Variant report

Variant	nsv540072
Chromosome Location	chr9:14805107-14859190
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr9:14846813-14847157	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr9:14812818-14813170	GM12878	blood:	n/a	n/a
3	BHLHE40	chr9:14822708-14823063	GM12878	blood:	n/a	n/a
4	BHLHE40	chr9:14831736-14831957	K562	blood:	n/a	n/a
5	CEBPB	chr9:14827709-14827960	HepG2	liver:	n/a	chr9:14827827-14827838
6	CEBPB	chr9:14827792-14827904	IMR90	lung:	n/a	chr9:14827827-14827838
7	CHD2	chr9:14846832-14847123	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr9:14846857-14847057	HepG2	liver:	n/a	n/a
9	CHD2	chr9:14818253-14818267	GM12878	blood:	n/a	n/a
10	CREB1	chr9:14846723-14847119	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr9:14846803-14847117	GM19238	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
12	CTCF	chr9:14846900-14847050	GM12872	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
13	CTCF	chr9:14846750-14847110	K562	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
14	CTCF	chr9:14846812-14847146	Medullo	brain:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
15	CTCF	chr9:14846793-14847102	GM19239	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
16	CTCF	chr9:14846880-14847030	HPAF	blood vessel:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
17	CTCF	chr9:14846900-14847050	AG10803	skin:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
18	CTCF	chr9:14846860-14847010	HRE	kidney:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
19	CTCF	chr9:14846880-14847030	NHDF-neo	bronchial:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
20	CTCF	chr9:14831820-14831970	AG09319	gingival:	n/a	n/a
21	CTCF	chr9:14846880-14847030	HCPEpiC	choroid plexus:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
22	CTCF	chr9:14846840-14846990	NHEK	skin:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846949-14846965 chr9:14846943-14846964
23	CTCF	chr9:14846859-14847081	Kidney_OC	kidney:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
24	CTCF	chr9:14831900-14832050	AG09319	gingival:	n/a	n/a
25	CTCF	chr9:14846745-14847152	H1-hESC	embryonic stem cell:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
26	CTCF	chr9:14846900-14847050	SK-N-SH_RA	brain:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
27	CTCF	chr9:14846820-14846970	HEEpiC	esophagus:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846949-14846965 chr9:14846943-14846964
28	CTCF	chr9:14846751-14847075	K562	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
29	CTCF	chr9:14847180-14847330	AG04449	skin:	n/a	n/a
30	CTCF	chr9:14846858-14847070	GM13976	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
31	CTCF	chr9:14846860-14847010	A549	lung:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
32	CTCF	chr9:14846880-14847030	GM06990	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
33	CTCF	chr9:14846860-14847010	HPAF	blood vessel:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
34	CTCF	chr9:14846480-14846630	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr9:14846854-14847091	GM10248	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
36	CTCF	chr9:14847160-14847310	HCT-116	colon:	n/a	n/a
37	CTCF	chr9:14846900-14847050	GM06990	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
38	CTCF	chr9:14846784-14847104	GM12892	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
39	CTCF	chr9:14846838-14847067	LNCaP	prostate:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
40	CTCF	chr9:14846880-14847030	HepG2	liver:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
41	CTCF	chr9:14846880-14847030	HRPEpiC	eye:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
42	CTCF	chr9:14846840-14846990	NHLF	lung:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846949-14846965 chr9:14846943-14846964
43	CTCF	chr9:14846900-14847050	HBMEC	blood vessel:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
44	CTCF	chr9:14846850-14847054	HepG2	liver:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
45	CTCF	chr9:14846900-14847050	HPF	lung:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
46	CTCF	chr9:14846900-14847050	GM12873	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
47	CTCF	chr9:14846860-14847010	MCF-7	breast:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
48	CTCF	chr9:14834251-14834297	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr9:14846807-14847066	ECC-1	luminal epithelium:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
50	CTCF	chr9:14847212-14847311	GM20000	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14838752-14838802	RPTEC	kidney:	n/a
2	chr9:14838752-14838802	HCM	heart:	n/a
3	chr9:14838752-14838802	NHBE	bronchial:	n/a
4	chr9:14838752-14838802	AoSMC	blood vessel:	n/a
5	chr9:14838752-14838802	PANC-1	pancreas:	n/a
6	chr9:14838752-14838802	AG10803	skin:	n/a
7	chr9:14838752-14838802	HL-60	blood:	n/a
8	chr9:14838752-14838802	HCF	heart:	n/a
9	chr9:14838752-14838802	Caco-2	colon:	n/a
10	chr9:14838752-14838802	SAEC	small airway:	n/a
11	chr9:14838752-14838802	A549	lung:	n/a
12	chr9:14838752-14838802	T-47D	breast:	n/a
13	chr9:14838752-14838802	SK-N-SH_RA	brain:	n/a
14	chr9:14838752-14838802	SK-N-SH	brain:	n/a
15	chr9:14838752-14838802	HMEC	breast:	n/a
16	chr9:14838752-14838802	SK-N-MC	brain:	n/a
17	chr9:14838752-14838802	NHDF-neo	bronchial:	n/a
