Variant report

Variant	nsv609002
Chromosome Location	chr7:150667210-150678080
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	BACH1	chr7:150675939-150675957	K562	blood:	n/a	n/a
2	BACH1	chr7:150671249-150671445	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:150671838-150672270	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:150671860-150671938	K562	blood:	n/a	n/a
5	BACH1	chr7:150674432-150674691	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr7:150671309-150672520	K562	blood:	n/a	chr7:150672357-150672373
7	BHLHE40	chr7:150671763-150672252	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:150675764-150675783	K562	blood:	n/a	n/a
9	BHLHE40	chr7:150675990-150676483	K562	blood:	n/a	chr7:150676280-150676296
10	BHLHE40	chr7:150673865-150674614	K562	blood:	n/a	n/a
11	CBX3	chr7:150671721-150672539	K562	blood:	n/a	n/a
12	CBX3	chr7:150673567-150674800	K562	blood:	n/a	n/a
13	CBX3	chr7:150675464-150676565	K562	blood:	n/a	n/a
14	CCNT2	chr7:150674541-150674744	K562	blood:	n/a	chr7:150674715-150674724
15	CCNT2	chr7:150674965-150675820	K562	blood:	n/a	chr7:150675703-150675712
16	CCNT2	chr7:150671495-150672456	K562	blood:	n/a	chr7:150672034-150672043
17	CCNT2	chr7:150676073-150676541	K562	blood:	n/a	chr7:150676330-150676339
18	CEBPB	chr7:150667468-150667703	K562	blood:	n/a	n/a
19	CEBPB	chr7:150667499-150667705	HepG2	liver:	n/a	n/a
20	CEBPB	chr7:150667431-150667683	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr7:150676284-150676464	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPD	chr7:150675762-150676300	K562	blood:	n/a	n/a
23	CHD2	chr7:150676082-150676396	K562	blood:	n/a	chr7:150676330-150676340
24	CHD2	chr7:150673915-150674483	K562	blood:	n/a	n/a
25	CHD2	chr7:150676684-150676880	K562	blood:	n/a	chr7:150676717-150676727
26	CHD2	chr7:150675620-150675770	GM12878	blood:	n/a	n/a
27	CHD2	chr7:150675514-150675810	K562	blood:	n/a	n/a
28	CHD2	chr7:150671805-150672059	K562	blood:	n/a	chr7:150672035-150672045
29	CHD2	chr7:150677771-150678280	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr7:150676008-150676490	H1-hESC	embryonic stem cell:	n/a	chr7:150676330-150676340
31	CHD2	chr7:150671834-150672142	GM12878	blood:	n/a	chr7:150672035-150672045
32	CHD2	chr7:150673493-150673715	K562	blood:	n/a	n/a
33	CHD2	chr7:150676108-150676368	GM12878	blood:	n/a	chr7:150676330-150676340
34	CHD2	chr7:150675560-150675802	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr7:150671723-150672321	A549	lung:	n/a	n/a
36	CTBP2	chr7:150676132-150676768	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr7:150672080-150672230	GM12867	blood:	n/a	chr7:150672164-150672173 chr7:150672161-150672179 chr7:150672162-150672178 chr7:150672166-150672176
38	CTCF	chr7:150672120-150672270	A549	lung:	n/a	chr7:150672164-150672173 chr7:150672161-150672179 chr7:150672162-150672178 chr7:150672166-150672176
39	CTCF	chr7:150672020-150672170	HMEC	breast:	n/a	n/a
40	CTCF	chr7:150672080-150672230	GM12868	blood:	n/a	chr7:150672164-150672173 chr7:150672161-150672179 chr7:150672162-150672178 chr7:150672166-150672176
41	CTCF	chr7:150672040-150672190	HPAF	blood vessel:	n/a	chr7:150672164-150672173 chr7:150672161-150672179 chr7:150672162-150672178 chr7:150672166-150672176
42	CTCF	chr7:150671960-150672250	WI-38	lung:	n/a	chr7:150672164-150672173 chr7:150672161-150672179 chr7:150672162-150672178 chr7:150672166-150672176
43	CTCF	chr7:150672060-150672210	AoAF	blood vessel:	n/a	chr7:150672164-150672173 chr7:150672161-150672179 chr7:150672162-150672178 chr7:150672166-150672176
44	CTCF	chr7:150672140-150672290	HCM	heart:	n/a	chr7:150672164-150672173 chr7:150672161-150672179 chr7:150672162-150672178 chr7:150672166-150672176
45	CTCF	chr7:150671772-150672472	K562	blood:	n/a	chr7:150672164-150672173 chr7:150672161-150672179 chr7:150672162-150672178 chr7:150672166-150672176
46	CTCF	chr7:150672080-150672230	GM12878	blood:	n/a	chr7:150672164-150672173 chr7:150672161-150672179 chr7:150672162-150672178 chr7:150672166-150672176
47	CTCF	chr7:150672140-150672290	AG04450	lung:	n/a	chr7:150672164-150672173 chr7:150672161-150672179 chr7:150672162-150672178 chr7:150672166-150672176
48	CTCF	chr7:150672078-150672255	MCF-7	breast:	n/a	chr7:150672164-150672173 chr7:150672161-150672179 chr7:150672162-150672178 chr7:150672166-150672176
49	CTCF	chr7:150672070-150672253	H1-hESC	embryonic stem cell:	n/a	chr7:150672164-150672173 chr7:150672161-150672179 chr7:150672162-150672178 chr7:150672166-150672176
50	CTCF	chr7:150672060-150672210	GM12865	blood:	n/a	chr7:150672164-150672173 chr7:150672161-150672179 chr7:150672162-150672178 chr7:150672166-150672176

