Variant report

Variant	nsv518862
Chromosome Location	chr5:7887478-7896511
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	ARID3A	chr5:7887185-7887551	HepG2	liver:	n/a	n/a
2	BATF	chr5:7894984-7895268	GM12878	blood:	n/a	n/a
3	BATF	chr5:7894979-7895288	GM12878	blood:	n/a	n/a
4	CEBPB	chr5:7892510-7892876	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr5:7892518-7892877	HepG2	liver:	n/a	n/a
6	CEBPB	chr5:7892528-7892870	IMR90	lung:	n/a	n/a
7	CEBPB	chr5:7892580-7892831	K562	blood:	n/a	n/a
8	CEBPB	chr5:7892534-7892945	A549	lung:	n/a	n/a
9	CTCF	chr5:7887400-7887550	HFF-Myc	foreskin:	n/a	n/a
10	CTCF	chr5:7887340-7887490	MCF-7	breast:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
11	CTCF	chr5:7887164-7887571	HepG2	liver:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
12	CTCF	chr5:7887222-7887527	HUVEC	blood vessel:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
13	CTCF	chr5:7887340-7887490	BJ	skin:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
14	CTCF	chr5:7887139-7887577	GM12878	blood:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
15	CTCF	chr5:7887340-7887490	GM12878	blood:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
16	CTCF	chr5:7887340-7887490	GM06990	blood:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
17	CTCF	chr5:7887272-7887527	SK-N-SH_RA	brain:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
18	CTCF	chr5:7887340-7887490	GM12867	blood:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
19	CTCF	chr5:7887360-7887510	HMEC	breast:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
20	CTCF	chr5:7887270-7887616	MCF-7	breast:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
21	CTCF	chr5:7887360-7887510	HRE	kidney:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
22	CTCF	chr5:7887340-7887490	GM12872	blood:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
23	CTCF	chr5:7887380-7887530	WI-38	lung:	n/a	chr5:7887381-7887402
24	CTCF	chr5:7887161-7887547	MCF-7	breast:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
25	CTCF	chr5:7887235-7887523	Spleen_OC	spleen:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
26	CTCF	chr5:7887340-7887490	HCPEpiC	choroid plexus:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
27	CTCF	chr5:7887260-7887550	MCF-7	breast:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
28	CTCF	chr5:7887303-7887489	LNCaP	prostate:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
29	CTCF	chr5:7887380-7887530	HAc	cerebellar:	n/a	chr5:7887381-7887402
30	CTCF	chr5:7887295-7887508	Lung_OC	lung:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
31	CTCF	chr5:7887270-7887493	Hela-S3	cervix:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
32	CTCF	chr5:7887400-7887550	GM12866	blood:	n/a	n/a
33	CTCF	chr5:7887256-7887489	GM12878	blood:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
34	CTCF	chr5:7887273-7887520	Medullo	brain:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
35	CTCF	chr5:7887360-7887510	K562	blood:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
36	CTCF	chr5:7886927-7887602	IMR90	lung:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
37	CTCF	chr5:7887360-7887510	NHDF-neo	bronchial:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
38	CTCF	chr5:7887360-7887510	GM12873	blood:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
39	CTCF	chr5:7887340-7887490	AoAF	blood vessel:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
40	CTCF	chr5:7887340-7887490	HVMF	connective:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
41	CTCF	chr5:7887181-7887587	K562	blood:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
42	CTCF	chr5:7887340-7887490	HUVEC	blood vessel:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
43	CTCF	chr5:7887177-7887550	H1-hESC	embryonic stem cell:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
44	CTCF	chr5:7887350-7887495	MCF-7	breast:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
45	CTCF	chr5:7886971-7887791	A549	lung:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
46	CTCF	chr5:7887147-7887543	A549	lung:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
47	CTCF	chr5:7887274-7887487	K562	blood:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
48	CTCF	chr5:7887360-7887510	GM12875	blood:	n/a	chr5:7887379-7887397 chr5:7887381-7887402
49	CUX1	chr5:7894842-7894878	K562	blood:	n/a	n/a
50	EBF1	chr5:7894933-7895216	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:7888576-7888626	HCPEpiC	choroid plexus:	n/a
2	chr5:7888576-7888626	HepG2	liver:	n/a
3	chr5:7888576-7888626	GM12891	blood:	n/a
4	chr5:7888576-7888626	U87	brain:	n/a
5	chr5:7888576-7888626	HAEpiC	amniotic membrane:	n/a
6	chr5:7888576-7888626	HRE	kidney:	n/a
7	chr5:7888576-7888626	ECC-1	luminal epithelium:	n/a
8	chr5:7888576-7888626	NH-A	brain:	n/a
9	chr5:7888576-7888626	Caco-2	colon:	n/a
10	chr5:7888576-7888626	HL-60	blood:	n/a
11	chr5:7888576-7888626	AG04449	skin:	fetal
12	chr5:7888576-7888626	MCF-7	breast:	n/a
13	chr5:7888576-7888626	PANC-1	pancreas:	n/a
