Variant report

Variant	nsv613646
Chromosome Location	chr9:14800779-14852141
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	chr9:14831736-14831957	K562	blood:	n/a	n/a
4	BHLHE40	chr9:14822708-14823063	GM12878	blood:	n/a	n/a
5	CEBPB	chr9:14827792-14827904	IMR90	lung:	n/a	chr9:14827827-14827838
6	CEBPB	chr9:14827709-14827960	HepG2	liver:	n/a	chr9:14827827-14827838
7	CHD2	chr9:14846857-14847057	HepG2	liver:	n/a	n/a
8	CHD2	chr9:14818253-14818267	GM12878	blood:	n/a	n/a
9	CHD2	chr9:14846832-14847123	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chr9:14846723-14847119	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr9:14846900-14847050	Hela-S3	cervix:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
12	CTCF	chr9:14846747-14847040	A549	lung:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
13	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
14	CTCF	chr9:14846900-14847050	AG09319	gingival:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
15	CTCF	chr9:14846860-14847010	GM12869	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
16	CTCF	chr9:14846860-14847010	AG09309	skin:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
17	CTCF	chr9:14846880-14847030	GM12869	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
18	CTCF	chr9:14846900-14847050	HCPEpiC	choroid plexus:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
19	CTCF	chr9:14847176-14847295	ProgFib	skin:	n/a	n/a
20	CTCF	chr9:14834251-14834297	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr9:14846860-14847010	HMF	breast:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
22	CTCF	chr9:14846778-14847109	GM12891	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
23	CTCF	chr9:14846799-14847116	GM12878	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
24	CTCF	chr9:14846880-14847030	HMF	breast:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
25	CTCF	chr9:14846554-14847343	A549	lung:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
26	CTCF	chr9:14846880-14847030	GM12873	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
27	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
28	CTCF	chr9:14846880-14847030	GM12864	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
29	CTCF	chr9:14846869-14847082	GM20000	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
30	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
31	CTCF	chr9:14847180-14847330	AG04449	skin:	n/a	n/a
32	CTCF	chr9:14831960-14832110	HFF	foreskin:	n/a	n/a
33	CTCF	chr9:14846798-14847109	GM19240	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
34	CTCF	chr9:14846860-14847010	NHDF-neo	bronchial:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
35	CTCF	chr9:14846773-14847111	Fibrobl	skin:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
36	CTCF	chr9:14846763-14847166	K562	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
37	CTCF	chr9:14846754-14847173	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
38	CTCF	chr9:14846860-14847010	GM12870	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	chr9:14846818-14847077	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
41	CTCF	chr9:14846900-14847050	HCFaa	heart:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
42	CTCF	chr9:14846900-14847050	AG04449	skin:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
43	CTCF	chr9:14847198-14847287	GM12878	blood:	n/a	n/a
44	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
45	CTCF	chr9:14846829-14847086	Hela-S3	cervix:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
46	CTCF	chr9:14846880-14847030	WI-38	lung:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
47	CTCF	chr9:14846880-14847030	GM12867	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
48	CTCF	chr9:14846900-14847050	AoAF	blood vessel:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964
49	CTCF	chr9:14846822-14847095	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
50	CTCF	chr9:14846880-14847030	GM12865	blood:	n/a	chr9:14846948-14846966 chr9:14846953-14846961 chr9:14846950-14846963 chr9:14846997-14847006 chr9:14846949-14846965 chr9:14846943-14846964

