Variant report

Variant	nsv1067861
Chromosome Location	chr8:53537321-53574220
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	ATF1	chr8:53571713-53571874	K562	blood:	n/a	n/a
2	ATF2	chr8:53541876-53542312	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr8:53541963-53542396	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr8:53541931-53542300	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr8:53538194-53538450	GM12878	blood:	n/a	n/a
6	BCL11A	chr8:53538553-53538791	GM12878	blood:	n/a	n/a
7	BCL11A	chr8:53541959-53542415	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr8:53541969-53542167	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr8:53560415-53560583	K562	blood:	n/a	chr8:53560511-53560524 chr8:53560511-53560522
10	CEBPB	chr8:53542026-53542177	HepG2	liver:	n/a	n/a
11	CEBPB	chr8:53547813-53547974	K562	blood:	n/a	n/a
12	CEBPB	chr8:53541912-53542424	MCF-7	breast:	n/a	n/a
13	CEBPB	chr8:53541795-53542303	H1-hESC	embryonic stem cell:	n/a	chr8:53541826-53541839
14	CEBPB	chr8:53559106-53559171	K562	blood:	n/a	n/a
15	CEBPB	chr8:53554677-53555064	IMR90	lung:	n/a	n/a
16	CEBPB	chr8:53541904-53542378	MCF-7	breast:	n/a	n/a
17	CEBPB	chr8:53541990-53542244	HepG2	liver:	n/a	n/a
18	CHD2	chr8:53542001-53542383	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr8:53538036-53538041	GM12878	blood:	n/a	n/a
20	CHD2	chr8:53566865-53567145	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr8:53537620-53537770	AG04450	lung:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
22	CTCF	chr8:53537600-53537750	MCF-7	breast:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
23	CTCF	chr8:53537500-53537650	NHEK	skin:	n/a	n/a
24	CTCF	chr8:53537565-53537785	HUVEC	blood vessel:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
25	CTCF	chr8:53537457-53537817	MCF-7	breast:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
26	CTCF	chr8:53537580-53537730	AG04449	skin:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
27	CTCF	chr8:53537640-53537790	WERI-Rb-1	eye:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
28	CTCF	chr8:53537560-53537710	HCT-116	colon:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
29	CTCF	chr8:53537640-53537790	GM06990	blood:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
30	CTCF	chr8:53537606-53537734	LNCaP	prostate:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
31	CTCF	chr8:53537600-53537750	BE2_C	brain:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
32	CTCF	chr8:53537580-53537730	NHDF-neo	bronchial:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
33	CTCF	chr8:53537560-53537710	AoAF	blood vessel:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
34	CTCF	chr8:53537434-53537854	MCF-7	breast:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
35	CTCF	chr8:53537601-53537738	GM12878	blood:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
36	CTCF	chr8:53537600-53537750	HPAF	blood vessel:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
37	CTCF	chr8:53537620-53537770	HBMEC	blood vessel:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
38	CTCF	chr8:53537580-53537730	WI-38	lung:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
39	CTCF	chr8:53537519-53537806	GM12878	blood:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
40	CTCF	chr8:53537586-53537765	Hela-S3	cervix:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
41	CTCF	chr8:53537620-53537770	HA-sp	spinal cord:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
42	CTCF	chr8:53537600-53537750	AG09319	gingival:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
43	CTCF	chr8:53537520-53537670	AG10803	skin:	n/a	n/a
44	CTCF	chr8:53537620-53537770	AG10803	skin:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
45	CTCF	chr8:53537640-53537790	AoAF	blood vessel:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
46	CTCF	chr8:53537580-53537730	AG09319	gingival:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
47	CTCF	chr8:53537560-53537710	MCF-7	breast:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
48	CTCF	chr8:53537500-53537650	HCT-116	colon:	n/a	n/a
49	CTCF	chr8:53537640-53537790	AG04449	skin:	n/a	chr8:53537672-53537688 chr8:53537666-53537687
50	CTCF	chr8:53537554-53537764	H1-hESC	embryonic stem cell:	n/a	chr8:53537672-53537688 chr8:53537666-53537687

