Variant report

Variant	nsv515488
Chromosome Location	chr6:36978745-36989587
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:795)
CpG islands
(count:61)
Chromatin interactive
region (count:72)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:36985997-36986807	K562	blood:	n/a	n/a
2	ARID3A	chr6:36986002-36986764	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:36989395-36989810	K562	blood:	n/a	n/a
4	ATF2	chr6:36986158-36986649	GM12878	blood:	n/a	n/a
5	ATF3	chr6:36989521-36989856	K562	blood:	n/a	n/a
6	ATF3	chr6:36979779-36980161	K562	blood:	n/a	n/a
7	BATF	chr6:36985866-36986237	GM12878	blood:	n/a	chr6:36985893-36985902
8	BCLAF1	chr6:36985916-36986759	GM12878	blood:	n/a	n/a
9	BCLAF1	chr6:36985945-36986799	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:36989486-36989851	K562	blood:	n/a	n/a
11	BHLHE40	chr6:36985940-36986736	K562	blood:	n/a	n/a
12	BRCA1	chr6:36985906-36986276	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr6:36985945-36986764	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr6:36989574-36989696	H1-hESC	embryonic stem cell:	n/a	n/a
15	CBX3	chr6:36985856-36986788	K562	blood:	n/a	n/a
16	CBX3	chr6:36989404-36989950	K562	blood:	n/a	n/a
17	CBX3	chr6:36989536-36989847	K562	blood:	n/a	n/a
18	CCNT2	chr6:36989580-36989901	K562	blood:	n/a	n/a
19	CEBPB	chr6:36979845-36980154	Hela-S3	cervix:	n/a	chr6:36980000-36980011 chr6:36980106-36980117
20	CEBPB	chr6:36979854-36980097	K562	blood:	n/a	chr6:36980000-36980011
21	CEBPB	chr6:36986848-36987319	MCF-7	breast:	n/a	n/a
22	CEBPB	chr6:36979752-36980179	K562	blood:	n/a	chr6:36980000-36980011 chr6:36980106-36980117
23	CEBPB	chr6:36979832-36980179	IMR90	lung:	n/a	chr6:36980000-36980011 chr6:36980106-36980117
24	CEBPB	chr6:36985491-36985625	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr6:36979843-36980152	HepG2	liver:	n/a	chr6:36980000-36980011 chr6:36980106-36980117
26	CEBPB	chr6:36979826-36980172	K562	blood:	n/a	chr6:36980000-36980011 chr6:36980106-36980117
27	CHD2	chr6:36985971-36986452	HepG2	liver:	n/a	n/a
28	CHD2	chr6:36985950-36986298	GM12878	blood:	n/a	n/a
29	CHD2	chr6:36985964-36986393	K562	blood:	n/a	n/a
30	CHD2	chr6:36985942-36986265	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr6:36989483-36989826	K562	blood:	n/a	n/a
32	CHD2	chr6:36985917-36986298	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr6:36986440-36986590	GM12868	blood:	n/a	n/a
34	CTCF	chr6:36986324-36986713	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr6:36985870-36986973	MCF-7	breast:	n/a	chr6:36986115-36986133
36	CTCF	chr6:36986366-36986716	HepG2	liver:	n/a	n/a
37	CTCF	chr6:36986460-36986610	AG09309	skin:	n/a	n/a
38	CTCF	chr6:36986500-36986650	GM12867	blood:	n/a	n/a
39	CTCF	chr6:36986060-36986210	GM12869	blood:	n/a	chr6:36986115-36986133
40	CTCF	chr6:36986560-36986710	HCT-116	colon:	n/a	n/a
41	CTCF	chr6:36986500-36986650	HepG2	liver:	n/a	n/a
42	CTCF	chr6:36986022-36986256	GM20000	blood:	n/a	chr6:36986115-36986133
43	CTCF	chr6:36986645-36986700	GM19238	blood:	n/a	n/a
44	CTCF	chr6:36989500-36989650	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:36985480-36985750	HepG2	liver:	n/a	n/a
46	CTCF	chr6:36986540-36986690	HepG2	liver:	n/a	n/a
47	CTCF	chr6:36989560-36989710	GM12864	blood:	n/a	n/a
48	CTCF	chr6:36986040-36986190	GM12867	blood:	n/a	chr6:36986115-36986133
49	CTCF	chr6:36989520-36989670	K562	blood:	n/a	n/a
50	CTCF	chr6:36986080-36986230	HMEC	breast:	n/a	chr6:36986115-36986133

