Variant report

Variant	nsv1033552
Chromosome Location	chr9:19104662-19131866
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1092)
CpG islands
(count:366)
Chromatin interactive
region (count:38)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1092 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:19112781-19112847	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:19127264-19127726	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:19114039-19114454	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:19129565-19129966	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:19114191-19114413	K562	blood:	n/a	n/a
6	ARID3A	chr9:19123956-19124382	K562	blood:	n/a	n/a
7	ATF2	chr9:19126871-19127725	GM12878	blood:	n/a	n/a
8	ATF2	chr9:19129790-19130332	GM12878	blood:	n/a	n/a
9	ATF2	chr9:19126887-19127266	GM12878	blood:	n/a	n/a
10	ATF2	chr9:19128464-19128720	GM12878	blood:	n/a	n/a
11	ATF3	chr9:19127427-19127709	HepG2	liver:	n/a	n/a
12	ATF3	chr9:19127394-19127634	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr9:19127439-19127606	GM12878	blood:	n/a	n/a
14	ATF3	chr9:19108108-19108328	GM12878	blood:	n/a	n/a
15	ATF3	chr9:19127382-19127679	K562	blood:	n/a	n/a
16	ATF3	chr9:19127310-19127776	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr9:19108062-19108335	K562	blood:	n/a	n/a
18	ATF3	chr9:19114070-19114411	K562	blood:	n/a	n/a
19	ATF3	chr9:19127327-19127661	HepG2	liver:	n/a	n/a
20	BACH1	chr9:19127170-19127647	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr9:19128611-19128947	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr9:19129737-19130077	GM12878	blood:	n/a	chr9:19129886-19129897
23	BATF	chr9:19129722-19130073	GM12878	blood:	n/a	chr9:19129886-19129897
24	BATF	chr9:19124112-19124423	GM12878	blood:	n/a	n/a
25	BCL3	chr9:19129751-19130332	GM12878	blood:	n/a	n/a
26	BCLAF1	chr9:19129959-19130301	GM12878	blood:	n/a	n/a
27	BCLAF1	chr9:19126919-19127957	GM12878	blood:	n/a	n/a
28	BCLAF1	chr9:19129937-19130396	GM12878	blood:	n/a	n/a
29	BHLHE40	chr9:19116465-19116711	K562	blood:	n/a	n/a
30	BHLHE40	chr9:19128618-19129000	GM12878	blood:	n/a	chr9:19128969-19128985
31	BHLHE40	chr9:19127346-19127734	HepG2	liver:	n/a	chr9:19127550-19127563 chr9:19127552-19127561 chr9:19127552-19127561 chr9:19127553-19127562
32	BHLHE40	chr9:19127397-19127709	HepG2	liver:	n/a	chr9:19127550-19127563 chr9:19127552-19127561 chr9:19127552-19127561 chr9:19127553-19127562
33	BHLHE40	chr9:19125993-19126344	HepG2	liver:	n/a	n/a
34	BHLHE40	chr9:19127057-19127851	K562	blood:	n/a	chr9:19127550-19127563 chr9:19127552-19127561 chr9:19127552-19127561 chr9:19127553-19127562
35	BHLHE40	chr9:19127045-19128054	GM12878	blood:	n/a	chr9:19127550-19127563 chr9:19127552-19127561 chr9:19127552-19127561 chr9:19127553-19127562
36	BHLHE40	chr9:19129713-19130322	GM12878	blood:	n/a	n/a
37	BHLHE40	chr9:19126637-19126650	GM12878	blood:	n/a	n/a
38	BHLHE40	chr9:19127320-19127727	A549	lung:	n/a	chr9:19127550-19127563 chr9:19127552-19127561 chr9:19127552-19127561 chr9:19127553-19127562
39	BHLHE40	chr9:19127069-19127972	HepG2	liver:	n/a	chr9:19127550-19127563 chr9:19127552-19127561 chr9:19127552-19127561 chr9:19127553-19127562
40	BRCA1	chr9:19120542-19120616	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr9:19128785-19128857	GM12878	blood:	n/a	n/a
42	BRCA1	chr9:19127219-19127831	GM12878	blood:	n/a	n/a
43	BRCA1	chr9:19127095-19127242	H1-hESC	embryonic stem cell:	n/a	n/a
44	CBX3	chr9:19116387-19116779	HCT-116	colon:	n/a	n/a
45	CCNT2	chr9:19127172-19127848	K562	blood:	n/a	chr9:19127346-19127355
46	CCNT2	chr9:19124068-19124420	K562	blood:	n/a	n/a
47	CEBPB	chr9:19114146-19114614	K562	blood:	n/a	n/a
48	CEBPB	chr9:19118886-19119207	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr9:19116283-19116853	HCT-116	colon:	n/a	n/a
50	CEBPB	chr9:19116436-19116796	IMR90	lung:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:19127804-19127854	GM12891	blood:	n/a
2	chr9:19125654-19125704	HCF	heart:	n/a
3	chr9:19127804-19127854	ProgFib	skin:	n/a
4	chr9:19125654-19125704	HEK293	kidney:	embryo
5	chr9:19127804-19127854	BE2_C	brain:	n/a
6	chr9:19127549-19127599	HCF	heart:	n/a
7	chr9:19126294-19126344	GM12891	blood:	n/a
8	chr9:19127549-19127599	HEK293	kidney:	embryo
9	chr9:19127804-19127854	HEK293	kidney:	embryo
10	chr9:19126294-19126344	Jurkat	blood:	n/a
11	chr9:19106953-19107003	LNCaP	prostate:	n/a
12	chr9:19127549-19127599	AoSMC	blood vessel:	n/a
13	chr9:19127804-19127854	MCF-7	breast:	n/a
