Variant report

Variant	nsv980655
Chromosome Location	chr5:68660597-68661996
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:52)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:52 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr5:68660258-68660668	K562	blood:	n/a	n/a
2	CEBPB	chr5:68660176-68660624	K562	blood:	n/a	chr5:68660260-68660271 chr5:68660260-68660271
3	CTCF	chr5:68660308-68660617	K562	blood:	n/a	n/a
4	CTCF	chr5:68660277-68660604	GM12878	blood:	n/a	n/a
5	CTCF	chr5:68660460-68660610	HFF-Myc	foreskin:	n/a	n/a
6	CTCF	chr5:68660460-68660610	NHLF	lung:	n/a	n/a
7	CTCF	chr5:68660291-68660644	K562	blood:	n/a	n/a
8	CTCF	chr5:68660840-68660990	BE2_C	brain:	n/a	n/a
9	CTCF	chr5:68660313-68660615	IMR90	lung:	n/a	n/a
10	CTCF	chr5:68660460-68660610	WI-38	lung:	n/a	n/a
11	FOS	chr5:68660771-68660966	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr5:68660771-68660983	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr5:68660711-68660970	MCF10A-Er-Src	breast:	n/a	n/a
14	HEY1	chr5:68660869-68661297	K562	blood:	n/a	n/a
15	JUN	chr5:68660680-68661004	HepG2	liver:	n/a	chr5:68660867-68660880
16	JUND	chr5:68660324-68661023	HepG2	liver:	n/a	chr5:68660842-68660853
17	MAFF	chr5:68660760-68661128	HepG2	liver:	n/a	chr5:68660934-68660952
18	MAFF	chr5:68660775-68661107	K562	blood:	n/a	chr5:68660934-68660952
19	MAFK	chr5:68660756-68661125	HepG2	liver:	n/a	chr5:68660936-68660951
20	MAFK	chr5:68660391-68661129	HepG2	liver:	n/a	chr5:68660936-68660951
21	MAFK	chr5:68660749-68661086	Hela-S3	cervix:	n/a	chr5:68660936-68660951
22	MAFK	chr5:68660763-68661010	H1-hESC	embryonic stem cell:	n/a	chr5:68660936-68660951
23	MAFK	chr5:68660359-68661129	K562	blood:	n/a	chr5:68660936-68660951
24	MAFK	chr5:68660758-68661162	IMR90	lung:	n/a	chr5:68660936-68660951
25	POLR2A	chr5:68660813-68661320	GM12878	blood:	n/a	n/a
26	POLR2A	chr5:68660766-68660818	HUVEC	blood vessel:	n/a	n/a
27	POLR2A	chr5:68660939-68661156	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr5:68660156-68660790	GM12878	blood:	n/a	n/a
29	POLR2A	chr5:68660181-68660709	A549	lung:	n/a	n/a
30	POLR2A	chr5:68660103-68661118	K562	blood:	n/a	n/a
31	POLR2A	chr5:68660141-68660646	GM12892	blood:	n/a	n/a
32	POLR2A	chr5:68660786-68661556	SK-N-MC	brain:	n/a	n/a
33	POLR2A	chr5:68660991-68661140	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr5:68660255-68661023	HepG2	liver:	n/a	n/a
35	POLR2A	chr5:68660658-68661167	GM12892	blood:	n/a	n/a
36	POLR2A	chr5:68659738-68662513	K562	blood:	n/a	n/a
37	POLR2A	chr5:68660305-68660620	GM12891	blood:	n/a	n/a
38	POLR2A	chr5:68660742-68661205	GM12891	blood:	n/a	n/a
39	POLR2A	chr5:68660092-68661244	K562	blood:	n/a	n/a
40	POLR2A	chr5:68660879-68661035	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr5:68661291-68661644	GM12891	blood:	n/a	n/a
42	POLR2A	chr5:68660169-68660620	GM12878	blood:	n/a	n/a
43	POLR2A	chr5:68661918-68662117	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr5:68660723-68661103	K562	blood:	n/a	n/a
45	POLR2A	chr5:68660839-68661196	GM12891	blood:	n/a	n/a
46	POLR2A	chr5:68660964-68661117	GM12878	blood:	n/a	n/a
47	POLR2A	chr5:68660733-68660876	H1-hESC	embryonic stem cell:	n/a	n/a
48	RAD21	chr5:68660292-68660599	Hela-S3	cervix:	n/a	chr5:68660451-68660458
49	RAD21	chr5:68660313-68660598	HepG2	liver:	n/a	chr5:68660451-68660458
50	STAT3	chr5:68660684-68660848	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:68661350-68661400	NHBE	bronchial:	n/a
2	chr5:68661350-68661400	A549	lung:	n/a
3	chr5:68661350-68661400	LNCaP	prostate:	n/a
4	chr5:68661350-68661400	AG04450	lung:	fetal
5	chr5:68661350-68661400	HepG2	liver:	n/a
6	chr5:68661350-68661400	BE2_C	brain:	n/a
7	chr5:68661350-68661400	PrEC	prostate:	n/a
8	chr5:68661350-68661400	Caco-2	colon:	n/a
9	chr5:68661350-68661400	HRE	kidney:	n/a
10	chr5:68661350-68661400	SKMC	muscle:	n/a
11	chr5:68661350-68661400	NH-A	brain:	n/a
12	chr5:68661350-68661400	HL-60	blood:	n/a
13	chr5:68661350-68661400	AG09319	gingival:	n/a
14	chr5:68661350-68661400	SK-N-MC	brain:	n/a
15	chr5:68661350-68661400	AG04449	skin:	fetal
16	chr5:68661350-68661400	NT2-D1	testis:	n/a
17	chr5:68661350-68661400	GM06990	blood:	n/a
18	chr5:68661350-68661400	HPAEpiC	pulmonary alveolar:	n/a
19	chr5:68661350-68661400	HCT-116	colon:	n/a
20	chr5:68661350-68661400	PFSK-1	brain:	n/a
21	chr5:68661350-68661400	GM12891	blood:	n/a
22	chr5:68661350-68661400	HAEpiC	amniotic membrane:	n/a
23	chr5:68661350-68661400	HEEpiC	esophagus:	n/a
24	chr5:68661350-68661400	SK-N-SH	brain:	n/a
25	chr5:68661350-68661400	Jurkat	blood:	n/a
26	chr5:68661350-68661400	MCF-7	breast:	n/a
27	chr5:68661350-68661400	NHDF-neo	bronchial:	n/a
28	chr5:68661350-68661400	HRPEpiC	eye:	n/a
29	chr5:68661350-68661400	HCPEpiC	choroid plexus:	n/a
30	chr5:68661350-68661400	ECC-1	luminal epithelium:	n/a
31	chr5:68661350-68661400	K562	blood:	n/a
32	chr5:68661350-68661400	ovcar-3	ovarian:	n/a
33	chr5:68661350-68661400	HUVEC	blood vessel:	n/a
34	chr5:68661350-68661400	GM12878	blood:	n/a
35	chr5:68661350-68661400	HRCEpiC	kidney:	n/a
36	chr5:68661350-68661400	HEK293	kidney:	embryo
37	chr5:68661350-68661400	IMR90	lung:	fetal
38	chr5:68661350-68661400	ProgFib	skin:	n/a
39	chr5:68661350-68661400	PANC-1	pancreas:	n/a
