Variant report

Variant	esv3351743
Chromosome Location	chr6:86286282-86308720
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:966)
CpG islands
(count:1160)
Chromatin interactive
region (count:57)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:966 , 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	chr6:86303651-86304076	K562	blood:	n/a	n/a
2	ARID3A	chr6:86303147-86303951	HepG2	liver:	n/a	n/a
3	ATF1	chr6:86302930-86304097	K562	blood:	n/a	n/a
4	ATF1	chr6:86290608-86290818	K562	blood:	n/a	n/a
5	ATF2	chr6:86303443-86304058	GM12878	blood:	n/a	n/a
6	ATF2	chr6:86303174-86304145	GM12878	blood:	n/a	n/a
7	ATF3	chr6:86303472-86303926	K562	blood:	n/a	n/a
8	ATF3	chr6:86303523-86303985	K562	blood:	n/a	n/a
9	ATF3	chr6:86290647-86291002	K562	blood:	n/a	n/a
10	BACH1	chr6:86303341-86303819	K562	blood:	n/a	n/a
11	BACH1	chr6:86290601-86290966	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr6:86303149-86304311	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr6:86290617-86290941	K562	blood:	n/a	n/a
14	BATF	chr6:86290611-86290964	GM12878	blood:	n/a	chr6:86290775-86290786
15	BCL3	chr6:86303192-86304290	A549	lung:	n/a	chr6:86303877-86303890
16	BCL3	chr6:86303130-86304600	A549	lung:	n/a	chr6:86304328-86304337 chr6:86303877-86303890
17	BCL3	chr6:86303182-86304153	GM12878	blood:	n/a	chr6:86303877-86303890
18	BCLAF1	chr6:86302945-86304489	GM12878	blood:	n/a	chr6:86304328-86304337 chr6:86303877-86303890
19	BCLAF1	chr6:86303514-86304059	K562	blood:	n/a	chr6:86303877-86303890
20	BCLAF1	chr6:86303382-86304101	K562	blood:	n/a	chr6:86303877-86303890
21	BCLAF1	chr6:86302737-86304189	GM12878	blood:	n/a	chr6:86303877-86303890
22	BHLHE40	chr6:86302952-86303999	HepG2	liver:	n/a	n/a
23	BHLHE40	chr6:86302752-86304466	K562	blood:	n/a	n/a
24	BHLHE40	chr6:86303506-86303846	A549	lung:	n/a	n/a
25	BHLHE40	chr6:86302896-86304488	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:86290583-86290948	K562	blood:	n/a	n/a
27	BRCA1	chr6:86303097-86304028	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr6:86303302-86303968	GM12878	blood:	n/a	n/a
29	BRCA1	chr6:86303844-86303894	HepG2	liver:	n/a	n/a
30	BRCA1	chr6:86303252-86303610	HepG2	liver:	n/a	n/a
31	CBX3	chr6:86292528-86292954	K562	blood:	n/a	n/a
32	CBX3	chr6:86302468-86304228	K562	blood:	n/a	n/a
33	CBX3	chr6:86291253-86291650	K562	blood:	n/a	n/a
34	CBX3	chr6:86290464-86292040	K562	blood:	n/a	n/a
35	CCNT2	chr6:86302926-86304172	K562	blood:	n/a	chr6:86304122-86304131 chr6:86303987-86303996 chr6:86303103-86303112
36	CEBPB	chr6:86307576-86307791	HepG2	liver:	n/a	chr6:86307693-86307704
37	CEBPB	chr6:86295443-86295846	HepG2	liver:	n/a	chr6:86295684-86295695 chr6:86295646-86295659 chr6:86295615-86295626 chr6:86295684-86295697 chr6:86295647-86295658
38	CEBPB	chr6:86303342-86304007	IMR90	lung:	n/a	n/a
39	CEBPB	chr6:86295591-86295702	HepG2	liver:	n/a	chr6:86295684-86295695 chr6:86295646-86295659 chr6:86295615-86295626 chr6:86295684-86295697 chr6:86295647-86295658
40	CEBPB	chr6:86302085-86302185	K562	blood:	n/a	n/a
41	CEBPB	chr6:86302930-86304368	Hela-S3	cervix:	n/a	chr6:86304352-86304365
42	CEBPB	chr6:86303567-86303979	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr6:86303633-86303944	K562	blood:	n/a	n/a
44	CEBPB	chr6:86295461-86295828	A549	lung:	n/a	chr6:86295684-86295695 chr6:86295646-86295659 chr6:86295615-86295626 chr6:86295684-86295697 chr6:86295647-86295658
45	CEBPB	chr6:86303593-86304033	K562	blood:	n/a	n/a
46	CEBPB	chr6:86295450-86295834	Hela-S3	cervix:	n/a	chr6:86295684-86295695 chr6:86295646-86295659 chr6:86295615-86295626 chr6:86295684-86295697 chr6:86295647-86295658
47	CEBPB	chr6:86295449-86295807	K562	blood:	n/a	chr6:86295684-86295695 chr6:86295646-86295659 chr6:86295615-86295626 chr6:86295684-86295697 chr6:86295647-86295658
