Variant report

Variant	nsv965728
Chromosome Location	chr6:56733888-56740633
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	CEBPB	chr6:56733324-56733947	HCT-116	colon:	n/a	n/a
2	EBF1	chr6:56734311-56734493	GM12878	blood:	n/a	n/a
3	EBF1	chr6:56736029-56736318	GM12878	blood:	n/a	n/a
4	EP300	chr6:56737956-56738245	SK-N-SH_RA	brain:	n/a	n/a
5	EP300	chr6:56733295-56734023	SK-N-SH	brain:	n/a	chr6:56733684-56733694 chr6:56733419-56733433
6	EP300	chr6:56733427-56733950	Hela-S3	cervix:	n/a	chr6:56733684-56733694
7	FOS	chr6:56733060-56734034	HUVEC	blood vessel:	n/a	chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733654-56733665 chr6:56733275-56733287 chr6:56733277-56733285 chr6:56733655-56733665 chr6:56733103-56733112
8	FOSL1	chr6:56733287-56734026	HCT-116	colon:	n/a	chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733655-56733665
9	FOSL1	chr6:56733406-56733982	HCT-116	colon:	n/a	chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733655-56733665
10	FOSL2	chr6:56740622-56741338	A549	lung:	n/a	chr6:56740888-56740902
11	FOSL2	chr6:56733327-56734050	SK-N-SH	brain:	n/a	chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733655-56733665
12	FOSL2	chr6:56733045-56733992	A549	lung:	n/a	chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733275-56733287 chr6:56733277-56733285 chr6:56733655-56733665 chr6:56733103-56733112
13	FOSL2	chr6:56733507-56733906	MCF-7	breast:	n/a	chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733655-56733665
14	FOSL2	chr6:56733454-56733895	SK-N-SH	brain:	n/a	chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733655-56733665
15	FOXA1	chr6:56733362-56733929	HepG2	liver:	n/a	chr6:56733447-56733459 chr6:56733683-56733698
16	FOXA1	chr6:56733493-56733938	HepG2	liver:	n/a	chr6:56733683-56733698
17	FOXA2	chr6:56733362-56734106	HepG2	liver:	n/a	chr6:56733447-56733459
18	FOXA2	chr6:56733372-56733986	A549	lung:	n/a	chr6:56733447-56733459
19	FOXM1	chr6:56733499-56733928	SK-N-SH	brain:	n/a	n/a
20	GATA2	chr6:56733450-56734024	HUVEC	blood vessel:	n/a	chr6:56733751-56733758 chr6:56733751-56733758 chr6:56733751-56733758 chr6:56733746-56733762 chr6:56733498-56733510 chr6:56733744-56733765 chr6:56733749-56733759
21	GATA3	chr6:56733281-56734097	SK-N-SH	brain:	n/a	chr6:56733751-56733758 chr6:56733751-56733758 chr6:56733751-56733758 chr6:56733746-56733762 chr6:56733498-56733510 chr6:56733750-56733758 chr6:56733744-56733765 chr6:56733749-56733759
22	GATA3	chr6:56733257-56734091	A549	lung:	n/a	chr6:56733751-56733758 chr6:56733751-56733758 chr6:56733751-56733758 chr6:56733746-56733762 chr6:56733498-56733510 chr6:56733750-56733758 chr6:56733744-56733765 chr6:56733749-56733759
23	GATA3	chr6:56733471-56733937	MCF-7	breast:	n/a	chr6:56733751-56733758 chr6:56733751-56733758 chr6:56733751-56733758 chr6:56733746-56733762 chr6:56733498-56733510 chr6:56733750-56733758 chr6:56733744-56733765 chr6:56733749-56733759
24	GATA3	chr6:56733229-56734275	SK-N-SH	brain:	n/a	chr6:56733751-56733758 chr6:56733751-56733758 chr6:56733751-56733758 chr6:56733746-56733762 chr6:56733498-56733510 chr6:56733750-56733758 chr6:56733744-56733765 chr6:56733749-56733759
25	GATA3	chr6:56737724-56738302	SK-N-SH	brain:	n/a	n/a
26	JUN	chr6:56733258-56734145	HUVEC	blood vessel:	n/a	chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733275-56733287 chr6:56733277-56733285 chr6:56733655-56733665
27	JUN	chr6:56739044-56739144	K562	blood:	n/a	n/a
28	JUND	chr6:56733336-56734028	SK-N-SH	brain:	n/a	chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733654-56733665
29	JUND	chr6:56733390-56733971	MCF-7	breast:	n/a	chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733654-56733665
30	JUND	chr6:56733450-56733971	Hela-S3	cervix:	n/a	chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733654-56733665
31	JUND	chr6:56733352-56734046	SK-N-SH	brain:	n/a	chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733654-56733665
32	JUND	chr6:56733464-56734304	SK-N-SH	brain:	n/a	chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733654-56733665
33	JUND	chr6:56733409-56734044	HCT-116	colon:	n/a	chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733655-56733665 chr6:56733654-56733665
34	MAFK	chr6:56733325-56734015	Hela-S3	cervix:	n/a	n/a
35	MAFK	chr6:56733599-56734176	IMR90	lung:	n/a	n/a
36	MAX	chr6:56740600-56741311	A549	lung:	n/a	n/a
37	MAZ	chr6:56737505-56737516	HepG2	liver:	n/a	n/a
38	MYC	chr6:56734539-56734613	MCF-7	breast:	n/a	n/a
39	NFIC	chr6:56733362-56734262	SK-N-SH	brain:	n/a	n/a
40	NR2F2	chr6:56733528-56733946	MCF-7	breast:	n/a	n/a
41	NR3C1	chr6:56735931-56736535	A549	lung:	n/a	n/a
42	NR3C1	chr6:56735934-56736523	A549	lung:	n/a	n/a
43	PBX3	chr6:56733497-56733977	SK-N-SH	brain:	n/a	n/a
44	PBX3	chr6:56733360-56734005	SK-N-SH	brain:	n/a	n/a
45	POLR2A	chr6:56733414-56734029	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr6:56735945-56736350	GM12878	blood:	n/a	n/a
47	POLR2A	chr6:56733482-56733900	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr6:56733342-56733952	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr6:56733507-56733901	SK-N-SH	brain:	n/a	n/a
50	POLR2A	chr6:56735988-56736240	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:56733843-56733893	NHDF-neo	bronchial:	n/a
