Variant report

Variant	nsv883387
Chromosome Location	chr6:2086679-2176239
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:975)
CpG islands
(count:306)
Chromatin interactive
region (count:40)
LncRNA
region (count:33)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:975 , 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	chr6:2104544-2104926	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:2159048-2159052	HepG2	liver:	n/a	n/a
3	ATF1	chr6:2124471-2124901	K562	blood:	n/a	n/a
4	ATF1	chr6:2155769-2155848	K562	blood:	n/a	n/a
5	ATF1	chr6:2127958-2128208	K562	blood:	n/a	n/a
6	ATF2	chr6:2111114-2112016	GM12878	blood:	n/a	n/a
7	ATF2	chr6:2110844-2112017	GM12878	blood:	n/a	n/a
8	ATF2	chr6:2129176-2129995	GM12878	blood:	n/a	n/a
9	ATF2	chr6:2129217-2129887	GM12878	blood:	n/a	n/a
10	ATF2	chr6:2127588-2128027	GM12878	blood:	n/a	n/a
11	ATF2	chr6:2158011-2158521	GM12878	blood:	n/a	n/a
12	ATF3	chr6:2111370-2111777	HCT-116	colon:	n/a	chr6:2111530-2111545 chr6:2111531-2111544
13	BACH1	chr6:2158879-2159189	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr6:2157291-2157615	GM12878	blood:	n/a	n/a
15	BATF	chr6:2161920-2162182	GM12878	blood:	n/a	chr6:2162063-2162074
16	BATF	chr6:2158074-2158348	GM12878	blood:	n/a	n/a
17	BATF	chr6:2111329-2111889	GM12878	blood:	n/a	chr6:2111639-2111650 chr6:2111531-2111544
18	BATF	chr6:2158049-2158395	GM12878	blood:	n/a	n/a
19	BATF	chr6:2111319-2111990	GM12878	blood:	n/a	chr6:2111639-2111650 chr6:2111531-2111544
20	BATF	chr6:2161935-2162214	GM12878	blood:	n/a	chr6:2162063-2162074
21	BCL11A	chr6:2111331-2111731	GM12878	blood:	n/a	chr6:2111638-2111647 chr6:2111639-2111648 chr6:2111589-2111598
22	BCL11A	chr6:2111264-2111905	GM12878	blood:	n/a	chr6:2111638-2111647 chr6:2111639-2111648 chr6:2111589-2111598 chr6:2111822-2111831
23	BCL11A	chr6:2158074-2158406	GM12878	blood:	n/a	n/a
24	BCL3	chr6:2129238-2129889	GM12878	blood:	n/a	n/a
25	BCL3	chr6:2157541-2157964	GM12878	blood:	n/a	chr6:2157712-2157721
26	BCLAF1	chr6:2104414-2104922	GM12878	blood:	n/a	n/a
27	BCLAF1	chr6:2158041-2158533	GM12878	blood:	n/a	n/a
28	BCLAF1	chr6:2129190-2129959	GM12878	blood:	n/a	n/a
29	BCLAF1	chr6:2111435-2111937	GM12878	blood:	n/a	chr6:2111638-2111647 chr6:2111639-2111648 chr6:2111589-2111598 chr6:2111822-2111831
30	BHLHE40	chr6:2124551-2124863	K562	blood:	n/a	n/a
31	BHLHE40	chr6:2095378-2095459	K562	blood:	n/a	n/a
32	BHLHE40	chr6:2110839-2111080	GM12878	blood:	n/a	n/a
33	BHLHE40	chr6:2087299-2087385	GM12878	blood:	n/a	n/a
34	BHLHE40	chr6:2111337-2111790	GM12878	blood:	n/a	n/a
35	BRCA1	chr6:2132596-2133098	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr6:2165702-2165774	GM12878	blood:	n/a	n/a
37	CBX3	chr6:2111370-2111903	HCT-116	colon:	n/a	n/a
38	CBX3	chr6:2132527-2133153	HCT-116	colon:	n/a	n/a
39	CCNT2	chr6:2126528-2126717	K562	blood:	n/a	n/a
40	CEBPB	chr6:2105462-2105680	HepG2	liver:	n/a	chr6:2105610-2105623
41	CEBPB	chr6:2158927-2159460	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr6:2104032-2104300	Hela-S3	cervix:	n/a	chr6:2104116-2104129
43	CEBPB	chr6:2102641-2102895	MCF-7	breast:	n/a	chr6:2102739-2102750
44	CEBPB	chr6:2111258-2111935	GM12878	blood:	n/a	chr6:2111391-2111404
45	CEBPB	chr6:2158921-2159444	A549	lung:	n/a	n/a
46	CEBPB	chr6:2162421-2162684	MCF-7	breast:	n/a	n/a
47	CEBPB	chr6:2161980-2162682	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr6:2159148-2159423	A549	lung:	n/a	n/a
49	CEBPB	chr6:2159064-2159519	A549	lung:	n/a	n/a
50	CEBPB	chr6:2157653-2158220	IMR90	lung:	n/a	chr6:2157963-2157974

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:2104322-2104372	NHDF-neo	bronchial:	n/a
