Variant report

Variant	nsv572980
Chromosome Location	chr16:75505046-75549885
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1145)
CpG islands
(count:1470)
Chromatin interactive
region (count:100)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1145 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:75543367-75543781	K562	blood:	n/a	n/a
2	ARID3A	chr16:75505682-75506080	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:75515556-75515577	K562	blood:	n/a	n/a
4	ARID3A	chr16:75540461-75540804	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:75505697-75506039	K562	blood:	n/a	n/a
6	ARID3A	chr16:75540441-75540853	K562	blood:	n/a	n/a
7	ATF1	chr16:75540441-75540853	K562	blood:	n/a	n/a
8	ATF1	chr16:75539875-75540195	K562	blood:	n/a	n/a
9	ATF1	chr16:75543362-75543935	K562	blood:	n/a	n/a
10	ATF2	chr16:75505640-75506042	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr16:75523217-75523680	GM12878	blood:	n/a	n/a
12	ATF3	chr16:75505746-75505953	K562	blood:	n/a	n/a
13	ATF3	chr16:75543263-75543677	K562	blood:	n/a	n/a
14	BACH1	chr16:75529192-75529506	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr16:75505594-75506008	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr16:75528737-75528745	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr16:75520552-75520972	GM12878	blood:	n/a	n/a
18	BATF	chr16:75520619-75520952	GM12878	blood:	n/a	n/a
19	BATF	chr16:75505750-75505994	GM12878	blood:	n/a	chr16:75505829-75505840
20	BCL3	chr16:75523221-75523575	GM12878	blood:	n/a	n/a
21	BCLAF1	chr16:75505648-75506077	GM12878	blood:	n/a	n/a
22	BHLHE40	chr16:75543277-75543975	K562	blood:	n/a	n/a
23	BHLHE40	chr16:75535302-75535565	HepG2	liver:	n/a	n/a
24	BHLHE40	chr16:75505736-75506089	HepG2	liver:	n/a	n/a
25	BHLHE40	chr16:75535379-75535401	K562	blood:	n/a	n/a
26	BRCA1	chr16:75540448-75540781	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr16:75518787-75519101	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr16:75517101-75517518	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr16:75540335-75541012	HCT-116	colon:	n/a	n/a
30	CBX3	chr16:75543145-75543731	K562	blood:	n/a	n/a
31	CBX3	chr16:75540292-75541038	HCT-116	colon:	n/a	n/a
32	CCNT2	chr16:75543308-75543999	K562	blood:	n/a	n/a
33	CEBPB	chr16:75540413-75540869	K562	blood:	n/a	chr16:75540740-75540753
34	CEBPB	chr16:75518572-75519002	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr16:75540526-75540869	HepG2	liver:	n/a	chr16:75540740-75540753
36	CEBPB	chr16:75537226-75537375	HepG2	liver:	n/a	chr16:75537332-75537343
37	CEBPB	chr16:75548019-75548165	HepG2	liver:	n/a	chr16:75548145-75548156 chr16:75548145-75548158 chr16:75548145-75548156
38	CEBPB	chr16:75540223-75541088	HCT-116	colon:	n/a	chr16:75540397-75540410 chr16:75540740-75540753
39	CEBPB	chr16:75537232-75537387	A549	lung:	n/a	chr16:75537332-75537343
40	CEBPB	chr16:75537218-75537418	HepG2	liver:	n/a	chr16:75537332-75537343
41	CEBPB	chr16:75540073-75541047	HCT-116	colon:	n/a	chr16:75540397-75540410 chr16:75540740-75540753
42	CEBPB	chr16:75506223-75506456	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr16:75540565-75540907	A549	lung:	n/a	chr16:75540740-75540753
44	CEBPB	chr16:75535826-75535905	K562	blood:	n/a	n/a
45	CEBPB	chr16:75540420-75540943	A549	lung:	n/a	chr16:75540740-75540753
46	CEBPB	chr16:75505680-75506059	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr16:75543235-75543689	K562	blood:	n/a	n/a
48	CEBPB	chr16:75540456-75540806	HepG2	liver:	n/a	chr16:75540740-75540753
49	CEBPB	chr16:75540438-75540917	HepG2	liver:	n/a	chr16:75540740-75540753
50	CEBPB	chr16:75537367-75537380	IMR90	lung:	n/a	n/a

(count:1470 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:75512273-75512323	HEEpiC	esophagus:	n/a
2	chr16:75529019-75529069	GM12878	blood:	n/a
3	chr16:75529346-75529396	HRCEpiC	kidney:	n/a
4	chr16:75520165-75520215	A549	lung:	n/a
5	chr16:75528813-75528863	HepG2	liver:	n/a
6	chr16:75512979-75513029	A549	lung:	n/a
7	chr16:75512273-75512323	HEEpiC	esophagus:	n/a
8	chr16:75529019-75529069	GM12878	blood:	n/a
9	chr16:75529346-75529396	HRCEpiC	kidney:	n/a
10	chr16:75520165-75520215	A549	lung:	n/a
11	chr16:75528813-75528863	HepG2	liver:	n/a
12	chr16:75512979-75513029	A549	lung:	n/a
13	chr16:75520165-75520215	HCF	heart:	n/a
14	chr16:75529504-75529554	HL-60	blood:	n/a
15	chr16:75528977-75529027	AG04449	skin:	fetal
16	chr16:75517052-75517102	HPAEpiC	pulmonary alveolar:	n/a
17	chr16:75529346-75529396	NH-A	brain:	n/a
18	chr16:75528920-75528970	A549	lung:	n/a
19	chr16:75508622-75508672	HepG2	liver:	n/a
20	chr16:75512979-75513029	AG10803	skin:	n/a
21	chr16:75528977-75529027	HPAEpiC	pulmonary alveolar:	n/a
