Variant report

Variant	esv1813223
Chromosome Location	chr8:58108686-58130419
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:601)
CpG islands
(count:1342)
Chromatin interactive
region (count:16)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:601 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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	chr8:58118159-58118698	K562	blood:	n/a	n/a
6	BHLHE40	chr8:58127590-58127948	K562	blood:	n/a	n/a
7	BRCA1	chr8:58127438-58127751	HepG2	liver:	n/a	n/a
8	BRCA1	chr8:58118301-58118654	GM12878	blood:	n/a	n/a
9	BRCA1	chr8:58127563-58127875	GM12878	blood:	n/a	n/a
10	BRCA1	chr8:58122208-58123016	GM12878	blood:	n/a	n/a
11	BRCA1	chr8:58122170-58122971	HepG2	liver:	n/a	n/a
12	CEBPB	chr8:58118253-58118637	K562	blood:	n/a	chr8:58118437-58118448
13	CEBPB	chr8:58122125-58123045	K562	blood:	n/a	n/a
14	CEBPB	chr8:58118292-58118614	HepG2	liver:	n/a	chr8:58118437-58118448
15	CEBPZ	chr8:58118279-58118527	HepG2	liver:	n/a	n/a
16	CHD1	chr8:58122169-58123189	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr8:58118485-58118679	GM12878	blood:	n/a	n/a
18	CHD2	chr8:58122614-58122989	GM12878	blood:	n/a	n/a
19	CHD2	chr8:58118259-58118697	HepG2	liver:	n/a	n/a
20	CHD2	chr8:58122153-58122987	K562	blood:	n/a	n/a
21	CHD2	chr8:58127562-58127861	HepG2	liver:	n/a	n/a
22	CHD2	chr8:58122268-58123011	HepG2	liver:	n/a	n/a
23	CHD2	chr8:58116729-58116763	K562	blood:	n/a	n/a
24	CTCF	chr8:58122200-58122350	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr8:58122180-58122330	BE2_C	brain:	n/a	n/a
26	CTCF	chr8:58122106-58122590	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr8:58122173-58122320	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr8:58127680-58127830	GM12867	blood:	n/a	n/a
29	CTCF	chr8:58127640-58127790	GM12872	blood:	n/a	n/a
30	CTCF	chr8:58122640-58122790	GM12866	blood:	n/a	n/a
31	CTCF	chr8:58122180-58122330	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr8:58118314-58118380	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr8:58118420-58118570	AG09309	skin:	n/a	n/a
34	CTCF	chr8:58127640-58127790	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr8:58118460-58118610	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr8:58125620-58125770	NB4	blood:	n/a	n/a
37	CTCF	chr8:58122220-58122370	HMF	breast:	n/a	n/a
38	CTCF	chr8:58118380-58118530	MCF-7	breast:	n/a	n/a
39	CTCF	chr8:58123320-58123470	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr8:58118280-58118430	GM12864	blood:	n/a	n/a
41	CTCF	chr8:58121540-58121690	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr8:58125520-58125670	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr8:58118280-58118430	GM12872	blood:	n/a	n/a
44	CTCF	chr8:58127540-58127690	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr8:58123240-58123390	GM12866	blood:	n/a	n/a
46	CTCF	chr8:58118200-58118350	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr8:58118520-58118670	HEK293	kidney:	n/a	n/a
48	CTCF	chr8:58118220-58118370	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr8:58126296-58126324	GM19239	blood:	n/a	n/a
50	CTCF	chr8:58118400-58118550	AG04450	lung:	n/a	n/a