40	chr5:68661350-68661400	HNPCEpiC	eye:	n/a
41	chr5:68661350-68661400	BJ	skin:	n/a
42	chr5:68661350-68661400	MCF10A-Er-Src	breast:	n/a
43	chr5:68661350-68661400	HMEC	breast:	n/a
44	chr5:68661350-68661400	HCF	heart:	n/a
45	chr5:68661350-68661400	U87	brain:	n/a
46	chr5:68661350-68661400	GM19239	blood:	n/a
47	chr5:68661350-68661400	Hela-S3	cervix:	n/a
48	chr5:68661350-68661400	AG10803	skin:	n/a
49	chr5:68661350-68661400	GM12892	blood:	n/a
50	chr5:68661350-68661400	NB4	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:68530945..68532461-chr5:68661059..68663307,2	K562	blood:
2	chr5:68659075..68661167-chr5:68788179..68790221,2	MCF-7	breast:
3	chr5:68644789..68648896-chr5:68660361..68665573,5	K562	blood:
4	chr5:68626792..68633026-chr5:68660168..68667090,13	MCF-7	breast:
5	chr5:68637589..68639798-chr5:68660289..68662388,2	MCF-7	breast:
6	chr5:68626462..68633259-chr5:68656360..68665608,14	MCF-7	breast:
7	chr5:68655369..68657333-chr5:68659094..68660959,2	MCF-7	breast:
8	chr5:68654797..68657370-chr5:68660109..68661621,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TAF9	hsa-miR-16-5p	chr5:68660699-68660722

Variant related genes	Relation type
RAD17	TF binding region
RAD17	CpG island
ENSG00000134058	chromatin interactions
ENSG00000183323	chromatin interactions
ENSG00000197822	chromatin interactions
ENSG00000271045	chromatin interactions
ENSG00000215006	chromatin interactions

Extended variants
information (count: 65 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:65 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202001793	chr5:68660721-68660722	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region miRNA target site	6 gene(s)	Overlapped CNVs	n/a
2	rs1802767	chr5:68660735-68660736	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs138549217	chr5:68660768-68660769	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs182239883	chr5:68660781-68660782	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs138635374	chr5:68660786-68660787	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs548057941	chr5:68660800-68660801	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs559947664	chr5:68660802-68660803	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs527471914	chr5:68660803-68660804	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs558584166	chr5:68660804-68660805	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs551896541	chr5:68660809-68660810	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs570480786	chr5:68660810-68660811	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs146996937	chr5:68660836-68660837	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs549714068	chr5:68660863-68660864	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs375540616	chr5:68660884-68660885	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs17849755	chr5:68660892-68660893	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs568680612	chr5:68660908-68660909	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs11542580	chr5:68660935-68660936	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs138121137	chr5:68660951-68660952	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs540368237	chr5:68660964-68660965	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs369915657	chr5:68660970-68660971	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs201594691	chr5:68660988-68660989	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs143694270	chr5:68661022-68661023	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs376232365	chr5:68661028-68661029	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs139529741	chr5:68661064-68661065	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs149658269	chr5:68661066-68661067	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs201579031	chr5:68661075-68661076	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs368866547	chr5:68661077-68661078	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs372574875	chr5:68661087-68661088	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs141432494	chr5:68661112-68661113	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs576827210	chr5:68661124-68661125	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs150848424	chr5:68661127-68661128	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs376343029	chr5:68661250-68661251	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs369843156	chr5:68661255-68661256	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs374084798	chr5:68661330-68661331	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs139330602	chr5:68661331-68661332	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs150010364	chr5:68661392-68661393	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs376721865	chr5:68661398-68661399	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs576444241	chr5:68661406-68661407	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs200198878	chr5:68661428-68661429	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs11542581	chr5:68661431-68661432	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs373908767	chr5:68661432-68661433	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs376244246	