14	chr5:7888576-7888626	BJ	skin:	n/a
15	chr5:7888576-7888626	LNCaP	prostate:	n/a
16	chr5:7888576-7888626	T-47D	breast:	n/a
17	chr5:7888576-7888626	NHBE	bronchial:	n/a
18	chr5:7888576-7888626	Jurkat	blood:	n/a
19	chr5:7888576-7888626	H1-hESC	embryonic stem cell:	embryo
20	chr5:7888576-7888626	HRPEpiC	eye:	n/a
21	chr5:7888576-7888626	HRCEpiC	kidney:	n/a
22	chr5:7888576-7888626	SK-N-SH	brain:	n/a
23	chr5:7888576-7888626	HMEC	breast:	n/a
24	chr5:7888576-7888626	HNPCEpiC	eye:	n/a
25	chr5:7888576-7888626	PrEC	prostate:	n/a
26	chr5:7888576-7888626	NHDF-neo	bronchial:	n/a
27	chr5:7888576-7888626	HIPEpiC	eye:	n/a
28	chr5:7888576-7888626	Hepatocyte	liver:	n/a
29	chr5:7888576-7888626	AG04450	lung:	fetal
30	chr5:7888576-7888626	HCM	heart:	n/a
31	chr5:7888576-7888626	SAEC	small airway:	n/a
32	chr5:7888576-7888626	A549	lung:	n/a
33	chr5:7888576-7888626	GM12892	blood:	n/a
34	chr5:7888576-7888626	PFSK-1	brain:	n/a
35	chr5:7888576-7888626	HUVEC	blood vessel:	n/a
36	chr5:7888576-7888626	SK-N-SH_RA	brain:	n/a
37	chr5:7888576-7888626	GM12878	blood:	n/a
38	chr5:7888576-7888626	NB4	blood:	n/a
39	chr5:7888576-7888626	SK-N-MC	brain:	n/a
40	chr5:7888576-7888626	RPTEC	kidney:	n/a
41	chr5:7888576-7888626	IMR90	lung:	fetal
42	chr5:7888576-7888626	AoSMC	blood vessel:	n/a
43	chr5:7888576-7888626	ProgFib	skin:	n/a
44	chr5:7888576-7888626	AG09319	gingival:	n/a
45	chr5:7888576-7888626	GM06990	blood:	n/a
46	chr5:7888576-7888626	NT2-D1	testis:	n/a
47	chr5:7888576-7888626	BE2_C	brain:	n/a
48	chr5:7888576-7888626	HPAEpiC	pulmonary alveolar:	n/a
49	chr5:7888576-7888626	AG09309	skin:	n/a
50	chr5:7888576-7888626	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:7873979..7876833-chr5:7886025..7888380,2	K562	blood:
2	chr5:7886573..7888723-chr5:7891916..7894639,3	K562	blood:
3	chr5:7867651..7870301-chr5:7886397..7888680,2	MCF-7	breast:
4	chr5:7887367..7887882-chr5:9207640..9208590,2	K562	blood:

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

Extended variants
information (count: 426 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs162040	chr5:7887478-7887479	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs13190084	chr5:7887488-7887489	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs533194390	chr5:7887509-7887510	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs544364801	chr5:7887568-7887569	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs564722699	chr5:7887591-7887592	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs2914032	chr5:7887650-7887651	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs577768398	chr5:7887651-7887652	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs416455	chr5:7887670-7887671	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs533386392	chr5:7887674-7887675	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs532744558	chr5:7887679-7887680	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs188434552	chr5:7887711-7887712	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs142548228	chr5:7887723-7887724	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs144069526	chr5:7887847-7887848	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs72162827	chr5:7887848-7887849	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs467102	chr5:7887849-7887850	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs200127709	chr5:7887855-7887856	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs146105409	chr5:7887868-7887869	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs140063418	chr5:7887871-7887872	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs466575	chr5:7887881-7887882	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs138411575	chr5:7887890-7887891	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs368560714	chr5:7887904-7887905	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs372829698	chr5:7887907-7887908	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs113778866	chr5:7887908-7887909	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs111247975	chr5:7887909-7887910	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs460625	chr5:7887913-7887914	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
26	rs568935911	chr5:7887920-7887921	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs371160132	chr5:7887922-7887923	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs537957711	chr5:7887924-7887925	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs60340929	chr5:7887943-7887944	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs62342529	chr5:7887944-7887945	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs569354527	chr5:7887945-7887946	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs568515769	chr5:7887946-7887947	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs374345190	chr5:7887947-7887948	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs113168263	chr5:7887962-7887963	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs192932719	chr5:7887980-7887981	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs326125	