Variant report

Variant	nsv1025381
Chromosome Location	chr7:6356704-6409818
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	ARID3A	chr7:6388618-6388920	K562	blood:	n/a	n/a
2	ARID3A	chr7:6403396-6403567	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:6388543-6388891	HepG2	liver:	n/a	n/a
4	ATF1	chr7:6388405-6388876	K562	blood:	n/a	n/a
5	ATF2	chr7:6388437-6388937	H1-hESC	embryonic stem cell:	n/a	chr7:6388596-6388607
6	ATF2	chr7:6388529-6388924	GM12878	blood:	n/a	chr7:6388596-6388607
7	ATF2	chr7:6388443-6388988	H1-hESC	embryonic stem cell:	n/a	chr7:6388596-6388607
8	ATF2	chr7:6388420-6388909	GM12878	blood:	n/a	chr7:6388596-6388607
9	ATF3	chr7:6388356-6388835	K562	blood:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607
10	ATF3	chr7:6388385-6388986	A549	lung:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607
11	ATF3	chr7:6388479-6388902	GM12878	blood:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607
12	ATF3	chr7:6388456-6389065	K562	blood:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607
13	ATF3	chr7:6388397-6388976	HepG2	liver:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607
14	ATF3	chr7:6388437-6389070	A549	lung:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607
15	ATF3	chr7:6388442-6388841	H1-hESC	embryonic stem cell:	n/a	chr7:6388594-6388609 chr7:6388598-6388605 chr7:6388595-6388608 chr7:6388595-6388606 chr7:6388595-6388608 chr7:6388596-6388607 chr7:6388598-6388606 chr7:6388596-6388607
16	ATF3	chr7:6398701-6398975	K562	blood:	n/a	n/a
17	BACH1	chr7:6388532-6388708	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL3	chr7:6371973-6372304	GM12878	blood:	n/a	n/a
19	BCL3	chr7:6388503-6388987	A549	lung:	n/a	n/a
20	BCLAF1	chr7:6388469-6388989	GM12878	blood:	n/a	n/a
21	BCLAF1	chr7:6362508-6363008	GM12878	blood:	n/a	n/a
22	BHLHE40	chr7:6362651-6362951	K562	blood:	n/a	n/a
23	BHLHE40	chr7:6407253-6407453	K562	blood:	n/a	n/a
24	BHLHE40	chr7:6357557-6357862	K562	blood:	n/a	n/a
25	BHLHE40	chr7:6357599-6357867	HepG2	liver:	n/a	n/a
26	BHLHE40	chr7:6388098-6388876	GM12878	blood:	n/a	chr7:6388115-6388131 chr7:6388446-6388462
27	BHLHE40	chr7:6383439-6383454	K562	blood:	n/a	n/a
28	BHLHE40	chr7:6387976-6388072	K562	blood:	n/a	n/a
29	BHLHE40	chr7:6388411-6388912	K562	blood:	n/a	chr7:6388446-6388462
30	BHLHE40	chr7:6357510-6357923	HepG2	liver:	n/a	n/a
31	BRCA1	chr7:6388496-6388723	GM12878	blood:	n/a	n/a
32	BRCA1	chr7:6388497-6388819	HepG2	liver:	n/a	n/a
33	BRCA1	chr7:6388593-6388823	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr7:6388417-6388923	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr7:6398439-6399054	K562	blood:	n/a	n/a
36	CBX3	chr7:6388389-6389002	K562	blood:	n/a	n/a
37	CBX3	chr7:6398593-6399013	K562	blood:	n/a	n/a
38	CCNT2	chr7:6388438-6388902	K562	blood:	n/a	chr7:6388639-6388648
39	CEBPB	chr7:6392958-6393082	HepG2	liver:	n/a	chr7:6393040-6393051
40	CEBPB	chr7:6390462-6390715	HepG2	liver:	n/a	chr7:6390575-6390586
41	CEBPB	chr7:6392836-6393267	MCF-7	breast:	n/a	chr7:6393040-6393051
42	CEBPB	chr7:6393016-6393102	Hela-S3	cervix:	n/a	chr7:6393040-6393051
43	CEBPB	chr7:6358279-6358602	HepG2	liver:	n/a	chr7:6358458-6358469 chr7:6358459-6358468 chr7:6358459-6358468 chr7:6358459-6358468 chr7:6358459-6358468 chr7:6358457-6358470
44	CEBPB	chr7:6390518-6390648	A549	lung:	n/a	chr7:6390575-6390586
45	CEBPB	chr7:6358288-6358619	K562	blood:	n/a	chr7:6358458-6358469 chr7:6358459-6358468 chr7:6358459-6358468 chr7:6358459-6358468 chr7:6358459-6358468 chr7:6358457-6358470
46	CEBPB	chr7:6392894-6393207	K562	blood:	n/a	chr7:6393040-6393051
47	CEBPB	chr7:6388622-6388888	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr7:6388607-6388900	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:6407493-6407918	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr7:6392904-6393211	A549	lung:	n/a	chr7:6393040-6393051

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6388618-6388668	HUVEC	blood vessel:	n/a
2	chr7:6369837-6369887	HEK293	kidney:	embryo
3	chr7:6370717-6370767	GM19239	blood:	n/a
4	chr7:6388618-6388668	HUVEC	blood vessel:	n/a
5	chr7:6369837-6369887	HEK293	kidney:	embryo
6	chr7:6370717-6370767	GM19239	blood:	n/a
7	chr7:6369837-6369887	GM12892	blood:	n/a
8	chr7:6389919-6389969	HEK293	kidney:	embryo
