Variant report

Variant	nsv1025847
Chromosome Location	chr9:6701133-6725007
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:698)
CpG islands
(count:610)
Chromatin interactive
region (count:30)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:698 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6702813-6703015	K562	blood:	n/a	n/a
2	ARID3A	chr9:6714320-6714869	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6716174-6716454	HepG2	liver:	n/a	n/a
4	ATF2	chr9:6703839-6704309	GM12878	blood:	n/a	n/a
5	ATF2	chr9:6715844-6716527	GM12878	blood:	n/a	chr9:6716129-6716140
6	ATF2	chr9:6722727-6723186	GM12878	blood:	n/a	n/a
7	ATF2	chr9:6722741-6723673	GM12878	blood:	n/a	n/a
8	ATF2	chr9:6703375-6704596	GM12878	blood:	n/a	n/a
9	ATF2	chr9:6703874-6704656	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr9:6703987-6704605	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr9:6715890-6716329	GM12878	blood:	n/a	chr9:6716129-6716140
12	ATF3	chr9:6703900-6704493	H1-hESC	embryonic stem cell:	n/a	chr9:6703954-6703967 chr9:6704101-6704111
13	ATF3	chr9:6703946-6704478	A549	lung:	n/a	chr9:6703954-6703967 chr9:6704101-6704111
14	ATF3	chr9:6703937-6704598	GM12878	blood:	n/a	chr9:6703954-6703967 chr9:6704101-6704111
15	ATF3	chr9:6704051-6704512	A549	lung:	n/a	chr9:6704101-6704111
16	ATF3	chr9:6704052-6704432	HepG2	liver:	n/a	chr9:6704101-6704111
17	ATF3	chr9:6703972-6704567	H1-hESC	embryonic stem cell:	n/a	chr9:6704101-6704111
18	ATF3	chr9:6704072-6704352	GM12878	blood:	n/a	chr9:6704101-6704111
19	ATF3	chr9:6703940-6704551	HepG2	liver:	n/a	chr9:6703954-6703967 chr9:6704101-6704111
20	BACH1	chr9:6703514-6704556	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr9:6722711-6723091	GM12878	blood:	n/a	n/a
22	BATF	chr9:6723227-6723565	GM12878	blood:	n/a	n/a
23	BCL11A	chr9:6723143-6723561	GM12878	blood:	n/a	n/a
24	BCL11A	chr9:6722699-6723018	GM12878	blood:	n/a	n/a
25	BCL3	chr9:6703998-6704656	A549	lung:	n/a	n/a
26	BCL3	chr9:6703922-6704535	A549	lung:	n/a	n/a
27	BCLAF1	chr9:6723281-6723701	GM12878	blood:	n/a	n/a
28	BCLAF1	chr9:6703931-6704678	GM12878	blood:	n/a	n/a
29	BCLAF1	chr9:6715879-6716683	GM12878	blood:	n/a	chr9:6716073-6716086 chr9:6716320-6716329 chr9:6716213-6716221
30	BCLAF1	chr9:6703280-6704665	GM12878	blood:	n/a	n/a
31	BHLHE40	chr9:6704046-6704437	A549	lung:	n/a	n/a
32	BHLHE40	chr9:6704234-6704320	K562	blood:	n/a	n/a
33	BHLHE40	chr9:6715913-6716873	GM12878	blood:	n/a	chr9:6716419-6716428 chr9:6716413-6716434 chr9:6716417-6716430 chr9:6716418-6716427 chr9:6716419-6716428
34	BHLHE40	chr9:6723433-6723669	GM12878	blood:	n/a	n/a
35	BHLHE40	chr9:6715802-6716907	HepG2	liver:	n/a	chr9:6716419-6716428 chr9:6716413-6716434 chr9:6716417-6716430 chr9:6716418-6716427 chr9:6716419-6716428
36	BHLHE40	chr9:6704026-6704494	HepG2	liver:	n/a	n/a
37	BHLHE40	chr9:6703524-6704514	GM12878	blood:	n/a	n/a
38	BRCA1	chr9:6715949-6716503	GM12878	blood:	n/a	n/a
39	BRCA1	chr9:6716101-6716288	HepG2	liver:	n/a	n/a
40	BRCA1	chr9:6702904-6703133	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr9:6704412-6704466	GM12878	blood:	n/a	n/a
42	CBX3	chr9:6708746-6709217	HCT-116	colon:	n/a	n/a
43	CEBPB	chr9:6715250-6715507	HepG2	liver:	n/a	chr9:6715355-6715366
44	CEBPB	chr9:6715178-6715580	MCF-7	breast:	n/a	chr9:6715355-6715366
45	CEBPB	chr9:6715155-6715503	MCF-7	breast:	n/a	chr9:6715355-6715366
46	CEBPB	chr9:6703872-6704529	GM12878	blood:	n/a	n/a
47	CEBPB	chr9:6711405-6711761	IMR90	lung:	n/a	n/a
48	CEBPB	chr9:6715714-6716369	MCF-7	breast:	n/a	chr9:6715961-6715972
49	CEBPB	chr9:6717843-6717863	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr9:6716043-6716801	GM12878	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6703605-6703655	HPAEpiC	pulmonary alveolar:	n/a
