Variant report

Variant	nsv869477
Chromosome Location	chrY:20063342-20961810
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1526)
CpG islands
(count:491)
Chromatin interactive
region (count:0)
LncRNA
region (count:75)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chrY:20812659-20812938	A549	lung:	n/a	n/a
2	CTCF	chrY:20831700-20831850	HCM	heart:	n/a	n/a
3	CTCF	chrY:20831720-20831870	NHLF	lung:	n/a	n/a
4	CTCF	chrY:20488475-20488701	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chrY:20862420-20862484	LNCaP	prostate:	n/a	n/a
6	CTCF	chrY:20831729-20831969	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chrY:20103445-20103493	HepG2	liver:	n/a	n/a
8	CTCF	chrY:20292637-20292677	Medullo	brain:	n/a	n/a
9	CTCF	chrY:20338170-20338243	GM19239	blood:	n/a	n/a
10	CTCF	chrY:20488462-20488773	HUVEC	blood vessel:	n/a	n/a
11	CTCF	chrY:20247840-20248114	A549	lung:	n/a	n/a
12	CTCF	chrY:20622380-20622600	GM10266	blood:	n/a	n/a
13	CTCF	chrY:20851456-20851497	GM10248	blood:	n/a	n/a
14	CTCF	chrY:20556034-20556226	LNCaP	prostate:	n/a	n/a
15	CTCF	chrY:20831704-20831989	Medullo	brain:	n/a	n/a
16	CTCF	chrY:20308428-20308675	Medullo	brain:	n/a	n/a
17	CTCF	chrY:20331720-20331788	GM10248	blood:	n/a	n/a
18	CTCF	chrY:20344137-20344225	LNCaP	prostate:	n/a	n/a
19	CTCF	chrY:20607806-20608110	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chrY:20274498-20274535	GM10266	blood:	n/a	n/a
21	CTCF	chrY:20247879-20247880	Medullo	brain:	n/a	n/a
22	CTCF	chrY:20399726-20399837	Medullo	brain:	n/a	n/a
23	CTCF	chrY:20399662-20399738	GM19239	blood:	n/a	n/a
24	CTCF	chrY:20831780-20831930	HepG2	liver:	n/a	n/a
25	CTCF	chrY:20674243-20674266	ProgFib	skin:	n/a	n/a
26	CTCF	chrY:20455118-20455164	GM20000	blood:	n/a	n/a
27	CTCF	chrY:20373034-20373112	GM10266	blood:	n/a	n/a
28	CTCF	chrY:20872126-20872184	Medullo	brain:	n/a	n/a
29	CTCF	chrY:20227167-20227226	GM20000	blood:	n/a	n/a
30	CTCF	chrY:20831820-20831970	GM12871	blood:	n/a	n/a
31	CTCF	chrY:20586197-20586462	GM19239	blood:	n/a	n/a
32	CTCF	chrY:20607834-20608134	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chrY:20873707-20873924	LNCaP	prostate:	n/a	n/a
34	CTCF	chrY:20117811-20117875	GM10266	blood:	n/a	n/a
35	CTCF	chrY:20292220-20292225	A549	lung:	n/a	n/a
36	CTCF	chrY:20777791-20777989	A549	lung:	n/a	n/a
37	CTCF	chrY:20500466-20500499	GM10266	blood:	n/a	n/a
38	CTCF	chrY:20793661-20793717	ProgFib	skin:	n/a	n/a
39	CTCF	chrY:20773890-20773981	LNCaP	prostate:	n/a	n/a
40	CTCF	chrY:20621100-20621415	Medullo	brain:	n/a	n/a
41	CTCF	chrY:20242093-20242329	Medullo	brain:	n/a	n/a
42	CTCF	chrY:20914878-20914927	LNCaP	prostate:	n/a	n/a
43	CTCF	chrY:20375819-20375870	HepG2	liver:	n/a	n/a
44	CTCF	chrY:20556014-20556205	HepG2	liver:	n/a	n/a
45	CTCF	chrY:20622143-20622182	GM10266	blood:	n/a	n/a
46	CTCF	chrY:20204981-20205077	LNCaP	prostate:	n/a	n/a
47	CTCF	chrY:20267792-20267841	GM20000	blood:	n/a	n/a
48	CTCF	chrY:20621916-20621966	GM10248	blood:	n/a	n/a
49	CTCF	chrY:20622399-20622570	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chrY:20504512-20504649	GM12891	blood:	n/a	n/a

