Variant report

Variant	nsv885816
Chromosome Location	chr6:36965099-36999682
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1771)
CpG islands
(count:489)
Chromatin interactive
region (count:153)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1771 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:36989395-36989810	K562	blood:	n/a	n/a
2	ARID3A	chr6:36997095-36997525	K562	blood:	n/a	n/a
3	ARID3A	chr6:36985997-36986807	K562	blood:	n/a	n/a
4	ARID3A	chr6:36991063-36991839	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:36986002-36986764	HepG2	liver:	n/a	n/a
6	ATF1	chr6:36997113-36997531	K562	blood:	n/a	n/a
7	ATF2	chr6:36972239-36972765	GM12878	blood:	n/a	n/a
8	ATF2	chr6:36975311-36976028	GM12878	blood:	n/a	n/a
9	ATF2	chr6:36986158-36986649	GM12878	blood:	n/a	n/a
10	ATF3	chr6:36997134-36997455	K562	blood:	n/a	n/a
11	ATF3	chr6:36997083-36997579	K562	blood:	n/a	n/a
12	ATF3	chr6:36989521-36989856	K562	blood:	n/a	n/a
13	ATF3	chr6:36979779-36980161	K562	blood:	n/a	n/a
14	BACH1	chr6:36997074-36997343	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr6:36997118-36997494	K562	blood:	n/a	n/a
16	BACH1	chr6:36989735-36989791	K562	blood:	n/a	n/a
17	BATF	chr6:36997059-36997417	GM12878	blood:	n/a	n/a
18	BATF	chr6:36985866-36986237	GM12878	blood:	n/a	chr6:36985893-36985902
19	BCLAF1	chr6:36985916-36986759	GM12878	blood:	n/a	n/a
20	BCLAF1	chr6:36996996-36997671	K562	blood:	n/a	n/a
21	BCLAF1	chr6:36973184-36973691	GM12878	blood:	n/a	n/a
22	BCLAF1	chr6:36985945-36986799	GM12878	blood:	n/a	n/a
23	BHLHE40	chr6:36973353-36973682	K562	blood:	n/a	n/a
24	BHLHE40	chr6:36989486-36989851	K562	blood:	n/a	n/a
25	BHLHE40	chr6:36967394-36967480	K562	blood:	n/a	n/a
26	BHLHE40	chr6:36985940-36986736	K562	blood:	n/a	n/a
27	BHLHE40	chr6:36971830-36972133	GM12878	blood:	n/a	n/a
28	BHLHE40	chr6:36975123-36975848	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:36997051-36997428	HepG2	liver:	n/a	n/a
30	BHLHE40	chr6:36972439-36972669	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:36997156-36997345	GM12878	blood:	n/a	n/a
32	BHLHE40	chr6:36973273-36973560	GM12878	blood:	n/a	n/a
33	BHLHE40	chr6:36996975-36997540	K562	blood:	n/a	n/a
34	BRCA1	chr6:36985945-36986764	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr6:36989574-36989696	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr6:36973517-36973609	GM12878	blood:	n/a	n/a
37	BRCA1	chr6:36972329-36972426	GM12878	blood:	n/a	n/a
38	BRCA1	chr6:36997205-36997413	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr6:36985906-36986276	H1-hESC	embryonic stem cell:	n/a	n/a
40	CBX3	chr6:36989536-36989847	K562	blood:	n/a	n/a
41	CBX3	chr6:36998225-36998994	K562	blood:	n/a	n/a
42	CBX3	chr6:36989404-36989950	K562	blood:	n/a	n/a
43	CBX3	chr6:36985856-36986788	K562	blood:	n/a	n/a
44	CBX3	chr6:36973277-36973639	K562	blood:	n/a	n/a
45	CBX3	chr6:36997034-36997599	K562	blood:	n/a	n/a
46	CBX3	chr6:36997951-36998980	K562	blood:	n/a	n/a
47	CBX3	chr6:36996893-36997854	K562	blood:	n/a	n/a
48	CCNT2	chr6:36997133-36997526	K562	blood:	n/a	n/a
49	CCNT2	chr6:36989580-36989901	K562	blood:	n/a	n/a
50	CEBPB	chr6:36991199-36991415	HepG2	liver:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:36966223-36966273	NHDF-neo	bronchial:	n/a
2	chr6:36966223-36966273	NHDF-neo	bronchial:	n/a
3	chr6:36966223-36966273	PANC-1	pancreas:	n/a
4	chr6:36972127-36972177	HRE	kidney:	n/a
5	chr6:36996068-36996118	Caco-2	colon:	n/a
6	chr6:36973448-36973498	HMEC	breast:	n/a
7	chr6:36972163-36972213	HEEpiC	esophagus:	n/a
8	chr6:36973448-36973498	H1-hESC	embryonic stem cell:	embryo
9	chr6:36973518-36973568	AG09309	skin:	n/a
10	chr6:36996068-36996118	U87	brain:	n/a
11	chr6:36996068-36996118	HUVEC	blood vessel:	n/a
12	chr6:36996068-36996118	NHBE	bronchial:	n/a
13	chr6:36972127-36972177	H1-hESC	embryonic stem cell:	embryo
14	chr6:36972027-36972077	HUVEC	blood vessel:	n/a
15	chr6:36973448-36973498	HAEpiC	amniotic membrane:	n/a
16	chr6:36996068-36996118	HRPEpiC	eye:	n/a
17	chr6:36972163-36972213	NHBE	bronchial:	n/a
18	chr6:36972163-36972213	ECC-1	luminal epithelium:	n/a
19	chr6:36973518-36973568	RPTEC	kidney:	n/a
20	chr6:36973448-36973498	HNPCEpiC	eye:	n/a
21	chr6:36996068-36996118	GM12892	blood:	n/a
22	chr6:36973518-36973568	SK-N-MC	brain:	n/a
23	chr6:36973448-36973498	NHBE	bronchial:	n/a
24	chr6:36966223-36966273	GM12891	blood:	n/a
