Variant report

Variant	nsv933954
Chromosome Location	chr5:7897495-7900858
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:51)
CpG islands
(count:62)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:51 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr5:7897139-7898076	A549	lung:	n/a	n/a
2	CTCF	chr5:7897005-7897702	SK-N-SH	brain:	n/a	n/a
3	CTCF	chr5:7897154-7897513	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr5:7897138-7897538	MCF-7	breast:	n/a	n/a
5	CTCF	chr5:7897133-7897559	MCF-7	breast:	n/a	n/a
6	CTCF	chr5:7897124-7897511	GM12878	blood:	n/a	n/a
7	CTCF	chr5:7897170-7897501	K562	blood:	n/a	n/a
8	CTCF	chr5:7897118-7897498	IMR90	lung:	n/a	n/a
9	ELK1	chr5:7898439-7898591	K562	blood:	n/a	n/a
10	FOS	chr5:7897168-7897551	MCF10A-Er-Src	breast:	n/a	chr5:7897362-7897369 chr5:7897359-7897370
11	FOS	chr5:7897145-7897553	MCF10A-Er-Src	breast:	n/a	chr5:7897362-7897369 chr5:7897359-7897370
12	FOS	chr5:7897203-7897551	MCF10A-Er-Src	breast:	n/a	chr5:7897362-7897369 chr5:7897359-7897370
13	FOS	chr5:7897179-7897550	MCF10A-Er-Src	breast:	n/a	chr5:7897362-7897369 chr5:7897359-7897370
14	FOS	chr5:7897191-7897613	HUVEC	blood vessel:	n/a	chr5:7897362-7897369 chr5:7897359-7897370
15	FOSL2	chr5:7897080-7897582	A549	lung:	n/a	chr5:7897362-7897369
16	FOSL2	chr5:7897095-7897557	SK-N-SH	brain:	n/a	chr5:7897362-7897369
17	JUN	chr5:7897212-7897495	K562	blood:	n/a	chr5:7897362-7897369
18	JUND	chr5:7897138-7897518	SK-N-SH	brain:	n/a	chr5:7897362-7897369 chr5:7897359-7897370
19	JUND	chr5:7897203-7897500	HepG2	liver:	n/a	chr5:7897362-7897369 chr5:7897359-7897370
20	JUND	chr5:7897157-7897540	K562	blood:	n/a	chr5:7897362-7897369 chr5:7897359-7897370
21	MXI1	chr5:7897925-7897926	GM12878	blood:	n/a	n/a
22	POLR2A	chr5:7898755-7898926	HepG2	liver:	n/a	n/a
23	POLR2A	chr5:7899549-7899628	HepG2	liver:	n/a	n/a
24	POLR2A	chr5:7898485-7900072	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr5:7898057-7905443	K562	blood:	n/a	n/a
26	POLR2A	chr5:7897195-7897695	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr5:7899680-7899723	GM12878	blood:	n/a	n/a
28	POLR2A	chr5:7899628-7899840	GM12878	blood:	n/a	n/a
29	POLR2A	chr5:7899588-7899778	GM12878	blood:	n/a	n/a
30	POLR2A	chr5:7899234-7900079	HepG2	liver:	n/a	n/a
31	POLR2A	chr5:7899568-7899880	HL-60	blood:	n/a	n/a
32	POLR2A	chr5:7900321-7900628	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr5:7899637-7899914	GM12878	blood:	n/a	n/a
34	POLR2A	chr5:7898620-7898820	HepG2	liver:	n/a	n/a
35	POLR2A	chr5:7900257-7900546	GM12878	blood:	n/a	n/a
36	POLR2A	chr5:7899488-7899860	GM12878	blood:	n/a	n/a
37	POLR2A	chr5:7898549-7900055	K562	blood:	n/a	n/a
38	POLR2A	chr5:7900500-7900697	HepG2	liver:	n/a	n/a
39	POLR2A	chr5:7898677-7898947	GM12878	blood:	n/a	n/a
40	POLR2A	chr5:7899692-7899850	K562	blood:	n/a	n/a
41	POLR2A	chr5:7899496-7899890	GM12891	blood:	n/a	n/a
42	RAD21	chr5:7897148-7897508	IMR90	lung:	n/a	n/a
43	RAD21	chr5:7897181-7897588	MCF-7	breast:	n/a	n/a
44	TBL1XR1	chr5:7897854-7898048	K562	blood:	n/a	n/a
45	TBL1XR1	chr5:7897150-7897527	K562	blood:	n/a	n/a
46	YY1	chr5:7896917-7897735	SK-N-SH	brain:	n/a	chr5:7897338-7897350
47	YY1	chr5:7897181-7897499	ECC-1	luminal epithelium:	n/a	chr5:7897338-7897350
48	YY1	chr5:7897169-7897534	SK-N-SH	brain:	n/a	chr5:7897338-7897350
49	YY1	chr5:7897111-7897504	A549	lung:	n/a	chr5:7897338-7897350
50	YY1	chr5:7897176-7897500	GM12878	blood:	n/a	chr5:7897338-7897350

