Variant report

Variant	esv2751567
Chromosome Location	chr16:34437589-34757071
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1354)
CpG islands
(count:2626)
Chromatin interactive
region (count:4)
LncRNA
region (count:67)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1354 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

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	chr16:34625774-34626005	K562	blood:	n/a	n/a
3	ATF1	chr16:34643912-34644196	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	chr16:34589373-34589390	K562	blood:	n/a	n/a
7	ATF1	chr16:34574452-34574460	K562	blood:	n/a	n/a
8	BATF	chr16:34536693-34536965	GM12878	blood:	n/a	chr16:34536834-34536845
9	BATF	chr16:34539887-34540221	GM12878	blood:	n/a	chr16:34540044-34540055
10	BATF	chr16:34539865-34540180	GM12878	blood:	n/a	chr16:34540044-34540055
11	BATF	chr16:34731793-34732055	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
12	BATF	chr16:34731803-34731989	GM12878	blood:	n/a	chr16:34731883-34731894 chr16:34731915-34731926
13	BHLHE40	chr16:34726730-34726951	K562	blood:	n/a	chr16:34726896-34726912
14	BHLHE40	chr16:34741044-34741235	K562	blood:	n/a	n/a
15	BHLHE40	chr16:34625401-34626021	K562	blood:	n/a	n/a
16	BHLHE40	chr16:34625806-34626006	GM12878	blood:	n/a	n/a
17	BHLHE40	chr16:34721874-34721912	GM12878	blood:	n/a	n/a
18	BHLHE40	chr16:34732021-34732023	GM12878	blood:	n/a	n/a
19	BHLHE40	chr16:34647001-34647022	GM12878	blood:	n/a	n/a
20	BHLHE40	chr16:34740335-34740524	K562	blood:	n/a	n/a
21	BHLHE40	chr16:34745112-34745352	K562	blood:	n/a	chr16:34745242-34745251
22	BHLHE40	chr16:34598011-34598017	K562	blood:	n/a	n/a
23	BHLHE40	chr16:34745103-34745432	GM12878	blood:	n/a	chr16:34745242-34745251
24	BRCA1	chr16:34666402-34666616	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr16:34666658-34666728	GM12878	blood:	n/a	n/a
26	CBX3	chr16:34625799-34625988	K562	blood:	n/a	n/a
27	CEBPB	chr16:34486670-34487169	HepG2	liver:	n/a	chr16:34486713-34486730
28	CEBPB	chr16:34662346-34662546	IMR90	lung:	n/a	n/a
29	CEBPB	chr16:34532934-34533739	IMR90	lung:	n/a	chr16:34533406-34533417
30	CEBPB	chr16:34603901-34604333	A549	lung:	n/a	n/a
31	CEBPB	chr16:34562362-34562531	A549	lung:	n/a	n/a
32	CEBPB	chr16:34542362-34542582	HepG2	liver:	n/a	n/a
33	CEBPB	chr16:34533242-34533527	Hela-S3	cervix:	n/a	chr16:34533406-34533417
34	CEBPB	chr16:34530917-34531822	A549	lung:	n/a	n/a
35	CEBPB	chr16:34483631-34483649	K562	blood:	n/a	n/a
36	CEBPB	chr16:34539085-34539474	HepG2	liver:	n/a	n/a
37	CEBPB	chr16:34685136-34685387	IMR90	lung:	n/a	n/a
38	CEBPB	chr16:34643898-34644263	HepG2	liver:	n/a	n/a
39	CEBPB	chr16:34662373-34662658	HepG2	liver:	n/a	n/a
40	CEBPB	chr16:34597947-34598296	A549	lung:	n/a	n/a
41	CEBPB	chr16:34730735-34731108	IMR90	lung:	n/a	n/a
42	CEBPB	chr16:34600114-34600449	MCF-7	breast:	n/a	chr16:34600335-34600346
43	CEBPB	chr16:34597883-34598280	HepG2	liver:	n/a	n/a
44	CEBPB	chr16:34600051-34600514	ECC-1	luminal epithelium:	n/a	chr16:34600335-34600346
45	CEBPB	chr16:34532878-34533767	A549	lung:	n/a	chr16:34533406-34533417
46	CEBPB	chr16:34532914-34533612	ECC-1	luminal epithelium:	n/a	chr16:34533406-34533417
47	CEBPB	chr16:34536217-34536514	HepG2	liver:	n/a	n/a
48	CEBPB	chr16:34598601-34599065	A549	lung:	n/a	n/a
49	CEBPB	chr16:34730661-34731121	HepG2	liver:	n/a	n/a
50	CEBPB	chr16:34715391-34715623	K562	blood:	n/a	n/a

(count:2626 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:34649152-34649202	PrEC	prostate:	n/a
2	chr16:34740520-34740570	A549	lung:	n/a
3	chr16:34578819-34578869	SK-N-MC	brain:	n/a
4	chr16:34649152-34649202	PrEC	prostate:	n/a
5	chr16:34740520-34740570	A549	lung:	n/a
6	chr16:34578819-34578869	SK-N-MC	brain:	n/a
7	chr16:34579002-34579052	NB4	blood:	n/a
8	chr16:34712713-34712763	AG04449	skin:	fetal