25	chr6:36973448-36973498	HEEpiC	esophagus:	n/a
26	chr6:36973518-36973568	SKMC	muscle:	n/a
27	chr6:36972127-36972177	NT2-D1	testis:	n/a
28	chr6:36966223-36966273	A549	lung:	n/a
29	chr6:36972027-36972077	CMK	blood:	n/a
30	chr6:36972027-36972077	HRE	kidney:	n/a
31	chr6:36996068-36996118	SK-N-SH_RA	brain:	n/a
32	chr6:36966223-36966273	AG10803	skin:	n/a
33	chr6:36972163-36972213	AG10803	skin:	n/a
34	chr6:36972163-36972213	HL-60	blood:	n/a
35	chr6:36973448-36973498	MCF-7	breast:	n/a
36	chr6:36966223-36966273	AG09319	gingival:	n/a
37	chr6:36972163-36972213	Hepatocyte	liver:	n/a
38	chr6:36973518-36973568	HEK293	kidney:	embryo
39	chr6:36973448-36973498	NB4	blood:	n/a
40	chr6:36972163-36972213	HIPEpiC	eye:	n/a
41	chr6:36972163-36972213	K562	blood:	n/a
42	chr6:36972163-36972213	MCF-7	breast:	n/a
43	chr6:36985879-36985929	AG04449	skin:	fetal
44	chr6:36966223-36966273	GM06990	blood:	n/a
45	chr6:36985879-36985929	HRCEpiC	kidney:	n/a
46	chr6:36972027-36972077	ovcar-3	ovarian:	n/a
47	chr6:36996068-36996118	AG10803	skin:	n/a
48	chr6:36972127-36972177	PFSK-1	brain:	n/a
49	chr6:36973448-36973498	NH-A	brain:	n/a
50	chr6:36972163-36972213	HRCEpiC	kidney:	n/a

(count:153 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:36759534..36760254-chr6:36985709..36986530,2	K562	blood:
2	chr6:36985158..36987310-chr6:37189028..37190861,2	K562	blood:
3	chr6:36950593..36954224-chr6:36982678..36985968,4	K562	blood:
4	chr6:36962998..36965678-chr6:36969207..36971647,3	K562	blood:
5	chr6:36990959..36991838-chr6:37139648..37140564,3	MCF-7	breast:
6	chr6:36996603..36998184-chr6:37175452..37176492,5	K562	blood:
7	chr6:36991470..36994009-chr6:36994154..36996007,2	K562	blood:
8	chr6:36967024..36973771-chr6:36979699..36986633,7	K562	blood:
9	chr6:36962998..36965678-chr6:36969207..36971647,3	K562	blood:
10	chr6:36807651..36808641-chr6:36985800..36986642,2	K562	blood:
11	chr6:36997259..36998862-chr6:37140083..37143068,2	K562	blood:
12	chr6:36951647..36954567-chr6:36984468..36987638,6	K562	blood:
13	chr6:36852005..36855458-chr6:36984429..36987560,3	K562	blood:
14	chr6:36991470..36994009-chr6:36994154..36996007,2	K562	blood:
15	chr6:36998448..37001378-chr6:37003343..37005292,2	K562	blood:
16	chr6:36987000..36988996-chr6:36992167..36994325,2	MCF-7	breast:
17	chr6:36964178..36967540-chr6:36970147..36973518,3	K562	blood:
18	chr6:36986189..36986703-chr6:36997156..36997970,2	K562	blood:
19	chr6:36989418..36991271-chr6:36992892..36995334,2	K562	blood:
20	chr6:36986189..36986703-chr6:36997156..36997970,2	K562	blood:
21	chr6:36952434..36955977-chr6:36983476..36987276,5	MCF-7	breast:
22	chr6:36952740..36955730-chr6:36990686..36992977,2	MCF-7	breast:
23	chr6:36970572..36972473-chr6:36980077..36981597,2	MCF-7	breast:
24	chr6:36985713..36987315-chr6:37177177..37178923,41	K562	blood:
25	chr6:36865240..36866025-chr6:36985626..36986520,4	MCF-7	breast:
26	chr6:36953080..36955220-chr6:36964655..36966214,2	MCF-7	breast:
27	chr6:36989705..36991355-chr6:37177906..37180017,2	K562	blood:
28	chr6:36996688..36999703-chr6:37014680..37019381,6	K562	blood:
29	chr6:36990515..36993191-chr6:37140306..37142032,2	K562	blood:
30	chr6:36951556..36954050-chr6:36967032..36970466,4	K562	blood:
31	chr6:36996464..36997699-chr6:37282346..37283344,3	K562	blood:
32	chr6:36886183..36886832-chr6:36986137..36986795,2	MCF-7	breast:
33	chr6:36990791..36991393-chr6:37175987..37176512,2	K562	blood:
34	chr6:36995858..36998070-chr6:37135401..37138146,2	K562	blood:
35	chr6:36998830..37003518-chr6:37005337..37008054,4	K562	blood:
36	chr6:36997224..37001862-chr6:37173680..37176936,6	K562	blood:
37	chr6:36953033..36955715-chr6:36997324..37000089,2	K562	blood:
38	chr6:36959704..36962585-chr6:36968931..36971107,3	K562	blood:
39	chr6:36990308..36994435-chr6:37135955..37142463,7	MCF-7	breast:
40	chr6:36881502..36882020-chr6:36986068..36986734,2	MCF-7	breast:
41	chr6:36990365..36993008-chr6:37173056..37174910,2	MCF-7	breast:
42	chr6:36996009..36998535-chr6:37144117..37146528,2	K562	blood:
43	chr6:36985258..36986956-chr6:37321041..37322902,2	MCF-7	breast:
44	chr6:36996735..36997557-chr6:37139677..37140272,3	MCF-7	breast:
45	chr6:36993138..36995327-chr6:37018553..37020815,2	MCF-7	breast:
46	chr6:36995255..36997450-chr6:37157746..37159592,2	K562	blood:
47	chr6:36951113..36952947-chr6:36995288..36997269,2	K562	blood:
48	chr6:36952074..36956895-chr6:36967839..36978010,11	MCF-7	breast:
49	chr6:36990980..36992588-chr6:37004025..37006241,2	MCF-7	breast:
50	chr6:36989691..36991271-chr6:36992892..36995062,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGD2-1	chr6:36976610-36977807	NONHSAT112246
2	lnc-FGD2-1	chr6:36973422-36973661	NONHSAT112246
3	lnc-COX6A1P2-2	chr6:36996385-36996653	expReg_chr6_4389_+

No data

Variant related genes	Relation type
FGD2	TF binding region
FGD2	CpG island
ENSG00000137409	chromatin interactions
ENSG00000137193	chromatin interactions
ENSG00000252687	chromatin interactions
ENSG00000112130	chromatin interactions
ENSG00000124496	chromatin interactions
ENSG00000146192	chromatin interactions
ENSG00000198663	chromatin interactions
ENSG00000172738	chromatin interactions
ENSG00000124772	chromatin interactions

Extended variants
information (count: 1662 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1662 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6930271	chr6:36965099-36965100	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74576955	chr6:36965131-36965132	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs541840920	chr6:36965132-36965133	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs180936048	chr6:36965133-36965134	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs35792696	chr6:36965138-36965139	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs561714703	chr6:36965147-36965148	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs147929365	chr6:36965148-36965149	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs141795154	chr6:36965157-36965158	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs543138651	chr6:36965176-36965177	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs562925656	chr6:36965177-36965178	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs76099781	chr6:36965189-36965190	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs114466620	chr6:36965246-36965247	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs148174962	chr6:36965247-36965248	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs115046255	chr6:36965254-36965255	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs555993632	chr6:36965258-36965259	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs11759019	chr6:36965282-36965283	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs375023131	chr6:36965283-36965284	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs566177617	chr6:36965292-36965293	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs369779689	chr6:36965318-36965319	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs373460606	chr6:36965324-36965325	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs708011	chr6:36965349-36965350	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs369565125	chr6:36965379-36965380	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs74729055	chr6:36965409-36965410	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs538065024	chr6:36965415-36965416	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs201134087	chr6:36965445-36965446	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs78745589	chr6:36965524-36965525	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs73733429	chr6:36965563-36965564	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs554189136	chr6:36965571-36965572	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs77935433	chr6:36965576-36965577	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs140922098	chr6:36965595-36965596	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs542720437	chr6:36965622-36965623	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs185882443	chr6:36965624-36965625	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs531765611	chr6:36965625-36965626	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs111269277	chr6:36965633-36965634	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs565178608	chr6:36965642-36965643	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs150197877	chr6:36965653-36965654	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs547711833	chr6:36965665-36965666	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs200566585	chr6:36965688-36965689	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs16889362	chr6:36965705-36965706	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs182978955	