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:7900364-7900414	AG04450	lung:	fetal
2	chr5:7900364-7900414	AG04450	lung:	fetal
3	chr5:7900364-7900414	SAEC	small airway:	n/a
4	chr5:7900364-7900414	NHDF-neo	bronchial:	n/a
5	chr5:7900364-7900414	GM12892	blood:	n/a
6	chr5:7900364-7900414	HAEpiC	amniotic membrane:	n/a
7	chr5:7900364-7900414	NB4	blood:	n/a
8	chr5:7900364-7900414	HCPEpiC	choroid plexus:	n/a
9	chr5:7900364-7900414	SK-N-MC	brain:	n/a
10	chr5:7900364-7900414	HIPEpiC	eye:	n/a
11	chr5:7900364-7900414	MCF-7	breast:	n/a
12	chr5:7900364-7900414	PANC-1	pancreas:	n/a
13	chr5:7900364-7900414	AoSMC	blood vessel:	n/a
14	chr5:7900364-7900414	U87	brain:	n/a
15	chr5:7900364-7900414	GM12891	blood:	n/a
16	chr5:7900364-7900414	HEK293	kidney:	embryo
17	chr5:7900364-7900414	Caco-2	colon:	n/a
18	chr5:7900364-7900414	LNCaP	prostate:	n/a
19	chr5:7900364-7900414	PrEC	prostate:	n/a
20	chr5:7900364-7900414	HEEpiC	esophagus:	n/a
21	chr5:7900364-7900414	Jurkat	blood:	n/a
22	chr5:7900364-7900414	HepG2	liver:	n/a
23	chr5:7900364-7900414	AG04449	skin:	fetal
24	chr5:7900364-7900414	GM12878	blood:	n/a
25	chr5:7900364-7900414	CMK	blood:	n/a
26	chr5:7900364-7900414	HRE	kidney:	n/a
27	chr5:7900364-7900414	SK-N-SH	brain:	n/a
28	chr5:7900364-7900414	HL-60	blood:	n/a
29	chr5:7900364-7900414	AG09309	skin:	n/a
30	chr5:7900364-7900414	HNPCEpiC	eye:	n/a
31	chr5:7900364-7900414	SK-N-SH_RA	brain:	n/a
32	chr5:7900364-7900414	T-47D	breast:	n/a
33	chr5:7900364-7900414	ProgFib	skin:	n/a
34	chr5:7900364-7900414	RPTEC	kidney:	n/a
35	chr5:7900364-7900414	SKMC	muscle:	n/a
36	chr5:7900364-7900414	AG09319	gingival:	n/a
37	chr5:7900364-7900414	HRPEpiC	eye:	n/a
38	chr5:7900364-7900414	Hela-S3	cervix:	n/a
39	chr5:7900364-7900414	BJ	skin:	n/a
40	chr5:7900364-7900414	HCT-116	colon:	n/a
41	chr5:7900364-7900414	HCF	heart:	n/a
42	chr5:7900364-7900414	AG10803	skin:	n/a
43	chr5:7900364-7900414	HRCEpiC	kidney:	n/a
44	chr5:7900364-7900414	NH-A	brain:	n/a
45	chr5:7900364-7900414	GM06990	blood:	n/a
46	chr5:7900364-7900414	NT2-D1	testis:	n/a
47	chr5:7900364-7900414	ECC-1	luminal epithelium:	n/a
48	chr5:7900364-7900414	NHBE	bronchial:	n/a
49	chr5:7900364-7900414	A549	lung:	n/a
50	chr5:7900364-7900414	GM19239	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:7867721..7870602-chr5:7899852..7901700,2	MCF-7	breast:
2	chr5:7867976..7870362-chr5:7899262..7901515,2	K562	blood:
3	chr5:7891090..7893015-chr5:7896688..7898784,2	K562	blood:
4	chr5:7896860..7897757-chr5:9207693..9208247,3	K562	blood:
5	chr5:7897166..7899613-chr5:7900650..7902755,2	MCF-7	breast:
6	chr5:7897897..7900344-chr5:7900899..7905029,3	MCF-7	breast:

No data

Variant related genes	Relation type
MTRR	TF binding region
MTRR	CpG island
ENSG00000124275	chromatin interactions
ENSG00000124279	chromatin interactions