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150676283-150676333	NT2-D1	testis:	n/a
2	chr7:150674972-150675022	GM12891	blood:	n/a
3	chr7:150675308-150675358	HCF	heart:	n/a
4	chr7:150676283-150676333	NT2-D1	testis:	n/a
5	chr7:150674972-150675022	GM12891	blood:	n/a
6	chr7:150675308-150675358	HCF	heart:	n/a
7	chr7:150671807-150671857	HNPCEpiC	eye:	n/a
8	chr7:150675025-150675075	HRPEpiC	eye:	n/a
9	chr7:150675025-150675075	CMK	blood:	n/a
10	chr7:150674980-150675030	AG09319	gingival:	n/a
11	chr7:150674012-150674062	ProgFib	skin:	n/a
12	chr7:150672768-150672818	HCF	heart:	n/a
13	chr7:150673192-150673242	GM12892	blood:	n/a
14	chr7:150676364-150676414	Hepatocyte	liver:	n/a
15	chr7:150670099-150670149	HIPEpiC	eye:	n/a
16	chr7:150674980-150675030	Jurkat	blood:	n/a
17	chr7:150673192-150673242	HAEpiC	amniotic membrane:	n/a
18	chr7:150674980-150675030	HepG2	liver:	n/a
19	chr7:150668669-150668719	ECC-1	luminal epithelium:	n/a
20	chr7:150675516-150675566	SK-N-SH_RA	brain:	n/a
21	chr7:150669058-150669108	NHDF-neo	bronchial:	n/a
22	chr7:150675859-150675909	IMR90	lung:	fetal
23	chr7:150677125-150677175	HIPEpiC	eye:	n/a
24	chr7:150670099-150670149	PANC-1	pancreas:	n/a
25	chr7:150675516-150675566	HEEpiC	esophagus:	n/a
26	chr7:150672267-150672317	NHBE	bronchial:	n/a
27	chr7:150676529-150676579	AG10803	skin:	n/a
28	chr7:150674972-150675022	SK-N-SH	brain:	n/a
29	chr7:150670099-150670149	U87	brain:	n/a
30	chr7:150672175-150672225	HEK293	kidney:	embryo
31	chr7:150675516-150675566	Hepatocyte	liver:	n/a
32	chr7:150669058-150669108	AG09309	skin:	n/a
33	chr7:150668669-150668719	NT2-D1	testis:	n/a
34	chr7:150674972-150675022	NH-A	brain:	n/a
35	chr7:150672768-150672818	AG04450	lung:	fetal
36	chr7:150670099-150670149	PrEC	prostate:	n/a
37	chr7:150675308-150675358	HAEpiC	amniotic membrane:	n/a
38	chr7:150674596-150674646	SK-N-SH_RA	brain:	n/a
39	chr7:150672175-150672225	U87	brain:	n/a
40	chr7:150668669-150668719	GM19239	blood:	n/a
41	chr7:150674012-150674062	Hepatocyte	liver:	n/a
42	chr7:150674972-150675022	HCM	heart:	n/a
43	chr7:150674753-150674803	HCPEpiC	choroid plexus:	n/a
44	chr7:150671500-150671550	HCF	heart:	n/a
45	chr7:150668669-150668719	LNCaP	prostate:	n/a
46	chr7:150675516-150675566	ECC-1	luminal epithelium:	n/a
47	chr7:150674972-150675022	HEEpiC	esophagus:	n/a
48	chr7:150671500-150671550	HRE	kidney:	n/a
49	chr7:150671807-150671857	CMK	blood:	n/a
50	chr7:150674012-150674062	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:150668944..150671861-chr7:150941507..150943455,2	MCF-7	breast:
2	chr16:85044766..85045536-chr7:150674758..150675258,2	HCT-116	colon:
3	chr7:150646673..150650094-chr7:150670937..150674779,4	MCF-7	breast:
4	chr7:150661579..150663428-chr7:150675690..150677350,2	MCF-7	breast:
5	chr11:592285..592822-chr7:150671646..150672236,2	MCF-7	breast:
6	chr7:150670321..150673113-chr7:150933266..150935781,2	MCF-7	breast:
7	chr7:150677750..150680138-chr7:150716469..150718503,2	MCF-7	breast:
8	chr7:150669264..150677850-chr7:150681612..150689209,13	MCF-7	breast:
9	chr7:150671887..150673971-chr7:150915991..150917932,2	K562	blood:
10	chr7:150661173..150665225-chr7:150669426..150673358,7	MCF-7	breast:
11	chr7:150019591..150022356-chr7:150674947..150677441,2	K562	blood:
12	chr7:150064708..150066870-chr7:150673905..150675576,2	MCF-7	breast:
13	chr7:150670508..150673387-chr7:150723224..150725668,3	MCF-7	breast:
14	chr7:150654869..150656816-chr7:150670691..150673405,2	MCF-7	breast:
15	chr7:150675423..150678179-chr7:150678935..150681223,3	MCF-7	breast:
16	chr12:65259282..65261612-chr7:150671119..150672990,2	MCF-7	breast:
17	chr7:150634464..150636964-chr7:150670317..150672404,2	MCF-7	breast:
18	chr7:150668903..150671561-chr7:150807024..150809833,2	MCF-7	breast:
19	chr7:150670110..150672033-chr7:150810426..150812934,2	MCF-7	breast:
20	chr7:150671455..150673565-chr7:150752052..150755338,3	MCF-7	breast:
21	chr7:150654976..150656696-chr7:150671274..150673215,2	MCF-7	breast:
22	chr7:150670653..150672364-chr7:150715220..150718108,2	MCF-7	breast:
23	chr7:150671805..150672600-chr7:150682853..150683837,2	K562	blood:
24	chr19:55918635..55919319-chr7:150671393..150672297,2	HCT-116	colon:
25	chr7:150675659..150676250-chr7:150705407..150706353,2	K562	blood:
26	chr7:150627605..150628492-chr7:150671224..150672069,2	K562	blood:
27	chr7:150671828..150674694-chr7:150692153..150695076,2	MCF-7	breast:
28	chr7:150594719..150596784-chr7:150671045..150673400,2	MCF-7	breast:
29	chr7:150661035..150665420-chr7:150665668..150673641,9	MCF-7	breast:
30	chr7:150673570..150675827-chr7:150725848..150727398,2	MCF-7	breast:
31	chr7:150654740..150658307-chr7:150674264..150676481,3	MCF-7	breast:
32	chr7:150670317..150671058-chr7:150682793..150683490,2	K562	blood:
33	chr7:150671324..150673603-chr7:150688182..150691343,3	MCF-7	breast:
34	chr7:150671778..150674151-chr7:150678272..150681379,4	MCF-7	breast:

Variant related genes	Relation type
KCNH2	TF binding region
KCNH2	CpG island
ENSG00000164889	chromatin interactions
ENSG00000211517	chromatin interactions
ENSG00000153786	chromatin interactions
ENSG00000055118	chromatin interactions
ENSG00000082014	chromatin interactions
ENSG00000197150	chromatin interactions
ENSG00000106526	chromatin interactions
ENSG00000164885	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000214022	chromatin interactions
ENSG00000196456	chromatin interactions
ENSG00000133612	chromatin interactions
ENSG00000127399	chromatin interactions
ENSG00000164867	chromatin interactions
ENSG00000243433	chromatin interactions
ENSG00000181652	chromatin interactions

Extended variants
information (count: 465 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:465 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3807375	chr7:150667210-150667211	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs544805947	chr7:150667217-150667218	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552118151	chr7:150667277-150667278	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs369043768	chr7:150667304-150667305	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs41308981	chr7:150667347-150667348	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs41308984	chr7:150667349-150667350	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs182514979	chr7:150667353-150667354	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372257847	chr7:150667354-150667355	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150286129	chr7:150667361-150667362	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs137909495	chr7:150667362-150667363	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs143492904	chr7:150667363-150667364	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs145888505	chr7:150667395-150667396	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549271497	chr7:150667398-150667399	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138755795	chr7:150667450-150667451	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs150987673	chr7:150667491-150667492	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569411981	chr7:150667498-150667499	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115564829	chr7:150667507-150667508	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs41307343	chr7:150667533-150667534	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7792983	chr7:150667639-150667640	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs528167743	chr7:150667643-150667644	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs118121666	chr7:150667664-150667665	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs575974241	chr7:150667683-150667684	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs544929398	chr7:150667711-150667712	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs115937974	chr7:150667712-150667713	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs574877658	chr7:150667748-150667749	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs142127098	chr7:150667755-150667756	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs560612596	chr7:150667774-150667775	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs146163983	chr7:150667778-150667779	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs552317715	chr7:150667834-150667835	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs562353611	chr7:150667858-150667859	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs75562728	chr7:150667869-150667870	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs548074824	chr7:150667878-150667879	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs568052884	chr7:150667879-150667880	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs147862727	chr7:150667880-150667881	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs547102681	chr7:150667930-150667931	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs572719880	chr7:150668027-150668028	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs189467962	chr7:150668069-150668070	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs10236214	chr7:150668070-150668071	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs578125157	chr7:150668126-150668127	