Variant report

Variant	esv3420572
Chromosome Location	chr6:167409162-167413360
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:951)
CpG islands
(count:672)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:951 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167412733-167413004	K562	blood:	n/a	n/a
2	ARID3A	chr6:167412830-167413052	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167409914-167410241	HepG2	liver:	n/a	n/a
4	ATF1	chr6:167412491-167413014	K562	blood:	n/a	n/a
5	ATF3	chr6:167412291-167413065	K562	blood:	n/a	chr6:167412794-167412803 chr6:167412658-167412667
6	BACH1	chr6:167412311-167413008	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:167411902-167411982	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr6:167410984-167411489	GM12878	blood:	n/a	n/a
9	BCLAF1	chr6:167412629-167413075	GM12878	blood:	n/a	chr6:167412650-167412663
10	BHLHE40	chr6:167409958-167410190	HepG2	liver:	n/a	n/a
11	BHLHE40	chr6:167412265-167413504	K562	blood:	n/a	chr6:167412603-167412619
12	BHLHE40	chr6:167411086-167411590	K562	blood:	n/a	n/a
13	BHLHE40	chr6:167410972-167411541	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:167412359-167413040	GM12878	blood:	n/a	chr6:167412603-167412619
15	BHLHE40	chr6:167410952-167411513	HepG2	liver:	n/a	n/a
16	BHLHE40	chr6:167413328-167413584	GM12878	blood:	n/a	n/a
17	BRCA1	chr6:167412356-167412502	HepG2	liver:	n/a	n/a
18	BRCA1	chr6:167412795-167413014	HepG2	liver:	n/a	n/a
19	BRCA1	chr6:167412538-167413026	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr6:167411138-167411549	GM12878	blood:	n/a	n/a
21	BRCA1	chr6:167411860-167411976	GM12878	blood:	n/a	n/a
22	CBX3	chr6:167412141-167413129	K562	blood:	n/a	n/a
23	CBX3	chr6:167411106-167411749	K562	blood:	n/a	n/a
24	CCNT2	chr6:167411773-167413668	K562	blood:	n/a	chr6:167412624-167412633 chr6:167412658-167412667
25	CEBPB	chr6:167409892-167410252	MCF-7	breast:	n/a	n/a
26	CEBPB	chr6:167409859-167410257	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:167409857-167410227	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:167409867-167410161	K562	blood:	n/a	n/a
29	CEBPB	chr6:167409814-167410253	K562	blood:	n/a	n/a
30	CEBPB	chr6:167412598-167412978	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr6:167410889-167411045	HepG2	liver:	n/a	chr6:167410991-167411003 chr6:167410982-167410995
32	CEBPB	chr6:167410828-167411172	HepG2	liver:	n/a	chr6:167410991-167411003 chr6:167410982-167410995
33	CEBPB	chr6:167409758-167410278	K562	blood:	n/a	n/a
34	CEBPB	chr6:167409921-167410163	HepG2	liver:	n/a	n/a
35	CEBPB	chr6:167409820-167410381	IMR90	lung:	n/a	n/a
36	CEBPB	chr6:167409902-167410280	HepG2	liver:	n/a	n/a
37	CEBPB	chr6:167409918-167410166	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr6:167409868-167410218	A549	lung:	n/a	n/a
39	CEBPD	chr6:167409904-167410181	HepG2	liver:	n/a	n/a
40	CEBPD	chr6:167413207-167413513	HepG2	liver:	n/a	n/a
41	CEBPD	chr6:167412289-167413081	HepG2	liver:	n/a	n/a
42	CEBPD	chr6:167413166-167413525	HepG2	liver:	n/a	n/a
43	CEBPD	chr6:167412767-167413036	HepG2	liver:	n/a	n/a
44	CHD1	chr6:167412286-167413059	GM12878	blood:	n/a	chr6:167412622-167412632
45	CHD1	chr6:167412917-167413605	H1-hESC	embryonic stem cell:	n/a	chr6:167413075-167413085
46	CHD1	chr6:167411221-167411603	GM12878	blood:	n/a	n/a
47	CHD2	chr6:167412692-167413021	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr6:167411993-167413175	K562	blood:	n/a	chr6:167413075-167413085 chr6:167412622-167412632