(count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrY:20508362-20508412	HCM	heart:	n/a
2	chrY:20508275-20508325	HepG2	liver:	n/a
3	chrY:20488280-20488330	T-47D	breast:	n/a
4	chrY:20508362-20508412	HCM	heart:	n/a
5	chrY:20508275-20508325	HepG2	liver:	n/a
6	chrY:20488280-20488330	T-47D	breast:	n/a
7	chrY:20508275-20508325	HRPEpiC	eye:	n/a
8	chrY:20508275-20508325	HEK293	kidney:	embryo
9	chrY:20736147-20736197	PrEC	prostate:	n/a
10	chrY:20488293-20488343	GM12891	blood:	n/a
11	chrY:20748782-20748832	HNPCEpiC	eye:	n/a
12	chrY:20736147-20736197	GM12891	blood:	n/a
13	chrY:20736147-20736197	Hepatocyte	liver:	n/a
14	chrY:20508362-20508412	A549	lung:	n/a
15	chrY:20488280-20488330	GM19239	blood:	n/a
16	chrY:20748782-20748832	AoSMC	blood vessel:	n/a
17	chrY:20488280-20488330	CMK	blood:	n/a
18	chrY:20748782-20748832	AG09319	gingival:	n/a
19	chrY:20501241-20501291	ECC-1	luminal epithelium:	n/a
20	chrY:20508275-20508325	AoSMC	blood vessel:	n/a
21	chrY:20488269-20488319	AG04450	lung:	fetal
22	chrY:20748782-20748832	AG04449	skin:	fetal
23	chrY:20736147-20736197	HIPEpiC	eye:	n/a
24	chrY:20748782-20748832	BJ	skin:	n/a
25	chrY:20748782-20748832	Jurkat	blood:	n/a
26	chrY:20736147-20736197	RPTEC	kidney:	n/a
27	chrY:20488280-20488330	HUVEC	blood vessel:	n/a
28	chrY:20508275-20508325	HCPEpiC	choroid plexus:	n/a
29	chrY:20508362-20508412	HL-60	blood:	n/a
30	chrY:20501241-20501291	HPAEpiC	pulmonary alveolar:	n/a
31	chrY:20508362-20508412	AG09309	skin:	n/a
32	chrY:20501241-20501291	CMK	blood:	n/a
33	chrY:20488280-20488330	K562	blood:	n/a
34	chrY:20501241-20501291	A549	lung:	n/a
35	chrY:20488293-20488343	HAEpiC	amniotic membrane:	n/a
36	chrY:20488280-20488330	SK-N-SH_RA	brain:	n/a
37	chrY:20501241-20501291	Caco-2	colon:	n/a
38	chrY:20488269-20488319	ProgFib	skin:	n/a
39	chrY:20488269-20488319	HCM	heart:	n/a
40	chrY:20748782-20748832	HCT-116	colon:	n/a
41	chrY:20736147-20736197	HCPEpiC	choroid plexus:	n/a
42	chrY:20508362-20508412	SK-N-SH_RA	brain:	n/a
43	chrY:20748782-20748832	GM12891	blood:	n/a
44	chrY:20508275-20508325	GM12891	blood:	n/a
45	chrY:20508362-20508412	HAEpiC	amniotic membrane:	n/a
46	chrY:20488280-20488330	AG04450	lung:	fetal
47	chrY:20748782-20748832	HL-60	blood:	n/a
48	chrY:20488293-20488343	HCM	heart:	n/a
49	chrY:20488293-20488343	SKMC	muscle:	n/a
50	chrY:20508362-20508412	AG09319	gingival:	n/a