2	chr6:56733843-56733893	HAEpiC	amniotic membrane:	n/a
3	chr6:56733843-56733893	K562	blood:	n/a
4	chr6:56733843-56733893	GM12892	blood:	n/a
5	chr6:56733843-56733893	U87	brain:	n/a
6	chr6:56733843-56733893	Hepatocyte	liver:	n/a
7	chr6:56733843-56733893	ProgFib	skin:	n/a
8	chr6:56733843-56733893	HEEpiC	esophagus:	n/a
9	chr6:56733843-56733893	HCT-116	colon:	n/a
10	chr6:56733843-56733893	Hela-S3	cervix:	n/a
11	chr6:56733843-56733893	SK-N-SH	brain:	n/a
12	chr6:56733843-56733893	ovcar-3	ovarian:	n/a
13	chr6:56733843-56733893	GM12891	blood:	n/a
14	chr6:56733843-56733893	AG09319	gingival:	n/a
15	chr6:56733843-56733893	HPAEpiC	pulmonary alveolar:	n/a
16	chr6:56733843-56733893	Caco-2	colon:	n/a
17	chr6:56733843-56733893	HCPEpiC	choroid plexus:	n/a
18	chr6:56733843-56733893	CMK	blood:	n/a
19	chr6:56733843-56733893	HL-60	blood:	n/a
20	chr6:56733843-56733893	HNPCEpiC	eye:	n/a
21	chr6:56733843-56733893	T-47D	breast:	n/a
22	chr6:56733843-56733893	HRPEpiC	eye:	n/a
23	chr6:56733843-56733893	GM19239	blood:	n/a
24	chr6:56733843-56733893	H1-hESC	embryonic stem cell:	embryo
25	chr6:56733843-56733893	PFSK-1	brain:	n/a
26	chr6:56733843-56733893	SKMC	muscle:	n/a
27	chr6:56733843-56733893	AG09309	skin:	n/a
28	chr6:56733843-56733893	HIPEpiC	eye:	n/a
29	chr6:56733843-56733893	AG04449	skin:	fetal
30	chr6:56733843-56733893	IMR90	lung:	fetal
31	chr6:56733843-56733893	MCF-7	breast:	n/a
32	chr6:56733843-56733893	RPTEC	kidney:	n/a
33	chr6:56733843-56733893	ECC-1	luminal epithelium:	n/a
34	chr6:56733843-56733893	HEK293	kidney:	embryo
35	chr6:56733843-56733893	Jurkat	blood:	n/a
36	chr6:56733843-56733893	HCM	heart:	n/a
37	chr6:56733843-56733893	AG04450	lung:	fetal
38	chr6:56733843-56733893	GM06990	blood:	n/a
39	chr6:56733843-56733893	HMEC	breast:	n/a
40	chr6:56733843-56733893	HepG2	liver:	n/a
41	chr6:56733843-56733893	AoSMC	blood vessel:	n/a
42	chr6:56733843-56733893	SK-N-SH_RA	brain:	n/a
43	chr6:56733843-56733893	NHBE	bronchial:	n/a
44	chr6:56733843-56733893	AG10803	skin:	n/a
45	chr6:56733843-56733893	HRCEpiC	kidney:	n/a
46	chr6:56733843-56733893	HRE	kidney:	n/a
47	chr6:56733843-56733893	BJ	skin:	n/a
48	chr6:56733843-56733893	SK-N-MC	brain:	n/a
49	chr6:56733843-56733893	NH-A	brain:	n/a
50	chr6:56733843-56733893	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:56725702..56727982-chr6:56732126..56734324,2	K562	blood:
2	chr6:56722965..56725223-chr6:56732847..56735248,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BEND6-2	chr6:56735989-56736541	NONHSAT113251

Variant related genes	Relation type
RPL17P26	TF binding region
RPL17P26	CpG island

Extended variants
information (count: 253 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535473007	chr6:56733927-56733928	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs186219410	chr6:56733943-56733944	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs150147147	chr6:56733960-56733961	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs553692996	chr6:56734031-56734032	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs111874504	chr6:56734045-56734046	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs13209099	chr6:56734052-56734053	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs189838514	chr6:56734081-56734082	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs182731896	chr6:56734222-56734223	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs568807539	chr6:56734254-56734255	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs185833527	chr6:56734257-56734258	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs571074586	chr6:56734303-56734304	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs567200230	chr6:56734359-56734360	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs547321165	chr6:56734386-56734387	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs76898153	chr6:56734390-56734391	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs539219591	chr6:56734393-56734394	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs71564864	chr6:56734394-56734395	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs74599206	chr6:56734403-56734404	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs554585226	chr6:56734435-56734436	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs575925349	chr6:56734458-56734459	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs536769891	chr6:56734471-56734472	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs191475754	chr6:56734546-56734547	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs143933968	chr6:56734578-56734579	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs540777202	chr6:56734586-56734587	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs114157888	chr6:56734607-56734608	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs113791952	chr6:56734616-56734617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541738229	chr6:56734631-56734632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559212611	chr6:56734632-56734633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373768570	chr6:56734637-56734638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563726254	