Variant report

Variant	nsv1057967
Chromosome Location	chr16:34479681-34784591
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1335)
CpG islands
(count:2320)
Chromatin interactive
region (count:5)
LncRNA
region (count:64)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1335 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr16:34573796-34574082	K562	blood:	n/a	n/a
2	ATF1	chr16:34574452-34574460	K562	blood:	n/a	n/a
3	ATF1	chr16:34589373-34589390	K562	blood:	n/a	n/a
4	ATF1	chr16:34486728-34487212	K562	blood:	n/a	n/a
5	ATF1	chr16:34715569-34715609	K562	blood:	n/a	n/a
6	ATF1	chr16:34625774-34626005	K562	blood:	n/a	n/a
7	ATF1	chr16:34643912-34644196	K562	blood:	n/a	n/a
8	ATF1	chr16:34765990-34765998	K562	blood:	n/a	n/a
9	ATF1	chr16:34768061-34768441	K562	blood:	n/a	n/a
10	BATF	chr16:34731793-34732055	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
11	BATF	chr16:34536693-34536965	GM12878	blood:	n/a	chr16:34536834-34536845
12	BATF	chr16:34539887-34540221	GM12878	blood:	n/a	chr16:34540044-34540055
13	BATF	chr16:34539865-34540180	GM12878	blood:	n/a	chr16:34540044-34540055
14	BATF	chr16:34731803-34731989	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
15	BHLHE40	chr16:34721874-34721912	GM12878	blood:	n/a	n/a
16	BHLHE40	chr16:34745112-34745352	K562	blood:	n/a	chr16:34745242-34745251
17	BHLHE40	chr16:34647001-34647022	GM12878	blood:	n/a	n/a
18	BHLHE40	chr16:34741044-34741235	K562	blood:	n/a	n/a
19	BHLHE40	chr16:34625401-34626021	K562	blood:	n/a	n/a
20	BHLHE40	chr16:34740335-34740524	K562	blood:	n/a	n/a
21	BHLHE40	chr16:34745103-34745432	GM12878	blood:	n/a	chr16:34745242-34745251
22	BHLHE40	chr16:34598011-34598017	K562	blood:	n/a	n/a
23	BHLHE40	chr16:34732021-34732023	GM12878	blood:	n/a	n/a
24	BHLHE40	chr16:34726730-34726951	K562	blood:	n/a	chr16:34726896-34726912
25	BHLHE40	chr16:34625806-34626006	GM12878	blood:	n/a	n/a
26	BRCA1	chr16:34666402-34666616	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr16:34666658-34666728	GM12878	blood:	n/a	n/a
28	CBX3	chr16:34625799-34625988	K562	blood:	n/a	n/a
29	CEBPB	chr16:34573739-34574089	IMR90	lung:	n/a	chr16:34573875-34573886
30	CEBPB	chr16:34537186-34537555	IMR90	lung:	n/a	n/a
31	CEBPB	chr16:34730731-34731119	A549	lung:	n/a	n/a
32	CEBPB	chr16:34514068-34514216	HepG2	liver:	n/a	n/a
33	CEBPB	chr16:34715391-34715623	K562	blood:	n/a	n/a
34	CEBPB	chr16:34486708-34487148	A549	lung:	n/a	chr16:34486713-34486730
35	CEBPB	chr16:34600160-34600470	ECC-1	luminal epithelium:	n/a	chr16:34600335-34600346
36	CEBPB	chr16:34603883-34604326	HepG2	liver:	n/a	n/a
37	CEBPB	chr16:34533242-34533527	Hela-S3	cervix:	n/a	chr16:34533406-34533417
38	CEBPB	chr16:34611205-34611346	A549	lung:	n/a	chr16:34611274-34611285
39	CEBPB	chr16:34530917-34531822	A549	lung:	n/a	n/a
40	CEBPB	chr16:34643966-34644271	IMR90	lung:	n/a	n/a
41	CEBPB	chr16:34486751-34487148	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr16:34598584-34598949	HepG2	liver:	n/a	n/a
43	CEBPB	chr16:34532926-34533600	ECC-1	luminal epithelium:	n/a	chr16:34533406-34533417
44	CEBPB	chr16:34535207-34535347	HepG2	liver:	n/a	n/a
45	CEBPB	chr16:34768061-34768461	IMR90	lung:	n/a	n/a
46	CEBPB	chr16:34731698-34731782	HepG2	liver:	n/a	n/a
47	CEBPB	chr16:34662346-34662546	IMR90	lung:	n/a	n/a
48	CEBPB	chr16:34540548-34540632	IMR90	lung:	n/a	n/a
49	CEBPB	chr16:34643905-34644193	A549	lung:	n/a	n/a
50	CEBPB	chr16:34532934-34533739	IMR90	lung:	n/a	chr16:34533406-34533417

(count:2320 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34489904-34489954	SKMC	muscle:	n/a
2	chr16:34587307-34587357	GM12891	blood:	n/a
3	chr16:34489904-34489954	SKMC	muscle:	n/a
4	chr16:34587307-34587357	GM12891	blood:	n/a
5	chr16:34777881-34777931	GM06990	blood:	n/a
6	chr16:34586837-34586887	ECC-1	luminal epithelium:	n/a
7	chr16:34741251-34741301	GM12878	blood:	n/a
8	chr16:34625446-34625496	HPAEpiC	pulmonary alveolar:	n/a
9	chr16:34777682-34777732	SK-N-SH	brain:	n/a
10	chr16:34596941-34596991	SK-N-MC	brain:	n/a
11	chr16:34712713-34712763	NHDF-neo	bronchial:	n/a