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14838752-14838802	T-47D	breast:	n/a
2	chr9:14838752-14838802	NT2-D1	testis:	n/a
3	chr9:14838752-14838802	NHBE	bronchial:	n/a
4	chr9:14838752-14838802	HUVEC	blood vessel:	n/a
5	chr9:14838752-14838802	AG04449	skin:	fetal
6	chr9:14838752-14838802	K562	blood:	n/a
7	chr9:14838752-14838802	HAEpiC	amniotic membrane:	n/a
8	chr9:14838752-14838802	SAEC	small airway:	n/a
9	chr9:14838752-14838802	HepG2	liver:	n/a
10	chr9:14838752-14838802	Jurkat	blood:	n/a
11	chr9:14838752-14838802	GM12891	blood:	n/a
12	chr9:14838752-14838802	HRCEpiC	kidney:	n/a
13	chr9:14838752-14838802	NH-A	brain:	n/a
14	chr9:14838752-14838802	HEK293	kidney:	embryo
15	chr9:14838752-14838802	BE2_C	brain:	n/a
16	chr9:14838752-14838802	MCF-7	breast:	n/a
17	chr9:14838752-14838802	U87	brain:	n/a
18	chr9:14838752-14838802	SKMC	muscle:	n/a
19	chr9:14838752-14838802	AG09319	gingival:	n/a
20	chr9:14838752-14838802	HCPEpiC	choroid plexus:	n/a
21	chr9:14838752-14838802	GM19239	blood:	n/a
22	chr9:14838752-14838802	GM12878	blood:	n/a
23	chr9:14838752-14838802	HNPCEpiC	eye:	n/a
24	chr9:14838752-14838802	AG04450	lung:	fetal
25	chr9:14838752-14838802	BJ	skin:	n/a
26	chr9:14838752-14838802	LNCaP	prostate:	n/a
27	chr9:14838752-14838802	HIPEpiC	eye:	n/a
28	chr9:14838752-14838802	HCF	heart:	n/a
29	chr9:14838752-14838802	SK-N-MC	brain:	n/a
30	chr9:14838752-14838802	ProgFib	skin:	n/a
31	chr9:14838752-14838802	Caco-2	colon:	n/a
32	chr9:14838752-14838802	GM12892	blood:	n/a
33	chr9:14838752-14838802	Hela-S3	cervix:	n/a
34	chr9:14838752-14838802	PFSK-1	brain:	n/a
35	chr9:14838752-14838802	HL-60	blood:	n/a
36	chr9:14838752-14838802	ECC-1	luminal epithelium:	n/a
37	chr9:14838752-14838802	HRE	kidney:	n/a
38	chr9:14838752-14838802	MCF10A-Er-Src	breast:	n/a
39	chr9:14838752-14838802	NB4	blood:	n/a
40	chr9:14838752-14838802	GM06990	blood:	n/a
41	chr9:14838752-14838802	CMK	blood:	n/a
42	chr9:14838752-14838802	HEEpiC	esophagus:	n/a
43	chr9:14838752-14838802	SK-N-SH_RA	brain:	n/a
44	chr9:14838752-14838802	AoSMC	blood vessel:	n/a
45	chr9:14838752-14838802	HCM	heart:	n/a
46	chr9:14838752-14838802	HMEC	breast:	n/a
47	chr9:14838752-14838802	ovcar-3	ovarian:	n/a
48	chr9:14838752-14838802	NHDF-neo	bronchial:	n/a
49	chr9:14838752-14838802	AG10803	skin:	n/a
50	chr9:14838752-14838802	SK-N-SH	brain:	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	chr9:14843588..14845441-chr9:14847451..14849631,2	K562	blood:
5	chr9:14846510..14847037-chr9:15142689..15143560,2	MCF-7	breast:
6	chr9:14843588..14845441-chr9:14847451..14849631,2	K562	blood:
7	chr9:14813259..14815238-chr9:14818255..14820615,2	K562	blood:
8	chr9:14691985..14694492-chr9:14845348..14847282,2	MCF-7	breast:

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

Extended variants
information (count: 2628 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2628 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10738379	chr9:14800779-14800780	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs1552897	chr9:14800780-14800781	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72614222	chr9:14800804-14800805	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs533909207	chr9:14800817-14800818	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555235890	chr9:14800956-14800957	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185345360	chr9:14800957-14800958	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs115817161	chr9:14800963-14800964	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545601203	chr9:14801028-14801029	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146109032	chr9:14801033-14801034	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189828872	chr9:14801104-14801105	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs578027500	chr9:14801116-14801117	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542352555	chr9:14801141-14801142	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563767953	chr9:14801156-14801157	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555764921	chr9:14801200-14801201	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181376023	chr9:14801211-14801212	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs373311109	chr9:14801244-14801245	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572423308	chr9:14801259-14801260	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543126276	chr9:14801291-14801292	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561286056	chr9:14801292-14801293	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531792752	chr9:14801350-14801351	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551527323	chr9:14801358-14801359	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149443131	chr9:14801371-14801372	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532702057	chr9:14801428-14801429	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184149639	chr9:14801431-14801432	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572498194	chr9:14801469-14801470	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533611072	chr9:14801475-14801476	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549063993	chr9:14801506-14801507	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567295106	chr9:14801527-14801528	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144834318	chr9:14801614-14801615	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs377093420	chr9:14801621-14801622	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75281180	chr9:14801678-14801679	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs376613541	chr9:14801680-14801681	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370147643	chr9:14801683-14801684	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10738380	chr9:14801687-14801688	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs370291465	chr9:14801688-14801689	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs35870000	chr9:14801710-14801711	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs267602184	chr9:14801712-14801713	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76714828	chr9:14801713-14801714	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs572415935	chr9:14801722-14801723	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs61744094	chr9:14801725-14801726	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200773791	chr9:14801730-14801731	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs16932300	chr9:14801738-14801739	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561432462	chr9:14801744-14801745	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372956703	chr9:14801746-14801747	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs374510376	chr9:14801750-14801751	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs113023231	chr9:14801751-14801752	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs201200414	chr9:14801753-14801754	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543595426	chr9:14801768-14801769	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79023327	chr9:14801769-14801770	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs371449178	chr9:14801770-14801771	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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

Chromatin state (count:337 , 50 per page) page: 1 2 3 4 5 6 7

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	chr9:14791200-14801600	Weak transcription	Small Intestine	intestine
13	chr9:14793000-14822600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr9:14794000-14806400	Weak transcription	Fetal Muscle Leg	muscle
15	chr9:14796800-14811800	Weak transcription	Aorta	Aorta
16	chr9:14797600-14805000	Weak transcription	Duodenum Mucosa	Duodenum
17	chr9:14797800-14801200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr9:14798600-14801400	Weak transcription	Fetal Kidney	kidney
19	chr9:14798600-14801800	Strong transcription	Colon Smooth Muscle	Colon
20	chr9:14799200-14801000	Weak transcription	HepG2	liver
21	chr9:14799400-14801000	Weak transcription	Adipose Nuclei	Adipose
22	chr9:14799400-14804600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr9:14799400-14812200	Weak transcription	Fetal Muscle Trunk	muscle
24	chr9:14799600-14803600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr9:14800200-14801800	Strong transcription	Fetal Stomach	stomach
26	chr9:14800200-14802000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr9:14801000-14801400	Enhancers	Psoas Muscle	Psoas
28	chr9:14801000-14801800	Genic enhancers	HepG2	liver
29	chr9:14801000-14802400	Strong transcription	Adipose Nuclei	Adipose
30	chr9:14801200-14801800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr9:14801400-14801800	Strong transcription	Fetal Kidney	kidney
32	chr9:14801800-14802800	Weak transcription	Fetal Kidney	kidney
33	chr9:14801800-14811800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr9:14801800-14811800	Weak transcription	Colon Smooth Muscle	Colon
35	chr9:14801800-14812600	Weak transcription	Fetal Stomach	stomach
36	chr9:14801800-14857200	Strong transcription	HepG2	liver
37	chr9:14802000-14806400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr9:14802400-14806800	Weak transcription	Adipose Nuclei	Adipose
39	chr9:14802800-14809600	Strong transcription	Fetal Kidney	kidney
40	chr9:14803600-14805600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr9:14803600-14818000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr9:14804400-14807200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr9:14804600-14805200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr9:14805000-14806200	Strong transcription	Duodenum Mucosa	Duodenum
45	chr9:14805200-14806600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr9:14805600-14810200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr9:14806200-14807000	Weak transcription	Duodenum Mucosa	Duodenum
48	chr9:14806200-14807400	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr9:14806400-14806800	Strong transcription	Fetal Muscle Leg	muscle
50	chr9:14806400-14807200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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