Variant report

Variant	nsv881586
Chromosome Location	chr5:9549386-9578794
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:116)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:116 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr5:9557108-9557308	K562	blood:	n/a	n/a
2	CEBPB	chr5:9558555-9558900	Hela-S3	cervix:	n/a	chr5:9558688-9558699
3	CEBPB	chr5:9564913-9565267	IMR90	lung:	n/a	chr5:9565088-9565101
4	CEBPB	chr5:9564845-9565219	MCF-7	breast:	n/a	chr5:9565088-9565101
5	CEBPB	chr5:9558600-9558733	H1-hESC	embryonic stem cell:	n/a	chr5:9558688-9558699
6	CEBPB	chr5:9564941-9565236	HepG2	liver:	n/a	chr5:9565088-9565101
7	CEBPB	chr5:9558453-9558957	MCF-7	breast:	n/a	chr5:9558688-9558699
8	CEBPB	chr5:9562155-9562763	MCF-7	breast:	n/a	n/a
9	CEBPB	chr5:9558462-9558999	MCF-7	breast:	n/a	chr5:9558688-9558699
10	CEBPB	chr5:9562148-9562681	MCF-7	breast:	n/a	n/a
11	CEBPB	chr5:9557858-9558133	IMR90	lung:	n/a	n/a
12	CHD2	chr5:9562343-9562506	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr5:9549960-9550110	HCPEpiC	choroid plexus:	n/a	n/a
14	CTCF	chr5:9549880-9550030	GM12873	blood:	n/a	n/a
15	CTCF	chr5:9551587-9551644	GM20000	blood:	n/a	n/a
16	CTCF	chr5:9562280-9562430	HEK293	kidney:	n/a	n/a
17	CTCF	chr5:9574100-9574250	HPF	lung:	n/a	n/a
18	CTCF	chr5:9553000-9553150	GM12866	blood:	n/a	n/a
19	CTCF	chr5:9574020-9574170	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr5:9574080-9574230	HepG2	liver:	n/a	n/a
21	CTCF	chr5:9549860-9550010	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr5:9564460-9564610	GM12869	blood:	n/a	n/a
23	CTCF	chr5:9549880-9550030	HEK293	kidney:	n/a	n/a
24	CTCF	chr5:9574020-9574170	BE2_C	brain:	n/a	n/a
25	CTCF	chr5:9549840-9549990	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr5:9574000-9574150	BE2_C	brain:	n/a	n/a
27	CTCF	chr5:9560680-9560830	NHDF-neo	bronchial:	n/a	n/a
28	E2F4	chr5:9569176-9569376	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr5:9562487-9562704	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr5:9575255-9575562	MCF10A-Er-Src	breast:	n/a	n/a
31	EP300	chr5:9560010-9560464	MCF-7	breast:	n/a	n/a
32	FOS	chr5:9562247-9562585	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr5:9562260-9562589	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr5:9575086-9575390	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr5:9575098-9575353	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr5:9557859-9558139	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr5:9562268-9562585	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr5:9557889-9558111	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr5:9557863-9558194	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr5:9575129-9575287	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr5:9562295-9562599	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr5:9575077-9575406	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr5:9557815-9558198	MCF10A-Er-Src	breast:	n/a	n/a
44	FOSL1	chr5:9562282-9562510	K562	blood:	n/a	chr5:9562433-9562444 chr5:9562409-9562420
45	FOSL1	chr5:9562311-9562591	HCT-116	colon:	n/a	chr5:9562433-9562444 chr5:9562409-9562420
46	FOSL2	chr5:9562250-9562734	MCF-7	breast:	n/a	n/a
47	FOSL2	chr5:9562205-9562624	A549	lung:	n/a	n/a
48	FOSL2	chr5:9562171-9562773	MCF-7	breast:	n/a	n/a
49	GATA3	chr5:9558700-9559012	MCF-7	breast:	n/a	n/a
50	GATA3	chr5:9558431-9559189	MCF-7	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:9557609-9557659	Hepatocyte	liver:	n/a
