Variant report

Variant	esv18554
Chromosome Location	chr6:29915735-29928841
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:151)
CpG islands
(count:1162)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:151 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:29922852-29922901	K562	blood:	n/a	n/a
2	BCLAF1	chr6:29916040-29916482	GM12878	blood:	n/a	n/a
3	BHLHE40	chr6:29920974-29921274	K562	blood:	n/a	n/a
4	BHLHE40	chr6:29920783-29921023	A549	lung:	n/a	n/a
5	CBX3	chr6:29920575-29921454	HCT-116	colon:	n/a	n/a
6	CEBPB	chr6:29919167-29919420	K562	blood:	n/a	n/a
7	CHD2	chr6:29915994-29916686	GM12878	blood:	n/a	n/a
8	CTCF	chr6:29917974-29918105	K562	blood:	n/a	n/a
9	CTCF	chr6:29917940-29918090	K562	blood:	n/a	n/a
10	EBF1	chr6:29927419-29927625	GM12878	blood:	n/a	n/a
11	EBF1	chr6:29927470-29927619	GM12878	blood:	n/a	n/a
12	EBF1	chr6:29925101-29925327	GM12878	blood:	n/a	chr6:29925150-29925161 chr6:29925167-29925178
13	EP300	chr6:29920979-29921212	SK-N-SH_RA	brain:	n/a	n/a
14	EP300	chr6:29920634-29921267	A549	lung:	n/a	n/a
15	EP300	chr6:29920738-29921236	A549	lung:	n/a	n/a
16	FOS	chr6:29920684-29921270	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr6:29920677-29921326	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr6:29920699-29921264	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr6:29920665-29921284	HUVEC	blood vessel:	n/a	n/a
20	FOS	chr6:29920685-29921275	MCF10A-Er-Src	breast:	n/a	n/a
21	FOSL1	chr6:29920649-29921461	HCT-116	colon:	n/a	n/a
22	FOSL1	chr6:29920598-29921295	HCT-116	colon:	n/a	n/a
23	FOSL2	chr6:29920758-29921244	A549	lung:	n/a	n/a
24	FOSL2	chr6:29920563-29921346	SK-N-SH	brain:	n/a	n/a
25	FOSL2	chr6:29920553-29921362	A549	lung:	n/a	n/a
26	GATA3	chr6:29918761-29919040	SH-SY5Y	brain:	n/a	n/a
27	GATA3	chr6:29920615-29921377	A549	lung:	n/a	n/a
28	JUN	chr6:29920751-29921344	HUVEC	blood vessel:	n/a	n/a
29	JUND	chr6:29920645-29921459	HCT-116	colon:	n/a	n/a
30	JUND	chr6:29920569-29921371	HCT-116	colon:	n/a	n/a
31	JUND	chr6:29921013-29921312	K562	blood:	n/a	n/a
32	JUND	chr6:29920600-29921304	SK-N-SH	brain:	n/a	n/a
33	MAX	chr6:29920664-29921326	A549	lung:	n/a	n/a
34	MAX	chr6:29920664-29921185	A549	lung:	n/a	n/a
35	MEF2A	chr6:29920703-29921365	SK-N-SH	brain:	n/a	n/a
36	MTA3	chr6:29913554-29917310	GM12878	blood:	n/a	n/a
37	MTA3	chr6:29917718-29918201	GM12878	blood:	n/a	n/a
38	MXI1	chr6:29926953-29927079	GM12878	blood:	n/a	n/a
39	MYC	chr6:29916885-29916943	H1-hESC	embryonic stem cell:	n/a	n/a
40	MYC	chr6:29920694-29921154	MCF10A-Er-Src	breast:	n/a	n/a
41	MYC	chr6:29920684-29921247	MCF10A-Er-Src	breast:	n/a	n/a
42	NFATC1	chr6:29914067-29917278	GM12878	blood:	n/a	n/a
43	NFATC1	chr6:29913967-29917024	GM12878	blood:	n/a	n/a
44	NFIC	chr6:29920630-29921363	SK-N-SH	brain:	n/a	n/a
45	NR3C1	chr6:29920695-29921318	A549	lung:	n/a	n/a
46	NR3C1	chr6:29920717-29921190	A549	lung:	n/a	n/a
47	NR3C1	chr6:29920739-29921166	A549	lung:	n/a	n/a
48	PBX3	chr6:29920611-29921325	SK-N-SH	brain:	n/a	n/a
49	PML	chr6:29913677-29917213	GM12878	blood:	n/a	n/a
50	POLR2A	chr6:29917885-29917906	HepG2	liver:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:29924407-29924457	HepG2	liver:	n/a
2	chr6:29920309-29920359	ovcar-3	ovarian:	n/a
3	chr6:29924067-29924117	T-47D	breast:	n/a
