Variant report

Variant	nsv882681
Chromosome Location	chr5:106508913-106573961
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	CEBPB	chr5:106536248-106536250	A549	lung:	n/a	n/a
2	CEBPB	chr5:106553359-106553826	MCF-7	breast:	n/a	chr5:106553578-106553591
3	CEBPB	chr5:106554529-106554950	A549	lung:	n/a	chr5:106554937-106554950
4	CEBPB	chr5:106553239-106553882	HCT-116	colon:	n/a	chr5:106553578-106553591
5	CEBPB	chr5:106572454-106572552	HepG2	liver:	n/a	chr5:106572514-106572525
6	CEBPB	chr5:106572383-106572599	A549	lung:	n/a	chr5:106572514-106572525 chr5:106572402-106572413 chr5:106572402-106572413
7	CEBPB	chr5:106521516-106521822	HepG2	liver:	n/a	n/a
8	CEBPB	chr5:106531529-106531741	HepG2	liver:	n/a	n/a
9	CEBPB	chr5:106554588-106555075	Hela-S3	cervix:	n/a	chr5:106554937-106554950
10	CEBPB	chr5:106531570-106531610	A549	lung:	n/a	n/a
11	CEBPB	chr5:106553331-106553810	MCF-7	breast:	n/a	chr5:106553578-106553591
12	CHD2	chr5:106517883-106517892	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr5:106530677-106530761	GM20000	blood:	n/a	n/a
14	CTCF	chr5:106573342-106573367	LNCaP	prostate:	n/a	n/a
15	CTCF	chr5:106560930-106560954	Medullo	brain:	n/a	n/a
16	CTCF	chr5:106558800-106558950	Caco-2	colon:	n/a	n/a
17	CTCF	chr5:106535580-106535730	NHDF-neo	bronchial:	n/a	n/a
18	CUX1	chr5:106539164-106539309	GM12878	blood:	n/a	n/a
19	E2F4	chr5:106554675-106554947	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr5:106514550-106514625	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr5:106511801-106512104	MCF10A-Er-Src	breast:	n/a	n/a
22	EP300	chr5:106548094-106550089	SK-N-SH	brain:	n/a	n/a
23	EP300	chr5:106551356-106551626	SK-N-SH_RA	brain:	n/a	chr5:106551422-106551431 chr5:106551497-106551506
24	EP300	chr5:106555660-106556131	SK-N-SH	brain:	n/a	n/a
25	EP300	chr5:106555658-106555910	SK-N-SH_RA	brain:	n/a	n/a
26	EP300	chr5:106553261-106553773	T-47D	breast:	n/a	chr5:106553576-106553590 chr5:106553676-106553689
27	EP300	chr5:106555705-106556042	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr5:106548776-106549084	SK-N-SH_RA	brain:	n/a	n/a
29	EP300	chr5:106548748-106549068	SK-N-SH_RA	brain:	n/a	n/a
30	EP300	chr5:106553313-106553769	T-47D	breast:	n/a	chr5:106553576-106553590 chr5:106553676-106553689
31	ESR1	chr5:106553311-106553683	T-47D	breast:	n/a	n/a
32	ESR1	chr5:106553302-106553698	T-47D	breast:	n/a	n/a
33	ESR1	chr5:106553312-106553661	T-47D	breast:	n/a	n/a
34	FOS	chr5:106519689-106520070	HUVEC	blood vessel:	n/a	chr5:106519858-106519867 chr5:106519859-106519866 chr5:106519858-106519866 chr5:106519856-106519867
35	FOS	chr5:106554172-106554880	MCF10A-Er-Src	breast:	n/a	chr5:106554320-106554328 chr5:106554318-106554330 chr5:106554704-106554713 chr5:106554319-106554328 chr5:106554321-106554332 chr5:106554318-106554329 chr5:106554320-106554327 chr5:106554715-106554727 chr5:106554320-106554329
36	FOS	chr5:106553457-106553583	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr5:106554259-106554966	MCF10A-Er-Src	breast:	n/a	chr5:106554320-106554328 chr5:106554318-106554330 chr5:106554704-106554713 chr5:106554319-106554328 chr5:106554321-106554332 chr5:106554318-106554329 chr5:106554320-106554327 chr5:106554715-106554727 chr5:106554320-106554329
38	FOS	chr5:106519849-106520049	MCF10A-Er-Src	breast:	n/a	chr5:106519858-106519867 chr5:106519859-106519866 chr5:106519858-106519866 chr5:106519856-106519867
39	FOS	chr5:106553941-106554787	HUVEC	blood vessel:	n/a	chr5:106554320-106554328 chr5:106554318-106554330 chr5:106554704-106554713 chr5:106554319-106554328 chr5:106554321-106554332 chr5:106554318-106554329 chr5:106554320-106554327 chr5:106554715-106554727 chr5:106554320-106554329
40	FOS	chr5:106551224-106551676	HUVEC	blood vessel:	n/a	n/a
41	FOS	chr5:106519757-106519971	MCF10A-Er-Src	breast:	n/a	chr5:106519858-106519867 chr5:106519859-106519866 chr5:106519858-106519866 chr5:106519856-106519867