9	chr7:6370368-6370418	HRE	kidney:	n/a
10	chr7:6385721-6385771	HCF	heart:	n/a
11	chr7:6388695-6388745	SK-N-SH	brain:	n/a
12	chr7:6388618-6388668	MCF10A-Er-Src	breast:	n/a
13	chr7:6391166-6391216	H1-hESC	embryonic stem cell:	embryo
14	chr7:6385721-6385771	NH-A	brain:	n/a
15	chr7:6388738-6388788	HL-60	blood:	n/a
16	chr7:6391166-6391216	ovcar-3	ovarian:	n/a
17	chr7:6388872-6388922	AG09309	skin:	n/a
18	chr7:6388130-6388180	NB4	blood:	n/a
19	chr7:6388591-6388641	GM12891	blood:	n/a
20	chr7:6388620-6388670	MCF-7	breast:	n/a
21	chr7:6388695-6388745	PANC-1	pancreas:	n/a
22	chr7:6369837-6369887	HEEpiC	esophagus:	n/a
23	chr7:6370717-6370767	NB4	blood:	n/a
24	chr7:6388620-6388670	A549	lung:	n/a
25	chr7:6388334-6388384	NH-A	brain:	n/a
26	chr7:6391166-6391216	A549	lung:	n/a
27	chr7:6370717-6370767	SK-N-MC	brain:	n/a
28	chr7:6388872-6388922	SK-N-SH	brain:	n/a
29	chr7:6385721-6385771	LNCaP	prostate:	n/a
30	chr7:6388872-6388922	HCPEpiC	choroid plexus:	n/a
31	chr7:6388827-6388877	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:6370717-6370767	ProgFib	skin:	n/a
33	chr7:6388563-6388613	Caco-2	colon:	n/a
34	chr7:6388334-6388384	RPTEC	kidney:	n/a
35	chr7:6388334-6388384	HepG2	liver:	n/a
36	chr7:6388618-6388668	AG04449	skin:	fetal
37	chr7:6388742-6388792	NHDF-neo	bronchial:	n/a
38	chr7:6388620-6388670	Hela-S3	cervix:	n/a
39	chr7:6388695-6388745	HAEpiC	amniotic membrane:	n/a
40	chr7:6388618-6388668	GM06990	blood:	n/a
41	chr7:6385721-6385771	MCF10A-Er-Src	breast:	n/a
42	chr7:6388738-6388788	GM12878	blood:	n/a
43	chr7:6388563-6388613	HCF	heart:	n/a
44	chr7:6370368-6370418	GM06990	blood:	n/a
45	chr7:6388591-6388641	HRCEpiC	kidney:	n/a
46	chr7:6388872-6388922	BJ	skin:	n/a
47	chr7:6388620-6388670	AG09319	gingival:	n/a
48	chr7:6389919-6389969	H1-hESC	embryonic stem cell:	embryo
49	chr7:6388618-6388668	AG09319	gingival:	n/a
50	chr7:6388742-6388792	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:6120676..6122302-chr7:6388312..6390000,2	MCF-7	breast:
2	chr7:6377795..6380161-chr7:6386976..6388780,2	MCF-7	breast:
3	chr7:6143046..6145933-chr7:6364932..6367512,2	K562	blood:
4	chr7:6375428..6379947-chr7:6381885..6385915,4	K562	blood:
5	chr7:6097568..6100190-chr7:6387069..6389785,3	MCF-7	breast:
6	chr7:6049082..6051960-chr7:6388689..6390680,2	MCF-7	breast:
7	chr7:6310552..6312369-chr7:6355817..6357966,2	K562	blood:
8	chr10:93169367..93170145-chr7:6388240..6389220,2	Hela-S3	cervix:
9	chr7:6379408..6381446-chr7:6384710..6386481,2	MCF-7	breast:
10	chr7:6390235..6392804-chr7:6397143..6398713,2	K562	blood:
11	chr7:6195894..6198040-chr7:6361741..6363493,2	MCF-7	breast:
12	chr7:6402943..6405122-chr7:6514612..6517402,2	K562	blood:
13	chr7:6362339..6362861-chr7:6969838..6970665,2	K562	blood:
14	chr7:6295108..6297565-chr7:6362435..6365344,2	MCF-7	breast:
15	chr7:6387247..6388755-chr7:6413232..6415374,2	MCF-7	breast:
16	chr7:6388682..6389270-chr7:6443357..6444249,2	MCF-7	breast:
17	chr7:6362326..6363972-chr7:6370986..6373639,2	MCF-7	breast:
18	chr7:6362326..6363972-chr7:6370986..6373639,2	MCF-7	breast:
19	chr7:6035426..6037082-chr7:6372151..6373884,2	MCF-7	breast:
20	chr7:6396326..6398264-chr7:6414179..6415764,2	MCF-7	breast:
21	chr7:6399153..6401648-chr7:6412367..6414838,2	K562	blood:
22	chr7:6386514..6388780-chr7:6439968..6442713,2	MCF-7	breast:
23	chr7:6364887..6367442-chr7:6388475..6390006,2	K562	blood:
24	chr7:6199558..6200447-chr7:6362313..6363284,3	MCF-7	breast:
25	chr7:6036973..6037538-chr7:6362378..6363229,3	K562	blood:
26	chr7:6046534..6048837-chr7:6387102..6390061,2	MCF-7	breast:
27	chr7:6377795..6380161-chr7:6386976..6388780,2	MCF-7	breast:
28	chr7:6047922..6050389-chr7:6388573..6391369,3	K562	blood:
29	chr2:101868629..101869217-chr7:6397500..6398000,2	Hela-S3	cervix:
30	chr7:6295381..6296000-chr7:6362330..6363265,2	MCF-7	breast:
31	chr7:6390235..6392804-chr7:6397143..6398713,2	K562	blood:
32	chr7:6199039..6200525-chr7:6362284..6363316,17	MCF-7	breast:
33	chr7:6408313..6409948-chr7:6425652..6428069,2	MCF-7	breast:
34	chr7:6383801..6385334-chr7:6385668..6388521,2	K562	blood:
35	chr7:6346440..6348361-chr7:6354558..6357169,2	K562	blood:
36	chr7:6381796..6384683-chr7:6387270..6389989,2	K562	blood:
37	chr7:6407358..6411182-chr7:6412675..6416929,4	K562	blood:
38	chr7:6200618..6201665-chr7:6361362..6362302,3	K562	blood:
39	chr7:6379408..6381446-chr7:6384710..6386481,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAC1-2	chr7:6369092-6369444	NONHSAT118994
2	lnc-RAC1-2	chr7:6370213-6370871	NONHSAT118994
3	lnc-RAC1-1	chr7:6405329-6405671	expReg_chr7_541_+

Variant related genes	Relation type
FAM220A	TF binding region
RAC1	TF binding region
FAM220A	CpG island
RAC1	CpG island
ENSG00000178397	chromatin interactions
ENSG00000122512	chromatin interactions
ENSG00000008256	chromatin interactions
ENSG00000165338	chromatin interactions
ENSG00000231704	chromatin interactions
ENSG00000106346	chromatin interactions
ENSG00000086232	chromatin interactions
ENSG00000136238	chromatin interactions
ENSG00000106305	chromatin interactions

Extended variants
information (count: 2859 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2859 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567438852	chr7:6356704-6356705	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs138882760	chr7:6356714-6356715	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs189927921	chr7:6356716-6356717	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs571450301	chr7:6356717-6356718	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs149414125	chr7:6356738-6356739	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs200193135	chr7:6356772-6356773	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs377519749	chr7:6356773-6356774	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs13229725	chr7:6356775-6356776	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs144838260	chr7:6356804-6356805	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs182520459	chr7:6356872-6356873	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs542287521	chr7:6356939-6356940	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs554758408	chr7:6356940-6356941	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs373731863	chr7:6356980-6356981	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs573137417	chr7:6356993-6356994	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs185633441	chr7:6356996-6356997	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs563488190	chr7:6357001-6357002	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs565616874	chr7:6357165-6357166	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs532685008	chr7:6357197-6357198	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs544603397	chr7:6357238-6357239	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs140139039	chr7:6357283-6357284	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs530237085	chr7:6357297-6357298	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs144104596	chr7:6357310-6357311	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs566954257	chr7:6357362-6357363	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs528321229	chr7:6357370-6357371	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs10247424	chr7:6357407-6357408	Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs571529371	chr7:6357413-6357414	Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs538513609	chr7:6357420-6357421	Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs556940550	chr7:6357438-6357439	Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs73339246	chr7:6357458-6357459	Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs373918545	chr7:6357487-6357488	Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs528834234	chr7:6357522-6357523	Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs147235914	chr7:6357576-6357577	Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs140743425	chr7:6357580-6357581	Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs534162967	chr7:6357591-6357592	Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs79301818	chr7:6357648-6357649	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs577468460	chr7:6357664-6357665	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs114596813	chr7:6357684-6357685	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs190440972	chr7:6357693-6357694	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs376907737	chr7:6357709-6357710	