(count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:58117794-58117844	GM12891	blood:	n/a
2	chr8:58114950-58115000	AG09319	gingival:	n/a
3	chr8:58115012-58115062	GM12878	blood:	n/a
4	chr8:58124249-58124299	GM19239	blood:	n/a
5	chr8:58117687-58117737	AG04450	lung:	fetal
6	chr8:58117794-58117844	IMR90	lung:	fetal
7	chr8:58122215-58122265	NB4	blood:	n/a
8	chr8:58122215-58122265	GM19239	blood:	n/a
9	chr8:58123513-58123563	MCF-7	breast:	n/a
10	chr8:58114950-58115000	HEEpiC	esophagus:	n/a
11	chr8:58120465-58120515	AG09319	gingival:	n/a
12	chr8:58129604-58129654	HNPCEpiC	eye:	n/a
13	chr8:58117541-58117591	HMEC	breast:	n/a
14	chr8:58122850-58122900	H1-hESC	embryonic stem cell:	embryo
15	chr8:58122850-58122900	GM19239	blood:	n/a
16	chr8:58117687-58117737	ovcar-3	ovarian:	n/a
17	chr8:58121215-58121265	U87	brain:	n/a
18	chr8:58121215-58121265	BJ	skin:	n/a
19	chr8:58116908-58116958	LNCaP	prostate:	n/a
20	chr8:58117794-58117844	Jurkat	blood:	n/a
21	chr8:58120465-58120515	SK-N-MC	brain:	n/a
22	chr8:58117687-58117737	HepG2	liver:	n/a
23	chr8:58118711-58118761	Hepatocyte	liver:	n/a
24	chr8:58118711-58118761	Jurkat	blood:	n/a
25	chr8:58114950-58115000	HRPEpiC	eye:	n/a
26	chr8:58114915-58114965	RPTEC	kidney:	n/a
27	chr8:58124249-58124299	GM12892	blood:	n/a
28	chr8:58128466-58128516	HPAEpiC	pulmonary alveolar:	n/a
29	chr8:58130323-58130373	U87	brain:	n/a
30	chr8:58118711-58118761	HRPEpiC	eye:	n/a
31	chr8:58129604-58129654	AG09319	gingival:	n/a
32	chr8:58126962-58127012	MCF-7	breast:	n/a
33	chr8:58117794-58117844	AoSMC	blood vessel:	n/a
34	chr8:58130041-58130091	SK-N-SH_RA	brain:	n/a
35	chr8:58126962-58127012	HMEC	breast:	n/a
36	chr8:58129604-58129654	HCT-116	colon:	n/a
37	chr8:58128724-58128774	GM06990	blood:	n/a
38	chr8:58130041-58130091	HCM	heart:	n/a
39	chr8:58130323-58130373	PANC-1	pancreas:	n/a
40	chr8:58126962-58127012	BE2_C	brain:	n/a
41	chr8:58120465-58120515	GM06990	blood:	n/a
42	chr8:58117687-58117737	HIPEpiC	eye:	n/a
43	chr8:58126962-58127012	HepG2	liver:	n/a
44	chr8:58117687-58117737	SK-N-MC	brain:	n/a
45	chr8:58114950-58115000	U87	brain:	n/a
46	chr8:58114950-58115000	HEK293	kidney:	embryo
47	chr8:58122215-58122265	Caco-2	colon:	n/a
48	chr8:58116908-58116958	MCF10A-Er-Src	breast:	n/a
49	chr8:58117541-58117591	Hepatocyte	liver:	n/a
50	chr8:58130323-58130373	HAEpiC	amniotic membrane:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
2	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
3	chr8:58121826..58122902-chr8:58255580..58256503,3	MCF-7	breast:
4	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
5	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:
6	chr8:58122191..58122786-chr8:58255142..58256110,2	K562	blood:
7	chr8:58104914..58107604-chr8:58109994..58112221,3	K562	blood:
8	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
9	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
10	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:
11	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
12	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:
13	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:
14	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
15	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
16	chr8:58127588..58129747-chr8:58135062..58137669,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-8	chr8:58121058-58121191	ENSG00000253301.1
2	lnc-FAM110B-8	chr8:58120568-58120763	ENSG00000253301.1

