Variant report

Variant	esv3521788
Chromosome Location	chr6:26334022-26356973
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:852)
CpG islands
(count:122)
Chromatin interactive
region (count:66)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:852 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:26351697-26352150	K562	blood:	n/a	n/a
2	ARID3A	chr6:26351223-26351344	K562	blood:	n/a	n/a
3	ARID3A	chr6:26348059-26348323	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:26350753-26350953	K562	blood:	n/a	n/a
5	ARID3A	chr6:26350342-26350719	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:26341880-26342096	K562	blood:	n/a	n/a
7	ARID3A	chr6:26333676-26334308	K562	blood:	n/a	chr6:26333756-26333772
8	ARID3A	chr6:26341883-26342145	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:26336479-26337361	K562	blood:	n/a	n/a
10	ARID3A	chr6:26351709-26352092	HepG2	liver:	n/a	n/a
11	ATF1	chr6:26351678-26352163	K562	blood:	n/a	n/a
12	ATF1	chr6:26336516-26337360	K562	blood:	n/a	n/a
13	ATF2	chr6:26341695-26342420	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr6:26341710-26342232	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr6:26351627-26352105	K562	blood:	n/a	n/a
16	ATF3	chr6:26341733-26342251	K562	blood:	n/a	chr6:26342011-26342025
17	ATF3	chr6:26341554-26342238	A549	lung:	n/a	chr6:26342011-26342025
18	ATF3	chr6:26336468-26337292	K562	blood:	n/a	n/a
19	BACH1	chr6:26348011-26348101	K562	blood:	n/a	n/a
20	BACH1	chr6:26347911-26348242	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr6:26341797-26342142	GM12878	blood:	n/a	n/a
22	BATF	chr6:26342194-26342848	GM12878	blood:	n/a	n/a
23	BATF	chr6:26342485-26342793	GM12878	blood:	n/a	n/a
24	BCLAF1	chr6:26341743-26342552	GM12878	blood:	n/a	n/a
25	BCLAF1	chr6:26341736-26342817	GM12878	blood:	n/a	n/a
26	BHLHE40	chr6:26341723-26342121	K562	blood:	n/a	n/a
27	BHLHE40	chr6:26341770-26342159	GM12878	blood:	n/a	n/a
28	BHLHE40	chr6:26342384-26342825	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:26351741-26352053	K562	blood:	n/a	n/a
30	BHLHE40	chr6:26352727-26352935	K562	blood:	n/a	n/a
31	BHLHE40	chr6:26336601-26337401	K562	blood:	n/a	n/a
32	BHLHE40	chr6:26341773-26342174	HepG2	liver:	n/a	n/a
33	BHLHE40	chr6:26345065-26345152	K562	blood:	n/a	n/a
34	BRCA1	chr6:26351731-26352104	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr6:26352490-26352618	HepG2	liver:	n/a	n/a
36	BRCA1	chr6:26341896-26342126	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr6:26341907-26342087	HepG2	liver:	n/a	n/a
38	CBX3	chr6:26351695-26352156	K562	blood:	n/a	n/a
39	CBX3	chr6:26341694-26342177	K562	blood:	n/a	n/a
40	CBX3	chr6:26341150-26342385	HCT-116	colon:	n/a	n/a
41	CBX3	chr6:26341436-26342402	HCT-116	colon:	n/a	n/a
42	CBX3	chr6:26336466-26337526	K562	blood:	n/a	n/a
43	CBX3	chr6:26351593-26352274	HCT-116	colon:	n/a	n/a
44	CBX3	chr6:26341528-26342240	K562	blood:	n/a	n/a
45	CCNT2	chr6:26336557-26337388	K562	blood:	n/a	n/a
46	CCNT2	chr6:26350542-26351033	K562	blood:	n/a	chr6:26350569-26350578
47	CCNT2	chr6:26341931-26342131	K562	blood:	n/a	n/a
48	CCNT2	chr6:26351784-26352173	K562	blood:	n/a	n/a
49	CCNT2	chr6:26352952-26353025	K562	blood:	n/a	n/a
50	CEBPB	chr6:26336507-26337020	A549	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26351915-26351965	Hela-S3	cervix:	n/a
2	chr6:26345053-26345103	AG04450	lung:	fetal
3	chr6:26345053-26345103	AG09309	skin:	n/a
4	chr6:26345053-26345103	MCF10A-Er-Src	breast:	n/a
5	chr6:26351915-26351965	SK-N-MC	brain:	n/a
6	chr6:26345053-26345103	CMK	blood:	n/a
7	chr6:26345053-26345103	HCPEpiC	choroid plexus:	n/a
8	chr6:26345053-26345103	HEK293	kidney:	embryo
9	chr6:26345053-26345103	ProgFib	skin:	n/a
10	chr6:26345053-26345103	GM12892	blood:	n/a
11	chr6:26351915-26351965	PANC-1	pancreas:	n/a
12	chr6:26351915-26351965	LNCaP	prostate:	n/a
13	chr6:26345053-26345103	HRE	kidney:	n/a
14	chr6:26351915-26351965	SAEC	small airway:	n/a
15	chr6:26351915-26351965	NHDF-neo	bronchial:	n/a
16	chr6:26345053-26345103	RPTEC	kidney:	n/a
17	chr6:26351915-26351965	NH-A	brain:	n/a
18	chr6:26345053-26345103	HIPEpiC	eye:	n/a
19	chr6:26351915-26351965	BJ	skin:	n/a
20	chr6:26351915-26351965	K562	blood:	n/a
21	chr6:26351915-26351965	H1-hESC	embryonic stem cell:	embryo
22	chr6:26345053-26345103	U87	brain:	n/a
23	chr6:26345053-26345103	HAEpiC	amniotic membrane:	n/a
24	chr6:26351915-26351965	GM12892	blood:	n/a
25	chr6:26345053-26345103	HRPEpiC	eye:	n/a
26	chr6:26345053-26345103	BE2_C	brain:	n/a
27	chr6:26351915-26351965	T-47D	breast:	n/a
28	chr6:26345053-26345103	HCT-116	colon:	n/a