12	chr16:34726734-34726784	HepG2	liver:	n/a
13	chr16:34726734-34726784	CMK	blood:	n/a
14	chr16:34741304-34741354	NT2-D1	testis:	n/a
15	chr16:34726734-34726784	Hepatocyte	liver:	n/a
16	chr16:34648842-34648892	HNPCEpiC	eye:	n/a
17	chr16:34598029-34598079	NH-A	brain:	n/a
18	chr16:34740520-34740570	GM12892	blood:	n/a
19	chr16:34586837-34586887	LNCaP	prostate:	n/a
20	chr16:34740934-34740984	HPAEpiC	pulmonary alveolar:	n/a
21	chr16:34579002-34579052	CMK	blood:	n/a
22	chr16:34587120-34587170	K562	blood:	n/a
23	chr16:34490033-34490083	CMK	blood:	n/a
24	chr16:34596941-34596991	HUVEC	blood vessel:	n/a
25	chr16:34741966-34742016	HRCEpiC	kidney:	n/a
26	chr16:34578819-34578869	SK-N-SH	brain:	n/a
27	chr16:34781451-34781501	BE2_C	brain:	n/a
28	chr16:34737523-34737573	NT2-D1	testis:	n/a
29	chr16:34741251-34741301	HRCEpiC	kidney:	n/a
30	chr16:34777881-34777931	SK-N-MC	brain:	n/a
31	chr16:34649152-34649202	NHBE	bronchial:	n/a
32	chr16:34741251-34741301	AoSMC	blood vessel:	n/a
33	chr16:34659664-34659714	IMR90	lung:	fetal
34	chr16:34777881-34777931	HPAEpiC	pulmonary alveolar:	n/a
35	chr16:34659771-34659821	HAEpiC	amniotic membrane:	n/a
36	chr16:34760531-34760581	IMR90	lung:	fetal
37	chr16:34777682-34777732	AG04449	skin:	fetal
38	chr16:34649152-34649202	SK-N-SH_RA	brain:	n/a
39	chr16:34596583-34596633	HCM	heart:	n/a
40	chr16:34596941-34596991	RPTEC	kidney:	n/a
41	chr16:34740520-34740570	HMEC	breast:	n/a
42	chr16:34648842-34648892	AG04449	skin:	fetal
43	chr16:34586894-34586944	AG09309	skin:	n/a
44	chr16:34726734-34726784	AG09319	gingival:	n/a
45	chr16:34740934-34740984	AG04450	lung:	fetal
46	chr16:34625446-34625496	SK-N-SH	brain:	n/a
47	chr16:34586894-34586944	NHDF-neo	bronchial:	n/a
48	chr16:34490033-34490083	LNCaP	prostate:	n/a
49	chr16:34726856-34726906	AoSMC	blood vessel:	n/a
50	chr16:34741493-34741543	GM19239	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:57024256..57026523-chr16:34752267..34754460,2	MCF-7	breast:
2	chr16:34726782..34727382-chr16:34760283..34761051,3	MCF-7	breast:
3	chr16:34726782..34727382-chr16:34760283..34761051,3	MCF-7	breast:
4	chr16:34422640..34423667-chr16:34625487..34626782,3	MCF-7	breast:
5	chr15:56788863..56789371-chr16:34759996..34760825,2	MCF-7	breast:

(count:64 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	NONHSAT142183
2	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616969	NONHSAT142183
3	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
4	lnc-CTD-2144E22.5.1-5	chr16:34487609-34488020	ENSG00000260958.2
5	lnc-CTD-2144E22.5.1-6	chr16:34617082-34617226	ENSG00000259841.2
6	lnc-LINC00273-27	chr16:34739464-34739785	ENSG00000260857.2
7	lnc-CTD-2144E22.5.1-6	chr16:34616840-34616969	ENSG00000259841.2
8	lnc-LINC00273-25	chr16:34712350-34712699	NONHSAT142191
9	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	NONHSAT142183
10	lnc-LINC00273-27	chr16:34739472-34739785	NONHSAT142200
11	lnc-LINC00273-27	chr16:34740697-34740840	NONHSAT142198
12	lnc-LINC00273-25	chr16:34714529-34714852	NONHSAT142191
13	lnc-CTD-2144E22.5.1-6	chr16:34615965-34616632	ENSG00000259841.2
14	lnc-LINC00273-25	chr16:34713636-34713735	NONHSAT142191
15	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616837	ENSG00000259841.2
16	lnc-LINC00273-24	chr16:34641562-34641720	NONHSAT142186
17	lnc-LINC00273-22	chr16:34570743-34570817	NONHSAT142179
18	lnc-LINC00273-23	chr16:34619259-34619457	NONHSAT142185
19	lnc-LINC00273-7	chr16:34729913-34729959	ENSG00000261445.1
20	lnc-CTD-2144E22.5.1-18	chr16:34493001-34494000	NONHSAT142176
21	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
22	lnc-LINC00273-24	chr16:34640118-34640617	NONHSAT142186
23	lnc-LINC00273-27	chr16:34740133-34740549	NONHSAT142200
24	lnc-LINC00273-7	chr16:34728125-34728568	ENSG00000261445.1
25	lnc-LINC00273-24	chr16:34640930-34641001	NONHSAT142186
26	lnc-CTD-2144E22.5.1-6	chr16:34597787-34597899	NONHSAT142183
27	lnc-CTD-2144E22.5.1-24	chr16:34581756-34582668	NONHSAT142180
28	lnc-LINC00273-23	chr16:34618515-34618930	NONHSAT142185
