Variant report

Variant	nsv520419
Chromosome Location	chr6:114285253-114306614
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1013)
CpG islands
(count:1100)
Chromatin interactive
region (count:33)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1013 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:114292324-114293464	K562	blood:	n/a	n/a
2	ARID3A	chr6:114292215-114292736	HepG2	liver:	n/a	n/a
3	ATF2	chr6:114292162-114292651	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr6:114292202-114292638	GM12878	blood:	n/a	n/a
5	ATF2	chr6:114292299-114292868	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr6:114292057-114292934	GM12878	blood:	n/a	n/a
7	ATF3	chr6:114292502-114292806	A549	lung:	n/a	n/a
8	BACH1	chr6:114291059-114292848	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr6:114292652-114292910	K562	blood:	n/a	n/a
10	BATF	chr6:114292357-114292809	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:114292309-114292811	GM12878	blood:	n/a	n/a
12	BCL3	chr6:114292219-114292794	A549	lung:	n/a	n/a
13	BCLAF1	chr6:114292468-114292936	K562	blood:	n/a	n/a
14	BCLAF1	chr6:114290887-114291280	GM12878	blood:	n/a	n/a
15	BCLAF1	chr6:114292067-114292958	GM12878	blood:	n/a	n/a
16	BCLAF1	chr6:114292074-114292821	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:114292078-114292916	HepG2	liver:	n/a	n/a
18	BHLHE40	chr6:114292140-114292977	GM12878	blood:	n/a	n/a
19	BHLHE40	chr6:114292250-114292739	A549	lung:	n/a	n/a
20	BHLHE40	chr6:114291327-114291912	GM12878	blood:	n/a	chr6:114291728-114291744
21	BHLHE40	chr6:114291068-114293199	K562	blood:	n/a	chr6:114291728-114291744
22	BRCA1	chr6:114292203-114292707	HepG2	liver:	n/a	n/a
23	BRCA1	chr6:114292150-114292816	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr6:114292314-114292626	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr6:114292277-114292680	GM12878	blood:	n/a	n/a
26	CBX3	chr6:114292020-114292935	K562	blood:	n/a	n/a
27	CBX3	chr6:114291871-114292851	HCT-116	colon:	n/a	n/a
28	CBX3	chr6:114292205-114292871	K562	blood:	n/a	n/a
29	CCNT2	chr6:114291480-114292869	K562	blood:	n/a	chr6:114292649-114292658
30	CEBPB	chr6:114292156-114292805	GM12878	blood:	n/a	n/a
31	CEBPB	chr6:114287915-114288151	HepG2	liver:	n/a	chr6:114288040-114288049 chr6:114288039-114288050 chr6:114288038-114288051 chr6:114288040-114288049 chr6:114288040-114288049 chr6:114288040-114288049 chr6:114288038-114288049
32	CEBPB	chr6:114292310-114292773	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr6:114292429-114292726	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr6:114293023-114293337	Hela-S3	cervix:	n/a	n/a
35	CEBPD	chr6:114292053-114292409	HepG2	liver:	n/a	n/a
36	CEBPD	chr6:114291446-114291721	HepG2	liver:	n/a	n/a
37	CEBPD	chr6:114292459-114292797	HepG2	liver:	n/a	n/a
38	CHD1	chr6:114292151-114292755	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD1	chr6:114290945-114291927	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr6:114291207-114292819	GM12878	blood:	n/a	n/a
41	CHD1	chr6:114290314-114290441	GM12878	blood:	n/a	n/a
42	CHD1	chr6:114289753-114293197	IMR90	lung:	n/a	n/a
43	CHD1	chr6:114290343-114290576	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr6:114290990-114292859	GM12878	blood:	n/a	n/a
45	CHD2	chr6:114302199-114302433	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr6:114291177-114293317	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr6:114292024-114292880	K562	blood:	n/a	n/a
48	CHD2	chr6:114291442-114291663	HepG2	liver:	n/a	n/a
49	CHD2	chr6:114292208-114292827	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr6:114291097-114291844	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:114292751-114292801	Caco-2	colon:	n/a
2	chr6:114292449-114292499	SK-N-MC	brain:	n/a
3	chr6:114292751-114292801	Caco-2	colon:	n/a
4	chr6:114292449-114292499	SK-N-MC	brain:	n/a
5	chr6:114287784-114287834	NHDF-neo	bronchial:	n/a
6	chr6:114289504-114289554	GM12892	blood:	n/a
7	chr6:114292723-114292773	AG09309	skin:	n/a
8	chr6:114295445-114295495	Jurkat	blood:	n/a
9	chr6:114291608-114291658	BE2_C	brain:	n/a
10	chr6:114289504-114289554	SK-N-SH	brain:	n/a
11	chr6:114289969-114290019	K562	blood:	n/a
12	chr6:114292723-114292773	BJ	skin:	n/a
13	chr6:114291252-114291302	K562	blood:	n/a
14	chr6:114289504-114289554	SK-N-SH_RA	brain:	n/a
15	chr6:114287784-114287834	HEEpiC	esophagus:	n/a
16	chr6:114292456-114292506	SK-N-SH	brain:	n/a
17	chr6:114292725-114292775	HCM	heart:	n/a
18	chr6:114291252-114291302	HEK293	kidney:	embryo
19	chr6:114291252-114291302	GM12891	blood:	n/a
20	chr6:114291608-114291658	HepG2	liver:	n/a
