n/a	n/a
9	CTCF	chr4:110598420-110598570	HFF-Myc	foreskin:	n/a	n/a
10	CTCF	chr4:110598177-110598273	GM12892	blood:	n/a	n/a
11	CTCF	chr4:110580240-110580390	MCF-7	breast:	n/a	n/a
12	CTCF	chr4:110580180-110580330	AG10803	skin:	n/a	n/a
13	CTCF	chr4:110591396-110591442	GM13976	blood:	n/a	n/a
14	CTCF	chr4:110598180-110598330	GM06990	blood:	n/a	n/a
15	CTCF	chr4:110598120-110598270	GM12864	blood:	n/a	n/a
16	CTCF	chr4:110598197-110598230	Fibrobl	skin:	n/a	n/a
17	CTCF	chr4:110580060-110580210	NHLF	lung:	n/a	n/a
18	CTCF	chr4:110580140-110580290	HMEC	breast:	n/a	n/a
19	CTCF	chr4:110598200-110598350	K562	blood:	n/a	n/a
20	CTCF	chr4:110597990-110598503	MCF-7	breast:	n/a	n/a
21	CTCF	chr4:110580120-110580270	RPTEC	kidney:	n/a	n/a
22	CTCF	chr4:110598223-110598282	Pancreas_OC	pancreas:	n/a	n/a
23	CTCF	chr4:110580160-110580310	HMF	breast:	n/a	n/a
24	CTCF	chr4:110598200-110598350	HCT-116	colon:	n/a	n/a
25	CTCF	chr4:110580157-110580303	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr4:110598162-110598357	Medullo	brain:	n/a	n/a
27	CTCF	chr4:110598147-110598338	HepG2	liver:	n/a	n/a
28	CTCF	chr4:110580080-110580230	AG09309	skin:	n/a	n/a
29	CTCF	chr4:110580080-110580230	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr4:110580069-110580402	GM12878	blood:	n/a	n/a
31	CTCF	chr4:110598160-110598310	AG10803	skin:	n/a	n/a
32	CTCF	chr4:110580011-110580330	HCT-116	colon:	n/a	n/a
33	CTCF	chr4:110580200-110580350	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr4:110580146-110580323	Medullo	brain:	n/a	n/a
35	CTCF	chr4:110580140-110580290	HCM	heart:	n/a	n/a
36	CTCF	chr4:110598152-110598317	MCF-7	breast:	n/a	n/a
37	CTCF	chr4:110598140-110598290	HMF	breast:	n/a	n/a
38	CTCF	chr4:110580200-110580350	RPTEC	kidney:	n/a	n/a
39	CTCF	chr4:110598168-110598310	GM12878	blood:	n/a	n/a
40	CTCF	chr4:110598180-110598330	SAEC	small airway:	n/a	n/a
41	CTCF	chr4:110598220-110598370	AG09309	skin:	n/a	n/a
42	CTCF	chr4:110598200-110598350	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr4:110580137-110580335	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr4:110598240-110598390	HFF	foreskin:	n/a	n/a
45	CTCF	chr4:110598160-110598410	RPTEC	kidney:	n/a	n/a
46	CTCF	chr4:110580060-110580210	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr4:110580180-110580330	AG04449	skin:	n/a	n/a
48	CTCF	chr4:110598140-110598290	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:110580200-110580350	HMEC	breast:	n/a	n/a
50	CTCF	chr4:110580188-110580303	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:110600020-110600070	GM12878	blood:	n/a
2	chr4:110599688-110599738	NB4	blood:	n/a
3	chr4:110599688-110599738	GM12878	blood:	n/a
4	chr4:110604090-110604140	SK-N-SH	brain:	n/a
5	chr4:110600020-110600070	A549	lung:	n/a
6	chr4:110604090-110604140	AG04450	lung:	fetal
7	chr4:110600020-110600070	HMEC	breast:	n/a
8	chr4:110600020-110600070	SK-N-SH_RA	brain:	n/a
9	chr4:110604090-110604140	IMR90	lung:	fetal
10	chr4:110604090-110604140	HCPEpiC	choroid plexus:	n/a
11	chr4:110583727-110583777	HepG2	liver:	n/a
12	chr4:110599688-110599738	PANC-1	pancreas:	n/a
13	chr4:110604090-110604140	HMEC	breast:	n/a
14	chr4:110599688-110599738	AG04449	skin:	fetal
15	chr4:110599688-110599738	HepG2	liver:	n/a
16	chr4:110583727-110583777	PFSK-1	brain:	n/a
17	chr4:110599688-110599738	LNCaP	prostate:	n/a
18	chr4:110583727-110583777	SK-N-MC	brain:	n/a
19	chr4:110583727-110583777	Caco-2	colon:	n/a
20	chr4:110604090-110604140	NH-A	brain:	n/a
21	chr4:110600020-110600070	NT2-D1	testis:	n/a
22	chr4:110604090-110604140	PFSK-1	brain:	n/a
23	chr4:110600020-110600070	Caco-2	colon:	n/a
24	chr4:110600020-110600070	GM19239	blood:	n/a
25	chr4:110599688-110599738	AoSMC	blood vessel:	n/a
26	chr4:110604090-110604140	HEEpiC	esophagus:	n/a
27	chr4:110604090-110604140	Caco-2	colon:	n/a
28	chr4:110600020-110600070	RPTEC	kidney:	n/a
29	chr4:110604090-110604140	HepG2	liver:	n/a
30	chr4:110583727-110583777	RPTEC	kidney:	n/a
31	chr4:110599688-110599738	MCF-7	breast:	n/a
32	chr4:110583727-110583777	PrEC	prostate:	n/a
33	chr4:110599688-110599738	BJ	skin:	n/a
34	chr4:110583727-110583777	A549	lung:	n/a
35	chr4:110599688-110599738	PrEC	prostate:	n/a
36	chr4:110599688-110599738	RPTEC	kidney:	n/a
37	chr4:110604090-110604140	HCF	heart:	n/a
38	chr4:110604090-110604140	BJ	skin:	n/a
39	chr4:110604090-110604140	HUVEC	blood vessel:	n/a
40	chr4:110583727-110583777	ECC-1	luminal epithelium:	n/a
41	chr4:110604090-110604140	GM12892	blood:	n/a
42	chr4:110600020-110600070	HNPCEpiC	eye:	n/a
43	chr4:110604090-110604140	T-47D	breast:	n/a
44	chr4:110599688-110599738	HRPEpiC	eye:	n/a
45	chr4:110604090-110604140	HIPEpiC	eye:	n/a
46	chr4:110599688-110599738	GM12892	blood:	n/a
47	chr4:110583727-110583777	HCT-116	colon:	n/a
48	chr4:110583727-110583777	LNCaP	prostate:	n/a
49	chr4:110599688-110599738	U87	brain:	n/a
50	chr4:110583727-110583777	BE2_C	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:110581396..110582917-chr4:110583378..110586264,2	MCF-7	breast:
2	chr4:110596739..110598343-chr4:110599981..110601558,2	MCF-7	breast:
3	chr4:110582260..110584595-chr4:110587879..110590432,2	K562	blood:
4	chr4:110353199..110355623-chr4:110596847..110599552,2	MCF-7	breast:
5	chr4:110592093..110594740-chr4:110602207..110604026,2	K562	blood:
6	chr4:110370787..110372375-chr4:110582316..110584517,2	MCF-7	breast:
7	chr4:110341049..110342014-chr4:110579969..110580500,2	MCF-7	breast:
8	chr4:110597890..110598667-chr4:110725301..110725981,3	MCF-7	breast:
9	chr4:110578534..110580904-chr4:110588408..110591184,2	K562	blood:
10	chr4:110568027..110570287-chr4:110582225..110584531,2	K562	blood:
11	chr4:110353269..110354820-chr4:110577196..110580148,2	MCF-7	breast:
12	chr4:110588789..110589289-chr8:43092779..43093429,2	MCF-7	breast:
13	chr4:110581396..110582917-chr4:110583378..110586264,2	MCF-7	breast:
14	chr4:110582184..110585367-chr4:110588932..110592046,3	K562	blood:
15	chr4:110582184..110585367-chr4:110588932..110592046,3	K562	blood:
16	chr4:110582260..110584595-chr4:110587879..110590432,2	K562	blood:
17	chr4:110596739..110598343-chr4:110599981..110601558,2	MCF-7	breast:
18	chr4:110578534..110580904-chr4:110588408..110591184,2	K562	blood:
19	chr4:110592093..110594740-chr4:110602207..110604026,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEC24B-2	chr4:110594999-110595280	NONHSAT097790

No data

Variant related genes	Relation type
CCDC109B	TF binding region
HIGD1AP14	TF binding region
CCDC109B	CpG island
HIGD1AP14	CpG island
ENSG00000138802	chromatin interactions
ENSG00000247950	chromatin interactions
ENSG00000243227	chromatin interactions

Extended variants
information (count: 943 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:943 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146881018	chr4:110579339-110579340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs561083372	chr4:110579381-110579382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs13435023	chr4:110579385-110579386	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs115296698	chr4:110579393-110579394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560462496	chr4:110579455-110579456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs111943469	chr4:110579458-110579459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371183133	chr4:110579475-110579476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532478359	chr4:110579484-110579485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs60182255	chr4:110579487-110579488	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs12511995	chr4:110579493-110579494	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs531269058	chr4:110579530-110579531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2158204	chr4:110579535-110579536	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs567690941	chr4:110579542-110579543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs180939085	chr4:110579546-110579547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566322089	chr4:110579558-110579559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544383981	chr4:110579574-110579575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547021616	chr4:110579576-110579577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs185766936	chr4:110579578-110579579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538993119	chr4:110579645-110579646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544972978	chr4:110579752-110579753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2107050	chr4:110579786-110579787	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs569440982	chr4:110579795-110579796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368854006	chr4:110579797-110579798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140230908	chr4:110579816-110579817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2107051	chr4:110579836-110579837	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs191496219	chr4:110579842-110579843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182540314	chr4:110579917-110579918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150317800	chr4:110579943-110579944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542610366	chr4:110579990-110579991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs1543812	chr4:110580084-110580085	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs576183150	chr4:110580125-110580126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs376679283	chr4:110580185-110580186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375249063	chr4:110580214-110580215	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544852646	chr4:110580245-110580246	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs113161118	chr4:110580251-110580252	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185634269	chr4:110580276-110580277	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190739225	chr4:110580293-110580294	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138159588	chr4:110580310-110580311	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567972526	