29	chr6:26351915-26351965	AG04450	lung:	fetal
30	chr6:26351915-26351965	HRCEpiC	kidney:	n/a
31	chr6:26345053-26345103	ovcar-3	ovarian:	n/a
32	chr6:26351915-26351965	HUVEC	blood vessel:	n/a
33	chr6:26345053-26345103	Hepatocyte	liver:	n/a
34	chr6:26351915-26351965	NB4	blood:	n/a
35	chr6:26345053-26345103	NHBE	bronchial:	n/a
36	chr6:26351915-26351965	ProgFib	skin:	n/a
37	chr6:26351915-26351965	AG04449	skin:	fetal
38	chr6:26345053-26345103	T-47D	breast:	n/a
39	chr6:26351915-26351965	HPAEpiC	pulmonary alveolar:	n/a
40	chr6:26351915-26351965	CMK	blood:	n/a
41	chr6:26351915-26351965	GM12878	blood:	n/a
42	chr6:26351915-26351965	GM19239	blood:	n/a
43	chr6:26351915-26351965	NT2-D1	testis:	n/a
44	chr6:26351915-26351965	SK-N-SH_RA	brain:	n/a
45	chr6:26345053-26345103	AG09319	gingival:	n/a
46	chr6:26345053-26345103	GM19239	blood:	n/a
47	chr6:26351915-26351965	HepG2	liver:	n/a
48	chr6:26345053-26345103	AoSMC	blood vessel:	n/a
49	chr6:26345053-26345103	HepG2	liver:	n/a
50	chr6:26351915-26351965	HCT-116	colon:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:26336969..26339316-chr6:26536636..26539094,2	K562	blood:
2	chr6:26272455..26274796-chr6:26340559..26343243,3	MCF-7	breast:
3	chr6:26346422..26348741-chr6:26456867..26458564,3	K562	blood:
4	chr6:26340224..26342444-chr6:26572464..26573981,2	K562	blood:
5	chr6:26340332..26342039-chr6:26569832..26571583,2	K562	blood:
6	chr6:26338579..26343405-chr6:26519686..26522615,5	K562	blood:
7	chr6:26337285..26338978-chr6:27114759..27116381,2	K562	blood:
8	chr6:26332412..26334494-chr6:26595085..26597642,2	K562	blood:
9	chr6:26340033..26342028-chr6:26415409..26417011,2	MCF-7	breast:
10	chr6:26335137..26336681-chr6:26520330..26522569,2	K562	blood:
11	chr6:26340224..26344158-chr6:26569567..26573981,6	K562	blood:
12	chr6:26339310..26342101-chr6:26554337..26555953,2	K562	blood:
13	chr6:26341837..26342412-chr6:26411698..26412292,2	MCF-7	breast:
14	chr6:26350529..26353058-chr6:26354416..26356563,2	K562	blood:
15	chr6:26335854..26338260-chr6:26521210..26523383,2	K562	blood:
16	chr6:26345077..26347178-chr6:26389815..26392658,2	K562	blood:
17	chr6:26332412..26338207-chr6:26594644..26597899,6	K562	blood:
18	chr6:26340367..26342068-chr6:26565730..26567496,2	K562	blood:
19	chr6:26341264..26342451-chr6:26569043..26570054,3	K562	blood:
20	chr6:26341478..26343917-chr6:26362438..26365038,2	K562	blood:
21	chr6:26346737..26349010-chr6:26483438..26485200,2	K562	blood:
22	chr6:26339658..26342406-chr6:26483476..26486207,2	K562	blood:
23	chr6:26335002..26338978-chr6:27114071..27116381,5	K562	blood:
24	chr6:26352176..26356420-chr6:26519489..26524545,4	K562	blood:
25	chr6:26334953..26336656-chr6:27103104..27105866,2	K562	blood:
26	chr6:26341882..26342492-chr6:26420774..26421520,2	MCF-7	breast:
27	chr6:26345126..26347534-chr6:26601972..26604774,2	K562	blood:
28	chr6:26350096..26351709-chr6:26521212..26523157,2	K562	blood:
29	chr6:26343594..26345212-chr6:26474079..26475915,2	K562	blood:
30	chr6:26338939..26342494-chr6:26519686..26522747,3	K562	blood:
31	chr6:26336805..26339023-chr6:26339169..26341807,3	MCF-7	breast:
32	chr6:26304711..26307029-chr6:26338839..26340987,2	MCF-7	breast:
33	chr6:26341984..26342515-chr6:26596029..26596572,2	MCF-7	breast:
34	chr6:26341496..26342438-chr6:26493055..26494222,5	K562	blood:
35	chr6:26339701..26341398-chr6:26520841..26522748,2	MCF-7	breast:
36	chr6:26350529..26353058-chr6:26354416..26356563,2	K562	blood:
37	chr6:26351127..26352720-chr6:26382336..26385327,2	K562	blood:
38	chr6:26328637..26334167-chr6:26519696..26523328,10	K562	blood:
39	chr6:26341644..26342483-chr6:26450003..26451206,4	MCF-7	breast:
40	chr6:26340614..26342213-chr6:26550720..26552761,2	K562	blood:
41	chr6:26327903..26334280-chr6:26553526..26557732,8	K562	blood:
42	chr6:26339036..26342767-chr6:26596200..26598139,3	K562	blood:
43	chr6:26342033..26344696-chr6:26521826..26523631,2	MCF-7	breast:
44	chr6:26342125..26345094-chr6:26474079..26475850,2	K562	blood:
45	chr1:17222072..17224236-chr6:26350716..26352236,2	K562	blood:
46	chr6:26341150..26343678-chr6:26575652..26577197,2	K562	blood:
47	chr6:26338721..26340808-chr6:27098381..27100563,2	MCF-7	breast:
48	chr6:26341603..26342500-chr6:26520725..26521500,3	K562	blood:
49	chr6:26340823..26342973-chr6:26490879..26493737,2	K562	blood:
50	chr6:26345080..26346941-chr6:26520838..26522730,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTN3A2-1	chr6:26334302-26334364	XLOC_005209
2	lnc-BTN3A2-1	chr6:26334302-26334364	XLOC_005209
