Variant report

Variant	nsv879661
Chromosome Location	chr4:100805207-100869635
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1488)
CpG islands
(count:1100)
Chromatin interactive
region (count:118)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1488 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:100866794-100867174	K562	blood:	n/a	n/a
2	ARID3A	chr4:100806281-100806595	K562	blood:	n/a	n/a
3	ARID3A	chr4:100868101-100868534	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:100806358-100806559	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:100815505-100815618	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:100868363-100868626	K562	blood:	n/a	n/a
7	ARID3A	chr4:100865222-100865553	K562	blood:	n/a	n/a
8	ATF1	chr4:100812609-100812809	K562	blood:	n/a	n/a
9	ATF1	chr4:100815425-100815767	K562	blood:	n/a	n/a
10	ATF2	chr4:100867812-100868613	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr4:100815272-100816060	GM12878	blood:	n/a	n/a
12	ATF2	chr4:100867529-100869163	GM12878	blood:	n/a	n/a
13	ATF2	chr4:100865124-100865491	GM12878	blood:	n/a	n/a
14	ATF2	chr4:100867849-100868786	GM12878	blood:	n/a	n/a
15	ATF2	chr4:100867642-100868933	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr4:100815406-100815871	K562	blood:	n/a	n/a
17	ATF3	chr4:100815406-100815641	HepG2	liver:	n/a	n/a
18	ATF3	chr4:100867751-100867975	K562	blood:	n/a	n/a
19	ATF3	chr4:100815353-100815815	GM12878	blood:	n/a	n/a
20	BACH1	chr4:100868024-100868492	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL11A	chr4:100867600-100868432	GM12878	blood:	n/a	chr4:100868305-100868314
22	BCL3	chr4:100867855-100868460	K562	blood:	n/a	chr4:100868305-100868314
23	BCL3	chr4:100867503-100869024	A549	lung:	n/a	chr4:100868305-100868314
24	BCL3	chr4:100815341-100816020	GM12878	blood:	n/a	n/a
25	BCL3	chr4:100867607-100868557	GM12878	blood:	n/a	chr4:100868305-100868314
26	BCL3	chr4:100867862-100868404	GM12878	blood:	n/a	chr4:100868305-100868314
27	BCL3	chr4:100867870-100868837	K562	blood:	n/a	chr4:100868305-100868314
28	BCL3	chr4:100867470-100868643	A549	lung:	n/a	chr4:100868305-100868314 chr4:100867499-100867512
29	BCL3	chr4:100815216-100815755	A549	lung:	n/a	n/a
30	BCLAF1	chr4:100867518-100868520	GM12878	blood:	n/a	chr4:100868305-100868314
31	BCLAF1	chr4:100815255-100816126	GM12878	blood:	n/a	n/a
32	BCLAF1	chr4:100867607-100868441	K562	blood:	n/a	chr4:100868305-100868314
33	BCLAF1	chr4:100867473-100868763	K562	blood:	n/a	chr4:100868305-100868314 chr4:100867499-100867512
34	BCLAF1	chr4:100867129-100868664	GM12878	blood:	n/a	chr4:100868305-100868314 chr4:100867499-100867512
35	BHLHE40	chr4:100868661-100868711	K562	blood:	n/a	n/a
36	BHLHE40	chr4:100815414-100816032	K562	blood:	n/a	n/a
37	BHLHE40	chr4:100815380-100815989	GM12878	blood:	n/a	n/a
38	BHLHE40	chr4:100867598-100868409	K562	blood:	n/a	n/a
39	BHLHE40	chr4:100867501-100868372	HepG2	liver:	n/a	n/a
40	BHLHE40	chr4:100865168-100865537	GM12878	blood:	n/a	n/a
41	BHLHE40	chr4:100815368-100816052	HepG2	liver:	n/a	n/a
42	BHLHE40	chr4:100867591-100868692	GM12878	blood:	n/a	n/a
43	BHLHE40	chr4:100867101-100867398	K562	blood:	n/a	chr4:100867361-100867377
44	BRCA1	chr4:100867936-100868635	H1-hESC	embryonic stem cell:	n/a	n/a
45	BRCA1	chr4:100867909-100868333	HepG2	liver:	n/a	n/a
46	BRCA1	chr4:100810770-100810790	GM12878	blood:	n/a	n/a
47	BRCA1	chr4:100815372-100815661	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr4:100867664-100867717	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr4:100867569-100867743	GM12878	blood:	n/a	n/a
50	CBX3	chr4:100815303-100815777	K562	blood:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:100868099-100868149	HIPEpiC	eye:	n/a
2	chr4:100868748-100868798	HPAEpiC	pulmonary alveolar:	n/a
3	chr4:100868099-100868149	HIPEpiC	eye:	n/a
4	chr4:100868748-100868798	HPAEpiC	pulmonary alveolar:	n/a
5	chr4:100815818-100815868	AG09309	skin:	n/a
6	chr4:100815442-100815492	PANC-1	pancreas:	n/a
7	chr4:100815590-100815640	T-47D	breast:	n/a
8	chr4:100868748-100868798	BE2_C	brain:	n/a
9	chr4:100867292-100867342	SAEC	small airway:	n/a
10	chr4:100816135-100816185	PrEC	prostate:	n/a
11	chr4:100867292-100867342	GM12878	blood:	n/a
12	chr4:100816135-100816185	CMK	blood:	n/a
13	chr4:100868132-100868182	PFSK-1	brain:	n/a
14	chr4:100815620-100815670	HCT-116	colon:	n/a
15	chr4:100815590-100815640	AG04449	skin:	fetal
16	chr4:100815570-100815620	HRPEpiC	eye:	n/a
17	chr4:100816135-100816185	HCPEpiC	choroid plexus:	n/a
18	chr4:100815570-100815620	Jurkat	blood:	n/a
19	chr4:100868099-100868149	PFSK-1	brain:	n/a
20	chr4:100815442-100815492	GM12878	blood:	n/a
21	chr4:100868318-100868368	Hepatocyte	liver:	n/a
22	chr4:100868318-100868368	ovcar-3	ovarian:	n/a
23	chr4:100867292-100867342	AG09319	gingival:	n/a
24	chr4:100815570-100815620	HNPCEpiC	eye:	n/a
