Variant report

Variant	nsv1033534
Chromosome Location	chr6:34516588-34555969
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1137)
CpG islands
(count:794)
Chromatin interactive
region (count:89)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1137 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:34537168-34537342	K562	blood:	n/a	n/a
2	ARID3A	chr6:34535143-34535361	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:34528420-34528567	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:34530717-34531006	K562	blood:	n/a	n/a
5	ARID3A	chr6:34528321-34529035	K562	blood:	n/a	n/a
6	ATF1	chr6:34528256-34528770	K562	blood:	n/a	n/a
7	ATF1	chr6:34530640-34531020	K562	blood:	n/a	n/a
8	BACH1	chr6:34528081-34528565	K562	blood:	n/a	n/a
9	BACH1	chr6:34525098-34525122	K562	blood:	n/a	n/a
10	BCL3	chr6:34543140-34543668	K562	blood:	n/a	chr6:34543350-34543359
11	BCL3	chr6:34541372-34541610	GM12878	blood:	n/a	n/a
12	BCL3	chr6:34522693-34523062	GM12878	blood:	n/a	n/a
13	BCL3	chr6:34522720-34523036	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:34526077-34526348	K562	blood:	n/a	n/a
15	BHLHE40	chr6:34535821-34536274	HepG2	liver:	n/a	n/a
16	BHLHE40	chr6:34528358-34529016	HepG2	liver:	n/a	n/a
17	BHLHE40	chr6:34527683-34529135	K562	blood:	n/a	n/a
18	BHLHE40	chr6:34535812-34536294	K562	blood:	n/a	n/a
19	BHLHE40	chr6:34530292-34531071	K562	blood:	n/a	n/a
20	BHLHE40	chr6:34525097-34525230	K562	blood:	n/a	n/a
21	BHLHE40	chr6:34531305-34531454	K562	blood:	n/a	n/a
22	BRCA1	chr6:34528656-34528787	HepG2	liver:	n/a	n/a
23	BRCA1	chr6:34539475-34539630	HepG2	liver:	n/a	n/a
24	BRCA1	chr6:34534813-34534889	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr6:34528383-34528433	HepG2	liver:	n/a	n/a
26	CBX3	chr6:34540358-34540680	K562	blood:	n/a	n/a
27	CBX3	chr6:34528147-34529296	K562	blood:	n/a	n/a
28	CBX3	chr6:34525886-34526725	K562	blood:	n/a	n/a
29	CBX3	chr6:34524227-34524720	K562	blood:	n/a	n/a
30	CBX3	chr6:34536960-34537774	K562	blood:	n/a	n/a
31	CBX3	chr6:34525771-34526610	K562	blood:	n/a	n/a
32	CBX3	chr6:34530537-34531593	K562	blood:	n/a	n/a
33	CBX3	chr6:34529829-34530430	K562	blood:	n/a	n/a
34	CBX3	chr6:34540332-34540766	K562	blood:	n/a	n/a
35	CBX3	chr6:34528238-34529132	K562	blood:	n/a	n/a
36	CCNT2	chr6:34530372-34531113	K562	blood:	n/a	n/a
37	CCNT2	chr6:34535428-34535454	K562	blood:	n/a	n/a
38	CCNT2	chr6:34524999-34525293	K562	blood:	n/a	n/a
39	CCNT2	chr6:34519480-34519561	K562	blood:	n/a	n/a
40	CCNT2	chr6:34551355-34551428	K562	blood:	n/a	n/a
41	CCNT2	chr6:34528207-34528986	K562	blood:	n/a	chr6:34528756-34528765
42	CEBPB	chr6:34535806-34536215	K562	blood:	n/a	chr6:34535938-34535949
43	CEBPB	chr6:34553219-34553507	K562	blood:	n/a	n/a
44	CEBPB	chr6:34535818-34536115	K562	blood:	n/a	chr6:34535938-34535949
45	CEBPB	chr6:34553230-34553567	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr6:34535785-34536006	K562	blood:	n/a	chr6:34535938-34535949
47	CEBPB	chr6:34530449-34530954	K562	blood:	n/a	n/a
48	CEBPB	chr6:34530630-34530986	K562	blood:	n/a	n/a
49	CEBPB	chr6:34553231-34553535	A549	lung:	n/a	n/a
50	CEBPB	chr6:34528245-34528702	K562	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:34523925-34523975	BJ	skin:	n/a
2	chr6:34523925-34523975	BJ	skin:	n/a
3	chr6:34524278-34524328	ovcar-3	ovarian:	n/a
4	chr6:34524278-34524328	GM19239	blood:	n/a
5	chr6:34528827-34528877	GM12878	blood:	n/a
6	chr6:34524597-34524647	GM12892	blood:	n/a
7	chr6:34523925-34523975	HCF	heart:	n/a
8	chr6:34524766-34524816	A549	lung:	n/a
9	chr6:34524766-34524816	HRCEpiC	kidney:	n/a
10	chr6:34535602-34535652	T-47D	breast:	n/a
11	chr6:34524095-34524145	NHDF-neo	bronchial:	n/a
12	chr6:34524766-34524816	HRE	kidney:	n/a
13	chr6:34523925-34523975	AG04449	skin:	fetal
14	chr6:34524097-34524147	PANC-1	pancreas:	n/a
15	chr6:34524698-34524748	Hela-S3	cervix:	n/a
16	chr6:34524698-34524748	GM12892	blood:	n/a
17	chr6:34554635-34554685	A549	lung:	n/a
18	chr6:34528827-34528877	SK-N-SH	brain:	n/a
19	chr6:34543055-34543105	MCF10A-Er-Src	breast:	n/a
20	chr6:34525026-34525076	Hepatocyte	liver:	n/a
21	chr6:34543055-34543105	BE2_C	brain:	n/a
22	chr6:34524766-34524816	LNCaP	prostate:	n/a
23	chr6:34524766-34524816	HEK293	kidney:	embryo
24	chr6:34528827-34528877	GM12891	blood:	n/a
25	chr6:34524097-34524147	MCF-7	breast:	n/a
26	chr6:34535602-34535652	A549	lung:	n/a
27	chr6:34524766-34524816	HCPEpiC	choroid plexus:	n/a
28	chr6:34524698-34524748	Jurkat	blood:	n/a