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53566460-53566510	AG04450	lung:	fetal
2	chr8:53566460-53566510	GM12891	blood:	n/a
3	chr8:53566460-53566510	NB4	blood:	n/a
4	chr8:53566460-53566510	ECC-1	luminal epithelium:	n/a
5	chr8:53566460-53566510	HCF	heart:	n/a
6	chr8:53566460-53566510	HAEpiC	amniotic membrane:	n/a
7	chr8:53566460-53566510	GM12892	blood:	n/a
8	chr8:53566460-53566510	U87	brain:	n/a
9	chr8:53566460-53566510	SK-N-SH_RA	brain:	n/a
10	chr8:53566460-53566510	MCF10A-Er-Src	breast:	n/a
11	chr8:53566460-53566510	LNCaP	prostate:	n/a
12	chr8:53566460-53566510	NT2-D1	testis:	n/a
13	chr8:53566460-53566510	HRPEpiC	eye:	n/a
14	chr8:53566460-53566510	GM06990	blood:	n/a
15	chr8:53566460-53566510	HNPCEpiC	eye:	n/a
16	chr8:53566460-53566510	AG04449	skin:	fetal
17	chr8:53566460-53566510	HEK293	kidney:	embryo
18	chr8:53566460-53566510	ovcar-3	ovarian:	n/a
19	chr8:53566460-53566510	HCPEpiC	choroid plexus:	n/a
20	chr8:53566460-53566510	AG09319	gingival:	n/a
21	chr8:53566460-53566510	Caco-2	colon:	n/a
22	chr8:53566460-53566510	SAEC	small airway:	n/a
23	chr8:53566460-53566510	Hela-S3	cervix:	n/a
24	chr8:53566460-53566510	PrEC	prostate:	n/a
25	chr8:53566460-53566510	IMR90	lung:	fetal
26	chr8:53566460-53566510	HIPEpiC	eye:	n/a
27	chr8:53566460-53566510	HRCEpiC	kidney:	n/a
28	chr8:53566460-53566510	Hepatocyte	liver:	n/a
29	chr8:53566460-53566510	AG09309	skin:	n/a
30	chr8:53566460-53566510	H1-hESC	embryonic stem cell:	embryo
31	chr8:53566460-53566510	NHBE	bronchial:	n/a
32	chr8:53566460-53566510	PFSK-1	brain:	n/a
33	chr8:53566460-53566510	BJ	skin:	n/a
34	chr8:53566460-53566510	HMEC	breast:	n/a
35	chr8:53566460-53566510	RPTEC	kidney:	n/a
36	chr8:53566460-53566510	SK-N-MC	brain:	n/a
37	chr8:53566460-53566510	AoSMC	blood vessel:	n/a
38	chr8:53566460-53566510	NH-A	brain:	n/a
39	chr8:53566460-53566510	T-47D	breast:	n/a
40	chr8:53566460-53566510	K562	blood:	n/a
41	chr8:53566460-53566510	SKMC	muscle:	n/a
42	chr8:53566460-53566510	SK-N-SH	brain:	n/a
43	chr8:53566460-53566510	BE2_C	brain:	n/a
44	chr8:53566460-53566510	MCF-7	breast:	n/a
45	chr8:53566460-53566510	AG10803	skin:	n/a
46	chr8:53566460-53566510	NHDF-neo	bronchial:	n/a
47	chr8:53566460-53566510	HepG2	liver:	n/a
48	chr8:53566460-53566510	GM19239	blood:	n/a
49	chr8:53566460-53566510	HL-60	blood:	n/a
50	chr8:53566460-53566510	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:53563732..53566107-chr8:53606822..53608530,2	K562	blood:
2	chr8:53544573..53546394-chr8:53550090..53551810,2	K562	blood:
3	chr8:53558929..53560566-chr8:53563756..53566639,2	K562	blood:
4	chr8:53568645..53570159-chr8:53571129..53573328,2	K562	blood:
5	chr8:53567898..53571839-chr8:53626186..53628473,3	K562	blood:
6	chr8:53558929..53560566-chr8:53563756..53566639,2	K562	blood:
7	chr8:53544573..53546394-chr8:53550090..53551810,2	K562	blood:
8	chr8:53568645..53570159-chr8:53571129..53573328,2	K562	blood:
9	chr8:53527707..53530232-chr8:53540269..53542754,2	K562	blood:
10	chr8:53558478..53560001-chr8:53562936..53564747,2	K562	blood:
11	chr8:53569082..53571374-chr8:53573595..53575990,2	K562	blood:
12	chr8:53527520..53529626-chr8:53537141..53539075,2	MCF-7	breast:
13	chr8:53558478..53560001-chr8:53562936..53564747,2	K562	blood:
14	chr8:53561775..53564480-chr8:53624857..53626585,2	K562	blood:
15	chr8:53557771..53561401-chr8:53624923..53627709,3	K562	blood:

Variant related genes	Relation type
RB1CC1	TF binding region
RB1CC1	CpG island
ENSG00000023287	chromatin interactions