Extended variants
information (count: 150 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:150 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555415091	chr5:7897502-7897503	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs17208190	chr5:7897529-7897530	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs41283147	chr5:7897536-7897537	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs563761185	chr5:7897539-7897540	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs576621404	chr5:7897590-7897591	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs576941820	chr5:7897596-7897597	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs111460700	chr5:7897599-7897600	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs545961392	chr5:7897602-7897603	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs559498621	chr5:7897630-7897631	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs528697093	chr5:7897646-7897647	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs548856887	chr5:7897704-7897705	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs568323452	chr5:7897770-7897771	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs180674476	chr5:7897781-7897782	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs530480796	chr5:7897871-7897872	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs150344238	chr5:7897878-7897879	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs370569066	chr5:7897887-7897888	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs138238044	chr5:7897888-7897889	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs368036664	chr5:7897901-7897902	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs17267793	chr5:7897946-7897947	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs368026517	chr5:7897969-7897970	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs535695326	chr5:7897994-7897995	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs565639889	chr5:7898001-7898002	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs142396918	chr5:7898003-7898004	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs79421232	chr5:7898030-7898031	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs10475398	chr5:7898051-7898052	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs537419498	chr5:7898054-7898055	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs10475399	chr5:7898094-7898095	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs576855695	chr5:7898123-7898124	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs545877450	chr5:7898125-7898126	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs559463596	chr5:7898181-7898182	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs146361524	chr5:7898331-7898332	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs71604190	chr5:7898475-7898476	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs116047888	chr5:7898506-7898507	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs562896432	chr5:7898535-7898536	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs202034941	chr5:7898547-7898548	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs34411979	chr5:7898548-7898549	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs398093168	chr5:7898550-7898551	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs111606024	chr5:7898552-7898553	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs114264198	chr5:7898554-7898555	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs375729309	chr5:7898569-7898570	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs564053956	chr5:7898571-7898572	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs368439307	chr5:7898593-7898594	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs74585692	chr5:7898636-7898637	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs13163363	chr5:7898640-7898641	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs114635330	chr5:7898664-7898665	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs566574531	chr5:7898710-7898711	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs72716538	chr5:7898731-7898732	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs16879367	chr5:7898733-7898734	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs181648879	chr5:7898737-7898738	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs537728160	chr5:7898804-7898805	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Lung cancer	21911935	CNVD
Cri-du chat syndrome	21549014	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Melanoma	22183965	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Ovarian cancer	19193619	CNVD
Hepatocellular carcinoma	16785998	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:7870200-7903400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:7871200-7903400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
3	chr5:7871200-7903600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
4	chr5:7871200-7903800	Strong transcription	HUES64 Cell Line	embryonic stem cell
5	chr5:7871400-7902400	Strong transcription	K562	blood
6	chr5:7871400-7903800	Strong transcription	HUES6 Cell Line	embryonic stem cell
7	chr5:7871600-7902800	Strong transcription	HUES48 Cell Line	embryonic stem cell
8	chr5:7871600-7905000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr5:7871600-7906400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr5:7871600-7906800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr5:7871800-7907400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
12	chr5:7873200-7903400	Strong transcription	Dnd41	blood
13	chr5:7873400-7904000	Strong transcription	Hela-S3	cervix
14	chr5:7874000-7905400	Strong transcription	Primary T cells from cord blood	blood
15	chr5:7874000-7909200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr5:7875000-7906600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:7875400-7903600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr5:7875400-7903800	Strong transcription	Primary B cells from peripheral blood	blood
19	chr5:7875400-7904200	Strong transcription	Primary hematopoietic stem cells	blood
20	chr5:7875400-7904400	Strong transcription	Fetal Muscle Trunk	muscle
21	chr5:7875600-7904400	Strong transcription	Left Ventricle	heart
22	chr5:7878600-7911800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr5:7879200-7901800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr5:7879200-7906400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr5:7879600-7900600	Strong transcription	Primary B cells from cord blood	blood
26	chr5:7880000-7903600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr5:7880400-7906600	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr5:7880600-7907000	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr5:7880800-7903800	Strong transcription	Rectal Mucosa Donor 29	rectum
30	chr5:7881000-7904400	Strong transcription	Fetal Intestine Large	intestine
31	chr5:7882200-7902200	Strong transcription	Primary T helper naive cells from peripheral blood	blood
32	chr5:7882400-7898600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr5:7882400-7905000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr5:7882600-7898600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr5:7885400-7904000	Strong transcription	A549	lung
36	chr5:7885400-7904800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr5:7887600-7906800	Strong transcription	Primary T helper cells PMA-I stimulated	--
38	chr5:7888000-7901400	Strong transcription	HSMM	muscle
39	chr5:7888200-7904000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr5:7888200-7904000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr5:7888200-7904200	Strong transcription	Liver	Liver
42	chr5:7888400-7903000	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr5:7888400-7904000	Strong transcription	Primary T cells fromperipheralblood	blood
44	chr5:7888400-7904200	Strong transcription	Placenta	Placenta
45	chr5:7888400-7906400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr5:7888600-7897600	Strong transcription	HSMMtube	muscle
47	chr5:7888600-7900600	Strong transcription	Stomach Smooth Muscle	stomach
48	chr5:7888600-7900600	Strong transcription	HepG2	liver
49	chr5:7888600-7900800	Strong transcription	H9 Cell Line	embryonic stem cell
50	chr5:7888600-7901800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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