49	CHD2	chr6:167412396-167413148	HepG2	liver:	n/a	chr6:167413075-167413085 chr6:167412622-167412632
50	CHD2	chr6:167411249-167411509	Hela-S3	cervix:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167412518-167412568	SK-N-SH_RA	brain:	n/a
2	chr6:167412518-167412568	SK-N-SH_RA	brain:	n/a
3	chr6:167412518-167412568	RPTEC	kidney:	n/a
4	chr6:167411361-167411411	NT2-D1	testis:	n/a
5	chr6:167412627-167412677	SKMC	muscle:	n/a
6	chr6:167412981-167413031	AG09309	skin:	n/a
7	chr6:167412704-167412754	HEEpiC	esophagus:	n/a
8	chr6:167412622-167412672	AG09319	gingival:	n/a
9	chr6:167409842-167409892	T-47D	breast:	n/a
10	chr6:167412529-167412579	HRPEpiC	eye:	n/a
11	chr6:167412518-167412568	SAEC	small airway:	n/a
12	chr6:167412622-167412672	ovcar-3	ovarian:	n/a
13	chr6:167412320-167412370	MCF-7	breast:	n/a
14	chr6:167411970-167412020	PANC-1	pancreas:	n/a
15	chr6:167411506-167411556	HCM	heart:	n/a
16	chr6:167412704-167412754	A549	lung:	n/a
17	chr6:167412981-167413031	AG04449	skin:	fetal
18	chr6:167412529-167412579	GM06990	blood:	n/a
19	chr6:167409842-167409892	GM19239	blood:	n/a
20	chr6:167412704-167412754	AoSMC	blood vessel:	n/a
21	chr6:167412622-167412672	PrEC	prostate:	n/a
22	chr6:167411361-167411411	HCT-116	colon:	n/a
23	chr6:167411970-167412020	GM12892	blood:	n/a
24	chr6:167412981-167413031	BE2_C	brain:	n/a
25	chr6:167412981-167413031	GM06990	blood:	n/a
26	chr6:167412320-167412370	K562	blood:	n/a
27	chr6:167412981-167413031	SKMC	muscle:	n/a
28	chr6:167411361-167411411	HRCEpiC	kidney:	n/a
29	chr6:167412627-167412677	NB4	blood:	n/a
30	chr6:167412704-167412754	GM19239	blood:	n/a
31	chr6:167412627-167412677	Caco-2	colon:	n/a
32	chr6:167411361-167411411	GM12878	blood:	n/a
33	chr6:167412529-167412579	CMK	blood:	n/a
34	chr6:167411970-167412020	HCPEpiC	choroid plexus:	n/a
35	chr6:167412622-167412672	NHBE	bronchial:	n/a
36	chr6:167412529-167412579	BE2_C	brain:	n/a
37	chr6:167412529-167412579	NHDF-neo	bronchial:	n/a
38	chr6:167412704-167412754	AG04449	skin:	fetal
39	chr6:167412704-167412754	ProgFib	skin:	n/a
40	chr6:167412320-167412370	CMK	blood:	n/a
41	chr6:167412704-167412754	H1-hESC	embryonic stem cell:	embryo
42	chr6:167412704-167412754	HCF	heart:	n/a
43	chr6:167412622-167412672	HepG2	liver:	n/a
44	chr6:167412981-167413031	AG04450	lung:	fetal
45	chr6:167412704-167412754	NHBE	bronchial:	n/a
46	chr6:167411506-167411556	NH-A	brain:	n/a
47	chr6:167412518-167412568	ovcar-3	ovarian:	n/a
48	chr6:167412704-167412754	HRPEpiC	eye:	n/a
49	chr6:167411506-167411556	HPAEpiC	pulmonary alveolar:	n/a
50	chr6:167412981-167413031	AoSMC	blood vessel:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:206936..207454-chr6:167411617..167412576,2	HCT-116	colon:
2	chr6:167409616..167411218-chr6:167423790..167425616,2	K562	blood:
3	chr6:167368335..167372073-chr6:167409735..167414257,6	K562	blood:
4	chr6:167368539..167373039-chr6:167409933..167412837,4	MCF-7	breast:
5	chr6:167353766..167357800-chr6:167411292..167413274,3	K562	blood:
6	chr6:167410797..167412644-chr6:167437633..167439150,2	MCF-7	breast:
7	chr6:167368436..167372370-chr6:167409956..167415121,7	MCF-7	breast:
8	chr19:3505580..3506338-chr6:167412062..167412777,2	NB4	blood:
9	chr6:167370155..167372073-chr6:167409744..167411701,2	K562	blood:
10	chr6:167369620..167371640-chr6:167412068..167415220,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNASET2-5	chr6:167410591-167411574	NONHSAT116067