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:36985879-36985929	HL-60	blood:	n/a
2	chr6:36985879-36985929	SK-N-SH_RA	brain:	n/a
3	chr6:36985879-36985929	SKMC	muscle:	n/a
4	chr6:36985879-36985929	GM12891	blood:	n/a
5	chr6:36985879-36985929	GM06990	blood:	n/a
6	chr6:36985879-36985929	HEEpiC	esophagus:	n/a
7	chr6:36985879-36985929	HIPEpiC	eye:	n/a
8	chr6:36985879-36985929	Hela-S3	cervix:	n/a
9	chr6:36985879-36985929	PrEC	prostate:	n/a
10	chr6:36985879-36985929	ECC-1	luminal epithelium:	n/a
11	chr6:36985879-36985929	K562	blood:	n/a
12	chr6:36985879-36985929	BE2_C	brain:	n/a
13	chr6:36985879-36985929	ProgFib	skin:	n/a
14	chr6:36985879-36985929	NB4	blood:	n/a
15	chr6:36985879-36985929	HUVEC	blood vessel:	n/a
16	chr6:36985879-36985929	HRPEpiC	eye:	n/a
17	chr6:36985879-36985929	Caco-2	colon:	n/a
18	chr6:36985879-36985929	GM19239	blood:	n/a
19	chr6:36985879-36985929	HRE	kidney:	n/a
20	chr6:36985879-36985929	HAEpiC	amniotic membrane:	n/a
21	chr6:36985879-36985929	NHBE	bronchial:	n/a
22	chr6:36985879-36985929	NH-A	brain:	n/a
23	chr6:36985879-36985929	PFSK-1	brain:	n/a
24	chr6:36985879-36985929	HCPEpiC	choroid plexus:	n/a
25	chr6:36985879-36985929	A549	lung:	n/a
26	chr6:36985879-36985929	HRCEpiC	kidney:	n/a
27	chr6:36985879-36985929	SAEC	small airway:	n/a
28	chr6:36985879-36985929	NHDF-neo	bronchial:	n/a
29	chr6:36985879-36985929	T-47D	breast:	n/a
30	chr6:36985879-36985929	U87	brain:	n/a
31	chr6:36985879-36985929	AG09319	gingival:	n/a
32	chr6:36985879-36985929	Hepatocyte	liver:	n/a
33	chr6:36985879-36985929	MCF-7	breast:	n/a
34	chr6:36985879-36985929	HCF	heart:	n/a
35	chr6:36985879-36985929	NT2-D1	testis:	n/a
36	chr6:36985879-36985929	GM12878	blood:	n/a
37	chr6:36985879-36985929	MCF10A-Er-Src	breast:	n/a
38	chr6:36985879-36985929	SK-N-MC	brain:	n/a
39	chr6:36985879-36985929	IMR90	lung:	fetal
40	chr6:36985879-36985929	LNCaP	prostate:	n/a
41	chr6:36985879-36985929	AoSMC	blood vessel:	n/a
42	chr6:36985879-36985929	HNPCEpiC	eye:	n/a
43	chr6:36985879-36985929	BJ	skin:	n/a
44	chr6:36985879-36985929	PANC-1	pancreas:	n/a
45	chr6:36985879-36985929	AG04449	skin:	fetal
46	chr6:36985879-36985929	ovcar-3	ovarian:	n/a
47	chr6:36985879-36985929	AG04450	lung:	fetal
48	chr6:36985879-36985929	AG09309	skin:	n/a
49	chr6:36985879-36985929	HCT-116	colon:	n/a
50	chr6:36985879-36985929	RPTEC	kidney:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:36960761..36964631-chr6:36974795..36978853,3	MCF-7	breast:
2	chr6:36986052..36986559-chr8:95912020..95912521,2	MCF-7	breast:
3	chr6:36853323..36855502-chr6:36984627..36986609,2	MCF-7	breast:
4	chr6:36952431..36954730-chr6:36980411..36983158,3	MCF-7	breast:
5	chr6:36985689..36987067-chr6:37174835..37176439,10	MCF-7	breast:
6	chr6:36986126..36987117-chr6:37176530..37177578,3	MCF-7	breast:
7	chr6:36881502..36882020-chr6:36986068..36986734,2	MCF-7	breast:
8	chr6:36986227..36987023-chr6:37179191..37179864,2	MCF-7	breast:
9	chr6:36865240..36866025-chr6:36985626..36986520,4	MCF-7	breast:
10	chr6:36984774..36987733-chr6:36993476..36997065,5	K562	blood:
11	chr6:36885661..36888291-chr6:36984443..36986353,2	MCF-7	breast:
12	chr6:36967024..36973771-chr6:36979699..36986633,7	K562	blood:
13	chr6:36976679..36978826-chr6:37225784..37227399,2	K562	blood:
14	chr6:36831717..36834035-chr6:36985083..36987828,2	K562	blood:
15	chr6:36733549..36734625-chr6:36985573..36986688,19	K562	blood:
16	chr6:36977300..36979509-chr6:36984947..36986503,2	K562	blood:
17	chr6:36989173..36991551-chr6:37137394..37139647,3	K562	blood:
18	chr6:36928588..36930558-chr6:36986253..36988587,2	K562	blood:
19	chr6:36989372..36991434-chr6:37069040..37071610,2	MCF-7	breast:
20	chr6:36882380..36882909-chr6:36985650..36986552,2	K562	blood:
21	chr6:36948207..36949609-chr6:36985741..36986646,4	MCF-7	breast:
22	chr6:36977300..36979509-chr6:36984947..36986503,2	K562	blood:
23	chr6:36886183..36886832-chr6:36986137..36986795,2	MCF-7	breast:
24	chr6:36926516..36929397-chr6:36985217..36986948,2	K562	blood:
25	chr6:36986109..36986997-chr6:37018972..37019835,3	MCF-7	breast:
26	chr6:36985833..36987427-chr6:37139677..37140666,12	MCF-7	breast:
27	chr6:36759534..36760254-chr6:36985709..36986530,2	K562	blood:
28	chr6:36986301..36987208-chr6:37139732..37140870,3	MCF-7	breast:
29	chr6:36733415..36734583-chr6:36985207..36986995,7	MCF-7	breast:
30	chr6:36989570..36992539-chr6:37178142..37179821,2	MCF-7	breast:
31	chr6:36980695..36984451-chr6:36985282..36988423,5	K562	blood:
32	chr6:36590724..36591717-chr6:36986052..36986604,2	K562	blood:
33	chr6:36985644..36987482-chr6:37177455..37178899,11	MCF-7	breast:
34	chr6:36986026..36986641-chr6:37144661..37145631,2	K562	blood:
35	chr6:36989098..36990112-chr6:37139646..37140588,5	K562	blood:
36	chr6:36985829..36988521-chr6:36988646..36990558,2	K562	blood:
37	chr6:36980162..36980663-chr6:106265143..106265643,2	MCF-7	breast:
38	chr6:36985713..36987315-chr6:37177177..37178923,41	K562	blood:
39	chr6:36986055..36987477-chr6:37177799..37178902,22	MCF-7	breast:
40	chr6:36944786..36946944-chr6:36988246..36989759,2	MCF-7	breast:
41	chr6:36986077..36986711-chr6:37180681..37181810,4	K562	blood:
42	chr6:36951647..36954567-chr6:36984468..36987638,6	K562	blood:
43	chr6:36987000..36988996-chr6:36992167..36994325,2	MCF-7	breast:
44	chr6:36943380..36943959-chr6:36986086..36986598,2	MCF-7	breast:
45	chr6:36987509..36988444-chr6:37177937..37178601,3	K562	blood:
46	chr6:36945041..36945795-chr6:36985646..36986592,2	MCF-7	breast:
47	chr6:36952577..36955767-chr6:36983861..36986521,4	MCF-7	breast:
48	chr6:36985158..36987310-chr6:37189028..37190861,2	K562	blood:
49	chr6:36985650..36986592-chr6:37282339..37282929,2	K562	blood:
50	chr6:36984736..36987348-chr6:37138212..37139729,2	K562	blood:

No data

Variant related genes	Relation type
FGD2	TF binding region
FGD2	CpG island
ENSG00000172738	chromatin interactions
ENSG00000112130	chromatin interactions
ENSG00000137409	chromatin interactions
ENSG00000124772	chromatin interactions
ENSG00000137193	chromatin interactions
ENSG00000198663	chromatin interactions
ENSG00000146192	chromatin interactions

Extended variants
information (count: 567 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1724088	chr6:36978745-36978746	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376101457	chr6:36978746-36978747	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs147833566	chr6:36978760-36978761	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs367720858	chr6:36978766-36978767	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs201342209	chr6:36978790-36978791	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs371671447	chr6:36978804-36978805	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs375895424	chr6:36978805-36978806	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs1753288	chr6:36978834-36978835	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs201539823	chr6:36978848-36978849	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563817565	chr6:36978855-36978856	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200428727	chr6:36978867-36978868	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1724087	chr6:36978879-36978880	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs1753289	chr6:36978954-36978955	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
14	rs34253327	chr6:36978986-36978987	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534381611	chr6:36979047-36979048	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547903898	chr6:36979073-36979074	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189730234	chr6:36979075-36979076	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1753290	chr6:36979084-36979085	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs528887243	chr6:36979089-36979090	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577045045	chr6:36979175-36979176	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538643149	chr6:36979186-36979187	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553367112	chr6:36979187-36979188	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146227314	chr6:36979239-36979240	Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138402504	chr6:36979323-36979324	Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562170740	chr6:36979346-36979347	Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575852262	chr6:36979350-36979351	Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs544790735	chr6:36979397-36979398	Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376729994	chr6:36979398-36979399	Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142985798	chr6:36979417-36979418	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533663734	chr6:36979421-36979422	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546994527	chr6:36979422-36979423	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs367821536	chr6:36979437-36979438	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558895696	chr6:36979445-36979446	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377133555	chr6:36979456-36979457	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs200847237	chr6:36979466-36979467	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369546579	chr6:36979468-36979469	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372998624	chr6:36979469-36979470	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs201414065	chr6:36979505-36979506	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371219616	chr6:36979512-36979513	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547840613	chr6:36979523-36979524	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567811602	chr6:36979532-36979533	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200637703	chr6:36979537-36979538	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs12202642	chr6:36979583-36979584	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs199827786	chr6:36979591-36979592	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181839126	chr6:36979601-36979602	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142895649	chr6:36979615-36979616	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs58465444	chr6:36979669-36979670	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566830080	chr6:36979790-36979791	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs535842471	chr6:36979826-36979827	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs72848059	chr6:36979875-36979876	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:91)

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
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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	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
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	19153074	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	21693616	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Breast cancer	16397240	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36974200-36987000	Weak transcription	Right Atrium	heart
2	chr6:36974400-36980800	Weak transcription	Lung	lung
3	chr6:36974800-36979400	Weak transcription	Pancreas	Pancrea
4	chr6:36974800-36984600	Weak transcription	Fetal Thymus	thymus
5	chr6:36974800-36985000	Weak transcription	Brain Substantia Nigra	brain
6	chr6:36975000-36985800	Weak transcription	Fetal Intestine Small	intestine
7	chr6:36975400-36979600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr6:36975400-36985400	Weak transcription	Right Ventricle	heart
9	chr6:36975400-36988600	Weak transcription	Gastric	stomach
10	chr6:36975600-36985800	Weak transcription	Stomach Mucosa	stomach
11	chr6:36975600-36988200	Weak transcription	Esophagus	oesophagus
12	chr6:36975600-36989600	Weak transcription	Thymus	Thymus
13	chr6:36976000-36985200	Weak transcription	Placenta	Placenta
14	chr6:36976000-36986200	Weak transcription	Colonic Mucosa	Colon
15	chr6:36976200-36979600	Genic enhancers	Primary B cells from peripheral blood	blood
16	chr6:36976200-36983200	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr6:36976200-36984800	Weak transcription	Brain Hippocampus Middle	brain
18	chr6:36976200-36985800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr6:36976200-36985800	Weak transcription	Rectal Smooth Muscle	rectum
20	chr6:36977000-36978800	Genic enhancers	Primary monocytes fromperipheralblood	blood
21	chr6:36977000-36981200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr6:36977000-36985800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr6:36977000-36986200	Weak transcription	Duodenum Mucosa	Duodenum
24	chr6:36977400-36979600	Strong transcription	GM12878-XiMat	blood
25	chr6:36977400-36979800	Genic enhancers	Monocytes-CD14+_RO01746	blood
26	chr6:36977400-36984800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr6:36977400-36986200	Weak transcription	Adipose Nuclei	Adipose
28	chr6:36977800-36984000	Strong transcription	Spleen	Spleen
29	chr6:36978000-36978800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr6:36978000-36980200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr6:36978000-36985600	Strong transcription	Primary B cells from cord blood	blood
32	chr6:36978800-36980000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr6:36978800-36985400	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr6:36979200-36979400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr6:36979400-36979600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr6:36979400-36979800	Enhancers	Pancreas	Pancrea
37	chr6:36979600-36980000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr6:36979600-36980200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr6:36979600-36980200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr6:36979600-36980200	Enhancers	Osteobl	bone
41	chr6:36979600-36980400	Weak transcription	GM12878-XiMat	blood
42	chr6:36979600-36985200	Strong transcription	Primary B cells from peripheral blood	blood
43	chr6:36979800-36985400	Strong transcription	Monocytes-CD14+_RO01746	blood
44	chr6:36980000-36981200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr6:36980200-36980600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr6:36980200-36980600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr6:36980200-36981200	Weak transcription	Osteobl	bone
48	chr6:36980400-36985600	Strong transcription	GM12878-XiMat	blood
49	chr6:36980600-36981000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr6:36980600-36982200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood

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