25	chr4:100867933-100867983	ECC-1	luminal epithelium:	n/a
26	chr4:100868318-100868368	HCPEpiC	choroid plexus:	n/a
27	chr4:100864777-100864827	PrEC	prostate:	n/a
28	chr4:100867853-100867903	AG04450	lung:	fetal
29	chr4:100864777-100864827	BE2_C	brain:	n/a
30	chr4:100815812-100815862	SAEC	small airway:	n/a
31	chr4:100815812-100815862	NHBE	bronchial:	n/a
32	chr4:100816515-100816565	HL-60	blood:	n/a
33	chr4:100864777-100864827	ovcar-3	ovarian:	n/a
34	chr4:100867461-100867511	SK-N-SH_RA	brain:	n/a
35	chr4:100864777-100864827	HL-60	blood:	n/a
36	chr4:100867292-100867342	HIPEpiC	eye:	n/a
37	chr4:100815570-100815620	GM06990	blood:	n/a
38	chr4:100868132-100868182	HEEpiC	esophagus:	n/a
39	chr4:100815818-100815868	H1-hESC	embryonic stem cell:	embryo
40	chr4:100815620-100815670	HMEC	breast:	n/a
41	chr4:100867461-100867511	HCF	heart:	n/a
42	chr4:100868318-100868368	PFSK-1	brain:	n/a
43	chr4:100867350-100867400	T-47D	breast:	n/a
44	chr4:100867853-100867903	LNCaP	prostate:	n/a
45	chr4:100816135-100816185	GM12892	blood:	n/a
46	chr4:100868099-100868149	ovcar-3	ovarian:	n/a
47	chr4:100815570-100815620	SK-N-SH	brain:	n/a
48	chr4:100815570-100815620	GM19239	blood:	n/a
49	chr4:100868748-100868798	HIPEpiC	eye:	n/a
50	chr4:100815590-100815640	HIPEpiC	eye:	n/a

(count:118 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr4:100768566..100770766-chr4:100839767..100842129,2	K562	blood:
2	chr4:100829302..100831359-chr4:100831716..100834419,2	K562	blood:
3	chr4:100837131..100839848-chr4:100866356..100868236,2	K562	blood:
4	chr4:100855120..100857614-chr4:100862703..100864671,2	K562	blood:
5	chr4:100802373..100804056-chr4:100811223..100813567,2	MCF-7	breast:
6	chr4:100733785..100736226-chr4:100868711..100870778,2	MCF-7	breast:
7	chr17:57970213..57970964-chr4:100815105..100815985,2	MCF-7	breast:
8	chr4:100840471..100849591-chr4:100866268..100873122,18	K562	blood:
9	chr4:100840471..100849591-chr4:100866268..100873122,18	K562	blood:
10	chr4:100813266..100817175-chr4:100865527..100871657,11	MCF-7	breast:
11	chr4:100732582..100733619-chr4:100805780..100806859,8	MCF-7	breast:
12	chr4:100814213..100816552-chr4:100866797..100868818,3	MCF-7	breast:
13	chr4:100819394..100821526-chr4:100823145..100825504,2	K562	blood:
14	chr4:100828518..100831140-chr4:100831923..100834406,2	MCF-7	breast:
15	chr4:100824278..100827001-chr4:100871760..100873443,2	K562	blood:
16	chr4:100851997..100854259-chr4:100861223..100863842,2	K562	blood:
17	chr4:100845037..100846550-chr4:100867903..100869729,2	MCF-7	breast:
18	chr4:100814600..100817376-chr4:100869817..100872742,4	MCF-7	breast:
19	chr4:100832439..100834484-chr4:100837119..100838825,2	MCF-7	breast:
20	chr4:100842980..100845246-chr4:100845585..100848805,3	K562	blood:
21	chr4:100815570..100818331-chr4:100848090..100849658,2	K562	blood:
22	chr4:100837896..100840734-chr4:100841683..100843412,2	MCF-7	breast:
23	chr4:100854185..100858103-chr4:100869055..100872773,4	MCF-7	breast:
24	chr4:100799869..100822436-chr4:100866015..100873106,54	K562	blood:
25	chr4:100856368..100857910-chr4:100866642..100868433,2	K562	blood:
26	chr4:100819072..100821321-chr4:100870712..100873019,2	MCF-7	breast:
27	chr4:100807450..100809212-chr4:100865402..100867857,2	K562	blood:
28	chr4:100837896..100840734-chr4:100841683..100843412,2	MCF-7	breast:
29	chr4:100810623..100827791-chr4:100865444..100874425,55	K562	blood:
30	chr4:100732741..100733588-chr4:100806987..100807845,2	MCF-7	breast:
31	chr4:100645156..100645805-chr4:100806019..100806629,2	MCF-7	breast:
32	chr4:100480938..100486909-chr4:100867873..100873651,15	K562	blood:
33	chr4:100842812..100845640-chr4:100851384..100853953,2	K562	blood:
34	chr4:100814647..100816517-chr4:100832549..100834839,2	K562	blood:
35	chr4:100829396..100833198-chr4:100836822..100839868,3	MCF-7	breast:
36	chr4:100815631..100818960-chr4:100821744..100826195,4	K562	blood:
37	chr4:100855120..100857614-chr4:100862703..100864671,2	K562	blood:
38	chr4:100850716..100855335-chr4:100865818..100872882,15	K562	blood:
39	chr4:100815138..100817913-chr4:100819745..100821681,2	K562	blood:
40	chr4:100482482..100485178-chr4:100807913..100810603,2	K562	blood:
41	chr4:100855576..100858012-chr4:100858356..100861147,2	MCF-7	breast:
42	chr4:100815570..100818331-chr4:100848090..100849658,2	K562	blood:
43	chr4:100832439..100834484-chr4:100837119..100838825,2	MCF-7	breast:
44	chr4:100483953..100487087-chr4:100868908..100871675,3	MCF-7	breast:
45	chr4:100008800..100012914-chr4:100866380..100869813,4	K562	blood:
46	chr4:100745759..100748161-chr4:100844127..100845854,2	K562	blood:
47	chr4:100849266..100851363-chr4:100851727..100854069,2	K562	blood:
48	chr4:100799869..100822436-chr4:100866015..100873106,54	K562	blood:
49	chr4:100856020..100858032-chr4:100868560..100871073,2	K562	blood:
50	chr4:100729924..100732920-chr4:100868919..100870955,3	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	DNAJB14	hsa-miR-30c-5p	chr4:100845804-100845826

Variant related genes	Relation type
DNAJB14	TF binding region
LAMTOR3	TF binding region
ENSG00000245322	TF binding region
DNAJB14	CpG island
LAMTOR3	CpG island
ENSG00000245322	CpG island
ENSG00000138814	chromatin interactions
ENSG00000138821	chromatin interactions
ENSG00000145331	chromatin interactions
ENSG00000164032	chromatin interactions
ENSG00000245322	chromatin interactions
ENSG00000108423	chromatin interactions
ENSG00000109270	chromatin interactions
ENSG00000120699	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000197894	chromatin interactions
ENSG00000248161	chromatin interactions
ENSG00000070190	chromatin interactions
ENSG00000254531	chromatin interactions
ENSG00000246090	chromatin interactions
ENSG00000138823	chromatin interactions
ENSG00000164022	chromatin interactions
ENSG00000120697	chromatin interactions
ENSG00000172493	chromatin interactions
ENSG00000164031	chromatin interactions

Extended variants
information (count: 2000 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:2000 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6532835	chr4:100805207-100805208	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs200308708	chr4:100805216-100805217	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs199686072	chr4:100805220-100805221	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs373077863	chr4:100805233-100805234	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs376575788	chr4:100805238-100805239	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs199789066	chr4:100805273-100805274	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs369290926	chr4:100805282-100805283	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs201259435	chr4:100805299-100805300	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs138870935	chr4:100805319-100805320	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs142750923	chr4:100805370-100805371	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs541217554	chr4:100805427-100805428	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs200574423	chr4:100805444-100805445	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs559473732	chr4:100805469-100805470	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs533488359	chr4:100805490-100805491	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs551549509	chr4:100805545-100805546	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs530773981	chr4:100805547-100805548	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs147379541	chr4:100805560-100805561	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs544332397	chr4:100805587-100805588	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs550092963	chr4:100805683-100805684	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs562449128	chr4:100805714-100805715	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs200423911	chr4:100805722-100805723	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs148392182	chr4:100805754-100805755	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs185362979	chr4:100805759-100805760	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs190210334	chr4:100805782-100805783	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs565852391	chr4:100805822-100805823	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs142520467	chr4:100805850-100805851	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs182172003	chr4:100805864-100805865	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs576017017	chr4:100805907-100805908	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs544622583	chr4:100805949-100805950	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs186083565	chr4:100806004-100806005	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs188242986	chr4:100806055-100806056	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs555682664	chr4:100806095-100806096	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs373320106	chr4:100806098-100806099	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs373077026	chr4:100806127-100806128	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs574003939	chr4:100806162-100806163	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs541296582	chr4:100806172-100806173	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs559535257	chr4:100806212-100806213	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs150897861	chr4:100806230-100806231	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs1365494	chr4:100806252-100806253	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs79559353	chr4:100806276-100806277	