chr6:56734646-56734647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs13195825	chr6:56734711-56734712	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs6926742	chr6:56734722-56734723	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs564525251	chr6:56734728-56734729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113329936	chr6:56734730-56734731	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374487859	chr6:56734735-56734736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs36048261	chr6:56734750-56734751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547256958	chr6:56734754-56734755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572879514	chr6:56734758-56734759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112756601	chr6:56734836-56734837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575221994	chr6:56734897-56734898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs13199024	chr6:56734950-56734951	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs550963315	chr6:56734991-56734992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569649307	chr6:56735072-56735073	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148502306	chr6:56735080-56735081	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs13213588	chr6:56735092-56735093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570257338	chr6:56735097-56735098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182814309	chr6:56735127-56735128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141851533	chr6:56735128-56735129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187531284	chr6:56735143-56735144	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192153140	chr6:56735145-56735146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542125392	chr6:56735148-56735149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:56725600-56734800	Enhancers	Hela-S3	cervix
2	chr6:56727200-56734600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:56727600-56734400	Enhancers	HMEC	breast
4	chr6:56727800-56734800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr6:56728000-56734800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr6:56728000-56735000	Enhancers	HSMM	muscle
7	chr6:56728000-56735000	Enhancers	NHDF-Ad	bronchial
8	chr6:56728800-56734800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr6:56730400-56740400	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr6:56731600-56734600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr6:56731800-56734600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr6:56731800-56734800	Enhancers	NH-A	brain
13	chr6:56732000-56734800	Enhancers	NHLF	lung
14	chr6:56732400-56734800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:56732600-56736000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr6:56732800-56734400	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr6:56733000-56734200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr6:56733000-56734200	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr6:56733000-56734200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr6:56733000-56734200	Flanking Active TSS	HUVEC	blood vessel
21	chr6:56733000-56734200	Enhancers	NHEK	skin
22	chr6:56733000-56734400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr6:56733000-56734400	Enhancers	HepG2	liver
24	chr6:56733000-56734600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr6:56733000-56734800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr6:56733200-56734200	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr6:56733200-56734400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr6:56733400-56734000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr6:56733600-56734000	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr6:56733600-56734400	Flanking Active TSS	GM12878-XiMat	blood
31	chr6:56733800-56734000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr6:56733800-56734000	Flanking Active TSS	A549	lung
33	chr6:56733800-56734000	Flanking Active TSS	HSMMtube	muscle
34	chr6:56733800-56734200	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr6:56733800-56734400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
36	chr6:56733800-56734400	Flanking Active TSS	Osteobl	bone
37	chr6:56733800-56735200	Enhancers	H1 Cell Line	embryonic stem cell
38	chr6:56734000-56734200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr6:56734000-56734200	Enhancers	HSMMtube	muscle
40	chr6:56734000-56734800	Enhancers	A549	lung
41	chr6:56734200-56734400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr6:56734200-56734400	Flanking Active TSS	HSMMtube	muscle
43	chr6:56734200-56734800	Enhancers	HUVEC	blood vessel
44	chr6:56734200-56755400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr6:56734400-56734600	Enhancers	HSMMtube	muscle
46	chr6:56734400-56735000	Enhancers	GM12878-XiMat	blood
47	chr6:56734400-56735000	Enhancers	Osteobl	bone
48	chr6:56734400-56735200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr6:56734400-56735200	Enhancers	Muscle Satellite Cultured Cells	--
50	chr6:56734400-56735600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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