Variant report

Variant	esv1793743
Chromosome Location	chr6:150167398-150170444
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:275)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:275 , 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	chr6:150168782-150169147	K562	blood:	n/a	n/a
2	ARID3A	chr6:150168290-150168454	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:150168716-150169082	HepG2	liver:	n/a	n/a
4	ATF1	chr6:150168706-150169270	K562	blood:	n/a	n/a
5	ATF3	chr6:150168612-150169050	K562	blood:	n/a	n/a
6	ATF3	chr6:150168738-150168916	K562	blood:	n/a	n/a
7	BACH1	chr6:150168873-150168948	K562	blood:	n/a	n/a
8	BACH1	chr6:150167601-150167781	H1-hESC	embryonic stem cell:	n/a	chr6:150167713-150167727
9	BATF	chr6:150168706-150168953	GM12878	blood:	n/a	chr6:150168857-150168868
10	BHLHE40	chr6:150167552-150167782	K562	blood:	n/a	n/a
11	BHLHE40	chr6:150168496-150168544	K562	blood:	n/a	n/a
12	BHLHE40	chr6:150168827-150169113	K562	blood:	n/a	n/a
13	BHLHE40	chr6:150168195-150169061	HepG2	liver:	n/a	n/a
14	BRCA1	chr6:150168141-150168320	HepG2	liver:	n/a	n/a
15	CCNT2	chr6:150167478-150167598	K562	blood:	n/a	n/a
16	CCNT2	chr6:150168743-150168947	K562	blood:	n/a	n/a
17	CEBPB	chr6:150168779-150169032	A549	lung:	n/a	n/a
18	CEBPB	chr6:150168711-150169234	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr6:150167414-150167744	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr6:150168674-150169066	K562	blood:	n/a	n/a
21	CEBPB	chr6:150168148-150168444	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr6:150168731-150169014	K562	blood:	n/a	n/a
23	CHD2	chr6:150168264-150168365	HepG2	liver:	n/a	n/a
24	CHD2	chr6:150167566-150167766	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr6:150169524-150169591	GM13977	blood:	n/a	n/a
26	CTCF	chr6:150168220-150168370	HepG2	liver:	n/a	n/a
27	CUX1	chr6:150168609-150169020	K562	blood:	n/a	chr6:150168920-150168934
28	E2F4	chr6:150168643-150168976	MCF10A-Er-Src	breast:	n/a	n/a
29	EGR1	chr6:150167524-150167766	K562	blood:	n/a	chr6:150167655-150167668
30	EGR1	chr6:150167253-150167951	ECC-1	luminal epithelium:	n/a	chr6:150167655-150167668
31	EGR1	chr6:150167213-150167875	MCF-7	breast:	n/a	chr6:150167655-150167668
32	EGR1	chr6:150167336-150167883	MCF-7	breast:	n/a	chr6:150167655-150167668
33	EGR1	chr6:150167406-150167856	ECC-1	luminal epithelium:	n/a	chr6:150167655-150167668
34	EGR1	chr6:150167480-150167787	K562	blood:	n/a	chr6:150167655-150167668
35	EGR1	chr6:150167077-150167865	HCT-116	colon:	n/a	chr6:150167655-150167668
36	EGR1	chr6:150167176-150167868	HCT-116	colon:	n/a	chr6:150167655-150167668
37	ELK1	chr6:150167550-150167657	Hela-S3	cervix:	n/a	n/a
38	EP300	chr6:150167349-150167909	SK-N-SH	brain:	n/a	chr6:150167715-150167724
39	EP300	chr6:150168725-150169027	SK-N-SH_RA	brain:	n/a	chr6:150168861-150168870
40	EP300	chr6:150168554-150169199	A549	lung:	n/a	chr6:150168861-150168870
41	EP300	chr6:150167404-150167769	SK-N-SH_RA	brain:	n/a	chr6:150167715-150167724
42	EP300	chr6:150168111-150169259	SK-N-SH	brain:	n/a	chr6:150168861-150168870
43	EP300	chr6:150165356-150169491	SK-N-SH	brain:	n/a	chr6:150167715-150167724 chr6:150168861-150168870
44	EP300	chr6:150168593-150169035	K562	blood:	n/a	chr6:150168861-150168870
45	EP300	chr6:150167685-150167732	K562	blood:	n/a	chr6:150167715-150167724
46	EP300	chr6:150168592-150169027	T-47D	breast:	n/a	chr6:150168861-150168870
47	EP300	chr6:150168528-150169154	A549	lung:	n/a	chr6:150168861-150168870
48	EP300	chr6:150168650-150169115	SK-N-SH_RA	brain:	n/a	chr6:150168861-150168870
49	EP300	chr6:150167404-150167773	SK-N-SH_RA	brain:	n/a	chr6:150167715-150167724
50	FOS	chr6:150167492-150168436	MCF10A-Er-Src	breast:	n/a	chr6:150168242-150168252 chr6:150167714-150167726 chr6:150167716-150167724 chr6:150168242-150168252 chr6:150167715-150167725 chr6:150167717-150167724 chr6:150167716-150167724 chr6:150168242-150168252

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150167359-150167409	HEK293	kidney:	embryo
2	chr6:150167359-150167409	ECC-1	luminal epithelium:	n/a
3	chr6:150167359-150167409	U87	brain:	n/a
4	chr6:150167359-150167409	SK-N-MC	brain:	n/a
5	chr6:150167359-150167409	PFSK-1	brain:	n/a
6	chr6:150167359-150167409	SK-N-SH_RA	brain:	n/a
7	chr6:150167359-150167409	GM06990	blood:	n/a
8	chr6:150167359-150167409	GM19239	blood:	n/a
9	chr6:150167359-150167409	NHBE	bronchial:	n/a
10	chr6:150167359-150167409	HCT-116	colon:	n/a
11	chr6:150167359-150167409	HNPCEpiC	eye:	n/a
12	chr6:150167359-150167409	AG09319	gingival:	n/a
13	chr6:150167359-150167409	AG04449	skin:	fetal
14	chr6:150167359-150167409	HEEpiC	esophagus:	n/a
15	chr6:150167359-150167409	NB4	blood:	n/a
16	chr6:150167359-150167409	HCF	heart:	n/a
17	chr6:150167359-150167409	ovcar-3	ovarian:	n/a
18	chr6:150167359-150167409	HRCEpiC	kidney:	n/a
19	chr6:150167359-150167409	PrEC	prostate:	n/a
20	chr6:150167359-150167409	HUVEC	blood vessel:	n/a
21	chr6:150167359-150167409	PANC-1	pancreas:	n/a
22	chr6:150167359-150167409	HCPEpiC	choroid plexus:	n/a
23	chr6:150167359-150167409	Caco-2	colon:	n/a
24	chr6:150167359-150167409	Hela-S3	cervix:	n/a
25	chr6:150167359-150167409	H1-hESC	embryonic stem cell:	embryo
26	chr6:150167359-150167409	NT2-D1	testis:	n/a
27	chr6:150167359-150167409	HRE	kidney:	n/a
28	chr6:150167359-150167409	BE2_C	brain:	n/a