18	chr9:14838752-14838802	AG04450	lung:	fetal
19	chr9:14838752-14838802	GM12891	blood:	n/a
20	chr9:14838752-14838802	SKMC	muscle:	n/a
21	chr9:14838752-14838802	NH-A	brain:	n/a
22	chr9:14838752-14838802	MCF-7	breast:	n/a
23	chr9:14838752-14838802	HIPEpiC	eye:	n/a
24	chr9:14838752-14838802	Hepatocyte	liver:	n/a
25	chr9:14838752-14838802	Hela-S3	cervix:	n/a
26	chr9:14838752-14838802	HCPEpiC	choroid plexus:	n/a
27	chr9:14838752-14838802	GM12878	blood:	n/a
28	chr9:14838752-14838802	PrEC	prostate:	n/a
29	chr9:14838752-14838802	GM12892	blood:	n/a
30	chr9:14838752-14838802	HCT-116	colon:	n/a
31	chr9:14838752-14838802	HPAEpiC	pulmonary alveolar:	n/a
32	chr9:14838752-14838802	HRE	kidney:	n/a
33	chr9:14838752-14838802	H1-hESC	embryonic stem cell:	embryo
34	chr9:14838752-14838802	GM19239	blood:	n/a
35	chr9:14838752-14838802	HEK293	kidney:	embryo
36	chr9:14838752-14838802	U87	brain:	n/a
37	chr9:14838752-14838802	LNCaP	prostate:	n/a
38	chr9:14838752-14838802	NT2-D1	testis:	n/a
39	chr9:14838752-14838802	HEEpiC	esophagus:	n/a
40	chr9:14838752-14838802	NB4	blood:	n/a
41	chr9:14838752-14838802	HNPCEpiC	eye:	n/a
42	chr9:14838752-14838802	K562	blood:	n/a
43	chr9:14838752-14838802	PFSK-1	brain:	n/a
44	chr9:14838752-14838802	BE2_C	brain:	n/a
45	chr9:14838752-14838802	CMK	blood:	n/a
46	chr9:14838752-14838802	AG09309	skin:	n/a
47	chr9:14838752-14838802	HAEpiC	amniotic membrane:	n/a
48	chr9:14838752-14838802	HRCEpiC	kidney:	n/a
49	chr9:14838752-14838802	GM06990	blood:	n/a
50	chr9:14838752-14838802	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:14842932..14845441-chr9:14846633..14848951,2	K562	blood:
2	chr9:14842932..14845441-chr9:14846633..14848951,2	K562	blood:
3	chr9:14813259..14815238-chr9:14818255..14820615,2	K562	blood:
4	chr9:14846510..14847037-chr9:15142689..15143560,2	MCF-7	breast:
5	chr9:14813259..14815238-chr9:14818255..14820615,2	K562	blood:
6	chr9:14691985..14694492-chr9:14845348..14847282,2	MCF-7	breast:
7	chr9:14843588..14845441-chr9:14847451..14849631,2	K562	blood:
8	chr9:14843588..14845441-chr9:14847451..14849631,2	K562	blood:
9	chr9:14850312..14853276-chr9:14856165..14857741,2	MCF-7	breast:

Variant related genes	Relation type
RNU6-1260P	TF binding region
RNU6-1260P	CpG island
ENSG00000199814	chromatin interactions
ENSG00000175893	chromatin interactions
ENSG00000251960	chromatin interactions

Extended variants
information (count: 2705 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2705 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376301776	chr9:14805118-14805119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs369918312	chr9:14805124-14805125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373880710	chr9:14805125-14805126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551654111	chr9:14805165-14805166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs199806558	chr9:14805172-14805173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs73644856	chr9:14805190-14805191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201413269	chr9:14805191-14805192	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181684043	chr9:14805204-14805205	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374983567	chr9:14805206-14805207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535075849	chr9:14805219-14805220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550588932	chr9:14805227-14805228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376554501	chr9:14805228-14805229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566345439	chr9:14805249-14805250	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568591752	chr9:14805264-14805265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs539543924	chr9:14805274-14805275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376829372	chr9:14805279-14805280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185972100	chr9:14805322-14805323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565241484	chr9:14805334-14805335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150080419	chr9:14805349-14805350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573003649	chr9:14805352-14805353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533800631	chr9:14805375-14805376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147233173	chr9:14805425-14805426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574018321	chr9:14805524-14805525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531940839	chr9:14805534-14805535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs79008101	chr9:14805552-14805553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs578006882	chr9:14805563-14805564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10117322	chr9:14805640-14805641	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs144764507	chr9:14805681-14805682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527881225	chr9:14805687-14805688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7038096	chr9:14805695-14805696	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs190296597	chr9:14805734-14805735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531912032	chr9:14805751-14805752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529829525	chr9:14805844-14805845	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550135293	