Variant report

Variant	nsv6470
Chromosome Location	chr9:6688118-6717908
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:761)
CpG islands
(count:671)
Chromatin interactive
region (count:33)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:761 , 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	chr9:6716174-6716454	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6702813-6703015	K562	blood:	n/a	n/a
3	ARID3A	chr9:6714320-6714869	HepG2	liver:	n/a	n/a
4	ATF2	chr9:6703874-6704656	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr9:6703987-6704605	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:6689798-6690646	GM12878	blood:	n/a	n/a
7	ATF2	chr9:6703839-6704309	GM12878	blood:	n/a	n/a
8	ATF2	chr9:6703375-6704596	GM12878	blood:	n/a	n/a
9	ATF2	chr9:6715890-6716329	GM12878	blood:	n/a	chr9:6716129-6716140
10	ATF2	chr9:6715844-6716527	GM12878	blood:	n/a	chr9:6716129-6716140
11	ATF3	chr9:6703946-6704478	A549	lung:	n/a	chr9:6703954-6703967 chr9:6704101-6704111
12	ATF3	chr9:6703900-6704493	H1-hESC	embryonic stem cell:	n/a	chr9:6703954-6703967 chr9:6704101-6704111
13	ATF3	chr9:6703940-6704551	HepG2	liver:	n/a	chr9:6703954-6703967 chr9:6704101-6704111
14	ATF3	chr9:6703972-6704567	H1-hESC	embryonic stem cell:	n/a	chr9:6704101-6704111
15	ATF3	chr9:6704051-6704512	A549	lung:	n/a	chr9:6704101-6704111
16	ATF3	chr9:6704072-6704352	GM12878	blood:	n/a	chr9:6704101-6704111
17	ATF3	chr9:6704052-6704432	HepG2	liver:	n/a	chr9:6704101-6704111
18	ATF3	chr9:6703937-6704598	GM12878	blood:	n/a	chr9:6703954-6703967 chr9:6704101-6704111
19	BACH1	chr9:6703514-6704556	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL11A	chr9:6689923-6690208	GM12878	blood:	n/a	n/a
21	BCL3	chr9:6703998-6704656	A549	lung:	n/a	n/a
22	BCL3	chr9:6703922-6704535	A549	lung:	n/a	n/a
23	BCLAF1	chr9:6689853-6690393	GM12878	blood:	n/a	n/a
24	BCLAF1	chr9:6715879-6716683	GM12878	blood:	n/a	chr9:6716073-6716086 chr9:6716320-6716329 chr9:6716213-6716221
25	BCLAF1	chr9:6690587-6691086	GM12878	blood:	n/a	n/a
26	BCLAF1	chr9:6703931-6704678	GM12878	blood:	n/a	n/a
27	BCLAF1	chr9:6703280-6704665	GM12878	blood:	n/a	n/a
28	BHLHE40	chr9:6704234-6704320	K562	blood:	n/a	n/a
29	BHLHE40	chr9:6715802-6716907	HepG2	liver:	n/a	chr9:6716419-6716428 chr9:6716413-6716434 chr9:6716417-6716430 chr9:6716418-6716427 chr9:6716419-6716428
30	BHLHE40	chr9:6689979-6690277	GM12878	blood:	n/a	n/a
31	BHLHE40	chr9:6704026-6704494	HepG2	liver:	n/a	n/a
32	BHLHE40	chr9:6704046-6704437	A549	lung:	n/a	n/a
33	BHLHE40	chr9:6703524-6704514	GM12878	blood:	n/a	n/a
34	BHLHE40	chr9:6715913-6716873	GM12878	blood:	n/a	chr9:6716419-6716428 chr9:6716413-6716434 chr9:6716417-6716430 chr9:6716418-6716427 chr9:6716419-6716428
35	BRCA1	chr9:6715949-6716503	GM12878	blood:	n/a	n/a
36	BRCA1	chr9:6716101-6716288	HepG2	liver:	n/a	n/a
37	BRCA1	chr9:6704412-6704466	GM12878	blood:	n/a	n/a
38	BRCA1	chr9:6702904-6703133	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr9:6708746-6709217	HCT-116	colon:	n/a	n/a
40	CEBPB	chr9:6715903-6716177	K562	blood:	n/a	chr9:6715961-6715972
41	CEBPB	chr9:6711405-6711761	IMR90	lung:	n/a	n/a
42	CEBPB	chr9:6705780-6705986	HepG2	liver:	n/a	chr9:6705845-6705856 chr9:6705846-6705857 chr9:6705809-6705821 chr9:6705845-6705858
43	CEBPB	chr9:6715972-6716139	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr9:6714351-6714473	K562	blood:	n/a	n/a
45	CEBPB	chr9:6715178-6715580	MCF-7	breast:	n/a	chr9:6715355-6715366
46	CEBPB	chr9:6715701-6716620	MCF-7	breast:	n/a	chr9:6715961-6715972
47	CEBPB	chr9:6712299-6712302	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr9:6689851-6690464	GM12878	blood:	n/a	n/a