29	chr6:34524095-34524145	PrEC	prostate:	n/a
30	chr6:34524095-34524145	Caco-2	colon:	n/a
31	chr6:34524278-34524328	PANC-1	pancreas:	n/a
32	chr6:34524097-34524147	HCM	heart:	n/a
33	chr6:34543055-34543105	Caco-2	colon:	n/a
34	chr6:34535602-34535652	IMR90	lung:	fetal
35	chr6:34535602-34535652	AG04449	skin:	fetal
36	chr6:34524698-34524748	GM19239	blood:	n/a
37	chr6:34524698-34524748	PFSK-1	brain:	n/a
38	chr6:34524278-34524328	NHBE	bronchial:	n/a
39	chr6:34524597-34524647	Caco-2	colon:	n/a
40	chr6:34524290-34524340	SK-N-SH	brain:	n/a
41	chr6:34524597-34524647	AG09319	gingival:	n/a
42	chr6:34528827-34528877	HCF	heart:	n/a
43	chr6:34524278-34524328	AG04450	lung:	fetal
44	chr6:34524097-34524147	AG04449	skin:	fetal
45	chr6:34524597-34524647	AG04450	lung:	fetal
46	chr6:34523925-34523975	MCF10A-Er-Src	breast:	n/a
47	chr6:34524766-34524816	ECC-1	luminal epithelium:	n/a
48	chr6:34524097-34524147	Hepatocyte	liver:	n/a
49	chr6:34524097-34524147	U87	brain:	n/a
50	chr6:34525026-34525076	PANC-1	pancreas:	n/a

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:34544544..34547164-chr6:34547916..34551672,4	K562	blood:
2	chr6:34520436..34525113-chr6:34525166..34530447,6	K562	blood:
3	chr6:34524749..34526335-chr6:34530684..34532317,2	K562	blood:
4	chr20:52484501..52486317-chr6:34526583..34529198,2	MCF-7	breast:
5	chr6:34426702..34428652-chr6:34520960..34523550,2	MCF-7	breast:
6	chr6:34528409..34535112-chr6:34539790..34543716,10	K562	blood:
7	chr6:34503128..34505845-chr6:34536309..34539232,2	K562	blood:
8	chr6:34528717..34530463-chr6:34574776..34577421,2	K562	blood:
9	chr6:34522438..34524089-chr6:34549801..34552822,3	MCF-7	breast:
10	chr6:34522370..34525112-chr6:34541822..34544372,2	MCF-7	breast:
11	chr6:34544544..34547164-chr6:34547916..34551672,4	K562	blood:
12	chr6:34514003..34515621-chr6:34528599..34531450,2	K562	blood:
13	chr6:34205000..34207351-chr6:34521778..34524214,3	MCF-7	breast:
14	chr6:34216270..34217861-chr6:34527614..34529829,2	MCF-7	breast:
15	chr6:34435937..34438924-chr6:34520705..34523320,2	MCF-7	breast:
16	chr6:34522438..34524089-chr6:34549801..34552822,3	MCF-7	breast:
17	chr6:34528906..34533005-chr6:34533870..34536568,4	MCF-7	breast:
18	chr6:34543493..34547191-chr6:34549783..34553774,3	MCF-7	breast:
19	chr6:34514809..34519137-chr6:34522826..34525341,4	K562	blood:
20	chr6:34204520..34207436-chr6:34522666..34524361,2	K562	blood:
21	chr6:34535096..34537769-chr6:34560989..34563955,2	K562	blood:
22	chr6:34514887..34517520-chr6:34540730..34542846,2	MCF-7	breast:
23	chr6:34514887..34517520-chr6:34540730..34542846,2	MCF-7	breast:
24	chr6:34528906..34533005-chr6:34533870..34536568,4	MCF-7	breast:
25	chr6:34481114..34483145-chr6:34525090..34526631,2	K562	blood:
26	chr6:34548787..34550337-chr6:34551862..34554295,2	K562	blood:
27	chr6:34518383..34520887-chr6:34564269..34566173,2	MCF-7	breast:
28	chr6:34552512..34555793-chr6:34557456..34559676,4	K562	blood:
29	chr6:34552512..34555793-chr6:34557456..34559676,3	K562	blood:
30	chr6:34531920..34532420-chr9:133836898..133837416,2	Hela-S3	cervix:
31	chr6:34535124..34537027-chr6:34540257..34543237,2	K562	blood:
32	chr6:34427383..34427978-chr6:34528004..34528902,2	MCF-7	breast:
33	chr6:34532465..34535112-chr6:34540040..34542974,2	K562	blood:
34	chr6:34538087..34543232-chr6:34543693..34548004,8	K562	blood:
35	chr6:34508152..34511012-chr6:34535080..34537020,2	K562	blood:
36	chr6:34509583..34511363-chr6:34518250..34520010,2	K562	blood:
37	chr6:34535538..34537048-chr6:34550660..34552218,2	K562	blood:
38	chr6:34535538..34537048-chr6:34550660..34552218,2	K562	blood:
39	chr6:34527129..34530623-chr6:34530939..34533511,3	K562	blood:
40	chr6:34536153..34538160-chr6:34545936..34548526,2	MCF-7	breast:
41	chr6:34529351..34531637-chr6:34540105..34542943,4	K562	blood:
42	chr6:34514736..34516500-chr6:34519380..34521095,2	K562	blood:
43	chr6:34529337..34532289-chr6:34533729..34536883,4	K562	blood:
44	chr6:34527129..34530623-chr6:34530939..34533511,3	K562	blood:
45	chr6:34548787..34550337-chr6:34551862..34554295,2	K562	blood:
46	chr6:34172530..34175474-chr6:34548744..34550732,2	K562	blood:
47	chr6:34527129..34529225-chr6:34531595..34533511,2	K562	blood:
48	chr6:34527602..34533050-chr6:34533572..34539589,8	K562	blood:
49	chr6:34528409..34535112-chr6:34539790..34543716,10	K562	blood:
50	chr6:34438209..34440665-chr6:34531080..34532692,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000196114	TF binding region