chr5:7888001-7888002	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs372145141	chr5:7888023-7888024	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs375482658	chr5:7888071-7888072	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs112040085	chr5:7888078-7888079	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs62342530	chr5:7888198-7888199	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs162041	chr5:7888218-7888219	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs162042	chr5:7888248-7888249	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs57240487	chr5:7888291-7888292	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs564455683	chr5:7888349-7888350	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs369121082	chr5:7888392-7888393	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs578115011	chr5:7888399-7888400	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs558065325	chr5:7888406-7888407	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs540519064	chr5:7888491-7888492	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs560793697	chr5:7888500-7888501	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs371574382	chr5:7888504-7888505	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:385 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:7870200-7903400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:7871000-7894000	Weak transcription	Fetal Heart	heart
3	chr5:7871200-7903400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
4	chr5:7871200-7903600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
5	chr5:7871200-7903800	Strong transcription	HUES64 Cell Line	embryonic stem cell
6	chr5:7871400-7902400	Strong transcription	K562	blood
7	chr5:7871400-7903800	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr5:7871600-7887600	Strong transcription	Placenta	Placenta
9	chr5:7871600-7902800	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr5:7871600-7905000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr5:7871600-7906400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr5:7871600-7906800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr5:7871800-7907400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
14	chr5:7872000-7895200	Strong transcription	Fetal Muscle Leg	muscle
15	chr5:7873200-7887600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr5:7873200-7903400	Strong transcription	Dnd41	blood
17	chr5:7873400-7904000	Strong transcription	Hela-S3	cervix
18	chr5:7874000-7890800	Strong transcription	Duodenum Smooth Muscle	Duodenum
19	chr5:7874000-7905400	Strong transcription	Primary T cells from cord blood	blood
20	chr5:7874000-7909200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr5:7874600-7894400	Strong transcription	Adipose Nuclei	Adipose
22	chr5:7874800-7887600	Strong transcription	Skeletal Muscle Female	skeletal muscle
23	chr5:7875000-7906600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:7875400-7895200	Strong transcription	H1 Cell Line	embryonic stem cell
25	chr5:7875400-7903600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr5:7875400-7903800	Strong transcription	Primary B cells from peripheral blood	blood
27	chr5:7875400-7904200	Strong transcription	Primary hematopoietic stem cells	blood
28	chr5:7875400-7904400	Strong transcription	Fetal Muscle Trunk	muscle
29	chr5:7875600-7904400	Strong transcription	Left Ventricle	heart
30	chr5:7878600-7911800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
31	chr5:7878800-7888600	Weak transcription	Psoas Muscle	Psoas
32	chr5:7878800-7890600	Strong transcription	NH-A	brain
33	chr5:7879200-7901800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr5:7879200-7906400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr5:7879400-7889800	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr5:7879600-7900600	Strong transcription	Primary B cells from cord blood	blood
37	chr5:7880000-7894400	Strong transcription	Duodenum Mucosa	Duodenum
38	chr5:7880000-7903600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr5:7880200-7887600	Strong transcription	Sigmoid Colon	Sigmoid Colon
40	chr5:7880200-7892000	Strong transcription	GM12878-XiMat	blood
41	chr5:7880200-7894200	Weak transcription	Stomach Mucosa	stomach
42	chr5:7880400-7906600	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr5:7880600-7907000	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr5:7880800-7903800	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr5:7881000-7904400	Strong transcription	Fetal Intestine Large	intestine
46	chr5:7882200-7902200	Strong transcription	Primary T helper naive cells from peripheral blood	blood
47	chr5:7882400-7898600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr5:7882400-7905000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr5:7882600-7898600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr5:7883800-7894400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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