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3939	chr6:167411318-167411339	MIMAT0018355

No data

Variant related genes	Relation type
ENSG00000272980	TF binding region
ENSG00000227598	TF binding region
FGFR1OP	TF binding region
MIR3939	TF binding region
ENSG00000272980	CpG island
ENSG00000227598	CpG island
FGFR1OP	CpG island
MIR3939	CpG island
ENSG00000177951	chromatin interactions
ENSG00000105325	chromatin interactions
ENSG00000249141	chromatin interactions
ENSG00000026297	chromatin interactions
ENSG00000213066	chromatin interactions

Extended variants
information (count: 202 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:202 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138052328	chr6:167409191-167409192	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs185719933	chr6:167409198-167409199	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs559140941	chr6:167409213-167409214	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs144264380	chr6:167409220-167409221	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs67500273	chr6:167409223-167409224	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs28856974	chr6:167409231-167409232	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs4710160	chr6:167409241-167409242	Weak transcription Strong transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs374952276	chr6:167409248-167409249	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs368822206	chr6:167409249-167409250	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs398110934	chr6:167409258-167409259	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs4710161	chr6:167409374-167409375	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs532312244	chr6:167409405-167409406	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373291466	chr6:167409425-167409426	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs377525512	chr6:167409469-167409470	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs200003715	chr6:167409506-167409507	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143102763	chr6:167409548-167409549	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565980614	chr6:167409558-167409559	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs388406	chr6:167409562-167409563	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs548211653	chr6:167409573-167409574	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190181645	chr6:167409610-167409611	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571592259	chr6:167409613-167409614	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374240370	chr6:167409628-167409629	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs377232	chr6:167409638-167409639	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs433191	chr6:167409662-167409663	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs7759776	chr6:167409744-167409745	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs387733	chr6:167409771-167409772	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs183111221	chr6:167409779-167409780	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs542075767	chr6:167409815-167409816	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs140752	chr6:167409824-167409825	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs397796083	chr6:167409827-167409828	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs431159	chr6:167409842-167409843	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs138715792	chr6:167409917-167409918	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs568641971	chr6:167409963-167409964	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs564588902	chr6:167409982-167409983	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs528544080	chr6:167410033-167410034	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs540432656	chr6:167410038-167410039	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs541242960	chr6:167410082-167410083	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs142704301	chr6:167410095-167410096	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs530026946	chr6:167410177-167410178	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs548496094	chr6:167410192-167410193	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs536094618	chr6:167410211-167410212	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs555538062	chr6:167410247-167410248	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs369787512	chr6:167410364-167410365	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs430145	chr6:167410369-167410370	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs34924499	chr6:167410390-167410391	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs566228280	chr6:167410400-167410401	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs530498903	chr6:167410422-167410423	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs188196213	chr6:167410424-167410425	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs147340943	chr6:167410428-167410429	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs73024229	chr6:167410443-167410444	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 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
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
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
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	22522925	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167371400-167411000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:167381200-167410000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:167381200-167411000	Weak transcription	Fetal Stomach	stomach
4	chr6:167382000-167411200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:167383200-167411200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:167383400-167411000	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr6:167384000-167410600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr6:167384000-167411000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr6:167384000-167411000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr6:167384400-167411000	Weak transcription	Fetal Muscle Leg	muscle
11	chr6:167384600-167409600	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr6:167385000-167411000	Weak transcription	Thymus	Thymus
13	chr6:167385400-167411000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr6:167386200-167409400	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr6:167388800-167410600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr6:167389600-167411000	Weak transcription	NHLF	lung
17	chr6:167390600-167411200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr6:167390800-167411000	Weak transcription	Gastric	stomach
19	chr6:167392200-167411000	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr6:167392600-167410800	Weak transcription	HUVEC	blood vessel
21	chr6:167395200-167410200	Weak transcription	Fetal Lung	lung
22	chr6:167396800-167410800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr6:167398800-167411000	Weak transcription	Esophagus	oesophagus
24	chr6:167401800-167411000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr6:167402000-167410800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr6:167402200-167410600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr6:167402600-167410000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr6:167402600-167411000	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr6:167402600-167411000	Weak transcription	Fetal Intestine Small	intestine
30	chr6:167402600-167411200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr6:167402800-167410800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr6:167402800-167411000	Weak transcription	NHEK	skin
33	chr6:167403000-167410800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:167403000-167411000	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr6:167403000-167411000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr6:167403000-167411200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr6:167403200-167409800	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr6:167403200-167410800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr6:167403200-167411000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
40	chr6:167403200-167411000	Weak transcription	Brain Angular Gyrus	brain
41	chr6:167403200-167411000	Weak transcription	Brain Germinal Matrix	brain
42	chr6:167403400-167410600	Weak transcription	Primary B cells from cord blood	blood
43	chr6:167403600-167410800	Weak transcription	Primary B cells from peripheral blood	blood
44	chr6:167403600-167410800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr6:167403600-167410800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr6:167403600-167411000	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr6:167403600-167411000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr6:167403800-167410600	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr6:167403800-167410800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr6:167403800-167410800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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