2	chr5:9557609-9557659	Caco-2	colon:	n/a
3	chr5:9549503-9549553	AG04449	skin:	fetal
4	chr5:9549503-9549553	HEK293	kidney:	embryo
5	chr5:9549503-9549553	HRCEpiC	kidney:	n/a
6	chr5:9557609-9557659	SKMC	muscle:	n/a
7	chr5:9549503-9549553	HCPEpiC	choroid plexus:	n/a
8	chr5:9557609-9557659	GM06990	blood:	n/a
9	chr5:9549503-9549553	GM12878	blood:	n/a
10	chr5:9549503-9549553	IMR90	lung:	fetal
11	chr5:9557609-9557659	GM12891	blood:	n/a
12	chr5:9549503-9549553	ovcar-3	ovarian:	n/a
13	chr5:9549503-9549553	NB4	blood:	n/a
14	chr5:9549503-9549553	HCF	heart:	n/a
15	chr5:9549503-9549553	AG10803	skin:	n/a
16	chr5:9557609-9557659	HepG2	liver:	n/a
17	chr5:9557609-9557659	AG04450	lung:	fetal
18	chr5:9557609-9557659	CMK	blood:	n/a
19	chr5:9549503-9549553	SK-N-MC	brain:	n/a
20	chr5:9549503-9549553	PANC-1	pancreas:	n/a
21	chr5:9557609-9557659	PrEC	prostate:	n/a
22	chr5:9557609-9557659	AoSMC	blood vessel:	n/a
23	chr5:9557609-9557659	H1-hESC	embryonic stem cell:	embryo
24	chr5:9549503-9549553	GM06990	blood:	n/a
25	chr5:9549503-9549553	ProgFib	skin:	n/a
26	chr5:9549503-9549553	PFSK-1	brain:	n/a
27	chr5:9549503-9549553	GM19239	blood:	n/a
28	chr5:9557609-9557659	U87	brain:	n/a
29	chr5:9549503-9549553	HPAEpiC	pulmonary alveolar:	n/a
30	chr5:9549503-9549553	SAEC	small airway:	n/a
31	chr5:9549503-9549553	NH-A	brain:	n/a
32	chr5:9557609-9557659	BE2_C	brain:	n/a
33	chr5:9549503-9549553	HAEpiC	amniotic membrane:	n/a
34	chr5:9549503-9549553	Caco-2	colon:	n/a
35	chr5:9557609-9557659	HIPEpiC	eye:	n/a
36	chr5:9549503-9549553	A549	lung:	n/a
37	chr5:9557609-9557659	BJ	skin:	n/a
38	chr5:9549503-9549553	GM12892	blood:	n/a
39	chr5:9557609-9557659	A549	lung:	n/a
40	chr5:9549503-9549553	T-47D	breast:	n/a
41	chr5:9549503-9549553	LNCaP	prostate:	n/a
42	chr5:9557609-9557659	NB4	blood:	n/a
43	chr5:9557609-9557659	HCM	heart:	n/a
44	chr5:9557609-9557659	HL-60	blood:	n/a
45	chr5:9549503-9549553	BJ	skin:	n/a
46	chr5:9557609-9557659	ECC-1	luminal epithelium:	n/a
47	chr5:9557609-9557659	T-47D	breast:	n/a
48	chr5:9549503-9549553	HUVEC	blood vessel:	n/a
49	chr5:9549503-9549553	PrEC	prostate:	n/a
50	chr5:9549503-9549553	Hela-S3	cervix:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:9419787..9421576-chr5:9562455..9564681,2	K562	blood:
2	chr5:9547276..9549709-chr5:9554757..9557488,2	K562	blood:
3	chr5:9546664..9548240-chr5:9561037..9563217,2	MCF-7	breast:
4	chr5:9548536..9550584-chr5:9558365..9560082,2	MCF-7	breast:
5	chr5:9545641..9548478-chr5:9550713..9552547,2	K562	blood:
6	chr5:9552447..9554138-chr5:9558237..9561822,3	MCF-7	breast:
7	chr5:9540715..9542331-chr5:9550727..9553558,2	MCF-7	breast:
8	chr5:9543479..9545232-chr5:9559885..9561800,2	MCF-7	breast:
9	chr5:9564209..9566573-chr5:9569585..9571107,2	K562	blood:
10	chr5:9552447..9554138-chr5:9558237..9561822,3	MCF-7	breast:
11	chr5:9546333..9547953-chr5:9549365..9551271,2	MCF-7	breast:
12	chr5:9546514..9548478-chr5:9550572..9552547,2	K562	blood:
13	chr5:9564209..9566573-chr5:9569585..9571107,2	K562	blood:
14	chr5:9546585..9548880-chr5:9563821..9566752,2	K562	blood:
15	chr5:7903532..7905536-chr5:9562936..9564513,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCT5-4	chr5:9549414-9550721	ENSG00000250786
2	lnc-CCT5-4	chr5:9549414-9549996	NONHSAT100369
3	lnc-CCT5-4	chr5:9548191-9550410	NONHSAT100370
4	lnc-CCT5-4	chr5:9549102-9549702	ENSG00000250786
5	lnc-CCT5-4	chr5:9549414-9550409	NR_045196