49	CEBPB	chr9:6715250-6715507	HepG2	liver:	n/a	chr9:6715355-6715366
50	CEBPB	chr9:6714282-6714602	Hela-S3	cervix:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6703605-6703655	HCM	heart:	n/a
2	chr9:6707115-6707165	HRCEpiC	kidney:	n/a
3	chr9:6706149-6706199	CMK	blood:	n/a
4	chr9:6716417-6716467	GM12892	blood:	n/a
5	chr9:6716007-6716057	HRPEpiC	eye:	n/a
6	chr9:6707115-6707165	NT2-D1	testis:	n/a
7	chr9:6703949-6703999	PrEC	prostate:	n/a
8	chr9:6703949-6703999	GM12892	blood:	n/a
9	chr9:6715032-6715082	BJ	skin:	n/a
10	chr9:6703949-6703999	HL-60	blood:	n/a
11	chr9:6716417-6716467	A549	lung:	n/a
12	chr9:6716417-6716467	HPAEpiC	pulmonary alveolar:	n/a
13	chr9:6706149-6706199	HPAEpiC	pulmonary alveolar:	n/a
14	chr9:6706149-6706199	ProgFib	skin:	n/a
15	chr9:6715032-6715082	IMR90	lung:	fetal
16	chr9:6703949-6703999	ProgFib	skin:	n/a
17	chr9:6703605-6703655	SKMC	muscle:	n/a
18	chr9:6700000-6700050	AG10803	skin:	n/a
19	chr9:6707115-6707165	AG10803	skin:	n/a
20	chr9:6703605-6703655	HRPEpiC	eye:	n/a
21	chr9:6715032-6715082	PANC-1	pancreas:	n/a
22	chr9:6715032-6715082	SK-N-SH_RA	brain:	n/a
23	chr9:6715032-6715082	NH-A	brain:	n/a
24	chr9:6703949-6703999	ECC-1	luminal epithelium:	n/a
25	chr9:6706149-6706199	GM06990	blood:	n/a
26	chr9:6704574-6704624	GM12878	blood:	n/a
27	chr9:6700000-6700050	U87	brain:	n/a
28	chr9:6703605-6703655	K562	blood:	n/a
29	chr9:6703949-6703999	SK-N-SH_RA	brain:	n/a
30	chr9:6716417-6716467	HUVEC	blood vessel:	n/a
31	chr9:6703605-6703655	SK-N-SH	brain:	n/a
32	chr9:6707115-6707165	ECC-1	luminal epithelium:	n/a
33	chr9:6700000-6700050	GM19239	blood:	n/a
34	chr9:6704574-6704624	ECC-1	luminal epithelium:	n/a
35	chr9:6700000-6700050	BJ	skin:	n/a
36	chr9:6704178-6704228	HEEpiC	esophagus:	n/a
37	chr9:6706149-6706199	AG10803	skin:	n/a
38	chr9:6706149-6706199	NHBE	bronchial:	n/a
39	chr9:6715032-6715082	Hela-S3	cervix:	n/a
40	chr9:6715032-6715082	HRPEpiC	eye:	n/a
41	chr9:6716007-6716057	SK-N-SH	brain:	n/a
42	chr9:6703949-6703999	GM19239	blood:	n/a
43	chr9:6707115-6707165	SK-N-SH_RA	brain:	n/a
44	chr9:6706149-6706199	H1-hESC	embryonic stem cell:	embryo
45	chr9:6707115-6707165	HNPCEpiC	eye:	n/a
46	chr9:6704574-6704624	GM12891	blood:	n/a
47	chr9:6715032-6715082	AG10803	skin:	n/a
48	chr9:6700000-6700050	HMEC	breast:	n/a
49	chr9:6716007-6716057	HepG2	liver:	n/a
50	chr9:6703949-6703999	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:6702847..6705575-chr9:6714326..6717882,7	MCF-7	breast:
2	chr9:6714309..6715981-chr9:6723655..6726584,2	MCF-7	breast:
3	chr9:6715258..6717463-chr9:6718537..6720528,2	MCF-7	breast:
4	chr2:32389334..32390859-chr9:6713099..6716031,2	MCF-7	breast:
5	chr9:6690617..6692723-chr9:6701607..6704265,2	MCF-7	breast:
6	chr9:6686168..6688293-chr9:6706461..6708275,2	MCF-7	breast:
7	chr9:6686168..6688293-chr9:6706461..6708275,2	MCF-7	breast:
8	chr9:6690617..6692723-chr9:6701607..6704265,2	MCF-7	breast:
9	chr9:6690536..6693350-chr9:6698647..6700189,2	MCF-7	breast:
10	chr9:6698340..6700152-chr9:6701946..6704339,2	MCF-7	breast:
11	chr9:6711589..6718151-chr9:6755774..6759657,12	MCF-7	breast:
12	chr9:6702551..6705246-chr9:6715022..6717677,6	MCF-7	breast:
13	chr9:6682207..6684667-chr9:6707689..6709841,2	K562	blood:
14	chr9:6702847..6705575-chr9:6714326..6717882,7	MCF-7	breast:
15	chr14:51410899..51411829-chr9:6715512..6716484,2	HCT-116	colon:
16	chr9:6681451..6683371-chr9:6705864..6707945,2	MCF-7	breast:
17	chr5:166256227..166256733-chr9:6703705..6704305,2	MCF-7	breast:
18	chr9:6698340..6700152-chr9:6701946..6704339,2	MCF-7	breast:
19	chr21:41708247..41710641-chr9:6714300..6715810,2	MCF-7	breast:
20	chr5:166255725..166256712-chr9:6703618..6704233,2	MCF-7	breast:
21	chr9:6702551..6705246-chr9:6715022..6717677,6	MCF-7	breast:
22	chr9:6713012..6714984-chr9:6718479..6720574,2	K562	blood:
23	chr9:6683289..6684884-chr9:6702645..6704262,2	MCF-7	breast:
24	chr9:6693828..6696318-chr9:6715075..6717694,2	MCF-7	breast:
25	chr9:6706468..6709007-chr9:6764056..6766511,2	MCF-7	breast:
26	chr9:6685820..6688107-chr9:6699923..6703311,3	MCF-7	breast:
27	chr9:6690536..6693350-chr9:6698647..6700189,2	MCF-7	breast:
28	chr9:6699861..6702298-chr9:6702749..6705225,2	MCF-7	breast:
29	chr1:100503108..100504085-chr9:6716038..6716673,2	NB4	blood:
30	chr9:6702391..6705446-chr9:6756717..6760058,5	MCF-7	breast:
31	chr9:6714844..6717578-chr9:6754943..6759087,4	MCF-7	breast:
32	chr9:6681423..6683704-chr9:6710640..6713020,2	MCF-7	breast:
33	chr9:6680639..6682955-chr9:6686831..6689135,2	MCF-7	breast:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KDM4C-11	chr9:6697542-6697780	NONHSAT130150
2	lnc-KDM4C-1	chr9:6709068-6709154	NONHSAT130156
3	lnc-KDM4C-1	chr9:6716946-6717438	NONHSAT130156
4	lnc-KDM4C-2	chr9:6704471-6704653	XLOC_007275
5	lnc-KDM4C-2	chr9:6707542-6707776	NONHSAT130153
6	lnc-KDM4C-1	chr9:6716548-6716616	ENSG00000225489.1
7	lnc-KDM4C-11	chr9:6694471-6694653	NONHSAT130150
8	lnc-KDM4C-1	chr9:6717873-6718981	ENSG00000225489.1
9	lnc-KDM4C-1	chr9:6709071-6709370	NONHSAT130155
10	lnc-KDM4C-1	chr9:6710863-6710997	NONHSAT130154
11	lnc-KDM4C-2	chr9:6704453-6704653	XLOC_007275
12	lnc-KDM4C-1	chr9:6708810-6708981	NONHSAT130155
13	lnc-KDM4C-1	chr9:6710863-6710997	NONHSAT130156
14	lnc-KDM4C-2	chr9:6704406-6704653	NONHSAT130153
15	lnc-KDM4C-1	chr9:6716503-6716619	NONHSAT130156
16	lnc-KDM4C-1	chr9:6716183-6716616	NONHSAT130157
17	lnc-KDM4C-1	chr9:6706548-6706616	NONHSAT130154
18	lnc-KDM4C-1	chr9:6707873-6708981	NONHSAT130154
19	lnc-KDM4C-1	chr9:6709071-6709154	NONHSAT130154
20	lnc-KDM4C-1	chr9:6716196-6716315	NONHSAT130158
21	lnc-KDM4C-1	chr9:6717873-6719234	NONHSAT130157
22	lnc-KDM4C-2	chr9:6704339-6704366	NONHSAT130152
23	lnc-KDM4C-1	chr9:6717873-6718149	NONHSAT130158
24	lnc-KDM4C-2	chr9:6707542-6707763	XLOC_007275
25	lnc-KDM4C-2	chr9:6704453-6704977	NONHSAT130152
26	lnc-KDM4C-2	chr9:6704179-6704343	XLOC_007275
27	lnc-KDM4C-2	chr9:6707542-6707780	XLOC_007275
28	lnc-KDM4C-1	chr9:6713527-6713630	NONHSAT130154

No data

Variant related genes	Relation type
ENSG00000229611	TF binding region
KDM4C	TF binding region
ENSG00000225489	TF binding region
ENSG00000229611	CpG island
KDM4C	CpG island
ENSG00000225489	CpG island
ENSG00000107077	chromatin interactions
ENSG00000100504	chromatin interactions
ENSG00000225489	chromatin interactions
ENSG00000229611	chromatin interactions
ENSG00000272716	chromatin interactions
ENSG00000156875	chromatin interactions
NXT2	miRNA target sites
DNMT3A	miRNA target sites

Extended variants
information (count: 1555 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1555 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571707226	chr9:6688136-6688137	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs118004031	chr9:6688147-6688148	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113599604	chr9:6688151-6688152	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374577734	chr9:6688153-6688154	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533521898	chr9:6688171-6688172	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs7853299	chr9:6688207-6688208	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs570321303	chr9:6688228-6688229	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs367579151	