Variant report

Variant	esv1839988
Chromosome Location	chr8:58122510-58130784
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:264)
CpG islands
(count:612)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:58122168-58122783	HepG2	liver:	n/a	n/a
2	ATF1	chr8:58122169-58123010	K562	blood:	n/a	n/a
3	BACH1	chr8:58122347-58122997	K562	blood:	n/a	n/a
4	BHLHE40	chr8:58122112-58123036	K562	blood:	n/a	n/a
5	BHLHE40	chr8:58127590-58127948	K562	blood:	n/a	n/a
6	BRCA1	chr8:58127563-58127875	GM12878	blood:	n/a	n/a
7	BRCA1	chr8:58122170-58122971	HepG2	liver:	n/a	n/a
8	BRCA1	chr8:58122208-58123016	GM12878	blood:	n/a	n/a
9	BRCA1	chr8:58127438-58127751	HepG2	liver:	n/a	n/a
10	CEBPB	chr8:58122125-58123045	K562	blood:	n/a	n/a
11	CHD1	chr8:58122169-58123189	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr8:58122268-58123011	HepG2	liver:	n/a	n/a
13	CHD2	chr8:58122614-58122989	GM12878	blood:	n/a	n/a
14	CHD2	chr8:58127562-58127861	HepG2	liver:	n/a	n/a
15	CHD2	chr8:58122153-58122987	K562	blood:	n/a	n/a
16	CTCF	chr8:58127540-58127690	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr8:58123380-58123530	GM12869	blood:	n/a	n/a
18	CTCF	chr8:58125600-58125750	HEEpiC	esophagus:	n/a	n/a
19	CTCF	chr8:58122880-58123030	GM12867	blood:	n/a	n/a
20	CTCF	chr8:58123240-58123390	GM12870	blood:	n/a	n/a
21	CTCF	chr8:58122860-58123010	HCT-116	colon:	n/a	n/a
22	CTCF	chr8:58122800-58122950	GM12864	blood:	n/a	n/a
23	CTCF	chr8:58122800-58122950	GM12878	blood:	n/a	n/a
24	CTCF	chr8:58122540-58122690	GM12871	blood:	n/a	n/a
25	CTCF	chr8:58124140-58124290	GM12866	blood:	n/a	n/a
26	CTCF	chr8:58123200-58123350	NHLF	lung:	n/a	n/a
27	CTCF	chr8:58122680-58122830	NHLF	lung:	n/a	n/a
28	CTCF	chr8:58126534-58126613	HepG2	liver:	n/a	n/a
29	CTCF	chr8:58122760-58122910	GM12875	blood:	n/a	n/a
30	CTCF	chr8:58122620-58122770	MCF-7	breast:	n/a	n/a
31	CTCF	chr8:58127640-58127790	GM12872	blood:	n/a	n/a
32	CTCF	chr8:58123320-58123470	HEEpiC	esophagus:	n/a	n/a
33	CTCF	chr8:58122680-58122830	GM12870	blood:	n/a	n/a
34	CTCF	chr8:58122640-58122790	GM12864	blood:	n/a	n/a
35	CTCF	chr8:58125560-58125710	GM12869	blood:	n/a	n/a
36	CTCF	chr8:58123340-58123490	HPF	lung:	n/a	n/a
37	CTCF	chr8:58122640-58122790	HCM	heart:	n/a	n/a
38	CTCF	chr8:58126544-58126631	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr8:58123320-58123470	GM12864	blood:	n/a	n/a
40	CTCF	chr8:58127560-58127710	GM12868	blood:	n/a	n/a
41	CTCF	chr8:58127680-58127830	K562	blood:	n/a	n/a
42	CTCF	chr8:58122620-58122770	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr8:58123260-58123410	AG10803	skin:	n/a	n/a
44	CTCF	chr8:58122860-58123010	GM12865	blood:	n/a	n/a
45	CTCF	chr8:58126535-58126668	K562	blood:	n/a	n/a
46	CTCF	chr8:58127680-58127830	AG10803	skin:	n/a	n/a
47	CTCF	chr8:58122500-58122650	NB4	blood:	n/a	n/a
48	CTCF	chr8:58122760-58122910	BE2_C	brain:	n/a	n/a
49	CTCF	chr8:58122880-58123030	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr8:58122740-58122890	MCF-7	breast:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:58130467-58130517	RPTEC	kidney:	n/a
2	chr8:58124249-58124299	K562	blood:	n/a
3	chr8:58130467-58130517	RPTEC	kidney:	n/a
4	chr8:58124249-58124299	K562	blood:	n/a
5	chr8:58122850-58122900	NHBE	bronchial:	n/a
6	chr8:58130323-58130373	AG10803	skin:	n/a
7	chr8:58130467-58130517	K562	blood:	n/a
8	chr8:58130323-58130373	LNCaP	prostate:	n/a
9	chr8:58123513-58123563	CMK	blood:	n/a
10	chr8:58129604-58129654	HMEC	breast:	n/a
11	chr8:58129604-58129654	AG10803	skin:	n/a
12	chr8:58126962-58127012	SAEC	small airway:	n/a
13	chr8:58128724-58128774	HEEpiC	esophagus:	n/a
14	chr8:58128724-58128774	NB4	blood:	n/a
15	chr8:58130323-58130373	RPTEC	kidney:	n/a
16	chr8:58128466-58128516	AG10803	skin:	n/a
17	chr8:58123513-58123563	HEK293	kidney:	embryo
18	chr8:58124249-58124299	H1-hESC	embryonic stem cell:	embryo
19	chr8:58130041-58130091	HPAEpiC	pulmonary alveolar:	n/a
20	chr8:58123513-58123563	NHBE	bronchial:	n/a
21	chr8:58122850-58122900	U87	brain:	n/a
22	chr8:58130467-58130517	HRE	kidney:	n/a
23	chr8:58130467-58130517	GM06990	blood:	n/a
24	chr8:58122850-58122900	HCPEpiC	choroid plexus:	n/a
25	chr8:58123513-58123563	AG09319	gingival:	n/a
26	chr8:58126962-58127012	HRCEpiC	kidney:	n/a
27	chr8:58124249-58124299	MCF10A-Er-Src	breast:	n/a
28	chr8:58124249-58124299	HIPEpiC	eye:	n/a
29	chr8:58123513-58123563	PANC-1	pancreas:	n/a
30	chr8:58130041-58130091	A549	lung:	n/a
31	chr8:58122850-58122900	Jurkat	blood:	n/a
32	chr8:58126962-58127012	LNCaP	prostate:	n/a
33	chr8:58123513-58123563	K562	blood:	n/a
34	chr8:58128466-58128516	HCM	heart:	n/a
35	chr8:58126962-58127012	BE2_C	brain:	n/a
36	chr8:58128466-58128516	PrEC	prostate:	n/a
37	chr8:58130467-58130517	NHDF-neo	bronchial:	n/a
38	chr8:58130041-58130091	GM19239	blood:	n/a
39	chr8:58130467-58130517	HL-60	blood:	n/a