3	lnc-BTN3A2-1	chr6:26334301-26334364	NONHSAT108266
4	lnc-BTN3A2-1	chr6:26339922-26340353	XLOC_005209
5	lnc-BTN3A2-1	chr6:26339922-26340353	NONHSAT108265
6	lnc-BTN3A2-1	chr6:26339921-26340507	NONHSAT108266
7	lnc-BTN3A2-1	chr6:26339929-26340507	XLOC_005209

No data

Variant related genes	Relation type
RNU6-1259P	TF binding region
RNU6-1259P	CpG island
ENSG00000218690	chromatin interactions
ENSG00000168242	chromatin interactions
ENSG00000197903	chromatin interactions
ENSG00000207005	chromatin interactions
ENSG00000228223	chromatin interactions
ENSG00000124508	chromatin interactions
ENSG00000146109	chromatin interactions
ENSG00000265565	chromatin interactions
ENSG00000184825	chromatin interactions
ENSG00000182952	chromatin interactions
ENSG00000124635	chromatin interactions
ENSG00000112763	chromatin interactions
ENSG00000199289	chromatin interactions
ENSG00000158406	chromatin interactions
CD46	miRNA target sites
CDC23	miRNA target sites

Extended variants
information (count: 816 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:816 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560000593	chr6:26334077-26334078	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs564924186	chr6:26334091-26334092	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs148447232	chr6:26334092-26334093	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs376254050	chr6:26334105-26334106	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs112958190	chr6:26334110-26334111	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs34536440	chr6:26334111-26334112	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs575400139	chr6:26334143-26334144	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs143207261	chr6:26334144-26334145	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs78698800	chr6:26334145-26334146	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs551077272	chr6:26334206-26334207	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs546467998	chr6:26334222-26334223	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs567621877	chr6:26334238-26334239	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs535639390	chr6:26334260-26334261	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs34569761	chr6:26334306-26334307	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs543004935	chr6:26334316-26334317	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs11755795	chr6:26334339-26334340	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs557814197	chr6:26334340-26334341	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs577588315	chr6:26334386-26334387	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs536607298	chr6:26334415-26334416	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs141727214	chr6:26334491-26334492	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs573610002	chr6:26334693-26334694	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542862177	chr6:26334732-26334733	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs190036725	chr6:26334816-26334817	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs112914796	chr6:26334930-26334931	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs182574995	chr6:26334936-26334937	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs565414751	chr6:26334979-26334980	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs150543661	chr6:26334989-26334990	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs544241910	chr6:26335009-26335010	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs368027927	chr6:26335035-26335036	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs371324183	chr6:26335139-26335140	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs184901275	chr6:26335140-26335141	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs190826580	chr6:26335141-26335142	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs549230111	chr6:26335188-26335189	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs565854421	chr6:26335195-26335196	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs77960387	chr6:26335269-26335270	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs74724022	chr6:26335271-26335272	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs9348708	chr6:26335276-26335277	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs6456714	chr6:26335346-26335347	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs183021704	chr6:26335349-26335350	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs537052010	chr6:26335351-26335352	