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs113064918	chr7:6357757-6357758	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs183563860	chr7:6357777-6357778	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs188956093	chr7:6357788-6357789	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs373310276	chr7:6357897-6357898	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142330292	chr7:6357913-6357914	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs544935349	chr7:6357920-6357921	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs564906213	chr7:6357926-6357927	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs377704680	chr7:6357938-6357939	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532452468	chr7:6357954-6357955	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs550635288	chr7:6357986-6357987	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs10248223	chr7:6358004-6358005	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:1190 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6348000-6357400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr7:6350000-6357200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr7:6353000-6357200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:6354000-6357200	Weak transcription	Placenta	Placenta
5	chr7:6354000-6357200	Weak transcription	NH-A	brain
6	chr7:6354200-6357400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr7:6354400-6357200	Weak transcription	HepG2	liver
8	chr7:6355600-6357200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr7:6355600-6357600	Enhancers	Fetal Muscle Leg	muscle
10	chr7:6355800-6357400	Weak transcription	K562	blood
11	chr7:6356000-6357000	Weak transcription	Fetal Muscle Trunk	muscle
12	chr7:6356000-6357400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr7:6356000-6357400	Weak transcription	Fetal Stomach	stomach
14	chr7:6356200-6356800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr7:6356200-6357200	Weak transcription	Ovary	ovary
16	chr7:6356200-6357200	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr7:6356200-6357400	Weak transcription	A549	lung
18	chr7:6356800-6357200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:6357000-6357200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr7:6357000-6357200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr7:6357000-6357200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr7:6357000-6357200	Enhancers	Adipose Nuclei	Adipose
23	chr7:6357000-6358400	Enhancers	Fetal Muscle Trunk	muscle
24	chr7:6357200-6357400	Enhancers	Primary hematopoietic stem cells	blood
25	chr7:6357200-6357400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr7:6357200-6357400	Enhancers	Aorta	Aorta
27	chr7:6357200-6357400	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr7:6357200-6357400	Active TSS	Right Atrium	heart
29	chr7:6357200-6357400	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr7:6357200-6357400	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr7:6357200-6357400	Enhancers	Small Intestine	intestine
32	chr7:6357200-6357400	Enhancers	Stomach Smooth Muscle	stomach
33	chr7:6357200-6357400	Enhancers	HepG2	liver
34	chr7:6357200-6357400	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr7:6357200-6357400	Enhancers	NHLF	lung
36	chr7:6357200-6357400	Enhancers	Osteobl	bone
37	chr7:6357200-6357600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr7:6357200-6357600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr7:6357200-6357600	Enhancers	Ovary	ovary
40	chr7:6357200-6357600	Enhancers	Stomach Mucosa	stomach
41	chr7:6357200-6357600	Enhancers	NH-A	brain
42	chr7:6357200-6357800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr7:6357200-6357800	Enhancers	Placenta	Placenta
44	chr7:6357200-6357800	Enhancers	Fetal Thymus	thymus
45	chr7:6357200-6358000	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr7:6357200-6358000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr7:6357200-6358000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr7:6357200-6358000	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr7:6357200-6358000	Enhancers	Spleen	Spleen
50	chr7:6357200-6358000	Enhancers	NHDF-Ad	bronchial

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