48	CEBPB	chr6:86303658-86303973	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:86295472-86295804	IMR90	lung:	n/a	chr6:86295684-86295695 chr6:86295646-86295659 chr6:86295615-86295626 chr6:86295684-86295697 chr6:86295647-86295658
50	CEBPD	chr6:86303289-86304091	K562	blood:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:86303887-86303937	ECC-1	luminal epithelium:	n/a
2	chr6:86303887-86303937	ECC-1	luminal epithelium:	n/a
3	chr6:86302926-86302976	Jurkat	blood:	n/a
4	chr6:86303771-86303821	MCF-7	breast:	n/a
5	chr6:86303744-86303794	HCM	heart:	n/a
6	chr6:86303781-86303831	HCF	heart:	n/a
7	chr6:86304180-86304230	HUVEC	blood vessel:	n/a
8	chr6:86303884-86303934	AG04449	skin:	fetal
9	chr6:86304180-86304230	ovcar-3	ovarian:	n/a
10	chr6:86302950-86303000	HCM	heart:	n/a
11	chr6:86303887-86303937	ProgFib	skin:	n/a
12	chr6:86303732-86303782	HRE	kidney:	n/a
13	chr6:86302950-86303000	PrEC	prostate:	n/a
14	chr6:86302888-86302938	GM12891	blood:	n/a
15	chr6:86290102-86290152	BE2_C	brain:	n/a
16	chr6:86302888-86302938	HCPEpiC	choroid plexus:	n/a
17	chr6:86303887-86303937	HMEC	breast:	n/a
18	chr6:86298769-86298819	BE2_C	brain:	n/a
19	chr6:86303669-86303719	H1-hESC	embryonic stem cell:	embryo
20	chr6:86303767-86303817	GM12878	blood:	n/a
21	chr6:86307053-86307103	HMEC	breast:	n/a
22	chr6:86303669-86303719	GM19239	blood:	n/a
23	chr6:86298769-86298819	A549	lung:	n/a
24	chr6:86303771-86303821	NHBE	bronchial:	n/a
25	chr6:86307053-86307103	RPTEC	kidney:	n/a
26	chr6:86304180-86304230	U87	brain:	n/a
27	chr6:86302926-86302976	SK-N-SH	brain:	n/a
28	chr6:86303159-86303209	AG10803	skin:	n/a
29	chr6:86303454-86303504	HMEC	breast:	n/a
30	chr6:86304180-86304230	Hela-S3	cervix:	n/a
31	chr6:86304180-86304230	HL-60	blood:	n/a
32	chr6:86304180-86304230	BJ	skin:	n/a
33	chr6:86302888-86302938	HCF	heart:	n/a
34	chr6:86303884-86303934	A549	lung:	n/a
35	chr6:86302926-86302976	HL-60	blood:	n/a
36	chr6:86290102-86290152	HIPEpiC	eye:	n/a
37	chr6:86303767-86303817	AG09309	skin:	n/a
38	chr6:86303159-86303209	AG04450	lung:	fetal
39	chr6:86303781-86303831	Hepatocyte	liver:	n/a
40	chr6:86303781-86303831	NT2-D1	testis:	n/a
41	chr6:86303462-86303512	RPTEC	kidney:	n/a
42	chr6:86303462-86303512	MCF-7	breast:	n/a
43	chr6:86303781-86303831	AG04449	skin:	fetal
44	chr6:86303767-86303817	GM06990	blood:	n/a
45	chr6:86303454-86303504	PrEC	prostate:	n/a
46	chr6:86303462-86303512	HEEpiC	esophagus:	n/a
47	chr6:86290102-86290152	AG09319	gingival:	n/a
48	chr6:86303781-86303831	NHBE	bronchial:	n/a
49	chr6:86303781-86303831	K562	blood:	n/a
50	chr6:86303887-86303937	AoSMC	blood vessel:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:63832950..63833773-chr6:86303351..86304176,2	NB4	blood:
2	chr6:86300873..86305245-chr6:86347697..86356641,19	K562	blood:
3	chr6:86304019..86306829-chr6:86313728..86315892,3	MCF-7	breast:
4	chr19:14247915..14248484-chr6:86303079..86303653,2	Hela-S3	cervix:
5	chr6:86307661..86310525-chr6:86316183..86318206,2	MCF-7	breast:
6	chr6:86252970..86255284-chr6:86299533..86301971,2	K562	blood:
7	chr6:86285488..86287926-chr6:86288888..86290773,2	MCF-7	breast:
8	chr6:86304731..86306825-chr6:86381702..86383409,2	K562	blood:
9	chr6:86287466..86289317-chr6:86353179..86355732,2	MCF-7	breast:
10	chr6:86294224..86298589-chr6:86301078..86306001,4	MCF-7	breast:
11	chr6:86305165..86307421-chr6:86382210..86384940,3	MCF-7	breast:
12	chr6:86296828..86298833-chr6:86383928..86385738,2	K562	blood:
13	chr10:17243018..17243990-chr6:86303214..86304214,3	Hela-S3	cervix:
14	chr6:86302271..86307129-chr6:86385631..86390073,11	MCF-7	breast:
15	chr6:86301325..86305014-chr6:86385299..86388840,4	MCF-7	breast:
16	chr6:86278096..86280709-chr6:86299065..86302030,2	K562	blood:
17	chr6:86303002..86303617-chr9:100745459..100746459,2	Hela-S3	cervix:
18	chr6:86286722..86289673-chr6:86387180..86389276,2	MCF-7	breast:
19	chr6:86284643..86286706-chr6:86299863..86303229,3	K562	blood:
20	chr6:86298683..86300956-chr6:86302311..86304856,2	MCF-7	breast:
21	chr6:86284643..86286706-chr6:86299863..86303229,3	K562	blood:
22	chr6:86299824..86305374-chr6:86350530..86356322,11	MCF-7	breast:
23	chr16:28936701..28937234-chr6:86303014..86303832,2	Hela-S3	cervix:
24	chr6:86301331..86304881-chr6:86350851..86355985,12	MCF-7	breast:
25	chr6:86300457..86307827-chr6:86347697..86356337,20	K562	blood:
26	chr6:86252970..86257934-chr6:86299533..86304034,5	K562	blood:
27	chr6:86287653..86290758-chr6:86386971..86389926,3	K562	blood:
28	chr6:86296961..86299849-chr6:86387985..86389629,2	K562	blood:
29	chr6:86279748..86283159-chr6:86286791..86290808,4	K562	blood:
30	chr6:86300286..86310605-chr6:86384413..86390498,39	K562	blood:
31	chr6:86306147..86310004-chr6:86351299..86354372,3	MCF-7	breast:
32	chr6:86288404..86291892-chr6:86352318..86354794,4	MCF-7	breast:
33	chr6:86287818..86291892-chr6:86385672..86390313,6	MCF-7	breast:
34	chr6:86285488..86287926-chr6:86288888..86290773,2	MCF-7	breast:
35	chr6:86295157..86296902-chr6:86297407..86299649,2	K562	blood:
36	chr6:86281475..86283897-chr6:86288113..86290341,2	K562	blood:
37	chr16:89630470..89633084-chr6:86301680..86303446,2	MCF-7	breast:
38	chr6:86191399..86193392-chr6:86300815..86302853,2	K562	blood:
39	chr6:86298806..86300763-chr6:86301374..86304077,2	MCF-7	breast:
40	chr6:86286697..86290056-chr6:86301886..86305465,5	MCF-7	breast:
41	chr6:86288385..86291520-chr6:86301409..86305260,7	K562	blood:
42	chr6:86298349..86307534-chr6:86383938..86391964,31	K562	blood:
43	chr6:86299850..86302872-chr6:86358961..86362964,3	K562	blood:
44	chr6:86294695..86297402-chr6:86376038..86378724,2	K562	blood:
45	chr6:86308147..86310058-chr6:86348388..86350658,2	K562	blood:
46	chr6:86298806..86300763-chr6:86301374..86304077,2	MCF-7	breast:
47	chr6:86306095..86308167-chr6:86335617..86337326,2	K562	blood:
48	chr6:86289336..86292710-chr6:86302948..86306481,4	MCF-7	breast:
49	chr6:86307722..86311863-chr6:86387029..86388748,3	MCF-7	breast:
50	chr6:86298683..86300956-chr6:86302311..86304856,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNX14-3	chr6:86304945-86305442	NONHSAT113844
2	lnc-SNX14-3	chr6:86305598-86305643	NONHSAT113844
3	lnc-SNX14-3	chr6:86307647-86307791	NONHSAT113844
4	lnc-SNX14-3	chr6:86306552-86307606	NONHSAT113844
5	lnc-SNX14-3	chr6:86307939-86309022	NONHSAT113844

No data

Variant related genes	Relation type
SNX14	TF binding region
SNX14	CpG island
ENSG00000203875	chromatin interactions
ENSG00000136938	chromatin interactions
ENSG00000267169	chromatin interactions
ENSG00000088035	chromatin interactions
ENSG00000137171	chromatin interactions
ENSG00000135317	chromatin interactions
ENSG00000107614	chromatin interactions
ENSG00000135316	chromatin interactions
ENSG00000112651	chromatin interactions
ENSG00000177548	chromatin interactions

Extended variants
information (count: 783 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:783 , 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	rs538809958	chr6:86286288-86286289	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs146049445	chr6:86286289-86286290	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs56134124	chr6:86286349-86286350	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs536562201	chr6:86286372-86286373	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs368441713	chr6:86286514-86286515	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs139430687	chr6:86286567-86286568	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs543885860	chr6:86286597-86286598	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs185765954	chr6:86286662-86286663	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs572680565	chr6:86286677-86286678	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs577417359	