29	lnc-LINC00273-22	chr16:34570437-34570514	NONHSAT142179
30	lnc-LINC00273-8	chr16:34766012-34766124	XLOC_011927
31	lnc-LINC00273-25	chr16:34713636-34713810	NONHSAT142192
32	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	ENSG00000259841.2
33	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	NONHSAT142183
34	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487411	NONHSAT142170
35	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	NONHSAT142183
36	lnc-CTD-2144E22.5.1-31	chr16:34751386-34751515	NONHSAT142207
37	lnc-LINC00273-28	chr16:34740963-34741308	NONHSAT142204
38	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
39	lnc-LINC00273-25	chr16:34713293-34713362	NONHSAT142192
40	lnc-LINC00273-27	chr16:34740697-34740833	ENSG00000260857.2
41	lnc-CTD-2144E22.5.1-5	chr16:34518127-34518517	ENSG00000260958.2
42	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
43	lnc-LINC00273-27	chr16:34739459-34739785	NONHSAT142198
44	lnc-LINC00273-22	chr16:34569648-34570147	NONHSAT142179
45	lnc-CTD-2144E22.5.1-6	chr16:34597902-34598201	ENSG00000259841.2
46	lnc-LINC00273-24	chr16:34641253-34641302	NONHSAT142186
47	lnc-LINC00273-8	chr16:34765218-34765705	XLOC_011927
48	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487506	ENSG00000260958.2
49	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
50	lnc-CTD-2144E22.5.1-5	chr16:34483054-34483172	ENSG00000260958.2

No data

Variant related genes	Relation type
ENSG00000259836	TF binding region
ENSG00000259897	TF binding region
ENSG00000221532	TF binding region
ENSG00000261752	TF binding region
ENSG00000260291	TF binding region
ENSG00000261299	TF binding region
ENSG00000261733	TF binding region
ENSG00000260857	TF binding region
ENSG00000261445	TF binding region
AGGF1P4	TF binding region
ENSG00000261350	TF binding region
ENSG00000214581	TF binding region
RARRES2P7	TF binding region
RARRES2P6	TF binding region
ENSG00000260480	TF binding region
RARRES2P9	TF binding region
ENSG00000261046	TF binding region
ENSG00000269622	TF binding region
ENSG00000260427	TF binding region
ENSG00000260341	TF binding region
ENSG00000260994	TF binding region
ENSG00000260598	TF binding region
ENSG00000260153	TF binding region
ENSG00000259841	TF binding region
RARRES2P8	TF binding region
ENSG00000261711	TF binding region
ENSG00000260680	TF binding region
ENSG00000260846	TF binding region
ENSG00000259836	CpG island
ENSG00000259897	CpG island
ENSG00000221532	CpG island
ENSG00000261752	CpG island
ENSG00000260291	CpG island
ENSG00000261299	CpG island
ENSG00000261733	CpG island
ENSG00000260857	CpG island
ENSG00000261445	CpG island
AGGF1P4	CpG island
ENSG00000261350	CpG island
ENSG00000214581	CpG island
RARRES2P7	CpG island
RARRES2P6	CpG island
ENSG00000260480	CpG island
RARRES2P9	CpG island
ENSG00000261046	CpG island
ENSG00000269622	CpG island
ENSG00000260427	CpG island
ENSG00000260341	CpG island
ENSG00000260994	CpG island
ENSG00000260598	CpG island
ENSG00000260153	CpG island
ENSG00000259841	CpG island
RARRES2P8	CpG island
ENSG00000261711	CpG island
ENSG00000260680	CpG island
ENSG00000260846	CpG island
ENSG00000137871	chromatin interactions
ZNF407	miRNA target sites
ZNF451	miRNA target sites

Extended variants
information (count: 5571 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5571 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143699922	chr16:34480407-34480408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs528086105	chr16:34480428-34480429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540183850	chr16:34480483-34480484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs72485962	chr16:34480515-34480516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs148123182	chr16:34480522-34480523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187671192	chr16:34480546-34480547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs35114919	chr16:34480553-34480554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550704680	