No data

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

Extended variants
information (count: 1435 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1435 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543704819	chr8:58108732-58108733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs117278780	chr8:58108743-58108744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112716591	chr8:58108744-58108745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189871539	chr8:58108768-58108769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181721489	chr8:58108811-58108812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528089638	chr8:58108823-58108824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs72649188	chr8:58108829-58108830	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs565039764	chr8:58108839-58108840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530731857	chr8:58108871-58108872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150060418	chr8:58108925-58108926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376696848	chr8:58108980-58108981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570149315	chr8:58108984-58108985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs79728051	chr8:58109051-58109052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201429902	chr8:58109053-58109054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs79416765	chr8:58109054-58109055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371580499	chr8:58109055-58109056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113415451	chr8:58109068-58109069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200246381	chr8:58109079-58109080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375374780	chr8:58109080-58109081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79897306	chr8:58109083-58109084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186494094	chr8:58109154-58109155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566038204	chr8:58109185-58109186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574717947	chr8:58109208-58109209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559329831	chr8:58109212-58109213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs17194995	chr8:58109220-58109221	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs188506771	chr8:58109249-58109250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73603879	chr8:58109344-58109345	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs557158420	chr8:58109370-58109371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117989061	chr8:58109375-58109376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373108728	chr8:58109379-58109380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542279205	chr8:58109380-58109381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559033982	chr8:58109412-58109413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181009089	chr8:58109423-58109424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147752063	chr8:58109462-58109463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs17195037	chr8:58109492-58109493	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs16921825	chr8:58109494-58109495	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs550729270	chr8:58109501-58109502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561037516	chr8:58109568-58109569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529930994	chr8:58109574-58109575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142332910	chr8:58109591-58109592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369164334	chr8:58109636-58109637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369236913	chr8:58109673-58109674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532055521	chr8:58109674-58109675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548579325	chr8:58109691-58109692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144630577	chr8:58109692-58109693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551518957	chr8:58109701-58109702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147891779	chr8:58109727-58109728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561760970	chr8:58109761-58109762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73680695	chr8:58109797-58109798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557246303	chr8:58109845-58109846	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:261 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58106200-58114800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:58111800-58112200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr8:58114800-58115400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:58115400-58118200	Weak transcription	Right Atrium	heart
5	chr8:58116000-58117400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:58116200-58117000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:58116200-58117200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr8:58116400-58117000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:58116400-58117000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:58116400-58117000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
11	chr8:58116400-58117200	ZNF genes & repeats	Spleen	Spleen
12	chr8:58116400-58117400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
13	chr8:58116400-58118000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr8:58116600-58116800	ZNF genes & repeats	Brain Hippocampus Middle	brain
15	chr8:58116600-58117000	Enhancers	Gastric	stomach
16	chr8:58116600-58117200	ZNF genes & repeats	Fetal Kidney	kidney
17	chr8:58116600-58117200	ZNF genes & repeats	Pancreas	Pancrea
18	chr8:58116600-58117600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr8:58116600-58118800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr8:58116800-58118200	Weak transcription	Brain Hippocampus Middle	brain
21	chr8:58117000-58118200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr8:58117000-58118200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr8:58117000-58118200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr8:58117000-58118200	Weak transcription	Gastric	stomach
25	chr8:58117000-58119000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr8:58117200-58118200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr8:58117200-58118200	Weak transcription	Fetal Kidney	kidney
28	chr8:58117400-58118200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr8:58117800-58118800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
30	chr8:58118000-58118800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
31	chr8:58118000-58118800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr8:58118000-58118800	ZNF genes & repeats	Brain Germinal Matrix	brain
33	chr8:58118000-58118800	ZNF genes & repeats	Pancreas	Pancrea
34	chr8:58118200-58118400	Bivalent/Poised TSS	Primary T killer memory cells from peripheral blood	blood
35	chr8:58118200-58118600	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
36	chr8:58118200-58118600	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
37	chr8:58118200-58118600	ZNF genes & repeats	Fetal Intestine Large	intestine
38	chr8:58118200-58118600	ZNF genes & repeats	Fetal Intestine Small	intestine
39	chr8:58118200-58118600	ZNF genes & repeats	Fetal Muscle Trunk	muscle
40	chr8:58118200-58118600	ZNF genes & repeats	Placenta	Placenta
41	chr8:58118200-58118600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
42	chr8:58118200-58118600	ZNF genes & repeats	NHEK	skin
43	chr8:58118200-58118800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
44	chr8:58118200-58118800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr8:58118200-58118800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:58118200-58118800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr8:58118200-58118800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:58118200-58118800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
49	chr8:58118200-58118800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
50	chr8:58118200-58118800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links