chr9:6688235-6688236	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192388878	chr9:6688254-6688255	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567293819	chr9:6688314-6688315	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7853417	chr9:6688317-6688318	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553006649	chr9:6688330-6688331	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7852525	chr9:6688334-6688335	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs145367569	chr9:6688349-6688350	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201817550	chr9:6688351-6688352	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7852535	chr9:6688352-6688353	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs372314677	chr9:6688355-6688356	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575585711	chr9:6688408-6688409	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142479734	chr9:6688446-6688447	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs3119843	chr9:6688472-6688473	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs116292913	chr9:6688491-6688492	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs193185595	chr9:6688502-6688503	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542023083	chr9:6688542-6688543	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555308739	chr9:6688550-6688551	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573639849	chr9:6688577-6688578	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185223728	chr9:6688604-6688605	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559489211	chr9:6688613-6688614	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs56122922	chr9:6688639-6688640	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533402165	chr9:6688661-6688662	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs551934675	chr9:6688666-6688667	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563854574	chr9:6688696-6688697	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189721224	chr9:6688712-6688713	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544256037	chr9:6688718-6688719	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150128546	chr9:6688780-6688781	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534650934	chr9:6688782-6688783	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546734399	chr9:6688783-6688784	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571703542	chr9:6688789-6688790	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs114915136	chr9:6688809-6688810	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557956642	chr9:6688816-6688817	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149322954	chr9:6688821-6688822	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540774758	chr9:6688905-6688906	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374849019	chr9:6688956-6688957	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113027628	chr9:6688968-6688969	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555655026	chr9:6688982-6688983	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144637740	chr9:6688984-6688985	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541018898	chr9:6689012-6689013	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs559218027	chr9:6689021-6689022	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371854251	chr9:6689045-6689046	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564064416	chr9:6689058-6689059	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140697414	chr9:6689094-6689095	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Dyslexia	22102821	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:757 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6682600-6689600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr9:6682600-6689800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr9:6682600-6691000	Weak transcription	Esophagus	oesophagus