SPDEF	TF binding region
ENSG00000196114	CpG island
SPDEF	CpG island
ENSG00000204256	chromatin interactions
ENSG00000223837	chromatin interactions
ENSG00000124507	chromatin interactions
ENSG00000186577	chromatin interactions
ENSG00000196114	chromatin interactions
ENSG00000221635	chromatin interactions
ENSG00000124664	chromatin interactions
ENSG00000204257	chromatin interactions
ENSG00000137309	chromatin interactions

Extended variants
information (count: 1686 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1686 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2395596	chr6:34516588-34516589	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577688084	chr6:34516598-34516599	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs545115603	chr6:34516605-34516606	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs373394379	chr6:34516609-34516610	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs377550094	chr6:34516615-34516616	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs34641105	chr6:34516706-34516707	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs560429659	chr6:34516756-34516757	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs527665721	chr6:34516799-34516800	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs542704002	chr6:34516847-34516848	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs145023881	chr6:34516848-34516849	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs531923965	chr6:34516867-34516868	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs550366811	chr6:34516877-34516878	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs138708116	chr6:34516888-34516889	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs529161507	chr6:34516920-34516921	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs532785619	chr6:34516968-34516969	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs542949623	chr6:34516972-34516973	Weak transcription Strong transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs547492088	chr6:34517000-34517001	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs112472303	chr6:34517015-34517016	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs565683998	chr6:34517020-34517021	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs3798551	chr6:34517069-34517070	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs547886001	chr6:34517082-34517083	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs569885968	chr6:34517110-34517111	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs536971871	chr6:34517114-34517115	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs558297527	chr6:34517121-34517122	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs184254233	chr6:34517152-34517153	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs534537751	chr6:34517190-34517191	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs35941266	chr6:34517223-34517224	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs554239579	chr6:34517225-34517226	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs6935147	chr6:34517226-34517227	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs3798550	chr6:34517229-34517230	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs199767993	chr6:34517233-34517234	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs112188406	chr6:34517234-34517235	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs189151391	chr6:34517238-34517239	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs9469800	chr6:34517255-34517256	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs544110626	chr6:34517283-34517284	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs192988521	chr6:34517287-34517288	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs532748242	chr6:34517339-34517340	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs377421490	chr6:34517389-34517390	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs548050339	chr6:34517390-34517391	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs552613882	chr6:34517395-34517396	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs3798549	chr6:34517425-34517426	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs3798548	chr6:34517428-34517429	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs143799411	chr6:34517437-34517438	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs59428262	chr6:34517463-34517464	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs368353892	chr6:34517499-34517500	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs536683817	chr6:34517570-34517571	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs184674937	chr6:34517611-34517612	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs571691355	chr6:34517620-34517621	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs570461909	chr6:34517622-34517623	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs374540990	chr6:34517751-34517752	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