14	chr9:19127804-19127854	AG09309	skin:	n/a
15	chr9:19106953-19107003	MCF10A-Er-Src	breast:	n/a
16	chr9:19127804-19127854	HRCEpiC	kidney:	n/a
17	chr9:19127804-19127854	NT2-D1	testis:	n/a
18	chr9:19127804-19127854	GM06990	blood:	n/a
19	chr9:19125654-19125704	HRCEpiC	kidney:	n/a
20	chr9:19128801-19128851	HRCEpiC	kidney:	n/a
21	chr9:19106953-19107003	HMEC	breast:	n/a
22	chr9:19106953-19107003	Caco-2	colon:	n/a
23	chr9:19106953-19107003	AG04450	lung:	fetal
24	chr9:19128801-19128851	NT2-D1	testis:	n/a
25	chr9:19126294-19126344	NH-A	brain:	n/a
26	chr9:19106953-19107003	BE2_C	brain:	n/a
27	chr9:19126294-19126344	HMEC	breast:	n/a
28	chr9:19126294-19126344	SK-N-MC	brain:	n/a
29	chr9:19128801-19128851	HepG2	liver:	n/a
30	chr9:19106953-19107003	ovcar-3	ovarian:	n/a
31	chr9:19125654-19125704	NT2-D1	testis:	n/a
32	chr9:19127549-19127599	HepG2	liver:	n/a
33	chr9:19127804-19127854	NHBE	bronchial:	n/a
34	chr9:19128801-19128851	AG09319	gingival:	n/a
35	chr9:19127549-19127599	Hela-S3	cervix:	n/a
36	chr9:19127549-19127599	HUVEC	blood vessel:	n/a
37	chr9:19126294-19126344	NHBE	bronchial:	n/a
38	chr9:19106953-19107003	HAEpiC	amniotic membrane:	n/a
39	chr9:19128801-19128851	AG04449	skin:	fetal
40	chr9:19127549-19127599	PANC-1	pancreas:	n/a
41	chr9:19125654-19125704	HCM	heart:	n/a
42	chr9:19125654-19125704	HIPEpiC	eye:	n/a
43	chr9:19126294-19126344	NB4	blood:	n/a
44	chr9:19127549-19127599	MCF-7	breast:	n/a
45	chr9:19125654-19125704	AG09319	gingival:	n/a
46	chr9:19126294-19126344	HRCEpiC	kidney:	n/a
47	chr9:19127804-19127854	PrEC	prostate:	n/a
48	chr9:19126294-19126344	NT2-D1	testis:	n/a
49	chr9:19125654-19125704	HRPEpiC	eye:	n/a
50	chr9:19126294-19126344	AG09309	skin:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:19114306..19116374-chr9:19119106..19120885,2	K562	blood:
2	chr9:19126615..19131871-chr9:19228040..19232542,7	MCF-7	breast:
3	chr9:19127602..19130118-chr9:19378923..19381565,2	MCF-7	breast:
4	chr9:19115262..19117243-chr9:19122204..19125901,3	K562	blood:
5	chr9:19121135..19123486-chr9:19230568..19232351,2	K562	blood:
6	chr9:19126391..19130012-chr9:19228888..19231863,3	MCF-7	breast:
7	chr9:19128414..19130954-chr9:19155486..19158249,2	MCF-7	breast:
8	chr9:19105131..19106902-chr9:19116559..19118325,2	MCF-7	breast:
9	chr9:19126218..19128183-chr9:19129523..19131340,2	MCF-7	breast:
10	chr9:19114306..19116374-chr9:19119106..19120885,2	K562	blood:
11	chr9:19125987..19127822-chr9:19460752..19462438,2	MCF-7	breast:
12	chr9:19047624..19049710-chr9:19124952..19127835,2	MCF-7	breast:
13	chr9:19128741..19130939-chr9:19361701..19364444,2	K562	blood:
14	chr9:19112623..19114448-chr9:19372527..19374995,2	MCF-7	breast:
15	chr9:19118229..19121028-chr9:19121588..19124316,4	K562	blood:
16	chr9:19101429..19104985-chr9:19125580..19131342,7	K562	blood:
17	chr9:19101429..19104985-chr9:19125580..19131342,7	K562	blood:
18	chr9:19128630..19131218-chr9:19137487..19139302,2	K562	blood:
19	chr9:19115262..19117243-chr9:19122204..19125901,3	K562	blood:
20	chr9:19102845..19104876-chr9:19230126..19231853,2	MCF-7	breast:
21	chr9:19119220..19121028-chr9:19122006..19124316,2	K562	blood:
22	chr9:19111300..19113114-chr9:19113556..19115992,2	K562	blood:
23	chr9:19062844..19065435-chr9:19102466..19104748,2	MCF-7	breast:
24	chr9:19101008..19104571-chr9:19119588..19122820,3	MCF-7	breast:
25	chr9:19101057..19103224-chr9:19126510..19128425,2	MCF-7	breast:
26	chr9:19119290..19121430-chr9:19125172..19128081,4	MCF-7	breast:
27	chr9:19125652..19127211-chr9:19148540..19150962,2	K562	blood:
28	chr9:19111300..19113114-chr9:19113556..19115992,2	K562	blood:
29	chr9:19119220..19121028-chr9:19122006..19124316,2	K562	blood:
30	chr9:19102335..19104420-chr9:19127605..19129443,2	MCF-7	breast:
31	chr9:19120570..19124590-chr9:19125970..19130053,4	MCF-7	breast:
32	chr9:19116586..19118716-chr9:19376796..19379635,2	K562	blood:
33	chr9:19100757..19103077-chr9:19112817..19114511,2	MCF-7	breast:
34	chr9:19124177..19125684-chr9:19126025..19128795,2	MCF-7	breast:
35	chr9:19047700..19050673-chr9:19122479..19124686,3	K562	blood:
36	chr9:19124716..19129711-chr9:19378738..19382022,6	K562	blood:
37	chr9:19127609..19129220-chr9:19207374..19210036,2	MCF-7	breast:
38	chr9:19047688..19050062-chr9:19125989..19129041,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PLIN2-2	chr9:19106479-19106788	NONHSAT130325
2	lnc-PLIN2-1	chr9:19129735-19131269	NONHSAT130327

No data

Variant related genes	Relation type
HAUS6	TF binding region