22	chr16:75528813-75528863	SAEC	small airway:	n/a
23	chr16:75512273-75512323	AoSMC	blood vessel:	n/a
24	chr16:75508622-75508672	GM12878	blood:	n/a
25	chr16:75513561-75513611	HPAEpiC	pulmonary alveolar:	n/a
26	chr16:75512616-75512666	HNPCEpiC	eye:	n/a
27	chr16:75513354-75513404	LNCaP	prostate:	n/a
28	chr16:75529197-75529247	HRE	kidney:	n/a
29	chr16:75512979-75513029	SAEC	small airway:	n/a
30	chr16:75529197-75529247	PFSK-1	brain:	n/a
31	chr16:75508622-75508672	CMK	blood:	n/a
32	chr16:75548557-75548607	A549	lung:	n/a
33	chr16:75528813-75528863	SK-N-SH_RA	brain:	n/a
34	chr16:75512273-75512323	GM19239	blood:	n/a
35	chr16:75532464-75532514	HAEpiC	amniotic membrane:	n/a
36	chr16:75528977-75529027	H1-hESC	embryonic stem cell:	embryo
37	chr16:75524926-75524976	CMK	blood:	n/a
38	chr16:75512979-75513029	Hepatocyte	liver:	n/a
39	chr16:75524926-75524976	HEK293	kidney:	embryo
40	chr16:75529504-75529554	IMR90	lung:	fetal
41	chr16:75528977-75529027	SKMC	muscle:	n/a
42	chr16:75515554-75515604	Hela-S3	cervix:	n/a
43	chr16:75532464-75532514	SKMC	muscle:	n/a
44	chr16:75529504-75529554	AoSMC	blood vessel:	n/a
45	chr16:75528813-75528863	BE2_C	brain:	n/a
46	chr16:75515554-75515604	HEEpiC	esophagus:	n/a
47	chr16:75505953-75506003	HCF	heart:	n/a
48	chr16:75528920-75528970	Jurkat	blood:	n/a
49	chr16:75548557-75548607	HRPEpiC	eye:	n/a
50	chr16:75512616-75512666	HRPEpiC	eye:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:75505406..75506311-chr16:75797784..75798667,3	MCF-7	breast:
2	chr16:75496239..75498624-chr16:75543687..75545847,2	MCF-7	breast:
3	chr16:75529289..75531150-chr16:75543079..75544974,2	K562	blood:
4	chr16:75523790..75524565-chr16:75542425..75543396,2	K562	blood:
5	chr16:75535711..75537222-chr16:75539478..75542235,2	MCF-7	breast:
6	chr16:75507460..75509082-chr16:75520993..75523733,2	MCF-7	breast:
7	chr16:75296409..75300528-chr16:75549238..75552790,3	MCF-7	breast:
8	chr16:75539405..75540962-chr16:75572342..75574110,2	K562	blood:
9	chr16:75535711..75537222-chr16:75539478..75542235,2	MCF-7	breast:
10	chr16:75505198..75507754-chr16:75508642..75511329,3	MCF-7	breast:
11	chr16:75523790..75524565-chr16:75542425..75543396,2	K562	blood:
12	chr16:75538464..75540762-chr16:75575477..75578098,2	MCF-7	breast:
13	chr16:75549723..75552104-chr16:75587869..75590374,4	MCF-7	breast:
14	chr16:75505427..75506354-chr16:75654710..75655557,4	MCF-7	breast:
15	chr16:75510774..75513332-chr16:75550628..75552832,2	MCF-7	breast:
16	chr16:75533525..75534182-chr16:75573663..75574408,2	MCF-7	breast:
17	chr16:75542394..75545244-chr16:75549898..75552701,3	K562	blood:
18	chr16:75538570..75543222-chr16:75547718..75552328,5	MCF-7	breast:
19	chr16:75285110..75287717-chr16:75517291..75520144,2	MCF-7	breast:
20	chr16:75546074..75547889-chr16:75549218..75551422,3	K562	blood:
21	chr16:75505900..75508078-chr16:75510609..75513420,3	MCF-7	breast:
22	chr16:75515909..75518493-chr16:75681322..75683050,2	MCF-7	breast:
23	chr16:75465026..75467989-chr16:75524514..75527095,2	MCF-7	breast:
24	chr16:75506243..75508903-chr16:75511656..75514124,2	K562	blood:
25	chr16:75516147..75519691-chr16:75524437..75526173,3	MCF-7	breast:
26	chr16:75506243..75508903-chr16:75511656..75514124,2	K562	blood:
27	chr16:75497399..75499829-chr16:75504719..75506935,2	K562	blood:
28	chr16:75549848..75551982-chr16:75681662..75683251,3	MCF-7	breast:
29	chr16:75497738..75499769-chr16:75549161..75551267,4	MCF-7	breast:
30	chr16:75509263..75511097-chr16:75511572..75513314,2	K562	blood:
31	chr16:75495533..75500726-chr16:75509549..75515784,9	MCF-7	breast:
32	chr16:75520122..75522617-chr16:75545167..75547600,2	MCF-7	breast:
33	chr16:75506694..75509130-chr16:75514124..75517050,2	MCF-7	breast:
34	chr16:75549686..75552508-chr16:75588605..75590350,2	MCF-7	breast:
35	chr16:75530551..75532986-chr16:75540003..75542944,2	K562	blood:
36	chr16:75505256..75507400-chr16:75525903..75527940,2	MCF-7	breast:
37	chr16:75497002..75498653-chr16:75549372..75551463,2	K562	blood:
38	chr16:75496707..75498493-chr16:75515933..75518742,2	MCF-7	breast:
39	chr16:75527053..75529439-chr16:75537012..75541443,4	K562	blood:
40	chr16:75505378..75506356-chr16:75797770..75798866,7	K562	blood:
41	chr16:75521011..75523844-chr16:75524605..75527828,4	MCF-7	breast:
42	chr16:75538570..75543222-chr16:75547718..75552328,5	MCF-7	breast:
43	chr16:75505393..75505919-chr16:75525499..75526021,2	MCF-7	breast:
44	chr16:75503553..75505745-chr16:75588650..75591373,2	MCF-7	breast:
45	chr16:75505348..75506153-chr16:75551055..75551869,3	MCF-7	breast:
46	chr16:75496250..75498914-chr16:75519937..75523724,3	MCF-7	breast:
47	chr16:75497139..75499689-chr16:75518408..75520806,2	K562	blood:
48	chr16:75539405..75541198-chr16:75546430..75548650,2	K562	blood:
49	chr16:75539405..75541198-chr16:75546430..75548650,2	K562	blood:
50	chr16:75505434..75506225-chr16:75525498..75526266,4	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GABARAPL2-1	chr16:75529158-75529305	ENSG00000203472.3
2	lnc-CHST6-2	chr16:75507025-75507817	NONHSAT143740
3	lnc-GABARAPL2-1	chr16:75509794-75510218	ENSG00000203472.3
4	lnc-CHST6-2	chr16:75528838-75528926	NONHSAT143740

No data

Variant related genes	Relation type
ENSG00000203472	TF binding region
CHST6	TF binding region
ENSG00000262583	TF binding region
ENSG00000203472	CpG island
CHST6	CpG island
ENSG00000262583	CpG island
ENSG00000203472	chromatin interactions
ENSG00000183196	chromatin interactions
ENSG00000196792	chromatin interactions
ENSG00000262583	chromatin interactions
ENSG00000065427	chromatin interactions
ENSG00000166848	chromatin interactions
ENSG00000166822	chromatin interactions
ENSG00000100478	chromatin interactions
ENSG00000153774	chromatin interactions
ENSG00000261717	chromatin interactions
ENSG00000205084	chromatin interactions
ENSG00000050820	chromatin interactions

Extended variants
information (count: 2147 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2147 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs37602	chr16:75505046-75505047	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534515676	chr16:75505136-75505137	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs371807820	chr16:75505150-75505151	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs185949021	chr16:75505184-75505185	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs11641864	chr16:75505190-75505191	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs536615165	chr16:75505234-75505235	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs76464622	chr16:75505267-75505268	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs375484002	chr16:75505283-75505284	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs573608644	chr16:75505299-75505300	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs375078615	chr16:75505321-75505322	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs561464417	chr16:75505330-75505331	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs376554209	chr16:75505331-75505332	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs117206697	chr16:75505405-75505406	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs150786925	chr16:75505421-75505422	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs139412791	chr16:75505472-75505473	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs529889455	chr16:75505491-75505492	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs191991782	chr16:75505492-75505493	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs551286770	chr16:75505507-75505508	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs561124458	chr16:75505543-75505544	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs77056230	chr16:75505553-75505554	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs546735216	chr16:75505558-75505559	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs76631269	chr16:75505561-75505562	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs37603	chr16:75505567-75505568	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs182021992	chr16:75505667-75505668	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs559640749	chr16:75505706-75505707	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs536924638	chr16:75505708-75505709	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs528737956	chr16:75505710-75505711	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs557268368	chr16:75505711-75505712	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs567112040	chr16:75505731-75505732	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs536248854	chr16:75505735-75505736	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs552765854	chr16:75505736-75505737	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs113841380	chr16:75505745-75505746	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs144092932	chr16:75505748-75505749	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs190760206	chr16:75505776-75505777	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs575959057	chr16:75505854-75505855	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs146010646	chr16:75505856-75505857	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs369481405	chr16:75505883-75505884	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs140065245	chr16:75505884-75505885	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs529993549	chr16:75505892-75505893	