Variant report

Variant	nsv437095
Chromosome Location	chr10:6649064-6666823
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	chr10:6663485-6663746	K562	blood:	n/a	n/a
2	BHLHE40	chr10:6666757-6666979	K562	blood:	n/a	n/a
3	CEBPB	chr10:6649802-6650100	Hela-S3	cervix:	n/a	chr10:6649944-6649955
4	CEBPB	chr10:6649894-6650028	K562	blood:	n/a	chr10:6649944-6649955
5	CEBPB	chr10:6657447-6657691	HepG2	liver:	n/a	n/a
6	CEBPB	chr10:6649828-6650094	HepG2	liver:	n/a	chr10:6649944-6649955
7	CTCF	chr10:6666802-6667190	K562	blood:	n/a	n/a
8	CTCF	chr10:6666801-6667126	K562	blood:	n/a	n/a
9	CTCF	chr10:6666803-6667042	K562	blood:	n/a	n/a
10	E2F4	chr10:6654393-6654902	MCF10A-Er-Src	breast:	n/a	n/a
11	E2F4	chr10:6653664-6654135	MCF10A-Er-Src	breast:	n/a	n/a
12	E2F4	chr10:6652961-6653161	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F6	chr10:6665965-6666397	H1-hESC	embryonic stem cell:	n/a	n/a
14	E2F6	chr10:6665870-6666471	H1-hESC	embryonic stem cell:	n/a	n/a
15	FOS	chr10:6651379-6651579	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr10:6663485-6663813	MCF10A-Er-Src	breast:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663648-6663656
17	FOS	chr10:6654259-6654588	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr10:6663466-6663829	MCF10A-Er-Src	breast:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663648-6663656
19	FOS	chr10:6654281-6654588	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr10:6661783-6661874	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr10:6649799-6650107	MCF10A-Er-Src	breast:	n/a	chr10:6649965-6649974
22	FOS	chr10:6651415-6651518	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr10:6663485-6663807	MCF10A-Er-Src	breast:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663648-6663656
24	FOS	chr10:6649836-6650030	MCF10A-Er-Src	breast:	n/a	chr10:6649965-6649974
25	FOS	chr10:6649810-6650097	MCF10A-Er-Src	breast:	n/a	chr10:6649965-6649974
26	FOS	chr10:6654272-6654782	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr10:6663471-6663830	MCF10A-Er-Src	breast:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663648-6663656
28	FOS	chr10:6654272-6654599	MCF10A-Er-Src	breast:	n/a	n/a
29	FOSL2	chr10:6661614-6661969	HepG2	liver:	n/a	n/a
30	FOSL2	chr10:6663419-6663739	SK-N-SH	brain:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663648-6663656
31	GATA3	chr10:6663444-6663521	SH-SY5Y	brain:	n/a	chr10:6663459-6663466 chr10:6663508-6663517 chr10:6663504-6663520 chr10:6663508-6663515 chr10:6663504-6663520 chr10:6663459-6663466 chr10:6663459-6663466 chr10:6663508-6663515 chr10:6663507-6663517 chr10:6663508-6663515 chr10:6663452-6663473
32	JUN	chr10:6663612-6663814	HepG2	liver:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663648-6663656
33	JUN	chr10:6663503-6663800	H1-hESC	embryonic stem cell:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663648-6663656
34	JUND	chr10:6663460-6663825	H1-hESC	embryonic stem cell:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663646-6663657 chr10:6663648-6663656
35	JUND	chr10:6663491-6663795	Hela-S3	cervix:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663646-6663657 chr10:6663648-6663656
36	JUND	chr10:6663404-6664010	SK-N-SH	brain:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663646-6663657 chr10:6663648-6663656
37	JUND	chr10:6663504-6663807	K562	blood:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663646-6663657 chr10:6663648-6663656
38	JUND	chr10:6663493-6663843	HepG2	liver:	n/a	chr10:6663647-6663657 chr10:6663647-6663656 chr10:6663649-6663656 chr10:6663648-6663657 chr10:6663646-6663657 chr10:6663648-6663656
39	KAP1	chr10:6663335-6664022	HEK293	kidney:	n/a	chr10:6663649-6663658
40	KAP1	chr10:6663095-6663993	U2OS	brain:	n/a	chr10:6663649-6663658
41	MAFF	chr10:6657616-6657628	HepG2	liver:	n/a	n/a
42	MAFK	chr10:6657451-6657756	HepG2	liver:	n/a	n/a
43	MAFK	chr10:6657422-6657626	HepG2	liver:	n/a	n/a
44	MAFK	chr10:6652715-6652916	HepG2	liver:	n/a	chr10:6652804-6652824 chr10:6652806-6652822 chr10:6652807-6652821 chr10:6652803-6652818
45	MAFK	chr10:6652761-6652961	HepG2	liver:	n/a	chr10:6652804-6652824 chr10:6652806-6652822 chr10:6652807-6652821 chr10:6652803-6652818
46	MYC	chr10:6649827-6650112	MCF10A-Er-Src	breast:	n/a	n/a
47	MYC	chr10:6654295-6654803	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr10:6663804-6664003	K562	blood:	n/a	n/a