42	FOS	chr5:106553369-106553656	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr5:106554140-106554969	MCF10A-Er-Src	breast:	n/a	chr5:106554320-106554328 chr5:106554318-106554330 chr5:106554704-106554713 chr5:106554319-106554328 chr5:106554321-106554332 chr5:106554318-106554329 chr5:106554320-106554327 chr5:106554715-106554727 chr5:106554320-106554329
44	FOS	chr5:106553456-106553667	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr5:106553413-106553720	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr5:106554135-106554980	MCF10A-Er-Src	breast:	n/a	chr5:106554320-106554328 chr5:106554318-106554330 chr5:106554704-106554713 chr5:106554319-106554328 chr5:106554321-106554332 chr5:106554318-106554329 chr5:106554320-106554327 chr5:106554715-106554727 chr5:106554320-106554329
47	FOS	chr5:106540805-106540957	MCF10A-Er-Src	breast:	n/a	chr5:106540855-106540864 chr5:106540855-106540862 chr5:106540853-106540865 chr5:106540854-106540864 chr5:106540854-106540864
48	FOSL1	chr5:106553206-106553822	HCT-116	colon:	n/a	n/a
49	FOSL2	chr5:106553274-106553760	MCF-7	breast:	n/a	n/a
50	FOXA1	chr5:106554789-106554967	T-47D	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:106530218-106530268	HL-60	blood:	n/a
2	chr5:106530218-106530268	K562	blood:	n/a
3	chr5:106530218-106530268	HCM	heart:	n/a
4	chr5:106530218-106530268	Jurkat	blood:	n/a
5	chr5:106530218-106530268	ECC-1	luminal epithelium:	n/a
6	chr5:106530218-106530268	HEEpiC	esophagus:	n/a
7	chr5:106530218-106530268	PANC-1	pancreas:	n/a
8	chr5:106530218-106530268	AG04449	skin:	fetal
9	chr5:106530218-106530268	NB4	blood:	n/a
10	chr5:106530218-106530268	AG10803	skin:	n/a
11	chr5:106530218-106530268	BE2_C	brain:	n/a
12	chr5:106530218-106530268	HAEpiC	amniotic membrane:	n/a
13	chr5:106530218-106530268	Hepatocyte	liver:	n/a
14	chr5:106530218-106530268	NHBE	bronchial:	n/a
15	chr5:106530218-106530268	T-47D	breast:	n/a
16	chr5:106530218-106530268	NHDF-neo	bronchial:	n/a
17	chr5:106530218-106530268	SAEC	small airway:	n/a
18	chr5:106530218-106530268	HPAEpiC	pulmonary alveolar:	n/a
19	chr5:106530218-106530268	SK-N-SH	brain:	n/a
20	chr5:106530218-106530268	HRPEpiC	eye:	n/a
21	chr5:106530218-106530268	GM06990	blood:	n/a
22	chr5:106530218-106530268	GM12891	blood:	n/a
23	chr5:106530218-106530268	HCPEpiC	choroid plexus:	n/a
24	chr5:106530218-106530268	AG09309	skin:	n/a
25	chr5:106530218-106530268	HCF	heart:	n/a
26	chr5:106530218-106530268	AG04450	lung:	fetal
27	chr5:106530218-106530268	PFSK-1	brain:	n/a
28	chr5:106530218-106530268	HCT-116	colon:	n/a
29	chr5:106530218-106530268	HUVEC	blood vessel:	n/a
30	chr5:106530218-106530268	Caco-2	colon:	n/a
31	chr5:106530218-106530268	SKMC	muscle:	n/a
32	chr5:106530218-106530268	GM19239	blood:	n/a
33	chr5:106530218-106530268	GM12892	blood:	n/a
34	chr5:106530218-106530268	A549	lung:	n/a
35	chr5:106530218-106530268	HepG2	liver:	n/a
36	chr5:106530218-106530268	AoSMC	blood vessel:	n/a
37	chr5:106530218-106530268	PrEC	prostate:	n/a
38	chr5:106530218-106530268	RPTEC	kidney:	n/a
39	chr5:106530218-106530268	LNCaP	prostate:	n/a
40	chr5:106530218-106530268	IMR90	lung:	fetal
41	chr5:106530218-106530268	GM12878	blood:	n/a
42	chr5:106530218-106530268	U87	brain:	n/a
43	chr5:106530218-106530268	ovcar-3	ovarian:	n/a
44	chr5:106530218-106530268	AG09319	gingival:	n/a
45	chr5:106530218-106530268	HRE	kidney:	n/a
46	chr5:106530218-106530268	CMK	blood:	n/a
47	chr5:106530218-106530268	HNPCEpiC	eye:	n/a
48	chr5:106530218-106530268	NH-A	brain:	n/a
49	chr5:106530218-106530268	SK-N-MC	brain:	n/a
50	chr5:106530218-106530268	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:105620861..105623100-chr5:106539185..106542118,2	MCF-7	breast:
2	chr5:106564448..106567221-chr5:106567347..106569105,2	K562	blood:
3	chr5:106525438..106528218-chr5:106529605..106532112,2	MCF-7	breast:
4	chr5:106564448..106567221-chr5:106567347..106569105,2	K562	blood:

Variant related genes	Relation type
PSMC1P5	TF binding region
PSMC1P5	CpG island
ENSG00000250273	chromatin interactions

Extended variants