No data

Variant related genes	Relation type
SEMA5A	TF binding region
SEMA5A	CpG island
ENSG00000250786	chromatin interactions
ENSG00000239112	chromatin interactions
ENSG00000112902	chromatin interactions

Extended variants
information (count: 1116 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1116 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17329485	chr5:9549386-9549387	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567469457	chr5:9549401-9549402	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs139140068	chr5:9549439-9549440	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs431288	chr5:9549459-9549460	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs569518429	chr5:9549489-9549490	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs369494063	chr5:9549504-9549505	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs35309345	chr5:9549527-9549528	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs538896688	chr5:9549541-9549542	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs557053441	chr5:9549601-9549602	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs187741971	chr5:9549660-9549661	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs386685338	chr5:9549739-9549740	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs185011199	chr5:9549741-9549742	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs12186736	chr5:9549755-9549756	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs143047846	chr5:9549823-9549824	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs543548113	chr5:9549827-9549828	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs187456578	chr5:9549867-9549868	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs11559051	chr5:9549941-9549942	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs536841051	chr5:9549970-9549971	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs565468904	chr5:9549987-9549988	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs554896153	chr5:9550034-9550035	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs527682178	chr5:9550046-9550047	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs193194228	chr5:9550080-9550081	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs560957754	chr5:9550128-9550129	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs369874441	chr5:9550133-9550134	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs372728681	chr5:9550259-9550260	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs184748024	chr5:9550260-9550261	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs549882699	chr5:9550267-9550268	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs569477378	chr5:9550276-9550277	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs538490746	chr5:9550283-9550284	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs189851783	chr5:9550303-9550304	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs113214114	chr5:9550323-9550324	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs1334	chr5:9550333-9550334	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs147457379	chr5:9550337-9550338	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs552820364	chr5:9550355-9550356	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs139839210	chr5:9550377-9550378	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs372907462	chr5:9550398-9550399	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs142016076	chr5:9550475-9550476	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs568031008	chr5:9550496-9550497	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs377494423	chr5:9550513-9550514	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs535598732	chr5:9550526-9550527	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs76832911	chr5:9550529-9550530	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs10462868	chr5:9550586-9550587	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs150688366	chr5:9550636-9550637	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs565563529	chr5:9550637-9550638	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs930076	chr5:9550642-9550643	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs7714356	chr5:9550703-9550704	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs414396	chr5:9550708-9550709	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs530050450	chr5:9550715-9550716	Weak transcription Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs16883128	chr5:9550770-9550771	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs116770697	chr5:9550786-9550787	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Cervical squamous cell carcinoma	21590768	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
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Ovarian cancer	19193619	CNVD
Hepatocellular carcinoma	16785998	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Lung adenocarcinoma	17982442	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:9547000-9554200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr5:9548000-9549400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:9548000-9549800	Weak transcription	Gastric	stomach
4	chr5:9548000-9551400	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr5:9548200-9549400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr5:9548200-9549400	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr5:9548200-9549400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr5:9548200-9549400	Weak transcription	Adipose Nuclei	Adipose
9	chr5:9548200-9549400	Weak transcription	Aorta	Aorta
10	chr5:9548200-9549400	Weak transcription	Brain Substantia Nigra	brain
11	chr5:9548200-9549400	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr5:9548200-9549600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr5:9548200-9549600	Weak transcription	Esophagus	oesophagus
14	chr5:9548200-9549600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr5:9548200-9549600	Weak transcription	Fetal Intestine Small	intestine
16	chr5:9548200-9549600	Weak transcription	Lung	lung
17	chr5:9548200-9549600	Weak transcription	Pancreas	Pancrea
18	chr5:9548200-9549800	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr5:9548200-9551000	Weak transcription	Ovary	ovary
20	chr5:9548200-9551800	Weak transcription	Brain Anterior Caudate	brain
21	chr5:9548200-9552400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr5:9548200-9552800	Weak transcription	Stomach Mucosa	stomach
23	chr5:9548200-9553000	Weak transcription	Fetal Kidney	kidney
24	chr5:9548200-9554000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr5:9548200-9554200	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr5:9548200-9556200	Weak transcription	Right Ventricle	heart
27	chr5:9548200-9558400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr5:9548200-9558400	Weak transcription	Liver	Liver
29	chr5:9548400-9549400	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr5:9548400-9549600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr5:9548400-9553600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr5:9548400-9558400	Weak transcription	Fetal Heart	heart
33	chr5:9548600-9552800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr5:9548600-9558400	Weak transcription	Brain Hippocampus Middle	brain
35	chr5:9548800-9549400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr5:9548800-9549400	Weak transcription	HMEC	breast
37	chr5:9548800-9549400	Genic enhancers	NHLF	lung
38	chr5:9548800-9549600	Enhancers	Placenta Amnion	Placenta Amnion
39	chr5:9548800-9550000	Genic enhancers	NHDF-Ad	bronchial
40	chr5:9548800-9551600	Strong transcription	HUES48 Cell Line	embryonic stem cell
41	chr5:9548800-9552800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr5:9549000-9550600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
43	chr5:9549000-9550600	Strong transcription	Left Ventricle	heart
44	chr5:9549000-9550800	Strong transcription	NHEK	skin
45	chr5:9549000-9552000	Strong transcription	Colonic Mucosa	Colon
46	chr5:9549000-9552200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr5:9549000-9552200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr5:9549000-9552200	Strong transcription	Duodenum Mucosa	Duodenum
49	chr5:9549000-9552400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr5:9549000-9552400	Strong transcription	Placenta	Placenta

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