No data

(count:75 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HSFY2-5	chrY:20938165-20938289	NONHSAT139595
2	lnc-HSFY1-8	chrY:20648080-20648236	NONHSAT139575
3	lnc-HSFY2-4	chrY:20553364-20553457	ENSG00000226362
4	lnc-HSFY2-4	chrY:20551156-20551882	ENSG00000226362
5	lnc-HSFY1-5	chrY:20691244-20691509	NONHSAT139580
6	lnc-CDY2A-2	chrY:20102823-20102907	NONHSAT139556
7	lnc-HSFY2-4	chrY:20552880-20553089	ENSG00000226362.2
8	lnc-HSFY1-2	chrY:20899941-20901083	ENSG00000131009.4
9	lnc-HSFY2-4	chrY:20553567-20553737	ENSG00000226362.2
10	lnc-HSFY1-6	chrY:20670463-20670954	NONHSAT139579
11	lnc-CDY2B-13	chrY:20438493-20438534	NONHSAT139566
12	lnc-HSFY2-2	chrY:20750492-20750592	ENSG00000131007.5
13	lnc-CDY2A-6	chrY:20278413-20278550	NONHSAT139560
14	lnc-HSFY2-2	chrY:20749298-20749434	ENSG00000131007.5
15	lnc-CDY2A-6	chrY:20279486-20279581	NONHSAT139560
16	lnc-HSFY2-5	chrY:20938702-20939447	NONHSAT139595
17	lnc-HSFY2-2	chrY:20743092-20744234	ENSG00000131007.5
18	lnc-HSFY1-10	chrY:20949636-20949966	NONHSAT139596
19	lnc-HSFY2-2	chrY:20749298-20749434	ENSG00000131007.5
20	lnc-CDY2B-9	chrY:20285560-20285685	NONHSAT139562
21	lnc-HSFY2-4	chrY:20566130-20566179	ENSG00000226362
22	lnc-CDY2A-2	chrY:20096229-20096449	NONHSAT139556
23	lnc-HSFY2-9	chrY:20694212-20694542	NONHSAT139581
24	lnc-CDY2B-13	chrY:20438909-20439381	NONHSAT139566
25	lnc-HSFY1-2	chrY:20893577-20893683	NONHSAT139592
26	lnc-CDY2B-5	chrY:20107081-20107289	NONHSAT139557
27	lnc-HSFY2-4	chrY:20552399-20552586	ENSG00000226362
28	lnc-HSFY1-4	chrY:20702866-20702995	NONHSAT139582
29	lnc-CDY2B-5	chrY:20108912-20109132	NONHSAT139557
30	lnc-HSFY2-2	chrY:20750017-20750130	ENSG00000131007.5
31	lnc-HSFY2-4	chrY:20566775-20566932	ENSG00000226362
32	lnc-HSFY1-2	chrY:20894045-20894158	NONHSAT139592
33	lnc-HSFY2-2	chrY:20750492-20750598	ENSG00000131007.5
34	lnc-HSFY2-4	chrY:20566130-20566179	ENSG00000226362.2
35	lnc-HSFY2-2	chrY:20743092-20744234	ENSG00000131007.5
36	lnc-HSFY2-4	chrY:20566775-20566932	ENSG00000226362.2
37	lnc-CDY2A-3	chrY:20063469-20063633	NONHSAT139555
38	lnc-CDY2A-3	chrY:20063942-20065380	NONHSAT139555
39	lnc-HSFY1-2	chrY:20894045-20894158	ENSG00000131009.4
40	lnc-HSFY2-2	chrY:20750017-20750130	ENSG00000131007.5
41	lnc-HSFY1-4	chrY:20704732-20705478	NONHSAT139582
42	lnc-HSFY2-4	chrY:20554672-20554800	ENSG00000226362
43	lnc-CDY2B-9	chrY:20283081-20283269	NONHSAT139562
44	lnc-HSFY2-11	chrY:20654896-20654988	NONHSAT139577
45	lnc-HSFY2-4	chrY:20551965-20552186	ENSG00000226362
46	lnc-HSFY2-11	chrY:20655067-20655191	NONHSAT139577
47	lnc-HSFY1-2	chrY:20891768-20891909	ENSG00000131009.4
48	lnc-HSFY1-2	chrY:20894741-20894877	ENSG00000131009.4
49	lnc-CDY2A-4	chrY:20230369-20230696	NONHSAT139558
50	lnc-HSFY1-2	chrY:20894741-20894877	NONHSAT139592