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
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	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
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	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
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	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
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:858 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34512400-34517600	Enhancers	Duodenum Mucosa	Duodenum
2	chr6:34512600-34522200	Enhancers	Stomach Mucosa	stomach
3	chr6:34512800-34517200	Enhancers	Colonic Mucosa	Colon
4	chr6:34513000-34517200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr6:34513000-34521400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr6:34513200-34524000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr6:34513800-34520600	Enhancers	Gastric	stomach
8	chr6:34514000-34517800	Enhancers	Fetal Muscle Leg	muscle
9	chr6:34514200-34516800	Enhancers	Pancreas	Pancrea
10	chr6:34514600-34521400	Weak transcription	K562	blood
11	chr6:34515000-34517800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:34515200-34516600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:34515200-34517000	Weak transcription	Fetal Stomach	stomach
14	chr6:34515200-34517600	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr6:34515200-34517800	Weak transcription	Adipose Nuclei	Adipose
16	chr6:34515200-34518000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr6:34515200-34518600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr6:34515200-34518800	Weak transcription	Spleen	Spleen
19	chr6:34515200-34520800	Weak transcription	Fetal Lung	lung
20	chr6:34515200-34527600	Weak transcription	Right Atrium	heart
21	chr6:34515800-34518600	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr6:34516000-34516800	Enhancers	A549	lung
23	chr6:34516000-34519800	Weak transcription	Fetal Intestine Small	intestine
24	chr6:34516000-34520800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr6:34516200-34516800	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr6:34516200-34518000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr6:34516400-34516600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr6:34516400-34517800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr6:34516400-34518800	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr6:34516600-34517800	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr6:34516800-34517600	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr6:34516800-34518000	Weak transcription	A549	lung
33	chr6:34517000-34517600	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr6:34517000-34517800	Enhancers	Placenta	Placenta
35	chr6:34517000-34517800	Enhancers	NHEK	skin
36	chr6:34517000-34518000	Genic enhancers	Fetal Stomach	stomach
37	chr6:34517200-34517800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr6:34517200-34517800	Enhancers	HMEC	breast
39	chr6:34517200-34518000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr6:34517200-34518400	Weak transcription	Colonic Mucosa	Colon
41	chr6:34517600-34519000	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr6:34517800-34518000	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr6:34517800-34518000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr6:34517800-34518200	Enhancers	Adipose Nuclei	Adipose
45	chr6:34517800-34518600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr6:34517800-34520800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr6:34518000-34518200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr6:34518000-34518800	Strong transcription	Fetal Stomach	stomach
49	chr6:34518000-34519200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr6:34518000-34519200	Enhancers	Fetal Thymus	thymus

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