4	chr9:6682600-6692000	Weak transcription	Fetal Stomach	stomach
5	chr9:6682600-6703200	Weak transcription	Thymus	Thymus
6	chr9:6682600-6703600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr9:6682800-6689600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr9:6682800-6690600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr9:6682800-6692400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr9:6682800-6693200	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr9:6682800-6693200	Weak transcription	Fetal Brain Male	brain
12	chr9:6683000-6691400	Weak transcription	Brain Cingulate Gyrus	brain
13	chr9:6683000-6691800	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr9:6683200-6688400	Weak transcription	HMEC	breast
15	chr9:6683400-6690600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr9:6683400-6692600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr9:6683600-6689200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr9:6683600-6689800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr9:6683600-6690600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr9:6683600-6690600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr9:6683600-6691000	Weak transcription	NHDF-Ad	bronchial
22	chr9:6683600-6692400	Weak transcription	HUVEC	blood vessel
23	chr9:6683600-6692600	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr9:6683600-6693000	Enhancers	Primary B cells from peripheral blood	blood
25	chr9:6683600-6693200	Weak transcription	Duodenum Mucosa	Duodenum
26	chr9:6683600-6703200	Weak transcription	Fetal Muscle Leg	muscle
27	chr9:6683800-6689600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr9:6683800-6690800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr9:6683800-6692600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr9:6683800-6692600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr9:6683800-6692800	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr9:6684000-6690800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr9:6684400-6689800	Weak transcription	Primary hematopoietic stem cells	blood
34	chr9:6684400-6689800	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr9:6684600-6690000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr9:6684800-6689800	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr9:6685000-6690000	Weak transcription	Dnd41	blood
38	chr9:6685000-6692000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr9:6686000-6692800	Enhancers	Primary B cells from cord blood	blood
40	chr9:6686600-6688800	Weak transcription	NHEK	skin
41	chr9:6686600-6690200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr9:6686600-6691800	Weak transcription	A549	lung
43	chr9:6686800-6690000	Weak transcription	Liver	Liver
44	chr9:6686800-6690000	Weak transcription	Osteobl	bone
45	chr9:6686800-6690200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr9:6686800-6691400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr9:6687400-6688600	Weak transcription	GM12878-XiMat	blood
48	chr9:6688000-6689200	Strong transcription	HSMM	muscle
49	chr9:6688000-6691400	Weak transcription	Fetal Intestine Small	intestine
50	chr9:6688600-6690000	Enhancers	GM12878-XiMat	blood

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