chr6:36965728-36965729	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs536129295	chr6:36965731-36965732	Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs548773648	chr6:36965810-36965811	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs114198888	chr6:36965823-36965824	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs112194750	chr6:36965833-36965834	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs186321388	chr6:36965837-36965838	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs571497700	chr6:36965855-36965856	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs527790431	chr6:36965883-36965884	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs113356791	chr6:36965908-36965909	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs554123926	chr6:36965942-36965943	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs708012	chr6:36965970-36965971	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36955400-36965200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:36955400-36965400	Weak transcription	Right Atrium	heart
3	chr6:36962200-36965200	Weak transcription	Brain Angular Gyrus	brain
4	chr6:36963000-36965600	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr6:36963600-36967800	Enhancers	Pancreas	Pancrea
6	chr6:36963800-36965200	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr6:36963800-36965400	Weak transcription	Right Ventricle	heart
8	chr6:36964400-36966000	Enhancers	Fetal Kidney	kidney
9	chr6:36964600-36965400	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr6:36964800-36967400	Enhancers	Fetal Muscle Trunk	muscle
11	chr6:36964800-36967600	Enhancers	Fetal Muscle Leg	muscle
12	chr6:36965000-36965200	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr6:36965000-36966800	Enhancers	Fetal Stomach	stomach
14	chr6:36965000-36967200	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr6:36965000-36967400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr6:36965000-36967600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:36965000-36967600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:36965200-36965400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:36965200-36965400	Enhancers	Stomach Smooth Muscle	stomach
20	chr6:36965200-36965600	Enhancers	Brain Substantia Nigra	brain
21	chr6:36965200-36966000	Enhancers	H1 Cell Line	embryonic stem cell
22	chr6:36965200-36966000	Enhancers	Brain Hippocampus Middle	brain
23	chr6:36965200-36966000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr6:36965200-36966200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:36965200-36966600	Enhancers	Ovary	ovary
26	chr6:36965200-36966800	Enhancers	Colon Smooth Muscle	Colon
27	chr6:36965200-36966800	Enhancers	Psoas Muscle	Psoas
28	chr6:36965200-36967000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
29	chr6:36965200-36967000	Enhancers	Spleen	Spleen
30	chr6:36965200-36967400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr6:36965200-36967400	Enhancers	Brain Angular Gyrus	brain
32	chr6:36965200-36967400	Enhancers	Brain Cingulate Gyrus	brain
33	chr6:36965200-36967400	Enhancers	Left Ventricle	heart
34	chr6:36965200-36967600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:36965200-36967600	Enhancers	Brain Anterior Caudate	brain
36	chr6:36965200-36967600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr6:36965400-36965800	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr6:36965400-36965800	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr6:36965400-36965800	Enhancers	Fetal Thymus	thymus
40	chr6:36965400-36966000	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr6:36965400-36966000	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr6:36965400-36966200	Flanking Active TSS	Stomach Smooth Muscle	stomach
43	chr6:36965400-36966600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr6:36965400-36966600	Enhancers	Gastric	stomach
45	chr6:36965400-36966600	Enhancers	Right Atrium	heart
46	chr6:36965400-36966600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
47	chr6:36965400-36966800	Enhancers	Adipose Nuclei	Adipose
48	chr6:36965400-36966800	Enhancers	Fetal Heart	heart
49	chr6:36965400-36966800	Enhancers	Fetal Lung	lung
50	chr6:36965400-36966800	Enhancers	Small Intestine	intestine

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