21	chr6:114287784-114287834	GM19239	blood:	n/a
22	chr6:114292459-114292509	AG04450	lung:	fetal
23	chr6:114291608-114291658	HRCEpiC	kidney:	n/a
24	chr6:114289969-114290019	GM12892	blood:	n/a
25	chr6:114292751-114292801	GM19239	blood:	n/a
26	chr6:114292051-114292101	RPTEC	kidney:	n/a
27	chr6:114292051-114292101	SK-N-MC	brain:	n/a
28	chr6:114292539-114292589	GM19239	blood:	n/a
29	chr6:114292802-114292852	GM12892	blood:	n/a
30	chr6:114291608-114291658	HCM	heart:	n/a
31	chr6:114291911-114291961	HCF	heart:	n/a
32	chr6:114292725-114292775	HCF	heart:	n/a
33	chr6:114290859-114290909	Hepatocyte	liver:	n/a
34	chr6:114289504-114289554	NH-A	brain:	n/a
35	chr6:114289969-114290019	GM12891	blood:	n/a
36	chr6:114292539-114292589	H1-hESC	embryonic stem cell:	embryo
37	chr6:114291911-114291961	HCT-116	colon:	n/a
38	chr6:114292539-114292589	A549	lung:	n/a
39	chr6:114292725-114292775	AG10803	skin:	n/a
40	chr6:114292456-114292506	PrEC	prostate:	n/a
41	chr6:114292051-114292101	AG09309	skin:	n/a
42	chr6:114292051-114292101	Jurkat	blood:	n/a
43	chr6:114292051-114292101	NT2-D1	testis:	n/a
44	chr6:114291911-114291961	HNPCEpiC	eye:	n/a
45	chr6:114291252-114291302	MCF10A-Er-Src	breast:	n/a
46	chr6:114291911-114291961	GM12892	blood:	n/a
47	chr6:114287784-114287834	HMEC	breast:	n/a
48	chr6:114290859-114290909	HCM	heart:	n/a
49	chr6:114292459-114292509	ovcar-3	ovarian:	n/a
50	chr6:114292449-114292499	HRPEpiC	eye:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:114270741..114273479-chr6:114282715..114285279,2	K562	blood:
2	chr6:114281941..114287220-chr6:114288215..114294270,10	MCF-7	breast:
3	chr6:114294440..114297186-chr6:114299827..114301682,2	K562	blood:
4	chr6:114295116..114299267-chr6:114302735..114304550,3	K562	blood:
5	chr6:114301698..114303779-chr6:114304752..114306956,2	MCF-7	breast:
6	chr6:114277709..114279245-chr6:114283228..114285269,2	MCF-7	breast:
7	chr6:114290174..114293671-chr6:114294895..114298600,4	K562	blood:
8	chr6:114293750..114295471-chr6:114297278..114299173,2	MCF-7	breast:
9	chr6:114291669..114294089-chr6:114295147..114298600,3	K562	blood:
10	chr6:114291224..114292783-chr6:114305550..114307576,2	MCF-7	breast:
11	chr6:114287247..114289431-chr6:114295805..114297955,2	K562	blood:
12	chr6:114287247..114289431-chr6:114295805..114297955,2	K562	blood:
13	chr6:114273569..114275934-chr6:114283284..114285737,2	K562	blood:
14	chr6:114287867..114290622-chr6:114290692..114293112,2	MCF-7	breast:
15	chr6:114293750..114295471-chr6:114297278..114299173,2	MCF-7	breast:
16	chr6:114291929..114293814-chr6:114301420..114303609,2	MCF-7	breast:
17	chr5:60627777..60628559-chr6:114292385..114293123,2	Hela-S3	cervix:
18	chr6:114247724..114249913-chr6:114294476..114297201,2	K562	blood:
19	chr12:49656786..49659396-chr6:114291007..114293085,2	MCF-7	breast:
20	chr6:114178671..114180639-chr6:114284210..114286994,2	MCF-7	breast:
21	chr6:114302031..114302848-chr6:116217639..116218164,2	MCF-7	breast:
22	chr6:114270434..114272529-chr6:114290878..114292915,2	K562	blood:
23	chr6:114294440..114297186-chr6:114299827..114301682,2	K562	blood:
24	chr6:114276746..114279489-chr6:114289754..114292765,3	MCF-7	breast:
25	chr6:114295116..114298801-chr6:114302591..114304550,3	K562	blood:
26	chr6:114296445..114297947-chr6:114301114..114303328,2	MCF-7	breast:
27	chr6:114296445..114297947-chr6:114301114..114303328,2	MCF-7	breast:
28	chr6:114287867..114290622-chr6:114290692..114293112,2	MCF-7	breast:
29	chr6:114291358..114292973-chr6:114297790..114299318,2	MCF-7	breast:
30	chr6:114295116..114298801-chr6:114302591..114304550,3	K562	blood:
31	chr6:114301698..114303779-chr6:114304752..114306956,2	MCF-7	breast:
32	chr6:114177680..114181410-chr6:114290377..114292499,3	MCF-7	breast:
33	chr6:114295116..114299267-chr6:114302735..114304550,3	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HS3ST5-4	chr6:114295876-114298201	ucscGeneNc_uc003pwa_2
2	lnc-HS3ST5-5	chr6:114288014-114288226	predAs_ge08_MARCKS_1
3	lnc-MARCKS-5	chr6:114291118-114291442	ENSG00000228624
4	lnc-HS3ST5-4	chr6:114300852-114301205	ucscGeneNc_uc003pwa_2
5	lnc-MARCKS-5	chr6:114292659-114292939	ENSG00000228624
6	lnc-MARCKS-5	chr6:114291178-114291487	NONHSAT114587
7	lnc-MARCKS-5	chr6:114291270-114291442	ENSG00000228624
8	lnc-HS3ST5-4	chr6:114298527-114298592	NONHSAT114592
9	lnc-HS3ST5-4	chr6:114297855-114298201	NONHSAT114592
10	lnc-MARCKS-5	chr6:114291399-114291487	ENSG00000228624
11	lnc-MARCKS-5	chr6:114292682-114292779	ENSG00000228624
12	lnc-HS3ST5-4	chr6:114298527-114298592	ucscGeneNc_uc003pwa_2
13	lnc-MARCKS-5	chr6:114292660-114292779	ENSG00000228624