2	chr9:6707115-6707165	HAEpiC	amniotic membrane:	n/a
3	chr9:6704574-6704624	HRE	kidney:	n/a
4	chr9:6716480-6716530	HCPEpiC	choroid plexus:	n/a
5	chr9:6716417-6716467	GM06990	blood:	n/a
6	chr9:6704178-6704228	AG04450	lung:	fetal
7	chr9:6704574-6704624	H1-hESC	embryonic stem cell:	embryo
8	chr9:6703605-6703655	HCF	heart:	n/a
9	chr9:6716417-6716467	HRE	kidney:	n/a
10	chr9:6704178-6704228	T-47D	breast:	n/a
11	chr9:6716480-6716530	SK-N-MC	brain:	n/a
12	chr9:6716007-6716057	AG09309	skin:	n/a
13	chr9:6706149-6706199	HEK293	kidney:	embryo
14	chr9:6703949-6703999	Hela-S3	cervix:	n/a
15	chr9:6707115-6707165	H1-hESC	embryonic stem cell:	embryo
16	chr9:6703949-6703999	HL-60	blood:	n/a
17	chr9:6703605-6703655	HCM	heart:	n/a
18	chr9:6703605-6703655	NHBE	bronchial:	n/a
19	chr9:6716480-6716530	MCF10A-Er-Src	breast:	n/a
20	chr9:6716007-6716057	PFSK-1	brain:	n/a
21	chr9:6716480-6716530	AG10803	skin:	n/a
22	chr9:6716480-6716530	NHDF-neo	bronchial:	n/a
23	chr9:6707115-6707165	PFSK-1	brain:	n/a
24	chr9:6715032-6715082	GM12878	blood:	n/a
25	chr9:6704574-6704624	NHDF-neo	bronchial:	n/a
26	chr9:6706149-6706199	GM12892	blood:	n/a
27	chr9:6703949-6703999	GM12891	blood:	n/a
28	chr9:6704574-6704624	MCF10A-Er-Src	breast:	n/a
29	chr9:6706149-6706199	AG04450	lung:	fetal
30	chr9:6716007-6716057	AG04450	lung:	fetal
31	chr9:6703949-6703999	Caco-2	colon:	n/a
32	chr9:6704178-6704228	HEK293	kidney:	embryo
33	chr9:6703605-6703655	T-47D	breast:	n/a
34	chr9:6715032-6715082	PFSK-1	brain:	n/a
35	chr9:6715032-6715082	SK-N-SH_RA	brain:	n/a
36	chr9:6704178-6704228	SK-N-MC	brain:	n/a
37	chr9:6716417-6716467	SK-N-SH	brain:	n/a
38	chr9:6703949-6703999	HRCEpiC	kidney:	n/a
39	chr9:6704574-6704624	AoSMC	blood vessel:	n/a
40	chr9:6703949-6703999	NHDF-neo	bronchial:	n/a
41	chr9:6703605-6703655	GM19239	blood:	n/a
42	chr9:6707115-6707165	PANC-1	pancreas:	n/a
43	chr9:6703605-6703655	PFSK-1	brain:	n/a
44	chr9:6715032-6715082	HCPEpiC	choroid plexus:	n/a
45	chr9:6716007-6716057	U87	brain:	n/a
46	chr9:6704574-6704624	GM12892	blood:	n/a
47	chr9:6716480-6716530	PANC-1	pancreas:	n/a
48	chr9:6706149-6706199	AoSMC	blood vessel:	n/a
49	chr9:6706149-6706199	U87	brain:	n/a
50	chr9:6704574-6704624	GM12878	blood:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6686168..6688293-chr9:6706461..6708275,2	MCF-7	breast:
2	chr9:6702847..6705575-chr9:6714326..6717882,7	MCF-7	breast:
3	chr5:166255725..166256712-chr9:6703618..6704233,2	MCF-7	breast:
4	chr9:6716286..6718322-chr9:6724305..6726614,2	MCF-7	breast:
5	chr9:6690617..6692723-chr9:6701607..6704265,2	MCF-7	breast:
6	chr5:166256227..166256733-chr9:6703705..6704305,2	MCF-7	breast:
7	chr9:6702551..6705246-chr9:6715022..6717677,6	MCF-7	breast:
8	chr21:41708247..41710641-chr9:6714300..6715810,2	MCF-7	breast:
9	chr9:6715258..6717463-chr9:6718537..6720528,2	MCF-7	breast:
10	chr9:6714309..6715981-chr9:6723655..6726584,2	MCF-7	breast:
11	chr9:6706468..6709007-chr9:6764056..6766511,2	MCF-7	breast:
12	chr9:6714309..6715981-chr9:6723655..6726584,2	MCF-7	breast:
13	chr9:6682207..6684667-chr9:6707689..6709841,2	K562	blood:
14	chr14:51410899..51411829-chr9:6715512..6716484,2	HCT-116	colon:
15	chr2:32389334..32390859-chr9:6713099..6716031,2	MCF-7	breast:
16	chr9:6681423..6683704-chr9:6710640..6713020,2	MCF-7	breast:
17	chr9:6711589..6718151-chr9:6755774..6759657,12	MCF-7	breast:
18	chr9:6698340..6700152-chr9:6701946..6704339,2	MCF-7	breast:
19	chr9:6722888..6726785-chr9:6754807..6757177,3	K562	blood:
20	chr9:6702391..6705446-chr9:6756717..6760058,5	MCF-7	breast:
21	chr9:6681451..6683371-chr9:6705864..6707945,2	MCF-7	breast:
22	chr9:6715258..6717463-chr9:6718537..6720528,2	MCF-7	breast:
23	chr9:6683289..6684884-chr9:6702645..6704262,2	MCF-7	breast:
24	chr1:100503108..100504085-chr9:6716038..6716673,2	NB4	blood:
25	chr9:6685820..6688107-chr9:6699923..6703311,3	MCF-7	breast:
26	chr9:6714844..6717578-chr9:6754943..6759087,4	MCF-7	breast:
27	chr9:6713012..6714984-chr9:6718479..6720574,2	K562	blood:
28	chr9:6702847..6705575-chr9:6714326..6717882,7	MCF-7	breast:
29	chr9:6702551..6705246-chr9:6715022..6717677,6	MCF-7	breast:
30	chr9:6699861..6702298-chr9:6702749..6705225,2	MCF-7	breast:

(count:36 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KDM4C-1	chr9:6719071-6719154	ENSG00000225489.2
2	lnc-KDM4C-2	chr9:6704179-6704343	XLOC_007275
3	lnc-KDM4C-1	chr9:6718965-6718981	ENSG00000225489.2
4	lnc-KDM4C-1	chr9:6720863-6720997	ENSG00000225489.2
5	lnc-KDM4C-1	chr9:6719068-6719154	ENSG00000225489.1
6	lnc-KDM4C-2	chr9:6704471-6704653	XLOC_007275
7	lnc-KDM4C-1	chr9:6709071-6709370	NONHSAT130155
8	lnc-KDM4C-1	chr9:6716548-6716616	ENSG00000225489.1
9	lnc-KDM4C-1	chr9:6717873-6718981	ENSG00000225489.1
10	lnc-KDM4C-1	chr9:6718810-6718981	ENSG00000225489.1
11	lnc-KDM4C-2	chr9:6707542-6707776	NONHSAT130153
12	lnc-KDM4C-1	chr9:6708810-6708981	NONHSAT130155
13	lnc-KDM4C-1	chr9:6720863-6720997	ENSG00000225489.1
14	lnc-KDM4C-1	chr9:6719071-6719370	ENSG00000225489.1
15	lnc-KDM4C-1	chr9:6713527-6713630	NONHSAT130154
16	lnc-KDM4C-2	chr9:6707542-6707763	XLOC_007275
17	lnc-KDM4C-1	chr9:6716946-6717438	NONHSAT130156
18	lnc-KDM4C-2	chr9:6707542-6707780	XLOC_007275
19	lnc-KDM4C-1	chr9:6710863-6710997	NONHSAT130154
20	lnc-KDM4C-1	chr9:6716196-6716315	NONHSAT130158
21	lnc-KDM4C-1	chr9:6716183-6716616	NONHSAT130157
22	lnc-KDM4C-1	chr9:6709071-6709154	NONHSAT130154
23	lnc-KDM4C-2	chr9:6704406-6704653	NONHSAT130153
24	lnc-KDM4C-1	chr9:6706548-6706616	NONHSAT130154
25	lnc-KDM4C-1	chr9:6720863-6720997	ENSG00000225489.1
26	lnc-KDM4C-2	chr9:6704453-6704653	XLOC_007275
27	lnc-KDM4C-1	chr9:6707873-6708981	NONHSAT130154
28	lnc-KDM4C-2	chr9:6704339-6704366	NONHSAT130152
29	lnc-KDM4C-1	chr9:6717873-6718149	NONHSAT130158
30	lnc-KDM4C-1	chr9:6723527-6723630	ENSG00000225489.1
31	lnc-KDM4C-1	chr9:6717873-6719234	NONHSAT130157
32	lnc-KDM4C-2	chr9:6704453-6704977	NONHSAT130152
33	lnc-KDM4C-1	chr9:6719071-6719154	ENSG00000225489.1
34	lnc-KDM4C-1	chr9:6709068-6709154	NONHSAT130156
35	lnc-KDM4C-1	chr9:6716503-6716619	NONHSAT130156
36	lnc-KDM4C-1	chr9:6710863-6710997	NONHSAT130156

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
ENSG00000225489	chromatin interactions
ENSG00000107077	chromatin interactions
ENSG00000100504	chromatin interactions
ENSG00000156875	chromatin interactions
ENSG00000229611	chromatin interactions
ENSG00000272716	chromatin interactions
DNMT3A	miRNA target sites
NXT2	miRNA target sites

Extended variants
information (count: 1312 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1312 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529727046	chr9:6701192-6701193	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs553869610	chr9:6701261-6701262	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs548781226	chr9:6701266-6701267	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs566913356	chr9:6701295-6701296	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs190688735	chr9:6701337-6701338	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs183189049	chr9:6701368-6701369	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs570901939	chr9:6701405-6701406	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs538224163	chr9:6701435-6701436	