chr6:86286695-86286696	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs545196000	chr6:86286696-86286697	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs535327457	chr6:86286702-86286703	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs558535627	chr6:86286773-86286774	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs560104540	chr6:86286893-86286894	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs532582883	chr6:86286935-86286936	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs79890604	chr6:86287004-86287005	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs527513347	chr6:86287005-86287006	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs548982037	chr6:86287014-86287015	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs561280502	chr6:86287025-86287026	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs531195846	chr6:86287043-86287044	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs376963243	chr6:86287093-86287094	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs144123708	chr6:86287121-86287122	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs570965656	chr6:86287122-86287123	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs11752795	chr6:86287129-86287130	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs547553844	chr6:86287130-86287131	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs545818672	chr6:86287209-86287210	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs190474112	chr6:86287227-86287228	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs536878617	chr6:86287269-86287270	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs569179872	chr6:86287281-86287282	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs35078819	chr6:86287314-86287315	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs554961994	chr6:86287356-86287357	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs183044551	chr6:86287371-86287372	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs146488095	chr6:86287396-86287397	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs139590734	chr6:86287429-86287430	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs577377673	chr6:86287509-86287510	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs541522275	chr6:86287510-86287511	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs201115701	chr6:86287523-86287524	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs149718227	chr6:86287550-86287551	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs572141909	chr6:86287673-86287674	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs145526977	chr6:86287741-86287742	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs560982891	chr6:86287744-86287745	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs531507865	chr6:86287795-86287796	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs542988853	chr6:86287798-86287799	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs564557449	chr6:86287822-86287823	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs532016778	chr6:86287867-86287868	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs73483557	chr6:86287868-86287869	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs115731820	chr6:86287903-86287904	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs530223778	chr6:86287955-86287956	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs188762276	chr6:86288048-86288049	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs570334451	chr6:86288082-86288083	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	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
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	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
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