2	chr6:2104322-2104372	NHDF-neo	bronchial:	n/a
3	chr6:2104322-2104372	ECC-1	luminal epithelium:	n/a
4	chr6:2110875-2110925	HCT-116	colon:	n/a
5	chr6:2141241-2141291	HCM	heart:	n/a
6	chr6:2168579-2168629	K562	blood:	n/a
7	chr6:2168579-2168629	AoSMC	blood vessel:	n/a
8	chr6:2134144-2134194	HCF	heart:	n/a
9	chr6:2168579-2168629	HPAEpiC	pulmonary alveolar:	n/a
10	chr6:2141241-2141291	HRPEpiC	eye:	n/a
11	chr6:2168579-2168629	HCT-116	colon:	n/a
12	chr6:2168579-2168629	NHDF-neo	bronchial:	n/a
13	chr6:2104322-2104372	HCM	heart:	n/a
14	chr6:2104322-2104372	K562	blood:	n/a
15	chr6:2168579-2168629	BE2_C	brain:	n/a
16	chr6:2110875-2110925	AG04450	lung:	fetal
17	chr6:2141241-2141291	BE2_C	brain:	n/a
18	chr6:2104322-2104372	HMEC	breast:	n/a
19	chr6:2104322-2104372	Jurkat	blood:	n/a
20	chr6:2168579-2168629	HNPCEpiC	eye:	n/a
21	chr6:2141241-2141291	K562	blood:	n/a
22	chr6:2134144-2134194	HL-60	blood:	n/a
23	chr6:2141241-2141291	SK-N-SH	brain:	n/a
24	chr6:2104322-2104372	A549	lung:	n/a
25	chr6:2110875-2110925	A549	lung:	n/a
26	chr6:2110875-2110925	SAEC	small airway:	n/a
27	chr6:2141241-2141291	PrEC	prostate:	n/a
28	chr6:2141241-2141291	GM06990	blood:	n/a
29	chr6:2104322-2104372	HCF	heart:	n/a
30	chr6:2104322-2104372	T-47D	breast:	n/a
31	chr6:2168579-2168629	PANC-1	pancreas:	n/a
32	chr6:2110875-2110925	Hepatocyte	liver:	n/a
33	chr6:2110875-2110925	SK-N-SH	brain:	n/a
34	chr6:2134144-2134194	SKMC	muscle:	n/a
35	chr6:2141241-2141291	LNCaP	prostate:	n/a
36	chr6:2168579-2168629	NHBE	bronchial:	n/a
37	chr6:2104322-2104372	AoSMC	blood vessel:	n/a
38	chr6:2134144-2134194	Caco-2	colon:	n/a
39	chr6:2110875-2110925	Hela-S3	cervix:	n/a
40	chr6:2141241-2141291	HL-60	blood:	n/a
41	chr6:2134144-2134194	HEK293	kidney:	embryo
42	chr6:2168579-2168629	LNCaP	prostate:	n/a
43	chr6:2104322-2104372	HAEpiC	amniotic membrane:	n/a
44	chr6:2168579-2168629	RPTEC	kidney:	n/a
45	chr6:2168579-2168629	AG09309	skin:	n/a
46	chr6:2168579-2168629	BJ	skin:	n/a
47	chr6:2141241-2141291	Hepatocyte	liver:	n/a
48	chr6:2104322-2104372	HNPCEpiC	eye:	n/a
49	chr6:2141241-2141291	HCF	heart:	n/a
50	chr6:2110875-2110925	ovcar-3	ovarian:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:2159025..2161764-chr6:2166698..2168603,2	MCF-7	breast:
2	chr6:2158821..2161883-chr6:2164038..2166971,3	K562	blood:
3	chr6:1604770..1605328-chr6:2158470..2159326,2	K562	blood:
4	chr6:2159018..2159546-chr6:2196064..2196713,2	K562	blood:
5	chr6:2158821..2161883-chr6:2164038..2166971,3	K562	blood:
6	chr6:2134081..2137218-chr6:2139617..2142589,3	K562	blood:
7	chr6:1604255..1605544-chr6:2104014..2105193,5	K562	blood:
8	chr6:2102993..2105699-chr6:2107973..2110016,2	K562	blood:
9	chr6:2107952..2110679-chr6:2111605..2113236,2	MCF-7	breast:
10	chr6:2165147..2167469-chr6:2167871..2169447,2	MCF-7	breast:
11	chr6:1606456..1608668-chr6:2173309..2175661,2	MCF-7	breast:
12	chr6:2040678..2043654-chr6:2103622..2106281,2	MCF-7	breast:
13	chr6:2162382..2163882-chr7:156518679..156520785,2	MCF-7	breast:
14	chr6:2133819..2135581-chr6:2140564..2142589,2	K562	blood:
15	chr6:2134081..2137218-chr6:2139617..2142589,3	K562	blood:
16	chr6:2130543..2132757-chr6:2133403..2136232,3	K562	blood:
17	chr6:2130543..2132757-chr6:2133403..2136232,3	K562	blood:
18	chr6:1616379..1619156-chr6:2096704..2099403,2	MCF-7	breast:
19	chr6:2133819..2135581-chr6:2140564..2142589,2	K562	blood:
20	chr6:1604456..1604957-chr6:2104229..2104835,2	MCF-7	breast:
21	chr6:2110933..2112552-chr6:2126239..2128267,2	MCF-7	breast:
22	chr6:1612494..1615565-chr6:2103145..2107069,5	MCF-7	breast:
23	chr6:2081922..2083588-chr6:2088961..2091628,2	MCF-7	breast:
24	chr6:2076391..2078469-chr6:2091267..2093676,2	MCF-7	breast:
25	chr6:1610117..1612459-chr6:2103517..2106482,4	MCF-7	breast:
26	chr6:2119577..2122402-chr6:2352666..2355381,2	MCF-7	breast:
27	chr6:2107952..2110679-chr6:2111605..2113236,2	MCF-7	breast:
28	chr6:2128247..2132613-chr6:2133683..2136448,4	K562	blood:
29	chr6:2161158..2164138-chr9:131314660..131316336,2	MCF-7	breast:
30	chr6:1608030..1611197-chr6:2098990..2102744,3	MCF-7	breast:
31	chr6:1607577..1610037-chr6:2107747..2109346,3	MCF-7	breast:
32	chr6:2102993..2105699-chr6:2107973..2110016,2	K562	blood:
33	chr6:2128247..2132613-chr6:2133683..2136448,4	K562	blood:
34	chr6:1609035..1611562-chr6:2103045..2105968,3	MCF-7	breast:
35	chr6:2040794..2041414-chr6:2132566..2133423,2	MCF-7	breast:
36	chr6:1596571..1597477-chr6:2104218..2105175,4	K562	blood:
37	chr6:2159025..2161764-chr6:2166698..2168603,2	MCF-7	breast:
38	chr6:1607774..1610426-chr6:2098410..2101344,2	MCF-7	breast:
39	chr6:2165147..2167469-chr6:2167871..2169447,2	MCF-7	breast:
40	chr6:2110933..2112552-chr6:2126239..2128267,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXC1-12	chr6:2106666-2106822	NONHSAT106599
2	lnc-FOXC1-12	chr6:2123357-2124499	NONHSAT106600
3	lnc-FOXC1-12	chr6:2122596-2124499	NONHSAT106601
4	lnc-FOXC1-12	chr6:2107681-2107741	NONHSAT106599
5	lnc-FOXC1-12	chr6:2107862-2107975	NONHSAT106601
6	lnc-FOXC1-12	chr6:2125895-2126649	NONHSAT106599
7	lnc-FOXC1-12	chr6:2120205-2120250	NONHSAT106600
8	lnc-FOXC1-12	chr6:2108159-2108260	NONHSAT106600
9	lnc-FOXC1-12	chr6:2122004-2122075	NONHSAT106599
10	lnc-FOXC1-12	chr6:2107862-2107975	NONHSAT106600
11	lnc-FOXC1-12	chr6:2108159-2108260	NONHSAT106601
12	lnc-FOXC1-12	chr6:2107466-2107557	NONHSAT106600
13	lnc-FOXC1-12	chr6:2107290-2107350	NONHSAT106600
14	lnc-FOXC1-12	chr6:2120205-2120250	NONHSAT106599
15	lnc-FOXC1-12	chr6:2107290-2107350	NONHSAT106601
16	lnc-FOXC1-12	chr6:2107862-2107975	NONHSAT106599
17	lnc-FOXC1-12	chr6:2107681-2107741	NONHSAT106600
18	lnc-FOXC1-12	chr6:2120363-2120431	NONHSAT106599
19	lnc-C6orf195-21	chr6:2152486-2152826	NONHSAT106605
20	lnc-FOXC1-12	chr6:2108159-2108260	NONHSAT106599
21	lnc-FOXC1-12	chr6:2120205-2120250	NONHSAT106601
22	lnc-FOXC1-12	chr6:2122004-2122075	NONHSAT106600
23	lnc-FOXC1-12	chr6:2125723-2125802	NONHSAT106599
24	lnc-FOXC1-12	chr6:2106666-2106822	NONHSAT106601
25	lnc-FOXC1-12	chr6:2107290-2107350	NONHSAT106599
26	lnc-FOXC1-12	chr6:2107466-2107557	NONHSAT106601
27	lnc-FOXC1-12	chr6:2106666-2106822	NONHSAT106600
28	lnc-FOXC1-12	chr6:2107681-2107741	NONHSAT106601
29	lnc-FOXC1-12	chr6:2122596-2122839	NONHSAT106600
30	lnc-C6orf195-21	chr6:2150891-2151124	NONHSAT106605
31	lnc-FOXC1-12	chr6:2107466-2107557	NONHSAT106599
32	lnc-C6orf195-20	chr6:2167900-2168389	NONHSAT106610
33	lnc-FOXC1-12	chr6:2122004-2122075	NONHSAT106601

No data

Variant related genes	Relation type
GMDS	TF binding region
GMDS	CpG island
ENSG00000228395	chromatin interactions
ENSG00000197694	chromatin interactions
ENSG00000054598	chromatin interactions
ENSG00000105983	chromatin interactions

Extended variants
information (count: 3240 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:3240 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7741331	chr6:2086679-2086680	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535576286	chr6:2086728-2086729	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371892139	chr6:2086734-2086735	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140762626	chr6:2086784-2086785	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs540933592	chr6:2086798-2086799	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558040947	chr6:2086824-2086825	