information (count: 977 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565980251	chr5:106510016-106510017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534489574	chr5:106510029-106510030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557932479	chr5:106510135-106510136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138975307	chr5:106510147-106510148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570916232	chr5:106510161-106510162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539977105	chr5:106510193-106510194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556591898	chr5:106510224-106510225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115968863	chr5:106510229-106510230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535860703	chr5:106510319-106510320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560205047	chr5:106510337-106510338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183771401	chr5:106510373-106510374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572704603	chr5:106510397-106510398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183866790	chr5:106525448-106525449	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs573771385	chr5:106525464-106525465	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs145016822	chr5:106525471-106525472	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs114523442	chr5:106525477-106525478	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs186822237	chr5:106525479-106525480	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs573126647	chr5:106525492-106525493	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs76422518	chr5:106525494-106525495	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs565398475	chr5:106525503-106525504	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs541632424	chr5:106525538-106525539	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs201193650	chr5:106525545-106525546	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs386690840	chr5:106525547-106525548	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs72780184	chr5:106525548-106525549	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs561500211	chr5:106525562-106525563	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530335555	chr5:106525565-106525566	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs566600680	chr5:106525588-106525589	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs560198577	chr5:106525599-106525600	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs187264522	chr5:106525601-106525602	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs192876265	chr5:106525615-106525616	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs569057139	chr5:106525669-106525670	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs201895952	chr5:106525684-106525685	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs537773953	chr5:106525724-106525725	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs376494903	chr5:106525766-106525767	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs567878365	chr5:106525801-106525802	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs74785795	chr5:106525805-106525806	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs397831293	chr5:106525811-106525812	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs199904784	chr5:106525812-106525813	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs200499251	chr5:106525817-106525818	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs533757468	chr5:106525850-106525851	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs185223666	chr5:106525867-106525868	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs542200362	chr5:106525882-106525883	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs190065458	chr5:106525888-106525889	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs182170712	chr5:106525956-106525957	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs563969966	chr5:106525977-106525978	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs558955924	chr5:106525982-106525983	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs575832778	chr5:106526002-106526003	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs544885455	chr5:106526008-106526009	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs72782142	chr5:106526029-106526030	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs56379720	chr5:106526071-106526072	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:106510000-106510400	Enhancers	Esophagus	oesophagus