4	chr6:29924407-29924457	HepG2	liver:	n/a
5	chr6:29920309-29920359	ovcar-3	ovarian:	n/a
6	chr6:29924067-29924117	T-47D	breast:	n/a
7	chr6:29924202-29924252	Hepatocyte	liver:	n/a
8	chr6:29924256-29924306	Jurkat	blood:	n/a
9	chr6:29923913-29923963	HMEC	breast:	n/a
10	chr6:29920309-29920359	HCM	heart:	n/a
11	chr6:29922522-29922572	NH-A	brain:	n/a
12	chr6:29923913-29923963	HCPEpiC	choroid plexus:	n/a
13	chr6:29924475-29924525	HMEC	breast:	n/a
14	chr6:29924207-29924257	GM12891	blood:	n/a
15	chr6:29924247-29924297	Caco-2	colon:	n/a
16	chr6:29924475-29924525	HRPEpiC	eye:	n/a
17	chr6:29922522-29922572	HCPEpiC	choroid plexus:	n/a
18	chr6:29924471-29924521	HUVEC	blood vessel:	n/a
19	chr6:29924067-29924117	AG09309	skin:	n/a
20	chr6:29924207-29924257	A549	lung:	n/a
21	chr6:29923952-29924002	AG10803	skin:	n/a
22	chr6:29924471-29924521	CMK	blood:	n/a
23	chr6:29924299-29924349	AG04449	skin:	fetal
24	chr6:29928362-29928412	AG09309	skin:	n/a
25	chr6:29921779-29921829	HCM	heart:	n/a
26	chr6:29924475-29924525	AG04450	lung:	fetal
27	chr6:29923695-29923745	HEK293	kidney:	embryo
28	chr6:29921779-29921829	BE2_C	brain:	n/a
29	chr6:29928362-29928412	H1-hESC	embryonic stem cell:	embryo
30	chr6:29923952-29924002	GM12892	blood:	n/a
31	chr6:29924247-29924297	ProgFib	skin:	n/a
32	chr6:29924471-29924521	HRPEpiC	eye:	n/a
33	chr6:29924471-29924521	AG04450	lung:	fetal
34	chr6:29923913-29923963	Caco-2	colon:	n/a
35	chr6:29924299-29924349	SKMC	muscle:	n/a
36	chr6:29923952-29924002	HRE	kidney:	n/a
37	chr6:29923954-29924004	HRPEpiC	eye:	n/a
38	chr6:29924207-29924257	AG09309	skin:	n/a
39	chr6:29924207-29924257	SK-N-SH_RA	brain:	n/a
40	chr6:29922522-29922572	HRCEpiC	kidney:	n/a
41	chr6:29928362-29928412	RPTEC	kidney:	n/a
42	chr6:29924067-29924117	MCF10A-Er-Src	breast:	n/a
43	chr6:29923913-29923963	AG09309	skin:	n/a
44	chr6:29924407-29924457	SAEC	small airway:	n/a
45	chr6:29923695-29923745	SKMC	muscle:	n/a
46	chr6:29924207-29924257	GM19239	blood:	n/a
47	chr6:29924202-29924252	Jurkat	blood:	n/a
48	chr6:29923695-29923745	HCF	heart:	n/a
49	chr6:29922522-29922572	SK-N-SH	brain:	n/a
50	chr6:29924475-29924525	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:29917413..29919975-chr6:29932108..29934788,2	K562	blood:
2	chr6:29917426..29919477-chr6:29924161..29925991,2	K562	blood:
3	chr6:29920527..29922060-chr6:29926055..29928693,2	K562	blood:
4	chr6:29920547..29922811-chr6:29925895..29928597,2	MCF-7	breast:
5	chr6:29909870..29912784-chr6:29914733..29916600,2	MCF-7	breast:
6	chr6:29917150..29919030-chr6:29920403..29922798,2	MCF-7	breast:
7	chr6:29926306..29930004-chr6:29943804..29947247,3	K562	blood:
8	chr6:29920527..29922060-chr6:29926055..29928693,2	K562	blood:
9	chr6:29860588..29861572-chr6:29915904..29916650,2	HCT-116	colon:
10	chr6:29820057..29821697-chr6:29920603..29922626,2	K562	blood:
11	chr6:29920547..29922811-chr6:29925895..29928597,2	MCF-7	breast:
12	chr6:29917150..29919030-chr6:29920403..29922798,2	MCF-7	breast:
13	chr6:29917977..29920432-chr6:29924161..29926474,2	K562	blood:
14	chr6:29921960..29924230-chr6:29934596..29936833,2	K562	blood:
15	chr6:29764926..29767618-chr6:29920990..29923179,3	MCF-7	breast:
16	chr6:29927397..29931336-chr6:29932208..29936273,8	K562	blood:

No data

Variant related genes	Relation type
HCG4P5	TF binding region
HLA-W	TF binding region
HCG4P5	CpG island
HLA-W	CpG island
ENSG00000233265	chromatin interactions
ENSG00000204625	chromatin interactions
ENSG00000206503	chromatin interactions
ENSG00000227766	chromatin interactions
ENSG00000235290	chromatin interactions

Extended variants
information (count: 1191 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:1191 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2735096	chr6:29915751-29915752	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs9260257	chr6:29915763-29915764	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs386698570	chr6:29915766-29915767	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs572291073	chr6:29915767-29915768	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs9260258	chr6:29915771-29915772	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs183696096	chr6:29915783-29915784	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs34095738	chr6:29915791-29915792	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs9260259	chr6:29915795-29915796	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs62390517	chr6:29915805-29915806	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs370401123	chr6:29915807-29915808	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs373571914	chr6:29915810-29915811	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs368051314	chr6:29915815-29915816	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs370417931	chr6:29915822-29915823	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs9260260	chr6:29915826-29915827	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs368297762	chr6:29915829-29915830	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs186541893	chr6:29915836-29915837	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs34016903	chr6:29915839-29915840	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs9260261	chr6:29915850-29915851	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs9260262	chr6:29915870-29915871	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs558990024	chr6:29915875-29915876	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs73725546	chr6:29915883-29915884	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs386698571	chr6:29915887-29915888	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs547539587	chr6:29915888-29915889	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs112377352	chr6:29915945-29915946	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
25	rs386698572	chr6:29915954-29915955	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs201130141	chr6:29915957-29915958	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs533446861	chr6:29915962-29915963	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs141566488	chr6:29915967-29915968	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs145060559	chr6:29915970-29915971	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs550182780	chr6:29915972-29915973	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs373481765	chr6:29915974-29915975	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs59675067	chr6:29915976-29915977	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs569928817	chr6:29915989-29915990	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs1632883	chr6:29915993-29915994	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs555910206	chr6:29916021-29916022	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs566136279	chr6:29916022-29916023	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs386698573	chr6:29916027-29916028	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs528660112	chr6:29916036-29916037	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs386698575	chr6:29916037-29916038	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs9260278	chr6:29916039-29916040	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs557438779	chr6:29916040-29916041	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs9260279	chr6:29916053-29916054	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs1655898	chr6:29916059-29916060	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs9260280	chr6:29916064-29916065	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs9260281	chr6:29916065-29916066	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs142496335	chr6:29916069-29916070	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs9260282	chr6:29916070-29916071	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs559026412	chr6:29916072-29916073	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs9260283	chr6:29916076-29916077	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs9260284	chr6:29916085-29916086	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:113)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
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
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
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD

Chromatin state (count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29911000-29915800	Weak transcription	Aorta	Aorta
2	chr6:29911200-29920200	Weak transcription	A549	lung
3	chr6:29911200-29921400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:29911600-29916200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr6:29911600-29920400	Weak transcription	Fetal Brain Male	brain
6	chr6:29911800-29916200	Genic enhancers	Left Ventricle	heart
7	chr6:29911800-29916800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr6:29911800-29917200	Strong transcription	Fetal Stomach	stomach
9	chr6:29911800-29917600	Strong transcription	Fetal Intestine Large	intestine
10	chr6:29912200-29916800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr6:29912400-29917200	Genic enhancers	Spleen	Spleen
12	chr6:29912400-29918000	Strong transcription	Fetal Intestine Small	intestine
13	chr6:29912600-29915800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr6:29912600-29916200	Weak transcription	Pancreas	Pancrea
15	chr6:29912600-29921000	Weak transcription	Psoas Muscle	Psoas
16	chr6:29912800-29916800	Strong transcription	Sigmoid Colon	Sigmoid Colon
17	chr6:29912800-29924200	Weak transcription	Right Atrium	heart
18	chr6:29913000-29917200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr6:29913000-29924000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr6:29913000-29924200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:29913200-29917000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr6:29913200-29917000	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr6:29913400-29915800	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr6:29913400-29916800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr6:29913400-29916800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr6:29913400-29916800	Strong transcription	HepG2	liver
27	chr6:29913400-29917000	Strong transcription	Stomach Smooth Muscle	stomach
28	chr6:29913400-29917800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr6:29913400-29917800	Weak transcription	Hela-S3	cervix
30	chr6:29913400-29918800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr6:29913400-29919600	Weak transcription	Fetal Muscle Trunk	muscle
32	chr6:29913400-29920800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr6:29913400-29932200	Weak transcription	Brain Anterior Caudate	brain
34	chr6:29913400-29932600	Weak transcription	Brain Substantia Nigra	brain
35	chr6:29913600-29916000	Weak transcription	Fetal Muscle Leg	muscle
36	chr6:29913600-29916200	Genic enhancers	Lung	lung
37	chr6:29913600-29916400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr6:29913600-29916800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr6:29913600-29917000	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr6:29913600-29917200	Strong transcription	Duodenum Mucosa	Duodenum
41	chr6:29913600-29918800	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr6:29913600-29919200	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr6:29913600-29920400	Weak transcription	HMEC	breast
44	chr6:29913600-29921600	Weak transcription	NHEK	skin
45	chr6:29913600-29924400	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr6:29913600-29925400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr6:29913800-29916400	Strong transcription	GM12878-XiMat	blood
48	chr6:29913800-29916800	Strong transcription	Rectal Mucosa Donor 31	rectum
49	chr6:29913800-29917200	Strong transcription	Adipose Nuclei	Adipose
50	chr6:29913800-29921000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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