RN7SL158P	TF binding region
PLIN2	TF binding region
HAUS6	CpG island
RN7SL158P	CpG island
PLIN2	CpG island
ENSG00000264126	chromatin interactions
ENSG00000231909	chromatin interactions
ENSG00000137154	chromatin interactions
ENSG00000137145	chromatin interactions
ENSG00000147874	chromatin interactions
ENSG00000147872	chromatin interactions
ENSG00000251733	chromatin interactions
ENSG00000155876	chromatin interactions

Extended variants
information (count: 1268 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1268 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9406759	chr9:19104662-19104663	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs191318085	chr9:19104664-19104665	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs563301665	chr9:19104671-19104672	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs148461540	chr9:19104679-19104680	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs530852020	chr9:19104687-19104688	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs558136554	chr9:19104702-19104703	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs181596069	chr9:19104710-19104711	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs570738805	chr9:19104734-19104735	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs559778807	chr9:19104740-19104741	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs532950736	chr9:19104742-19104743	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs185672976	chr9:19104744-19104745	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs546611413	chr9:19104756-19104757	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs190480787	chr9:19104766-19104767	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs535156119	chr9:19104785-19104786	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs200190665	chr9:19104823-19104824	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs555154354	chr9:19104825-19104826	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs576525731	chr9:19104845-19104846	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs537366711	chr9:19104857-19104858	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs558848036	chr9:19104871-19104872	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs534857595	chr9:19104892-19104893	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs557647491	chr9:19104919-19104920	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs142598726	chr9:19104933-19104934	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs150979952	chr9:19104982-19104983	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs375158849	chr9:19104998-19104999	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs563759064	chr9:19105032-19105033	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs559277669	chr9:19105043-19105044	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs72696500	chr9:19105079-19105080	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs552705525	chr9:19105107-19105108	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs139531474	chr9:19105120-19105121	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs563522731	chr9:19105135-19105136	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs571093433	chr9:19105138-19105139	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs552385052	chr9:19105147-19105148	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs564413976	chr9:19105222-19105223	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs112905457	chr9:19105230-19105231	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs528739857	chr9:19105288-19105289	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs546619921	chr9:19105321-19105322	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs567922650	chr9:19105342-19105343	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs528999381	chr9:19105347-19105348	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs577564226	chr9:19105353-19105354	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs370004207	chr9:19105381-19105382	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs550375681	chr9:19105383-19105384	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs183416415	chr9:19105405-19105406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs371172542	chr9:19105407-19105408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537279951	chr9:19105487-19105488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146905757	chr9:19105544-19105545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs546795520	chr9:19105548-19105549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570815394	chr9:19105566-19105567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534947528	chr9:19105574-19105575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553349731	chr9:19105577-19105578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566579835	chr9:19105588-19105589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	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