chr9:14805889-14805890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182526969	chr9:14805908-14805909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74760159	chr9:14805968-14805969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs369099066	chr9:14806017-14806018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539120909	chr9:14806023-14806024	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112896758	chr9:14806058-14806059	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566493259	chr9:14806083-14806084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533972159	chr9:14806098-14806099	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555626766	chr9:14806110-14806111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112805629	chr9:14806146-14806147	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs538153334	chr9:14806148-14806149	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556554871	chr9:14806151-14806152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs80180800	chr9:14806176-14806177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545117026	chr9:14806235-14806236	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554227630	chr9:14806246-14806247	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs150712536	chr9:14806250-14806251	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs35603165	chr9:14806252-14806253	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
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
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
Intellectual disability	22102821	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
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14745000-14809800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr9:14755800-14812400	Weak transcription	Pancreas	Pancrea
3	chr9:14764800-14809600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr9:14768600-14808800	Weak transcription	Fetal Intestine Small	intestine
5	chr9:14779800-14853200	Weak transcription	Placenta	Placenta
6	chr9:14780400-14843200	Weak transcription	Fetal Heart	heart
7	chr9:14782000-14822000	Weak transcription	Fetal Brain Male	brain
8	chr9:14782800-14822000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr9:14786800-14814400	Strong transcription	Fetal Lung	lung
10	chr9:14788400-14806800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr9:14789400-14809200	Weak transcription	Fetal Intestine Large	intestine
12	chr9:14793000-14822600	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr9:14794000-14806400	Weak transcription	Fetal Muscle Leg	muscle
14	chr9:14796800-14811800	Weak transcription	Aorta	Aorta
15	chr9:14799400-14812200	Weak transcription	Fetal Muscle Trunk	muscle
16	chr9:14801800-14811800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr9:14801800-14811800	Weak transcription	Colon Smooth Muscle	Colon
18	chr9:14801800-14812600	Weak transcription	Fetal Stomach	stomach
19	chr9:14801800-14857200	Strong transcription	HepG2	liver
20	chr9:14802000-14806400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr9:14802400-14806800	Weak transcription	Adipose Nuclei	Adipose
22	chr9:14802800-14809600	Strong transcription	Fetal Kidney	kidney
23	chr9:14803600-14805600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr9:14803600-14818000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr9:14804400-14807200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr9:14804600-14805200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr9:14805000-14806200	Strong transcription	Duodenum Mucosa	Duodenum
28	chr9:14805200-14806600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr9:14805600-14810200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr9:14806200-14807000	Weak transcription	Duodenum Mucosa	Duodenum
31	chr9:14806200-14807400	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr9:14806400-14806800	Strong transcription	Fetal Muscle Leg	muscle
33	chr9:14806400-14807200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr9:14806600-14807000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr9:14806600-14807000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr9:14806600-14813400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr9:14806800-14807000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr9:14806800-14810200	Weak transcription	Fetal Muscle Leg	muscle
39	chr9:14806800-14814000	Strong transcription	Adipose Nuclei	Adipose
40	chr9:14807000-14807400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr9:14807000-14807400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr9:14807000-14807400	Strong transcription	Duodenum Mucosa	Duodenum
43	chr9:14807200-14808000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr9:14807200-14822800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr9:14807400-14809800	Weak transcription	Duodenum Mucosa	Duodenum
46	chr9:14807400-14868600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr9:14807800-14811800	Weak transcription	Left Ventricle	heart
48	chr9:14807800-14813400	Weak transcription	Right Ventricle	heart
49	chr9:14808000-14808200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr9:14808000-14810000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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