chr4:110580343-110580344	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561429243	chr4:110580349-110580350	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527411669	chr4:110580355-110580356	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs72616574	chr4:110580435-110580436	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs5860986	chr4:110580436-110580437	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201496309	chr4:110580437-110580438	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs78809144	chr4:110580469-110580470	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533727067	chr4:110580513-110580514	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114958506	chr4:110580531-110580532	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114721731	chr4:110580559-110580560	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183013778	chr4:110580565-110580566	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs79141868	chr4:110580606-110580607	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Esophageal cancer	21851588	CNVD
Melanoma	20688739	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16397240	CNVD
Schizophrenia	19546859	CNVD
Colorectal cancer	16272173	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110546600-110580600	Weak transcription	Thymus	Thymus
2	chr4:110570400-110582000	Weak transcription	HSMM	muscle
3	chr4:110571000-110605400	Weak transcription	Left Ventricle	heart
4	chr4:110572600-110623200	Weak transcription	Esophagus	oesophagus
5	chr4:110573200-110588200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:110574000-110586600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr4:110574200-110580200	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr4:110574200-110580400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr4:110574200-110580400	Weak transcription	Fetal Thymus	thymus
10	chr4:110574200-110581000	Weak transcription	Primary B cells from peripheral blood	blood
11	chr4:110574200-110583200	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr4:110574200-110583200	Weak transcription	Dnd41	blood
13	chr4:110574200-110587400	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr4:110574200-110587600	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr4:110574200-110592600	Weak transcription	Primary hematopoietic stem cells	blood
16	chr4:110574200-110598400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr4:110574400-110581400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr4:110574600-110580800	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr4:110574600-110584800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr4:110574800-110581200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr4:110574800-110585000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr4:110576000-110580800	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr4:110576200-110579400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr4:110576200-110580400	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr4:110576200-110580600	Enhancers	Primary T cells fromperipheralblood	blood
26	chr4:110576200-110580800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
27	chr4:110576600-110589200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr4:110576800-110585000	Weak transcription	Primary B cells from cord blood	blood
29	chr4:110577000-110583200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr4:110577200-110580000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr4:110577200-110580800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr4:110577200-110582800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr4:110577400-110580000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr4:110577400-110587000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr4:110578200-110579400	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr4:110578800-110579400	Enhancers	HepG2	liver
37	chr4:110578800-110579800	Weak transcription	Primary T cells from cord blood	blood
38	chr4:110578800-110580000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr4:110579200-110608400	Weak transcription	Ovary	ovary
40	chr4:110579400-110579800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr4:110579400-110579800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr4:110579400-110581600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr4:110579400-110582600	Weak transcription	HepG2	liver
44	chr4:110579800-110580000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr4:110579800-110580400	Enhancers	Primary T cells from cord blood	blood
46	chr4:110579800-110580600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr4:110580000-110580200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr4:110580000-110580400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr4:110580000-110583800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr4:110580000-110585000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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