chr5:68661455-68661456	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs573934024	chr5:68661472-68661473	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs377584422	chr5:68661529-68661530	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs573124907	chr5:68661539-68661540	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs4252233	chr5:68661548-68661549	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs560008557	chr5:68661634-68661635	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs527486320	chr5:68661663-68661664	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs551912653	chr5:68661671-68661672	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs564040390	chr5:68661675-68661676	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ovarian cancer	21781307	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
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	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
Hepatocellular carcinoma	16750200	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
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21990379	CNVD
Hirschsprung''s Disease	21712996	CNVD
Apoptosis	19488400	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Acute monocytic leukemia	16498392	CNVD
Colorectal cancer	20459617	CNVD
Gastric adenocarcinoma	19115996	CNVD
Spinal muscular atrophy	17160897	CNVD
Spinal muscular atrophy	17668391	CNVD
Spinal muscular atrophy	17668395	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68639200-68663400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr5:68643000-68664400	Weak transcription	Colonic Mucosa	Colon
3	chr5:68643200-68663200	Weak transcription	Small Intestine	intestine
4	chr5:68643800-68660800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr5:68643800-68663600	Weak transcription	Brain Angular Gyrus	brain
6	chr5:68644000-68660600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr5:68644800-68660800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr5:68645200-68660600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr5:68645800-68660800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr5:68645800-68663400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr5:68646200-68661000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr5:68646200-68661000	Weak transcription	Pancreas	Pancrea
13	chr5:68646400-68660800	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr5:68646600-68661000	Weak transcription	Psoas Muscle	Psoas
15	chr5:68647400-68663400	Weak transcription	Fetal Brain Male	brain
16	chr5:68647400-68663800	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr5:68648400-68663400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr5:68649200-68663600	Weak transcription	Brain Substantia Nigra	brain
19	chr5:68649400-68663400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr5:68651400-68660800	Weak transcription	Left Ventricle	heart
21	chr5:68651400-68660800	Weak transcription	Rectal Smooth Muscle	rectum
22	chr5:68651400-68663600	Weak transcription	Right Ventricle	heart
23	chr5:68651400-68664400	Weak transcription	Aorta	Aorta
24	chr5:68653200-68664600	Weak transcription	Esophagus	oesophagus
25	chr5:68654400-68663200	Strong transcription	Primary B cells from peripheral blood	blood
26	chr5:68654800-68663400	Strong transcription	Fetal Muscle Leg	muscle
27	chr5:68655600-68662400	Strong transcription	Primary T cells from cord blood	blood
28	chr5:68656000-68663400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr5:68656000-68663400	Strong transcription	Fetal Thymus	thymus
30	chr5:68656600-68660600	Weak transcription	Primary hematopoietic stem cells	blood
31	chr5:68657000-68663200	Strong transcription	Primary monocytes fromperipheralblood	blood
32	chr5:68657800-68663200	Strong transcription	HUES64 Cell Line	embryonic stem cell
33	chr5:68657800-68663200	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr5:68657800-68663400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr5:68657800-68663400	Strong transcription	Fetal Muscle Trunk	muscle
36	chr5:68658000-68661600	Strong transcription	Fetal Brain Female	brain
37	chr5:68658000-68662000	Strong transcription	A549	lung
38	chr5:68658000-68662200	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr5:68658000-68662400	Strong transcription	HUVEC	blood vessel
40	chr5:68658000-68662400	Strong transcription	K562	blood
41	chr5:68658000-68662600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr5:68658000-68663000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:68658000-68663000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr5:68658000-68663000	Strong transcription	Liver	Liver
45	chr5:68658000-68663200	Strong transcription	Primary B cells from cord blood	blood
46	chr5:68658000-68663200	Strong transcription	Placenta	Placenta
47	chr5:68658000-68663400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr5:68658000-68663400	Strong transcription	HUES6 Cell Line	embryonic stem cell
49	chr5:68658000-68663400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr5:68658200-68660600	Strong transcription	GM12878-XiMat	blood

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