14	lnc-MARCKS-5	chr6:114290865-114291442	ENSG00000228624
15	lnc-MARCKS-5	chr6:114291178-114291487	NONHSAT114586

No data

Variant related genes	Relation type
HDAC2	TF binding region
ENSG00000228624	TF binding region
HDAC2	CpG island
ENSG00000228624	CpG island
ENSG00000228624	chromatin interactions
ENSG00000130449	chromatin interactions
ENSG00000196591	chromatin interactions
ENSG00000258101	chromatin interactions
ENSG00000167553	chromatin interactions
ENSG00000155130	chromatin interactions
GATA6	miRNA target sites
FOXJ3	miRNA target sites
EGFR	miRNA target sites
SOX4	miRNA target sites
BAZ1B	miRNA target sites
WDR77	miRNA target sites
CTPS	miRNA target sites

Extended variants
information (count: 789 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:789 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2499618	chr6:114285253-114285254	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs116926974	chr6:114285254-114285255	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs554253800	chr6:114285283-114285284	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs569452900	chr6:114285322-114285323	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs181279597	chr6:114285325-114285326	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs146337094	chr6:114285371-114285372	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs577108474	chr6:114285417-114285418	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs536404738	chr6:114285425-114285426	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs11435750	chr6:114285426-114285427	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs541728759	chr6:114285565-114285566	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs35678472	chr6:114285594-114285595	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs186386115	chr6:114285765-114285766	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs112623181	chr6:114285778-114285779	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs542095980	chr6:114285799-114285800	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs563766358	chr6:114285822-114285823	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs531052470	chr6:114285857-114285858	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs546202984	chr6:114285892-114285893	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs564486889	chr6:114285925-114285926	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs144428540	chr6:114285932-114285933	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs547671741	chr6:114285992-114285993	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs189902043	chr6:114286018-114286019	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs146602296	chr6:114286164-114286165	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs182411985	chr6:114286173-114286174	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs548028220	chr6:114286193-114286194	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs79396393	chr6:114286355-114286356	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs569743371	chr6:114286358-114286359	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs199810216	chr6:114286419-114286420	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs373903517	chr6:114286436-114286437	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs77838525	chr6:114286456-114286457	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs570450358	chr6:114286461-114286462	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs537139872	chr6:114286470-114286471	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs201834950	chr6:114286532-114286533	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs77692469	chr6:114286543-114286544	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs574594455	chr6:114286549-114286550	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs186717874	chr6:114286618-114286619	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs553619263	chr6:114286628-114286629	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs575075526	chr6:114286635-114286636	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs113861112	chr6:114286642-114286643	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs536022321	chr6:114286679-114286680	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs559043721	chr6:114286693-114286694	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs2499619	chr6:114286694-114286695	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs532341131	chr6:114286700-114286701	