2	chr5:106528200-106528600	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr5:106528200-106528800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr5:106528800-106531200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr5:106529400-106529600	Bivalent/Poised TSS	Liver	Liver
6	chr5:106530200-106530400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:106532000-106533000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr5:106534400-106534800	Enhancers	Muscle Satellite Cultured Cells	--
9	chr5:106538800-106539200	Enhancers	Fetal Brain Male	brain
10	chr5:106539000-106539400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr5:106539000-106539400	Active TSS	NHDF-Ad	bronchial
12	chr5:106539000-106539600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr5:106539000-106539600	Active TSS	Pancreatic Islets	Pancreatic Islet
14	chr5:106539000-106539800	Enhancers	GM12878-XiMat	blood
15	chr5:106540200-106540400	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr5:106547000-106547800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr5:106547200-106547800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr5:106547400-106547800	Enhancers	Brain Germinal Matrix	brain
19	chr5:106547800-106553200	Weak transcription	Brain Germinal Matrix	brain
20	chr5:106548800-106549000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr5:106548800-106549000	Enhancers	Aorta	Aorta
22	chr5:106548800-106549200	Enhancers	Left Ventricle	heart
23	chr5:106548800-106550400	Enhancers	Fetal Heart	heart
24	chr5:106549000-106549200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr5:106549000-106549200	Enhancers	Right Ventricle	heart
26	chr5:106549200-106551400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr5:106549200-106551600	Weak transcription	Right Ventricle	heart
28	chr5:106549200-106552000	Weak transcription	Left Ventricle	heart
29	chr5:106549200-106552400	Weak transcription	Aorta	Aorta
30	chr5:106550200-106552000	Enhancers	HUVEC	blood vessel
31	chr5:106550400-106551400	Weak transcription	Fetal Heart	heart
32	chr5:106551000-106551800	Enhancers	Muscle Satellite Cultured Cells	--
33	chr5:106551000-106554600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr5:106551000-106555000	Enhancers	NHEK	skin
35	chr5:106551200-106554200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr5:106551200-106555200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr5:106551400-106551600	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr5:106551400-106551600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr5:106551400-106551600	Enhancers	HSMM	muscle
40	chr5:106551400-106551600	Enhancers	NH-A	brain
41	chr5:106551400-106554800	Enhancers	Fetal Heart	heart
42	chr5:106551400-106555200	Enhancers	HMEC	breast
43	chr5:106551600-106551800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr5:106551600-106551800	Enhancers	Right Ventricle	heart
45	chr5:106551600-106552400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr5:106551600-106552800	Enhancers	Psoas Muscle	Psoas
47	chr5:106551600-106555400	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr5:106551800-106553000	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr5:106551800-106553200	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr5:106551800-106557200	Weak transcription	Right Ventricle	heart

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