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs35516000	chr6:2086830-2086831	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs114377354	chr6:2086860-2086861	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs78315420	chr6:2086909-2086910	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562584733	chr6:2086913-2086914	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531676755	chr6:2086999-2087000	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575988802	chr6:2087037-2087038	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs80335210	chr6:2087041-2087042	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs28483545	chr6:2087055-2087056	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561919918	chr6:2087057-2087058	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527903871	chr6:2087173-2087174	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183809867	chr6:2087200-2087201	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147892800	chr6:2087210-2087211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373665931	chr6:2087329-2087330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533505273	chr6:2087338-2087339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141662804	chr6:2087374-2087375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188577710	chr6:2087419-2087420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs535512946	chr6:2087433-2087434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555514900	chr6:2087444-2087445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs565838292	chr6:2087448-2087449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs142154444	chr6:2087638-2087639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs9503094	chr6:2087815-2087816	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs577859218	chr6:2087829-2087830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs543386641	chr6:2087859-2087860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556117715	chr6:2087864-2087865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9501802	chr6:2087888-2087889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541888039	chr6:2087890-2087891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561858645	chr6:2087891-2087892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372899064	chr6:2087910-2087911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73414503	chr6:2087936-2087937	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs73716936	chr6:2087940-2087941	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs151204526	chr6:2087987-2087988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559838073	chr6:2088000-2088001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs533653362	chr6:2088001-2088002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181506642	chr6:2088089-2088090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569634533	chr6:2088106-2088107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs186894622	chr6:2088136-2088137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192226762	chr6:2088145-2088146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528587218	chr6:2088146-2088147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73414507	chr6:2088196-2088197	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs551708164	chr6:2088199-2088200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77170071	chr6:2088229-2088230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571381697	chr6:2088235-2088236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571690434	chr6:2088280-2088281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs79964803	chr6:2088288-2088289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Prader-willi syndrome	20588305	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