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs186500858	chr9:6701436-6701437	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs112204540	chr9:6701439-6701440	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs535542879	chr9:6701478-6701479	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs554757069	chr9:6701483-6701484	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs572654579	chr9:6701510-6701511	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs540182286	chr9:6701529-6701530	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs820501	chr9:6701530-6701531	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs576458966	chr9:6701553-6701554	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs191492275	chr9:6701570-6701571	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs562312404	chr9:6701582-6701583	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs112429024	chr9:6701583-6701584	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs547931194	chr9:6701621-6701622	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs377021681	chr9:6701675-6701676	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs820500	chr9:6701706-6701707	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs527881826	chr9:6701772-6701773	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs544518032	chr9:6701780-6701781	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs571135850	chr9:6701783-6701784	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs371544427	chr9:6701784-6701785	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs111780368	chr9:6701785-6701786	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182467444	chr9:6701786-6701787	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs535946601	chr9:6701789-6701790	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs372702386	chr9:6701795-6701796	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs140420334	chr9:6701796-6701797	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs10975762	chr9:6701800-6701801	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs576742878	chr9:6701810-6701811	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs2779741	chr9:6701824-6701825	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs71490280	chr9:6701828-6701829	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs369504404	chr9:6701832-6701833	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs2779742	chr9:6701833-6701834	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs820499	chr9:6701840-6701841	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs187441326	chr9:6701845-6701846	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs820498	chr9:6701850-6701851	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs564634439	chr9:6701853-6701854	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs532039470	chr9:6701854-6701855	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs550159471	chr9:6701856-6701857	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs372514828	chr9:6701857-6701858	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs192290764	chr9:6701858-6701859	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs185343460	chr9:6701861-6701862	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539513867	chr9:6701863-6701864	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs189456972	chr9:6701864-6701865	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs570508417	chr9:6701868-6701869	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs538184242	chr9:6701869-6701870	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Breast cancer	22522925	CNVD