craniofacial dysmorphism	21918468	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
abnormal development	18461090	CNVD
Myelodysplastic syndrome	18508791	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1082 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:86208800-86289200	Weak transcription	Pancreas	Pancrea
2	chr6:86222600-86289400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:86224200-86302600	Weak transcription	Colonic Mucosa	Colon
4	chr6:86233800-86289200	Weak transcription	Spleen	Spleen
5	chr6:86243400-86301400	Weak transcription	Thymus	Thymus
6	chr6:86244200-86289200	Weak transcription	Gastric	stomach
7	chr6:86252800-86289600	Weak transcription	Esophagus	oesophagus
8	chr6:86254800-86287800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr6:86263000-86289400	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr6:86263000-86289600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr6:86265600-86288200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr6:86265600-86289800	Weak transcription	Stomach Smooth Muscle	stomach
13	chr6:86266400-86290000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr6:86272000-86290200	Weak transcription	Fetal Muscle Leg	muscle
15	chr6:86273400-86288000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr6:86275200-86286400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr6:86277600-86289200	Weak transcription	Lung	lung
18	chr6:86278200-86302600	Weak transcription	Ovary	ovary
19	chr6:86278400-86291400	Weak transcription	Adipose Nuclei	Adipose
20	chr6:86279200-86289200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr6:86280000-86301400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr6:86280200-86290200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr6:86281200-86288800	Weak transcription	Fetal Stomach	stomach
24	chr6:86281200-86289600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr6:86281400-86289200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr6:86281400-86301600	Weak transcription	Fetal Thymus	thymus
27	chr6:86281600-86288000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr6:86281600-86288000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr6:86281600-86288200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr6:86281600-86290000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr6:86281600-86290000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr6:86281600-86290200	Weak transcription	GM12878-XiMat	blood
33	chr6:86281600-86291800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr6:86281800-86287800	Weak transcription	Primary B cells from peripheral blood	blood
35	chr6:86281800-86290400	Weak transcription	Fetal Muscle Trunk	muscle
36	chr6:86282000-86289200	Weak transcription	Fetal Intestine Large	intestine
37	chr6:86282200-86290400	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr6:86282200-86291600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr6:86282400-86290200	Weak transcription	Placenta	Placenta
40	chr6:86282600-86288200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr6:86282800-86288000	Weak transcription	Primary T cells from cord blood	blood
42	chr6:86283000-86288800	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr6:86283000-86290200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr6:86283200-86288000	Weak transcription	Fetal Intestine Small	intestine
45	chr6:86283400-86289000	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr6:86283600-86290200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr6:86284200-86286800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr6:86284200-86286800	Enhancers	NHDF-Ad	bronchial
49	chr6:86284400-86286600	Enhancers	HepG2	liver
50	chr6:86284400-86286600	Enhancers	HUVEC	blood vessel

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