9	chr16:34442090-34442140	HUVEC	blood vessel:	n/a
10	chr16:34439811-34439861	HPAEpiC	pulmonary alveolar:	n/a
11	chr16:34663929-34663979	HCM	heart:	n/a
12	chr16:34596583-34596633	SK-N-SH_RA	brain:	n/a
13	chr16:34659771-34659821	NT2-D1	testis:	n/a
14	chr16:34648955-34649005	AG09319	gingival:	n/a
15	chr16:34726856-34726906	NB4	blood:	n/a
16	chr16:34445785-34445835	AG10803	skin:	n/a
17	chr16:34587307-34587357	HCM	heart:	n/a
18	chr16:34583045-34583095	NT2-D1	testis:	n/a
19	chr16:34586837-34586887	PFSK-1	brain:	n/a
20	chr16:34625446-34625496	HCT-116	colon:	n/a
21	chr16:34741304-34741354	HCPEpiC	choroid plexus:	n/a
22	chr16:34586894-34586944	SK-N-SH	brain:	n/a
23	chr16:34583045-34583095	HepG2	liver:	n/a
24	chr16:34441787-34441837	BE2_C	brain:	n/a
25	chr16:34598029-34598079	HRPEpiC	eye:	n/a
26	chr16:34443120-34443170	AG09319	gingival:	n/a
27	chr16:34489904-34489954	HNPCEpiC	eye:	n/a
28	chr16:34586894-34586944	BE2_C	brain:	n/a
29	chr16:34740934-34740984	T-47D	breast:	n/a
30	chr16:34649152-34649202	HRE	kidney:	n/a
31	chr16:34741966-34742016	A549	lung:	n/a
32	chr16:34489904-34489954	AG04449	skin:	fetal
33	chr16:34442373-34442423	MCF10A-Er-Src	breast:	n/a
34	chr16:34583045-34583095	NHBE	bronchial:	n/a
35	chr16:34598029-34598079	SK-N-SH	brain:	n/a
36	chr16:34586837-34586887	SKMC	muscle:	n/a
37	chr16:34741304-34741354	MCF-7	breast:	n/a
38	chr16:34659771-34659821	IMR90	lung:	fetal
39	chr16:34456429-34456479	HCM	heart:	n/a
40	chr16:34648842-34648892	MCF10A-Er-Src	breast:	n/a
41	chr16:34737523-34737573	HCM	heart:	n/a
42	chr16:34712713-34712763	BJ	skin:	n/a
43	chr16:34443612-34443662	HCPEpiC	choroid plexus:	n/a
44	chr16:34663929-34663979	U87	brain:	n/a
45	chr16:34578819-34578869	NT2-D1	testis:	n/a
46	chr16:34490033-34490083	AG04449	skin:	fetal
47	chr16:34663929-34663979	PANC-1	pancreas:	n/a
48	chr16:34587307-34587357	HNPCEpiC	eye:	n/a
49	chr16:34740934-34740984	AG04450	lung:	fetal
50	chr16:34741304-34741354	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr16:34726782..34727382-chr16:34760283..34761051,3	MCF-7	breast:
2	chr16:34429328..34431681-chr16:34466203..34469132,2	K562	blood:
3	chr15:57024256..57026523-chr16:34752267..34754460,2	MCF-7	breast:
4	chr16:34422640..34423667-chr16:34625487..34626782,3	MCF-7	breast:

(count:67 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LINC00273-22	chr16:34570743-34570817	NONHSAT142179
2	lnc-CTD-2144E22.5.1-6	chr16:34615965-34616632	ENSG00000259841.2
3	lnc-LINC00273-27	chr16:34739459-34739785	NONHSAT142198
4	lnc-LINC00273-27	chr16:34740133-34740549	NONHSAT142200
5	lnc-LINC00273-28	chr16:34740963-34741308	NONHSAT142204
6	lnc-CTD-2144E22.5.1-29	chr16:34723608-34724583	NONHSAT142194
7	lnc-CTD-2144E22.5.1-5	chr16:34442330-34442392	ENSG00000260958.2
8	lnc-LINC00273-24	chr16:34640118-34640617	NONHSAT142186
9	lnc-LINC00273-27	chr16:34739472-34739785	NONHSAT142200
10	lnc-CTD-2144E22.5.1-31	chr16:34743025-34743136	NONHSAT142207
11	lnc-CTD-2144E22.5.1-6	chr16:34616795-34616969	NONHSAT142183
12	lnc-LINC00273-23	chr16:34619259-34619457	NONHSAT142185
13	lnc-CTD-2144E22.5.1-6	chr16:34597783-34597899	ENSG00000259841.2
14	lnc-LINC00273-7	chr16:34728125-34728568	ENSG00000261445.1
15	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	NONHSAT142183
16	lnc-CTD-2144E22.5.1-6	chr16:34617082-34617226	ENSG00000259841.2
17	lnc-LINC00273-27	chr16:34740697-34740840	NONHSAT142198
18	lnc-CTD-2144E22.5.1-5	chr16:34487252-34487506	ENSG00000260958.2
19	lnc-CTD-2144E22.5.1-4	chr16:34477761-34477848	XLOC_011699
20	lnc-CTD-2144E22.5.1-5	chr16:34483054-34483172	ENSG00000260958.2
21	lnc-LINC00273-22	chr16:34571082-34571260	NONHSAT142179
22	lnc-CTD-2144E22.5.1-31	chr16:34756490-34756676	NONHSAT142207
23	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	ENSG00000259841.2
24	lnc-LINC00273-24	chr16:34641562-34641720	NONHSAT142186