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs539175232	chr7:150668164-150668165	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs559153806	chr7:150668167-150668168	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs11763131	chr7:150668182-150668183	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs576503557	chr7:150668221-150668222	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs543535440	chr7:150668227-150668228	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs545040329	chr7:150668228-150668229	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs3807374	chr7:150668346-150668347	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs141429994	chr7:150668355-150668356	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs560303391	chr7:150668380-150668381	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs577229085	chr7:150668381-150668382	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs150434008	chr7:150668405-150668406	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150657200-150669600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr7:150658200-150670800	Enhancers	Rectal Smooth Muscle	rectum
3	chr7:150658800-150670400	Enhancers	Duodenum Smooth Muscle	Duodenum
4	chr7:150660200-150668200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr7:150660400-150668000	Weak transcription	Brain Substantia Nigra	brain
6	chr7:150661800-150670400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr7:150662600-150667400	Weak transcription	Spleen	Spleen
8	chr7:150663400-150668200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:150664000-150670000	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr7:150664400-150673600	Enhancers	Fetal Lung	lung
11	chr7:150664600-150674000	Enhancers	Fetal Brain Male	brain
12	chr7:150665200-150671800	Genic enhancers	Fetal Stomach	stomach
13	chr7:150665400-150668400	Bivalent Enhancer	Placenta	Placenta
14	chr7:150665400-150671800	Enhancers	Left Ventricle	heart
15	chr7:150665600-150667800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
16	chr7:150665600-150669800	Enhancers	Fetal Brain Female	brain
17	chr7:150665600-150671200	Enhancers	Right Ventricle	heart
18	chr7:150665800-150669200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr7:150665800-150669200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:150665800-150669600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr7:150666000-150668600	Enhancers	Brain Germinal Matrix	brain
22	chr7:150666000-150668800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr7:150666000-150669600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:150666000-150669600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr7:150666000-150670200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr7:150666000-150670400	Enhancers	Fetal Intestine Small	intestine
27	chr7:150666200-150667800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr7:150666200-150668400	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr7:150666200-150669800	Enhancers	Ovary	ovary
30	chr7:150666200-150670000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr7:150666200-150670800	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr7:150666400-150668200	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr7:150666400-150669600	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr7:150666400-150669600	Enhancers	Brain Angular Gyrus	brain
35	chr7:150666400-150669800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr7:150666400-150670400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr7:150666400-150671400	Enhancers	Fetal Thymus	thymus
38	chr7:150666600-150668200	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr7:150666600-150669600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr7:150666800-150668000	Weak transcription	Brain Anterior Caudate	brain
41	chr7:150666800-150668400	Weak transcription	Right Atrium	heart
42	chr7:150666800-150668600	Enhancers	Fetal Muscle Leg	muscle
43	chr7:150666800-150670200	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr7:150666800-150671400	Enhancers	Fetal Intestine Large	intestine
45	chr7:150667000-150668000	Weak transcription	Brain Hippocampus Middle	brain
46	chr7:150667000-150668000	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr7:150667000-150668800	Enhancers	Colon Smooth Muscle	Colon
48	chr7:150667200-150667600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr7:150667200-150667600	Enhancers	Stomach Smooth Muscle	stomach
50	chr7:150667200-150667600	Weak transcription	HSMMtube	muscle

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