49	POLR2A	chr10:6656339-6656382	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr10:6656347-6656418	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:6665001-6665051	AG04450	lung:	fetal
2	chr10:6665001-6665051	AG04450	lung:	fetal
3	chr10:6665001-6665051	HMEC	breast:	n/a
4	chr10:6665001-6665051	GM12892	blood:	n/a
5	chr10:6665001-6665051	NHBE	bronchial:	n/a
6	chr10:6665001-6665051	AG04449	skin:	fetal
7	chr10:6665001-6665051	HIPEpiC	eye:	n/a
8	chr10:6665001-6665051	H1-hESC	embryonic stem cell:	embryo
9	chr10:6665001-6665051	Hepatocyte	liver:	n/a
10	chr10:6665001-6665051	RPTEC	kidney:	n/a
11	chr10:6665001-6665051	HCF	heart:	n/a
12	chr10:6665001-6665051	SK-N-SH	brain:	n/a
13	chr10:6665001-6665051	Caco-2	colon:	n/a
14	chr10:6665001-6665051	NT2-D1	testis:	n/a
15	chr10:6665001-6665051	CMK	blood:	n/a
16	chr10:6665001-6665051	GM12878	blood:	n/a
17	chr10:6665001-6665051	SAEC	small airway:	n/a
18	chr10:6665001-6665051	BE2_C	brain:	n/a
19	chr10:6665001-6665051	GM06990	blood:	n/a
20	chr10:6665001-6665051	K562	blood:	n/a
21	chr10:6665001-6665051	HAEpiC	amniotic membrane:	n/a
22	chr10:6665001-6665051	SK-N-MC	brain:	n/a
23	chr10:6665001-6665051	AG10803	skin:	n/a
24	chr10:6665001-6665051	NHDF-neo	bronchial:	n/a
25	chr10:6665001-6665051	ProgFib	skin:	n/a
26	chr10:6665001-6665051	T-47D	breast:	n/a
27	chr10:6665001-6665051	LNCaP	prostate:	n/a
28	chr10:6665001-6665051	HPAEpiC	pulmonary alveolar:	n/a
29	chr10:6665001-6665051	AG09319	gingival:	n/a
30	chr10:6665001-6665051	HCT-116	colon:	n/a
31	chr10:6665001-6665051	IMR90	lung:	fetal
32	chr10:6665001-6665051	NH-A	brain:	n/a
33	chr10:6665001-6665051	HRPEpiC	eye:	n/a
34	chr10:6665001-6665051	ECC-1	luminal epithelium:	n/a
35	chr10:6665001-6665051	HL-60	blood:	n/a
36	chr10:6665001-6665051	HEK293	kidney:	embryo
37	chr10:6665001-6665051	Jurkat	blood:	n/a
38	chr10:6665001-6665051	GM12891	blood:	n/a
39	chr10:6665001-6665051	SKMC	muscle:	n/a
40	chr10:6665001-6665051	MCF-7	breast:	n/a
41	chr10:6665001-6665051	U87	brain:	n/a
42	chr10:6665001-6665051	HepG2	liver:	n/a
43	chr10:6665001-6665051	PrEC	prostate:	n/a
44	chr10:6665001-6665051	GM19239	blood:	n/a
45	chr10:6665001-6665051	BJ	skin:	n/a
46	chr10:6665001-6665051	SK-N-SH_RA	brain:	n/a
47	chr10:6665001-6665051	AG09309	skin:	n/a
48	chr10:6665001-6665051	Hela-S3	cervix:	n/a
49	chr10:6665001-6665051	HRE	kidney:	n/a
50	chr10:6665001-6665051	HRCEpiC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:6622287..6623956-chr10:6655441..6657087,2	K562	blood:
2	chr10:6614415..6616986-chr10:6653036..6655207,2	K562	blood:
3	chr10:6624097..6625900-chr10:6665858..6667657,2	K562	blood:
4	chr10:6657794..6661242-chr10:6661759..6664532,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL137145.1-2	chr10:6657332-6657599	ENSG00000237943.2
2	lnc-AL137145.1-3	chr10:6662880-6663135	ENSG00000225948.2
3	lnc-AL137145.1-3	chr10:6662976-6663135	XLOC_008371
4	lnc-AL137145.1-3	chr10:6662880-6663135	XLOC_008371
5	lnc-AL137145.1-2	chr10:6657725-6657810	XLOC_008370
6	lnc-AL137145.1-2	chr10:6650310-6650370	ENSG00000237943.2
7	lnc-AL137145.1-2	chr10:6657725-6657886	ENSG00000237943.2
8	lnc-AL137145.1-2	chr10:6650310-6650370	ENSG00000237943.2
9	lnc-AL137145.1-2	chr10:6657725-6657921	ENSG00000237943.2
10	lnc-AL137145.1-2	chr10:6657968-6658273	XLOC_008370
11	lnc-AL137145.1-2	chr10:6650310-6650370	ENSG00000237943.2
12	lnc-AL137145.1-3	chr10:6663672-6663911	XLOC_008371
13	lnc-AL137145.1-3	chr10:6660678-6660738	ENSG00000225948.2
14	lnc-AL137145.1-2	chr10:6655593-6655651	ENSG00000237943.2
15	lnc-AL137145.1-2	chr10:6657693-6657797	FPKM1_group_2866_transcript_7
16	lnc-AL137145.1-3	chr10:6663672-6663824	ENSG00000225948.2
17	lnc-AL137145.1-3	chr10:6665644-6666266	ucscGeneNc_uc001ijl_2
18	lnc-AL137145.1-2	chr10:6657388-6657599	XLOC_008370
19	lnc-AL137145.1-2	chr10:6649249-6649377	ENSG00000237943.2
20	lnc-AL137145.1-2	chr10:6657332-6657409	XLOC_008370
21	lnc-AL137145.1-2	chr10:6657968-6658359	ENSG00000237943.2
22	lnc-AL137145.1-2	chr10:6657190-6657643	NONHSAT011239
23	lnc-AL137145.1-2	chr10:6657481-6657599	ENSG00000237943.2
24	lnc-AL137145.1-2	chr10:6657190-6657643	FPKM1_group_2866_transcript_7
25	lnc-AL137145.1-2	chr10:6657693-6658742	NONHSAT011239
26	lnc-AL137145.1-3	chr10:6662507-6662895	ucscGeneNc_uc001ijl_2
27	lnc-AL137145.1-3	chr10:6663672-6663911	XLOC_008371
28	lnc-AL137145.1-2	chr10:6657725-6657912	ENSG00000237943.2
29	lnc-AL137145.1-2	chr10:6657725-6657886	ENSG00000237943.2
30	lnc-AL137145.1-2	chr10:6657725-6657886	XLOC_008370
31	lnc-AL137145.1-2	chr10:6649283-6649377	ENSG00000237943.2