25	lnc-CTD-2144E22.5.1-6	chr16:34620250-34620420	NONHSAT142183
26	lnc-LINC00273-25	chr16:34712988-34713065	NONHSAT142192
27	lnc-LINC00273-7	chr16:34730748-34730828	ENSG00000261445.1
28	lnc-LINC00273-25	chr16:34713293-34713362	NONHSAT142192
29	lnc-LINC00273-27	chr16:34740697-34740833	ENSG00000260857.2
30	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	NONHSAT142183
31	lnc-CTD-2144E22.5.1-4	chr16:34478641-34479038	XLOC_011699
32	lnc-CTD-2144E22.5.1-6	chr16:34614340-34614458	ENSG00000259841.2
33	lnc-CTD-2144E22.5.1-6	chr16:34597787-34597899	NONHSAT142183
34	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	ENSG00000259841.2
35	lnc-LINC00273-7	chr16:34729913-34729959	ENSG00000261445.1
36	lnc-CTD-2144E22.5.1-5	chr16:34487609-34488020	ENSG00000260958.2
37	lnc-LINC00273-25	chr16:34712350-34712699	NONHSAT142191
38	lnc-CTD-2144E22.5.1-6	chr16:34616840-34616969	ENSG00000259841.2
39	lnc-CTD-2144E22.5.1-5	chr16:34471671-34474425	NONHSAT142170
40	lnc-CTD-2144E22.5.1-6	chr16:34610877-34611020	ENSG00000259841.2
41	lnc-LINC00273-18	chr16:34455954-34456419	NONHSAT142168
42	lnc-LINC00273-22	chr16:34569648-34570147	NONHSAT142179
43	lnc-CTD-2144E22.5.1-6	chr16:34597902-34598201	ENSG00000259841.2
44	lnc-LINC00273-24	chr16:34641253-34641302	NONHSAT142186
45	lnc-LINC00273-22	chr16:34570437-34570514	NONHSAT142179
46	lnc-LINC00273-27	chr16:34739464-34739785	ENSG00000260857.2
47	lnc-CTD-2144E22.5.1-6	chr16:34612943-34613184	NONHSAT142183
48	lnc-CTD-2144E22.5.1-5	chr16:34518127-34518517	ENSG00000260958.2
49	lnc-CTD-2144E22.5.1-6	chr16:34624074-34624955	ENSG00000259841.2
50	lnc-CTD-2144E22.5.1-5	chr16:34482858-34483251	NONHSAT142170

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
ENSG00000260857	TF binding region
ENSG00000261445	TF binding region
AGGF1P4	TF binding region
ENSG00000261350	TF binding region
ENSG00000214581	TF binding region
RARRES2P5	TF binding region
ENSG00000261274	TF binding region
RARRES2P7	TF binding region
RARRES2P6	TF binding region
ENSG00000260480	TF binding region
FGFR3P5	TF binding region
RARRES2P9	TF binding region
ENSG00000264479	TF binding region
ENSG00000269622	TF binding region
ENSG00000260427	TF binding region
ENSG00000260341	TF binding region
ENSG00000260598	TF binding region
ENSG00000260958	TF binding region
ENSG00000260153	TF binding region
ENSG00000259841	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
ENSG00000260857	CpG island
ENSG00000261445	CpG island
AGGF1P4	CpG island
ENSG00000261350	CpG island
ENSG00000214581	CpG island
RARRES2P5	CpG island
ENSG00000261274	CpG island
RARRES2P7	CpG island
RARRES2P6	CpG island
ENSG00000260480	CpG island
FGFR3P5	CpG island
RARRES2P9	CpG island
ENSG00000264479	CpG island
ENSG00000269622	CpG island
ENSG00000260427	CpG island
ENSG00000260341	CpG island
ENSG00000260598	CpG island
ENSG00000260958	CpG island
ENSG00000260153	CpG island
ENSG00000259841	CpG island
ENSG00000261711	CpG island
ENSG00000260680	CpG island
ENSG00000260846	CpG island
ENSG00000260073	chromatin interactions
ENSG00000137871	chromatin interactions
ENSG00000261398	chromatin interactions

Extended variants
information (count: 5792 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5792 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs748250	chr16:34437589-34437590	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564485522	chr16:34437617-34437618	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs576318846	chr16:34437618-34437619	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs541025275	chr16:34437631-34437632	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs559769634	chr16:34437684-34437685	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs543641894	chr16:34437707-34437708	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs562284931	