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs530971493	chr4:100806291-100806292	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs549406127	chr4:100806299-100806300	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs180721575	chr4:100806323-100806324	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs185024649	chr4:100806365-100806366	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs547681284	chr4:100806460-100806461	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs565903959	chr4:100806478-100806479	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs139400028	chr4:100806479-100806480	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs199884420	chr4:100806483-100806484	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs549180859	chr4:100806497-100806498	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs144547057	chr4:100806519-100806520	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2840 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100789600-100814200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr4:100790400-100814600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr4:100797000-100809600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr4:100797600-100809000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr4:100797800-100808400	Strong transcription	Adipose Nuclei	Adipose
6	chr4:100798000-100806200	Strong transcription	Primary B cells from peripheral blood	blood
7	chr4:100798000-100808200	Strong transcription	Liver	Liver
8	chr4:100798000-100809600	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr4:100798000-100810800	Strong transcription	Primary T helper cells fromperipheralblood	blood
10	chr4:100798200-100808400	Strong transcription	Placenta	Placenta
11	chr4:100798400-100806400	Strong transcription	HSMM	muscle
12	chr4:100798400-100814200	Weak transcription	Stomach Mucosa	stomach
13	chr4:100798600-100807600	Strong transcription	Duodenum Mucosa	Duodenum
14	chr4:100798600-100809000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr4:100798800-100808400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr4:100799000-100805600	Strong transcription	Rectal Mucosa Donor 29	rectum
17	chr4:100799000-100805800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr4:100799000-100806200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr4:100799000-100806600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr4:100799000-100806600	Strong transcription	Osteobl	bone
21	chr4:100799000-100808200	Strong transcription	NHDF-Ad	bronchial
22	chr4:100799000-100813400	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr4:100799200-100806200	Strong transcription	Dnd41	blood
24	chr4:100799200-100807200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr4:100799200-100808400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:100799200-100808400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr4:100799200-100811000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr4:100799400-100805600	Strong transcription	Primary T helper cells PMA-I stimulated	--
29	chr4:100799400-100806200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr4:100799400-100812200	Weak transcription	HepG2	liver
31	chr4:100799600-100805800	Strong transcription	NH-A	brain
32	chr4:100799600-100808200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr4:100799600-100814800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:100799800-100806600	Strong transcription	Muscle Satellite Cultured Cells	--
35	chr4:100799800-100808200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:100800000-100805400	Strong transcription	HUES48 Cell Line	embryonic stem cell
37	chr4:100800000-100805400	Strong transcription	Brain Anterior Caudate	brain
38	chr4:100800000-100806200	Strong transcription	Rectal Mucosa Donor 31	rectum
39	chr4:100800000-100810400	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr4:100800200-100814200	Weak transcription	Hela-S3	cervix
41	chr4:100800600-100805400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr4:100800600-100805600	Strong transcription	Colon Smooth Muscle	Colon
43	chr4:100800600-100808200	Strong transcription	HUVEC	blood vessel
44	chr4:100800800-100805600	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr4:100801400-100806200	Strong transcription	Primary neutrophils fromperipheralblood	blood
46	chr4:100801400-100809000	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr4:100801800-100814400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr4:100801800-100814600	Weak transcription	Psoas Muscle	Psoas
49	chr4:100802000-100809000	Weak transcription	Gastric	stomach
50	chr4:100802000-100812200	Weak transcription	Brain Angular Gyrus	brain

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