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs540641911	chr16:75505895-75505896	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs560178767	chr16:75505919-75505920	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs552569059	chr16:75505926-75505927	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs373688238	chr16:75505927-75505928	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs149791164	chr16:75505938-75505939	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs558897834	chr16:75505953-75505954	Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs145770993	chr16:75505954-75505955	Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs182301740	chr16:75505985-75505986	Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs550555498	chr16:75505998-75505999	Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs567573370	chr16:75506017-75506018	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs578043291	chr16:75506026-75506027	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:1020 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:75498600-75506800	Weak transcription	Brain Substantia Nigra	brain
2	chr16:75498600-75511800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr16:75498800-75505200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr16:75498800-75505600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr16:75498800-75505600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr16:75498800-75507200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr16:75498800-75518600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr16:75499000-75511000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr16:75499000-75511200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr16:75499000-75511200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr16:75499200-75505800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr16:75499200-75505800	Weak transcription	Fetal Heart	heart
13	chr16:75499200-75506000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr16:75499200-75506200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr16:75499200-75511400	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr16:75499200-75511400	Weak transcription	Brain Anterior Caudate	brain
17	chr16:75499200-75519600	Weak transcription	Fetal Intestine Small	intestine
18	chr16:75499400-75505600	Weak transcription	Hela-S3	cervix
19	chr16:75501400-75506000	Weak transcription	HepG2	liver
20	chr16:75502400-75518200	Weak transcription	Aorta	Aorta
21	chr16:75504000-75506800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr16:75504400-75505400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr16:75505000-75505800	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr16:75505000-75507000	Enhancers	H1 Cell Line	embryonic stem cell
25	chr16:75505200-75505400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr16:75505200-75506000	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr16:75505400-75505800	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr16:75505400-75507200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr16:75505400-75512600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr16:75505600-75505800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr16:75505600-75506000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr16:75505600-75506000	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr16:75505600-75506200	Enhancers	Brain Cingulate Gyrus	brain
34	chr16:75505600-75506200	Enhancers	Brain Hippocampus Middle	brain
35	chr16:75505600-75506200	Enhancers	A549	lung
36	chr16:75505600-75506400	Enhancers	Hela-S3	cervix
37	chr16:75505600-75506800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr16:75505800-75506000	Enhancers	H9 Cell Line	embryonic stem cell
39	chr16:75505800-75506000	Enhancers	Primary B cells from peripheral blood	blood
40	chr16:75505800-75506000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
41	chr16:75505800-75506200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr16:75505800-75506200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr16:75505800-75506200	Enhancers	Fetal Heart	heart
44	chr16:75505800-75506200	Enhancers	Fetal Kidney	kidney
45	chr16:75505800-75506600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr16:75506000-75506200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr16:75506000-75506200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr16:75506000-75506200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr16:75506000-75506200	Enhancers	Fetal Brain Male	brain
50	chr16:75506000-75506200	Enhancers	HepG2	liver

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