chr16:34437738-34437739	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs60580821	chr16:34437768-34437769	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs369373796	chr16:34437772-34437773	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs559097979	chr16:34437775-34437776	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs532912346	chr16:34437811-34437812	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs189843444	chr16:34437854-34437855	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs60943089	chr16:34437855-34437856	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs530402743	chr16:34437856-34437857	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs537328205	chr16:34437896-34437897	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs7404459	chr16:34437898-34437899	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs372544081	chr16:34437910-34437911	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs193260909	chr16:34437987-34437988	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs7404474	chr16:34438015-34438016	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs554190775	chr16:34438070-34438071	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs572204025	chr16:34438079-34438080	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs369084964	chr16:34438119-34438120	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs539487242	chr16:34438155-34438156	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs185366996	chr16:34438164-34438165	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs576353955	chr16:34438217-34438218	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs543678849	chr16:34438221-34438222	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs562156967	chr16:34438223-34438224	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs574134900	chr16:34438225-34438226	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs540774554	chr16:34438267-34438268	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs189632997	chr16:34438297-34438298	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs1843651	chr16:34438299-34438300	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs545057999	chr16:34438332-34438333	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs563253434	chr16:34438333-34438334	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs572390974	chr16:34438404-34438405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546600266	chr16:34438437-34438438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552210341	chr16:34438607-34438608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530848787	chr16:34438662-34438663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549227118	chr16:34438720-34438721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7186710	chr16:34438740-34438741	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs528335139	chr16:34438758-34438759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373340818	chr16:34438782-34438783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565869283	chr16:34438798-34438799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs180790252	chr16:34438809-34438810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539523802	chr16:34438816-34438817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557749471	chr16:34438836-34438837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs151129286	chr16:34438863-34438864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185594557	chr16:34438910-34438911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555982589	chr16:34438956-34438957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574250203	chr16:34438989-34438990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568398520	chr16:34439017-34439018	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	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:174 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34437400-34438400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:34438400-34441200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr16:34441200-34442800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr16:34441400-34442600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