Extended variants
information (count: 1422 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1422 , 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	rs371451246	chr8:53537322-53537323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs34169001	chr8:53537352-53537353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545108949	chr8:53537432-53537433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544028093	chr8:53537457-53537458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112823807	chr8:53537481-53537482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530728498	chr8:53537501-53537502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542900615	chr8:53537534-53537535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563914787	chr8:53537658-53537659	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145688040	chr8:53537673-53537674	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546807276	chr8:53537682-53537683	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs111230630	chr8:53537693-53537694	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs184916989	chr8:53537787-53537788	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529466426	chr8:53537790-53537791	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532213030	chr8:53537818-53537819	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374319915	chr8:53537855-53537856	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187039926	chr8:53537860-53537861	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568801871	chr8:53537962-53537963	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563372592	chr8:53537985-53537986	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192246714	chr8:53537996-53537997	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184629420	chr8:53538001-53538002	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138331474	chr8:53538090-53538091	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75788295	chr8:53538167-53538168	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143247716	chr8:53538189-53538190	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs207469174	chr8:53538203-53538204	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573639218	chr8:53538228-53538229	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542270271	chr8:53538229-53538230	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539085654	chr8:53538252-53538253	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189001053	chr8:53538269-53538270	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549427690	chr8:53538332-53538333	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs57896620	chr8:53538405-53538406	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs561205921	chr8:53538426-53538427	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4394416	chr8:53538462-53538463	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs566056967	chr8:53538472-53538473	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7825939	chr8:53538495-53538496	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs565062844	chr8:53538502-53538503	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs551305681	chr8:53538518-53538519	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs182551256	chr8:53538536-53538537	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185536457	chr8:53538547-53538548	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529689751	chr8:53538555-53538556	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547776442	chr8:53538648-53538649	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77991958	chr8:53538650-53538651	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs551387245	chr8:53538651-53538652	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs180725319	chr8:53538656-53538657	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546802740	chr8:53538691-53538692	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185544558	chr8:53538727-53538728	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs116813942	chr8:53538732-53538733	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs16918011	chr8:53538733-53538734	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs141566495	chr8:53538769-53538770	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77366320	chr8:53538802-53538803	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs575639401	chr8:53538803-53538804	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	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
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
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	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
Uveal melanoma	20484589	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1238 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53525400-53543800	Weak transcription	Lung	lung
2	chr8:53528400-53603600	Weak transcription	Small Intestine	intestine
3	chr8:53529000-53542000	Weak transcription	Aorta	Aorta
4	chr8:53529200-53538400	Weak transcription	A549	lung
5	chr8:53529600-53540800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr8:53529800-53538600	Weak transcription	Left Ventricle	heart
7	chr8:53529800-53546400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr8:53529800-53546400	Weak transcription	Psoas Muscle	Psoas
9	chr8:53529800-53554800	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr8:53530000-53541000	Weak transcription	NHEK	skin
11	chr8:53530000-53541200	Weak transcription	HMEC	breast
12	chr8:53530000-53565200	Weak transcription	Right Ventricle	heart
13	chr8:53530200-53541000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr8:53530200-53541200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr8:53530200-53543400	Weak transcription	HSMMtube	muscle
16	chr8:53530200-53544400	Weak transcription	NH-A	brain
17	chr8:53530400-53539200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr8:53530400-53565800	Weak transcription	Rectal Smooth Muscle	rectum
19	chr8:53530600-53569400	Weak transcription	NHLF	lung
20	chr8:53531000-53541200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr8:53531000-53569400	Weak transcription	Brain Cingulate Gyrus	brain
22	chr8:53531600-53540200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr8:53532000-53550600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr8:53532000-53569800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr8:53532200-53558000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr8:53532200-53562600	Weak transcription	Brain Angular Gyrus	brain
27	chr8:53532400-53538600	Weak transcription	Brain Hippocampus Middle	brain
28	chr8:53533000-53541000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr8:53533000-53544200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr8:53533400-53538600	Strong transcription	HSMM	muscle
31	chr8:53533400-53544600	Weak transcription	NHDF-Ad	bronchial
32	chr8:53533600-53543400	Strong transcription	Monocytes-CD14+_RO01746	blood
33	chr8:53533800-53547800	Strong transcription	Primary neutrophils fromperipheralblood	blood
34	chr8:53534000-53544200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr8:53534200-53538800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr8:53534200-53543000	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr8:53534200-53543800	Weak transcription	Brain Germinal Matrix	brain
38	chr8:53534200-53550600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr8:53534400-53538800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr8:53534400-53541000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr8:53534400-53541400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr8:53534400-53543400	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr8:53534400-53543600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr8:53534600-53539200	Weak transcription	Fetal Muscle Leg	muscle
45	chr8:53534600-53540000	Strong transcription	Adipose Nuclei	Adipose
46	chr8:53534600-53543000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr8:53534600-53543400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr8:53534600-53543600	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr8:53534800-53539400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr8:53534800-53539400	Weak transcription	HepG2	liver

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