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs113218058	chr6:26335373-26335374	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs567397370	chr6:26335374-26335375	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs535928333	chr6:26335376-26335377	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs553180626	chr6:26335413-26335414	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs75927883	chr6:26335420-26335421	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs532950761	chr6:26335434-26335435	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs545166748	chr6:26335506-26335507	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs188774581	chr6:26335539-26335540	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs78365581	chr6:26335579-26335580	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs551677907	chr6:26335593-26335594	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Williams-beuren syndrome	16971481	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Autism	22495309	CNVD
Lung cancer	21569311	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	19100363	CNVD

Chromatin state (count:535 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26332400-26336000	Weak transcription	HSMMtube	muscle
2	chr6:26332600-26336200	Weak transcription	HSMM	muscle
3	chr6:26332600-26336400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr6:26333000-26335800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:26333000-26336000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr6:26333000-26336000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr6:26333000-26336000	Weak transcription	Osteobl	bone
8	chr6:26333000-26336200	Weak transcription	NH-A	brain
9	chr6:26333000-26336200	Weak transcription	NHLF	lung
10	chr6:26333000-26336400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr6:26333000-26337200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:26333000-26341600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:26333000-26342200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr6:26333200-26335600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr6:26333200-26336000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:26333200-26336000	Weak transcription	GM12878-XiMat	blood
17	chr6:26333200-26336000	Weak transcription	NHEK	skin
18	chr6:26333200-26336400	Weak transcription	HMEC	breast
19	chr6:26333400-26334400	Enhancers	HepG2	liver
20	chr6:26333400-26335600	Weak transcription	Hela-S3	cervix
21	chr6:26333600-26334600	Flanking Active TSS	K562	blood
22	chr6:26333600-26335800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr6:26333800-26334200	Weak transcription	A549	lung
24	chr6:26334200-26334400	Enhancers	A549	lung
25	chr6:26334400-26335600	Weak transcription	A549	lung
26	chr6:26334400-26335600	Weak transcription	HepG2	liver
27	chr6:26334600-26336200	Enhancers	K562	blood
28	chr6:26335600-26336200	Enhancers	H9 Cell Line	embryonic stem cell
29	chr6:26335600-26336400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr6:26335600-26336400	Enhancers	A549	lung
31	chr6:26335600-26336400	Enhancers	Hela-S3	cervix
32	chr6:26335600-26337400	Enhancers	HepG2	liver
33	chr6:26335600-26337600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr6:26335800-26336200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr6:26335800-26336600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:26335800-26337000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr6:26335800-26337200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:26335800-26337400	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr6:26335800-26337400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr6:26335800-26337600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr6:26335800-26337600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr6:26336000-26336200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr6:26336000-26336200	Enhancers	Primary T cells fromperipheralblood	blood
44	chr6:26336000-26336200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr6:26336000-26336400	Enhancers	Muscle Satellite Cultured Cells	--
46	chr6:26336000-26336400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr6:26336000-26336600	Enhancers	GM12878-XiMat	blood
48	chr6:26336000-26336800	Enhancers	NHEK	skin
49	chr6:26336000-26337000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr6:26336000-26337000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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