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
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164919	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1085 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:2064200-2094000	Weak transcription	Gastric	stomach
2	chr6:2065000-2117400	Weak transcription	Pancreas	Pancrea
3	chr6:2078800-2103800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:2079000-2108800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr6:2081000-2108800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr6:2081200-2104000	Weak transcription	Primary hematopoietic stem cells	blood
7	chr6:2081200-2104200	Weak transcription	Duodenum Mucosa	Duodenum
8	chr6:2081200-2113000	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr6:2081600-2131800	Weak transcription	Fetal Intestine Small	intestine
10	chr6:2082800-2091600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr6:2082800-2092400	Weak transcription	Thymus	Thymus
12	chr6:2082800-2109000	Weak transcription	Primary T cells from cord blood	blood
13	chr6:2084000-2090000	Weak transcription	HepG2	liver
14	chr6:2086400-2086800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:2086400-2086800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr6:2086400-2086800	Enhancers	Aorta	Aorta
17	chr6:2086400-2087000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:2086400-2087000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr6:2086400-2087400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr6:2086600-2086800	Enhancers	Fetal Kidney	kidney
21	chr6:2086600-2087000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:2086600-2087000	Flanking Active TSS	NHDF-Ad	bronchial
23	chr6:2086600-2087400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr6:2086800-2087000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr6:2086800-2087000	Flanking Active TSS	Aorta	Aorta
26	chr6:2086800-2087000	Enhancers	Osteobl	bone
27	chr6:2086800-2087200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr6:2086800-2102600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr6:2087000-2087200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr6:2087000-2087400	Enhancers	Aorta	Aorta
31	chr6:2087000-2087400	Enhancers	NHDF-Ad	bronchial
32	chr6:2087000-2087600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr6:2087000-2097800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr6:2087400-2090000	Weak transcription	Aorta	Aorta
35	chr6:2087400-2104200	Weak transcription	NHDF-Ad	bronchial
36	chr6:2088800-2112200	Weak transcription	Small Intestine	intestine
37	chr6:2090000-2090200	Enhancers	Aorta	Aorta
38	chr6:2090000-2092000	Strong transcription	HepG2	liver
39	chr6:2090200-2094200	Weak transcription	Aorta	Aorta
40	chr6:2092000-2104200	Weak transcription	HepG2	liver
41	chr6:2092400-2092600	Enhancers	Thymus	Thymus
42	chr6:2094200-2094600	Enhancers	Thymus	Thymus
43	chr6:2094200-2095400	Enhancers	Aorta	Aorta
44	chr6:2094200-2095600	Enhancers	Fetal Thymus	thymus
45	chr6:2094600-2095400	Flanking Active TSS	Thymus	Thymus
46	chr6:2095400-2095600	Enhancers	Thymus	Thymus
47	chr6:2095400-2097400	Weak transcription	Aorta	Aorta
48	chr6:2097400-2098000	Active TSS	Aorta	Aorta
49	chr6:2097800-2098000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:2098000-2099800	Enhancers	HUES48 Cell Line	embryonic stem cell

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