29	chr6:150167359-150167409	MCF10A-Er-Src	breast:	n/a
30	chr6:150167359-150167409	NH-A	brain:	n/a
31	chr6:150167359-150167409	BJ	skin:	n/a
32	chr6:150167359-150167409	RPTEC	kidney:	n/a
33	chr6:150167359-150167409	MCF-7	breast:	n/a
34	chr6:150167359-150167409	HL-60	blood:	n/a
35	chr6:150167359-150167409	GM12891	blood:	n/a
36	chr6:150167359-150167409	GM12878	blood:	n/a
37	chr6:150167359-150167409	SAEC	small airway:	n/a
38	chr6:150167359-150167409	HIPEpiC	eye:	n/a
39	chr6:150167359-150167409	GM12892	blood:	n/a
40	chr6:150167359-150167409	IMR90	lung:	fetal
41	chr6:150167359-150167409	AG10803	skin:	n/a
42	chr6:150167359-150167409	SKMC	muscle:	n/a
43	chr6:150167359-150167409	Hepatocyte	liver:	n/a
44	chr6:150167359-150167409	HCM	heart:	n/a
45	chr6:150167359-150167409	T-47D	breast:	n/a
46	chr6:150167359-150167409	HAEpiC	amniotic membrane:	n/a
47	chr6:150167359-150167409	AG09309	skin:	n/a
48	chr6:150167359-150167409	HMEC	breast:	n/a
49	chr6:150167359-150167409	HPAEpiC	pulmonary alveolar:	n/a
50	chr6:150167359-150167409	CMK	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:150167839..150171816-chr6:150186693..150189063,3	K562	blood:
2	chr6:150164423..150166949-chr6:150167300..150169014,3	MCF-7	breast:
3	chr6:150166079..150172408-chr6:150181587..150186360,13	MCF-7	breast:
4	chr6:150168933..150170448-chr6:150175749..150177376,2	K562	blood:
5	chr6:150164239..150168667-chr6:150168889..150173398,4	K562	blood:
6	chr6:150147289..150147851-chr6:150168101..150168897,2	K562	blood:
7	chr6:150166110..150169897-chr6:150177295..150181208,4	MCF-7	breast:
8	chr6:150169785..150171423-chr6:150184398..150186335,2	K562	blood:
9	chr6:150159974..150162858-chr6:150163125..150167505,4	K562	blood:
10	chr6:150160714..150164051-chr6:150166023..150170073,4	MCF-7	breast:
11	chr6:150164239..150168667-chr6:150168889..150173398,4	K562	blood:
12	chr6:150166972..150170448-chr6:150175876..150178840,3	K562	blood:
13	chr6:150166050..150170337-chr6:150173456..150176763,5	MCF-7	breast:
14	chr6:150168942..150171816-chr6:150186693..150188431,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000273132	TF binding region
ENSG00000273132	CpG island
ENSG00000268592	chromatin interactions
ENSG00000273132	chromatin interactions
ENSG00000120256	chromatin interactions

Extended variants
information (count: 100 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:100 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs880245	chr6:150167398-150167399	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs554261628	chr6:150167418-150167419	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs370585264	chr6:150167434-150167435	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs543278298	chr6:150167489-150167490	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs116720136	chr6:150167495-150167496	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs191498006	chr6:150167529-150167530	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs547557763	chr6:150167564-150167565	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs62439678	chr6:150167566-150167567	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs567437118	chr6:150167579-150167580	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs527708964	chr6:150167593-150167594	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs536733588	chr6:150167619-150167620	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs74388002	chr6:150167696-150167697	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs570031505	chr6:150167702-150167703	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs561401454	chr6:150167722-150167723	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs530209425	chr6:150167812-150167813	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs550149349	chr6:150167817-150167818	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs570240371	chr6:150167827-150167828	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs2210683	chr6:150167871-150167872	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs77556923	chr6:150167925-150167926	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs527240785	chr6:150167942-150167943	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs558094594	chr6:150168014-150168015	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs534352590	chr6:150168015-150168016	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs577964372	chr6:150168057-150168058	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs187255439	chr6:150168071-150168072	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs9397034	chr6:150168087-150168088	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs9397035	chr6:150168089-150168090	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs200702427	chr6:150168090-150168091	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs111904172	chr6:150168099-150168100	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs145943634	chr6:150168108-150168109	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs71010876	chr6:150168153-150168154	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs117493821	chr6:150168154-150168155	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs201595086	chr6:150168156-150168157	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs537138319	