chr16:34480574-34480575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570172380	chr16:34480592-34480593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141823547	chr16:34480599-34480600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192883853	chr16:34480628-34480629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34700380	chr16:34480652-34480653	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs567693807	chr16:34480734-34480735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535003699	chr16:34480756-34480757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112019904	chr16:34480772-34480773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185823710	chr16:34480780-34480781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188677254	chr16:34480805-34480806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs370902042	chr16:34480813-34480814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540834610	chr16:34480815-34480816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557089141	chr16:34480844-34480845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575422609	chr16:34480853-34480854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542358929	chr16:34480861-34480862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371888749	chr16:34480886-34480887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs375847859	chr16:34480950-34480951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146042920	chr16:34482083-34482084	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs11380923	chr16:34482146-34482147	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs397825826	chr16:34482157-34482158	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs72485963	chr16:34482158-34482159	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs199748071	chr16:34482161-34482162	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs144233613	chr16:34482185-34482186	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs183963833	chr16:34482192-34482193	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs72485964	chr16:34482201-34482202	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs569171922	chr16:34482223-34482224	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs542052512	chr16:34482909-34482910	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs560333015	chr16:34482933-34482934	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs539428596	chr16:34482943-34482944	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs144477088	chr16:34482969-34482970	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs192017253	chr16:34482976-34482977	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs148434331	chr16:34483011-34483012	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs532384859	chr16:34483091-34483092	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs551742645	chr16:34483114-34483115	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs567178069	chr16:34483115-34483116	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs374534472	chr16:34483139-34483140	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs534358480	chr16:34483142-34483143	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs550532535	chr16:34483189-34483190	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs562845830	chr16:34483200-34483201	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs117552212	chr16:34483243-34483244	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs537847150	chr16:34483515-34483516	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs556157578	chr16:34483518-34483519	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs10871269	chr16:34483547-34483548	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
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
Ductal carcinoma	22052326	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Disorders of sex development	21048976	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18194544	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	20967226	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19214233	CNVD