Chromatin state (count:660 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6682600-6703200	Weak transcription	Thymus	Thymus
2	chr9:6682600-6703600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr9:6683600-6703200	Weak transcription	Fetal Muscle Leg	muscle
4	chr9:6692000-6703400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr9:6693600-6702800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:6695800-6703000	Weak transcription	Primary B cells from cord blood	blood
7	chr9:6696800-6702800	Weak transcription	Primary B cells from peripheral blood	blood
8	chr9:6702200-6702800	Enhancers	GM12878-XiMat	blood
9	chr9:6702200-6703600	Enhancers	Hela-S3	cervix
10	chr9:6702400-6703000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr9:6702600-6702800	Weak transcription	A549	lung
12	chr9:6702800-6703000	Enhancers	A549	lung
13	chr9:6702800-6703200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr9:6702800-6703200	Enhancers	Primary B cells from peripheral blood	blood
15	chr9:6702800-6703400	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr9:6702800-6703600	Flanking Active TSS	GM12878-XiMat	blood
17	chr9:6703000-6703200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr9:6703000-6703200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr9:6703000-6703200	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr9:6703000-6703200	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr9:6703000-6703200	Enhancers	Primary T cells from cord blood	blood
22	chr9:6703000-6703200	Active TSS	Primary hematopoietic stem cells	blood
23	chr9:6703000-6703200	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr9:6703000-6703200	Enhancers	Primary T helper cells PMA-I stimulated	--
25	chr9:6703000-6703200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr9:6703000-6703200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr9:6703000-6703200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr9:6703000-6703200	Enhancers	Colonic Mucosa	Colon
29	chr9:6703000-6703200	Enhancers	Duodenum Mucosa	Duodenum
30	chr9:6703000-6703200	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr9:6703000-6703200	Enhancers	Rectal Mucosa Donor 29	rectum
32	chr9:6703000-6703200	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr9:6703000-6703200	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr9:6703000-6703400	Active TSS	H1 Cell Line	embryonic stem cell
35	chr9:6703000-6703400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr9:6703000-6703400	Flanking Active TSS	A549	lung
37	chr9:6703000-6703800	Flanking Active TSS	Primary B cells from cord blood	blood
38	chr9:6703000-6704600	Active TSS	Primary T killer memory cells from peripheral blood	blood
39	chr9:6703000-6704600	Active TSS	Placenta Amnion	Placenta Amnion
40	chr9:6703200-6703400	Enhancers	H9 Cell Line	embryonic stem cell
41	chr9:6703200-6703400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
42	chr9:6703200-6703400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr9:6703200-6703400	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr9:6703200-6703400	Enhancers	Primary T cells fromperipheralblood	blood
45	chr9:6703200-6703400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr9:6703200-6703400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr9:6703200-6703400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
48	chr9:6703200-6703400	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
49	chr9:6703200-6703400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr9:6703200-6703400	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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