chr6:150168222-150168223	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs369029118	chr6:150168235-150168236	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs192180053	chr6:150168285-150168286	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs12214670	chr6:150168307-150168308	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs9383862	chr6:150168356-150168357	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs34752666	chr6:150168360-150168361	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs185599052	chr6:150168404-150168405	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs573691439	chr6:150168507-150168508	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs372934129	chr6:150168516-150168517	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs573158780	chr6:150168533-150168534	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs541485604	chr6:150168597-150168598	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs561326880	chr6:150168648-150168649	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs530001745	chr6:150168661-150168662	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs539845277	chr6:150168663-150168664	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs377145982	chr6:150168749-150168750	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs34471863	chr6:150168780-150168781	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs543902002	chr6:150168787-150168788	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs6936403	chr6:150168826-150168827	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	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
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:216 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150073800-150182400	Weak transcription	Fetal Brain Male	brain
2	chr6:150105800-150176400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr6:150152800-150172600	Weak transcription	Aorta	Aorta
4	chr6:150153000-150167800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr6:150155800-150182600	Weak transcription	Dnd41	blood
6	chr6:150156400-150168400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr6:150158800-150176400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:150159200-150172800	Weak transcription	Spleen	Spleen
9	chr6:150161400-150168200	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr6:150162000-150167400	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr6:150162200-150167400	Weak transcription	HUVEC	blood vessel
12	chr6:150162200-150168400	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr6:150162200-150175800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:150162600-150168200	Weak transcription	Brain Substantia Nigra	brain
15	chr6:150162600-150168200	Weak transcription	Fetal Intestine Large	intestine
16	chr6:150162600-150172000	Weak transcription	Liver	Liver
17	chr6:150162600-150177200	Weak transcription	Fetal Lung	lung
18	chr6:150163400-150169200	Enhancers	Placenta	Placenta
19	chr6:150163600-150175800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr6:150164200-150168200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr6:150164200-150171800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:150164400-150167400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr6:150164400-150167400	Genic enhancers	NHLF	lung
24	chr6:150164400-150168400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr6:150164400-150169000	Weak transcription	Ovary	ovary
26	chr6:150164400-150181800	Weak transcription	Brain Germinal Matrix	brain
27	chr6:150164600-150167400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr6:150164600-150167400	Weak transcription	HepG2	liver
29	chr6:150164600-150169600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr6:150164800-150168200	Enhancers	Muscle Satellite Cultured Cells	--
31	chr6:150164800-150168200	Enhancers	NH-A	brain
32	chr6:150164800-150169400	Enhancers	HMEC	breast
33	chr6:150165000-150181800	Weak transcription	Fetal Brain Female	brain
34	chr6:150165400-150167400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr6:150165400-150167600	Genic enhancers	NHEK	skin
36	chr6:150165400-150167800	Genic enhancers	Fetal Stomach	stomach
37	chr6:150165400-150168600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr6:150165400-150168800	Enhancers	Stomach Smooth Muscle	stomach
39	chr6:150166000-150167400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr6:150166000-150167600	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr6:150166000-150169200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr6:150166000-150169400	Enhancers	Brain Angular Gyrus	brain
43	chr6:150166200-150167400	Genic enhancers	A549	lung
44	chr6:150166200-150169200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr6:150166200-150169400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:150166400-150167400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr6:150166400-150168800	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr6:150166400-150169600	Enhancers	Placenta Amnion	Placenta Amnion
49	chr6:150166600-150168800	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr6:150166800-150167400	Enhancers	Hela-S3	cervix

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