early-passage human iPS cells	21368824	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Rett syndrome	21593744	CNVD
Myelofibrosis	22110671	CNVD
Autism	19287141	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Autism	18414403	CNVD

Chromatin state (count:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34480400-34481000	Enhancers	Adipose Nuclei	Adipose
2	chr16:34489600-34490400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
3	chr16:34489600-34490800	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr16:34489800-34490200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
5	chr16:34492800-34493400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
6	chr16:34505000-34507800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
7	chr16:34517800-34518400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
8	chr16:34531200-34534000	Enhancers	HMEC	breast
9	chr16:34531400-34534200	Enhancers	NHEK	skin
10	chr16:34531800-34532400	Active TSS	Fetal Heart	heart
11	chr16:34533800-34534000	Enhancers	Esophagus	oesophagus
12	chr16:34534200-34538800	Weak transcription	NHEK	skin
13	chr16:34535000-34537200	Weak transcription	Esophagus	oesophagus
14	chr16:34537000-34537400	ZNF genes & repeats	Fetal Heart	heart
15	chr16:34537200-34537400	Enhancers	Esophagus	oesophagus
16	chr16:34537400-34542200	Weak transcription	Esophagus	oesophagus
17	chr16:34538000-34538800	Active TSS	Fetal Heart	heart
18	chr16:34538600-34544000	Enhancers	HMEC	breast
19	chr16:34538800-34539600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
20	chr16:34538800-34543800	Enhancers	NHEK	skin
21	chr16:34539400-34539800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr16:34539800-34540200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr16:34540200-34540400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr16:34540400-34542800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr16:34542200-34543000	Enhancers	Esophagus	oesophagus
26	chr16:34542200-34546800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr16:34542800-34543000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr16:34542800-34543600	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr16:34543000-34543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr16:34543200-34544000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr16:34543400-34543800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr16:34543600-34543800	Enhancers	Esophagus	oesophagus
33	chr16:34545200-34552000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
34	chr16:34545400-34546800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr16:34545400-34552000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
36	chr16:34546200-34546400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
37	chr16:34549000-34549200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
38	chr16:34550000-34550200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
39	chr16:34553800-34554800	Enhancers	Brain Hippocampus Middle	brain
40	chr16:34554200-34554600	Enhancers	Brain Angular Gyrus	brain
41	chr16:34554200-34554600	Enhancers	Brain Cingulate Gyrus	brain
42	chr16:34554200-34554600	Enhancers	Brain Substantia Nigra	brain
43	chr16:34562400-34562800	Active TSS	Fetal Heart	heart
44	chr16:34571600-34577800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
45	chr16:34578400-34579200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr16:34578600-34579000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr16:34578800-34579000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr16:34578800-34579200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr16:34586600-34587000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
50	chr16:34586600-34587000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

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