32	lnc-AL137145.1-3	chr10:6663672-6663824	XLOC_008371
33	lnc-AL137145.1-2	chr10:6650338-6650370	ENSG00000237943.2
34	lnc-AL137145.1-2	chr10:6650310-6650370	XLOC_008370
35	lnc-AL137145.1-3	chr10:6660597-6660738	XLOC_008371
36	lnc-AL137145.1-3	chr10:6660678-6660738	XLOC_008371
37	lnc-AL137145.1-3	chr10:6662881-6663135	XLOC_008371
38	lnc-AL137145.1-2	chr10:6657968-6658414	ENSG00000237943.2

Variant related genes	Relation type
ENSG00000225948	TF binding region
PRKCQ-AS1	TF binding region
ENSG00000225948	CpG island
PRKCQ-AS1	CpG island
ENSG00000237943	chromatin interactions
ENSG00000225948	chromatin interactions
DDX6	miRNA target sites
EPHA4	miRNA target sites
RNF145	miRNA target sites
TOMM70A	miRNA target sites

Extended variants
information (count: 764 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:764 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2478866	chr10:6649064-6649065	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs575508869	chr10:6649091-6649092	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs17138640	chr10:6649100-6649101	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
4	rs9423942	chr10:6649132-6649133	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs11253614	chr10:6649160-6649161	Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs539900969	chr10:6649215-6649216	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561842773	chr10:6649216-6649217	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529064394	chr10:6649266-6649267	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs4748197	chr10:6649267-6649268	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs569100797	chr10:6649276-6649277	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs533261836	chr10:6649281-6649282	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs556822131	chr10:6649330-6649331	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs192329874	chr10:6649331-6649332	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs183237258	chr10:6649347-6649348	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs571829973	chr10:6649349-6649350	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs77988705	chr10:6649361-6649362	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs78098098	chr10:6649374-6649375	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs187589136	chr10:6649383-6649384	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568197276	chr10:6649432-6649433	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572806830	chr10:6649459-6649460	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535579502	chr10:6649461-6649462	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114182086	chr10:6649467-6649468	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575472283	chr10:6649468-6649469	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191658102	chr10:6649487-6649488	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184096309	chr10:6649528-6649529	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558429963	chr10:6649557-6649558	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572722419	chr10:6649596-6649597	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372929756	chr10:6649602-6649603	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139176634	chr10:6649622-6649623	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1409871	chr10:6649635-6649636	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs4747249	chr10:6649655-6649656	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs544371154	chr10:6649671-6649672	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200442011	chr10:6649712-6649713	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1409872	chr10:6649713-6649714	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs201374442	chr10:6649715-6649716	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142663007	chr10:6649730-6649731	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551341547	chr10:6649734-6649735	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560422096	chr10:6649740-6649741	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528445295	chr10:6649746-6649747	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546948632	chr10:6649781-6649782	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192293903	chr10:6649799-6649800	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs114275907	chr10:6649807-6649808	