40	chr8:58130323-58130373	AG04449	skin:	fetal
41	chr8:58126962-58127012	HCM	heart:	n/a
42	chr8:58129604-58129654	HCT-116	colon:	n/a
43	chr8:58130467-58130517	ECC-1	luminal epithelium:	n/a
44	chr8:58124249-58124299	Hepatocyte	liver:	n/a
45	chr8:58128724-58128774	GM12878	blood:	n/a
46	chr8:58130323-58130373	ovcar-3	ovarian:	n/a
47	chr8:58128724-58128774	MCF10A-Er-Src	breast:	n/a
48	chr8:58130467-58130517	AG09309	skin:	n/a
49	chr8:58123513-58123563	H1-hESC	embryonic stem cell:	embryo
50	chr8:58126962-58127012	AG10803	skin:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
2	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
3	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
4	chr8:58127588..58129747-chr8:58135062..58137669,2	K562	blood:
5	chr8:58122191..58122786-chr8:58255142..58256110,2	K562	blood:
6	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:
7	chr8:58121826..58122902-chr8:58255580..58256503,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000253301	TF binding region
ENSG00000253301	CpG island
ENSG00000253871	chromatin interactions

Extended variants
information (count: 629 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:629 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7013554	chr8:58122510-58122511	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs58684012	chr8:58122632-58122633	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs533150914	chr8:58122637-58122638	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs148357319	chr8:58122680-58122681	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs367929704	chr8:58122725-58122726	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs28504275	chr8:58122740-58122741	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs112188902	chr8:58122745-58122746	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs6996550	chr8:58122750-58122751	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs57312308	chr8:58122759-58122760	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs375644563	chr8:58122768-58122769	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs529561355	chr8:58122782-58122783	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs140680715	chr8:58122908-58122909	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs549267013	chr8:58122939-58122940	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs369725152	chr8:58122950-58122951	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs7015511	chr8:58122975-58122976	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs373965140	chr8:58123018-58123019	ZNF genes & repeats Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs11992325	chr8:58123028-58123029	ZNF genes & repeats Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs538535660	chr8:58123051-58123052	ZNF genes & repeats Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs75899248	chr8:58123052-58123053	ZNF genes & repeats Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs77241898	chr8:58123053-58123054	ZNF genes & repeats Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs371165402	chr8:58123130-58123131	ZNF genes & repeats Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs62513463	chr8:58123187-58123188	ZNF genes & repeats Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs373669946	chr8:58123199-58123200	ZNF genes & repeats Weak transcription Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs113482295	chr8:58123237-58123238	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs62513464	chr8:58123241-58123242	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs145770673	chr8:58123274-58123275	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200820482	chr8:58123280-58123281	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs60582150	chr8:58123284-58123285	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556889390	chr8:58123290-58123291	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143049076	chr8:58123293-58123294	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113783076	chr8:58123321-58123322	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148282646	chr8:58123387-58123388	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536511016	chr8:58123447-58123448	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs145941875	chr8:58123466-58123467	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs141254465	chr8:58123511-58123512	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs368136307	chr8:58123529-58123530	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs150784517	chr8:58123545-58123546	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs139665571	chr8:58123577-58123578	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs138355524	