Chronic lymphocytic leukemia	21546498	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Myelofibrosis	22110671	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Pancreatic cancer	21811587	CNVD
Renal cell carcinoma	21215367	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:1346 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:19103000-19113800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:19103400-19104800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr9:19103400-19104800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr9:19103400-19104800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr9:19103400-19104800	Weak transcription	Colon Smooth Muscle	Colon
6	chr9:19103400-19104800	Weak transcription	Fetal Kidney	kidney
7	chr9:19103400-19105000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr9:19103400-19107400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr9:19103400-19108200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr9:19103400-19110000	Weak transcription	Fetal Stomach	stomach
11	chr9:19103400-19111800	Weak transcription	Left Ventricle	heart
12	chr9:19103400-19114000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr9:19103400-19114000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr9:19103400-19114000	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr9:19103400-19114200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr9:19103400-19114200	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr9:19103400-19114200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr9:19103400-19114200	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr9:19103400-19114400	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr9:19103400-19114400	Weak transcription	Lung	lung
21	chr9:19103400-19114600	Weak transcription	NHLF	lung
22	chr9:19103400-19114800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:19103400-19114800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr9:19103400-19114800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr9:19103400-19114800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr9:19103400-19114800	Weak transcription	Brain Substantia Nigra	brain
27	chr9:19103400-19114800	Weak transcription	HSMM	muscle
28	chr9:19103400-19114800	Weak transcription	NHDF-Ad	bronchial
29	chr9:19103400-19115000	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr9:19103400-19115400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr9:19103400-19115600	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr9:19103400-19115600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr9:19103400-19115600	Weak transcription	Fetal Lung	lung
34	chr9:19103400-19115600	Weak transcription	Ovary	ovary
35	chr9:19103400-19115800	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr9:19103400-19115800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr9:19103400-19115800	Weak transcription	Gastric	stomach
38	chr9:19103400-19116000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr9:19103400-19116000	Weak transcription	Brain Germinal Matrix	brain
40	chr9:19103400-19116000	Weak transcription	Small Intestine	intestine
41	chr9:19103400-19116200	Weak transcription	Aorta	Aorta
42	chr9:19103400-19116200	Weak transcription	Esophagus	oesophagus
43	chr9:19103400-19120200	Weak transcription	Pancreas	Pancrea
44	chr9:19103400-19126400	Weak transcription	Fetal Brain Male	brain
45	chr9:19103600-19104800	Weak transcription	Fetal Muscle Leg	muscle
46	chr9:19103600-19105000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr9:19103600-19108000	Weak transcription	Primary T cells from cord blood	blood
48	chr9:19103600-19108400	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr9:19103600-19111400	Weak transcription	Adipose Nuclei	Adipose
50	chr9:19103600-19113800	Weak transcription	Fetal Intestine Small	intestine

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