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs550667555	chr10:6649888-6649889	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs4748198	chr10:6649935-6649936	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs184633481	chr10:6650026-6650027	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs5782918	chr10:6650076-6650077	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs397764419	chr10:6650077-6650078	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs562415214	chr10:6650128-6650129	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs190211540	chr10:6650141-6650142	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573467059	chr10:6650156-6650157	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Mantle cell lymphoma	19029149	CNVD

Chromatin state (count:234 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:6642400-6650400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr10:6642800-6651600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr10:6644400-6650400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr10:6644600-6650400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr10:6645400-6650600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr10:6645600-6650000	Weak transcription	Brain Germinal Matrix	brain
7	chr10:6645600-6650400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr10:6645800-6649200	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr10:6645800-6650600	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr10:6646400-6650400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr10:6646600-6649200	Weak transcription	Brain Hippocampus Middle	brain
12	chr10:6646600-6652600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr10:6648000-6649800	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr10:6648000-6649800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr10:6648200-6649200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr10:6648200-6649800	Enhancers	Primary T cells fromperipheralblood	blood
17	chr10:6648200-6649800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr10:6648200-6649800	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr10:6648200-6649800	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr10:6648200-6650000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr10:6648600-6649800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr10:6648800-6649400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr10:6648800-6649400	Enhancers	Dnd41	blood
24	chr10:6648800-6649800	Enhancers	Fetal Thymus	thymus
25	chr10:6648800-6650000	Enhancers	Thymus	Thymus
26	chr10:6649000-6649200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
27	chr10:6649000-6649200	Enhancers	Brain Cingulate Gyrus	brain
28	chr10:6649000-6649400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr10:6649000-6649400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr10:6649000-6649400	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr10:6649000-6649800	Genic enhancers	Primary T cells from cord blood	blood
32	chr10:6649000-6650200	Genic enhancers	Primary T helper cells PMA-I stimulated	--
33	chr10:6649000-6650800	Enhancers	Brain Angular Gyrus	brain
34	chr10:6649000-6650800	Enhancers	Brain Anterior Caudate	brain
35	chr10:6649000-6650800	Enhancers	Fetal Muscle Leg	muscle
36	chr10:6649200-6649400	Flanking Active TSS	Brain Cingulate Gyrus	brain
37	chr10:6649200-6649800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr10:6649200-6650000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
39	chr10:6649200-6650600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr10:6649200-6650600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr10:6649200-6650800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr10:6649200-6650800	Enhancers	Brain Hippocampus Middle	brain
43	chr10:6649200-6650800	Enhancers	Brain Substantia Nigra	brain
44	chr10:6649200-6651200	Strong transcription	Skeletal Muscle Female	skeletal muscle
45	chr10:6649400-6649800	Active TSS	Brain Inferior Temporal Lobe	brain
46	chr10:6649400-6650200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr10:6649400-6650800	Enhancers	Brain Cingulate Gyrus	brain
48	chr10:6649400-6650800	Enhancers	NHEK	skin
49	chr10:6649400-6651600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr10:6649400-6652600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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