5	chr16:34442000-34443200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
6	chr16:34442200-34443000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
7	chr16:34442200-34443000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr16:34442600-34442800	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr16:34456000-34456800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr16:34456200-34456400	ZNF genes & repeats	Gastric	stomach
11	chr16:34456200-34456600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr16:34465600-34466200	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr16:34465600-34466200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
14	chr16:34466600-34472200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr16:34466800-34467000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr16:34466800-34469400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr16:34467000-34468200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr16:34467000-34470200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr16:34468200-34469400	ZNF genes & repeats	Brain Germinal Matrix	brain
20	chr16:34474800-34476000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr16:34478600-34479000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
22	chr16:34480400-34481000	Enhancers	Adipose Nuclei	Adipose
23	chr16:34489600-34490400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
24	chr16:34489600-34490800	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr16:34489800-34490200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
26	chr16:34492800-34493400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
27	chr16:34505000-34507800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
28	chr16:34517800-34518400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
29	chr16:34531200-34534000	Enhancers	HMEC	breast
30	chr16:34531400-34534200	Enhancers	NHEK	skin
31	chr16:34531800-34532400	Active TSS	Fetal Heart	heart
32	chr16:34533800-34534000	Enhancers	Esophagus	oesophagus
33	chr16:34534200-34538800	Weak transcription	NHEK	skin
34	chr16:34535000-34537200	Weak transcription	Esophagus	oesophagus
35	chr16:34537000-34537400	ZNF genes & repeats	Fetal Heart	heart
36	chr16:34537200-34537400	Enhancers	Esophagus	oesophagus
37	chr16:34537400-34542200	Weak transcription	Esophagus	oesophagus
38	chr16:34538000-34538800	Active TSS	Fetal Heart	heart
39	chr16:34538600-34544000	Enhancers	HMEC	breast
40	chr16:34538800-34539600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
41	chr16:34538800-34543800	Enhancers	NHEK	skin
42	chr16:34539400-34539800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr16:34539800-34540200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr16:34540200-34540400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr16:34540400-34542800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr16:34542200-34543000	Enhancers	Esophagus	oesophagus
47	chr16:34542200-34546800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
48	chr16:34542800-34543000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr16:34542800-34543600	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr16:34543000-34543400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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