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs191222099	chr6:114286709-114286710	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs546341490	chr6:114286767-114286768	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs564425782	chr6:114286771-114286772	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs9488291	chr6:114286781-114286782	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs540310753	chr6:114286783-114286784	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs552715178	chr6:114286801-114286802	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs56168685	chr6:114286814-114286815	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs35445040	chr6:114286832-114286833	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:119)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	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
Ependymoma	16718352	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
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114253000-114289800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:114253400-114290600	Weak transcription	Aorta	Aorta
3	chr6:114258600-114291000	Weak transcription	Lung	lung
4	chr6:114258800-114285600	Weak transcription	Right Ventricle	heart
5	chr6:114258800-114289800	Weak transcription	Spleen	Spleen
6	chr6:114259000-114289200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr6:114264800-114289800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr6:114266000-114289600	Weak transcription	Esophagus	oesophagus
9	chr6:114266200-114285600	Weak transcription	Psoas Muscle	Psoas
10	chr6:114266400-114285600	Weak transcription	Small Intestine	intestine
11	chr6:114266400-114289800	Weak transcription	Pancreas	Pancrea
12	chr6:114267400-114286200	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr6:114267400-114287200	Weak transcription	Fetal Brain Male	brain
14	chr6:114267400-114288800	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr6:114267400-114289000	Weak transcription	Brain Angular Gyrus	brain
16	chr6:114267400-114289200	Weak transcription	Ovary	ovary
17	chr6:114267400-114289800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr6:114270400-114289800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr6:114273600-114289200	Weak transcription	Stomach Smooth Muscle	stomach
20	chr6:114275400-114289200	Weak transcription	Left Ventricle	heart
21	chr6:114275800-114286000	Weak transcription	Primary T cells from cord blood	blood
22	chr6:114276000-114289200	Weak transcription	A549	lung
23	chr6:114276000-114289200	Weak transcription	HMEC	breast
24	chr6:114276000-114289400	Weak transcription	NHEK	skin
25	chr6:114276000-114289800	Weak transcription	NHLF	lung
26	chr6:114276800-114289000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr6:114277000-114288400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr6:114277000-114288600	Weak transcription	Fetal Intestine Small	intestine
29	chr6:114277000-114289200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr6:114277000-114289200	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr6:114277000-114289400	Weak transcription	Fetal Stomach	stomach
32	chr6:114277000-114289800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr6:114277200-114289000	Weak transcription	Brain Cingulate Gyrus	brain
34	chr6:114277200-114289200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr6:114277400-114288800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr6:114277400-114288800	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr6:114277400-114289600	Weak transcription	Thymus	Thymus
38	chr6:114277400-114290200	Weak transcription	Fetal Muscle Trunk	muscle
39	chr6:114277600-114289800	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr6:114277800-114289800	Weak transcription	HSMMtube	muscle
41	chr6:114278000-114289200	Weak transcription	Liver	Liver
42	chr6:114278200-114288200	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr6:114278600-114288200	Weak transcription	Fetal Kidney	kidney
44	chr6:114278600-114289800	Weak transcription	Placenta	Placenta
45	chr6:114278800-114289800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr6:114279000-114289200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr6:114279000-114289800	Weak transcription	Brain Anterior Caudate	brain
48	chr6:114279400-114289200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr6:114279400-114289400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr6:114279600-114288600	Weak transcription	H1 Cell Line	embryonic stem cell

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