chr8:58123620-58123621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2172942	chr8:58123653-58123654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113660654	chr8:58123674-58123675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111930634	chr8:58123688-58123689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144676584	chr8:58123713-58123714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149276915	chr8:58123742-58123743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200857345	chr8:58123851-58123852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201995818	chr8:58123854-58123855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs144477315	chr8:58123871-58123872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148425101	chr8:58123876-58123877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147486725	chr8:58123933-58123934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143658103	chr8:58123937-58123938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	22183965	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58120200-58123400	ZNF genes & repeats	Brain Germinal Matrix	brain
2	chr8:58122000-58123200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:58122000-58123200	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
4	chr8:58122000-58123200	ZNF genes & repeats	Fetal Brain Female	brain
5	chr8:58122000-58123200	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
6	chr8:58122000-58123400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:58122000-58123400	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:58122000-58123400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
9	chr8:58122000-58123400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr8:58122000-58123400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr8:58122200-58122600	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
12	chr8:58122200-58122800	ZNF genes & repeats	Brain Angular Gyrus	brain
13	chr8:58122200-58122800	ZNF genes & repeats	Fetal Heart	heart
14	chr8:58122200-58123000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
15	chr8:58122200-58123000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr8:58122200-58123000	ZNF genes & repeats	Adipose Nuclei	Adipose
17	chr8:58122200-58123000	ZNF genes & repeats	Aorta	Aorta
18	chr8:58122200-58123000	ZNF genes & repeats	Brain Anterior Caudate	brain
19	chr8:58122200-58123000	ZNF genes & repeats	Brain Hippocampus Middle	brain
20	chr8:58122200-58123000	ZNF genes & repeats	Brain Substantia Nigra	brain
21	chr8:58122200-58123000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
22	chr8:58122200-58123000	ZNF genes & repeats	Fetal Lung	lung
23	chr8:58122200-58123000	Bivalent Enhancer	Fetal Stomach	stomach
24	chr8:58122200-58123000	ZNF genes & repeats	Ovary	ovary
25	chr8:58122200-58123000	ZNF genes & repeats	Placenta Amnion	Placenta Amnion
26	chr8:58122200-58123000	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
27	chr8:58122200-58123000	ZNF genes & repeats	Right Atrium	heart
28	chr8:58122200-58123000	ZNF genes & repeats	Right Ventricle	heart
29	chr8:58122200-58123000	ZNF genes & repeats	Stomach Mucosa	stomach
30	chr8:58122200-58123000	ZNF genes & repeats	NHDF-Ad	bronchial
31	chr8:58122200-58123200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr8:58122200-58123200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
33	chr8:58122200-58123200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr8:58122200-58123200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr8:58122200-58123200	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
36	chr8:58122200-58123200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr8:58122200-58123200	ZNF genes & repeats	Primary mononuclear cells fromperipheralblood	Blood
38	chr8:58122200-58123200	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
39	chr8:58122200-58123200	ZNF genes & repeats	Duodenum Mucosa	Duodenum
40	chr8:58122200-58123200	ZNF genes & repeats	Fetal Brain Male	brain
41	chr8:58122200-58123200	ZNF genes & repeats	Fetal Intestine Small	intestine
42	chr8:58122200-58123200	ZNF genes & repeats	Gastric	stomach
43	chr8:58122200-58123200	ZNF genes & repeats	Rectal Smooth Muscle	rectum
44	chr8:58122200-58123200	ZNF genes & repeats	NHLF	lung
45	chr8:58122200-58123400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
46	chr8:58122200-58123400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr8:58122200-58123400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
48	chr8:58122200-58123400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
49	chr8:58122200-58123400	ZNF genes & repeats	Esophagus	oesophagus
50	chr8:58122200-58123400	ZNF genes & repeats	Fetal Kidney	kidney

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