No data

Variant related genes	Relation type
OFD1P6Y	TF binding region
TTTY9B	TF binding region
USP9YP15	TF binding region
XKRYP1	TF binding region
TRAPPC2P8	TF binding region
CDY9P	TF binding region
PRYP2	TF binding region
USP9YP5	TF binding region
TAF9P2	TF binding region
ENSG00000244646	TF binding region
USP9YP16	TF binding region
USP9YP34	TF binding region
TCEB1P7	TF binding region
RNU1-48P	TF binding region
CDY7P	TF binding region
RNU1-95P	TF binding region
USP9YP2	TF binding region
RNA5SP522	TF binding region
USP9YP1	TF binding region
CLUHP2	TF binding region
OFD1P2Y	TF binding region
TCEB1P14	TF binding region
OFD1P4Y	TF binding region
ACTG1P11	TF binding region
FAM41AY2	TF binding region
USP9YP14	TF binding region
PRYP6	TF binding region
HSFY1	TF binding region
USP9YP32	TF binding region
TCEB1P12	TF binding region
TUBB1P1	TF binding region
CDY2A	TF binding region
TRAPPC2P7	TF binding region
RNA5SP523	TF binding region
CDY8P	TF binding region
ENSG00000251510	TF binding region
FAM224A	TF binding region
OFD1P5Y	TF binding region
RAB9AP4	TF binding region
ENSG00000252439	TF binding region
TCEB1P26	TF binding region
PRYP5	TF binding region
HSFY2	TF binding region
GPM6BP2	TF binding region
TCEB1P13	TF binding region
GPM6BP1	TF binding region
OFD1P6Y	CpG island
TTTY9B	CpG island
USP9YP15	CpG island
XKRYP1	CpG island
TRAPPC2P8	CpG island
CDY9P	CpG island
PRYP2	CpG island
USP9YP5	CpG island
TAF9P2	CpG island
ENSG00000244646	CpG island
USP9YP16	CpG island
USP9YP34	CpG island
TCEB1P7	CpG island
RNU1-48P	CpG island
CDY7P	CpG island
RNU1-95P	CpG island
USP9YP2	CpG island
RNA5SP522	CpG island
USP9YP1	CpG island
CLUHP2	CpG island
OFD1P2Y	CpG island
TCEB1P14	CpG island
OFD1P4Y	CpG island
ACTG1P11	CpG island
FAM41AY2	CpG island
USP9YP14	CpG island
PRYP6	CpG island
HSFY1	CpG island
USP9YP32	CpG island
TCEB1P12	CpG island
TUBB1P1	CpG island
CDY2A	CpG island
TRAPPC2P7	CpG island
RNA5SP523	CpG island
CDY8P	CpG island
ENSG00000251510	CpG island
FAM224A	CpG island
OFD1P5Y	CpG island
RAB9AP4	CpG island
ENSG00000252439	CpG island
TCEB1P26	CpG island
PRYP5	CpG island
HSFY2	CpG island
GPM6BP2	CpG island
TCEB1P13	CpG island
GPM6BP1	CpG island

Extended variants
information (count: 51 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:51 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375489037	chrY:20064944-20064945	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs35610792	chrY:20065054-20065055	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs113335840	chrY:20095681-20095682	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs199628740	chrY:20104256-20104257	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs200350179	chrY:20104258-20104259	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs111470346	chrY:20285577-20285578	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs113020839	chrY:20287283-20287284	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs111759873	chrY:20487378-20487379	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs112796730	chrY:20487829-20487830	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs113471154	chrY:20545229-20545230	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs112601695	chrY:20571899-20571900	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs112435279	chrY:20571921-20571922	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs372004785	chrY:20659368-20659369	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs376329594	chrY:20659369-20659370	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs368336148	chrY:20659370-20659371	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs372923477	chrY:20659374-20659375	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs35597989	chrY:20807206-20807207	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs67053054	chrY:20811307-20811308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs374694350	chrY:20811364-20811365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs367826259	chrY:20811376-20811377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs13304791	chrY:20815730-20815731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs13305190	chrY:20815738-20815739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs13305470	chrY:20815739-20815740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs13305347	chrY:20815765-20815766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs377676703	chrY:20815816-20815817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs112594658	chrY:20815834-20815835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs13303921	chrY:20815886-20815887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs13303924	chrY:20815888-20815889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs369852836	chrY:20816211-20816212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374662939	chrY:20816516-20816517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376484921	chrY:20826983-20826984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34760176	chrY:20827177-20827178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374240543	chrY:20827796-20827797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76389735	chrY:20828172-20828173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368408685	chrY:20828486-20828487	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs372214569	chrY:20828549-20828550	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs9786501	chrY:20828795-20828796	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs35125699	chrY:20831549-20831550	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs13303953	chrY:20832009-20832010	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs13304468	chrY:20832033-20832034	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs13304003	chrY:20832034-20832035	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs13304438	chrY:20832062-20832063	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs13304954	chrY:20832066-20832067	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs13304582	chrY:20832076-20832077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs13305244	chrY:20832084-20832085	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs13304603	chrY:20832092-20832093	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs13305335	chrY:20832125-20832126	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs13304693	chrY:20832126-20832127	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs13305363	chrY:20832136-20832137	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs13304715	chrY:20832137-20832138	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Testicular failure	20966427	CNVD
Honadal dysgenesis	22138850	CNVD
severe oligozoospermia and azoospermia	19731213	CNVD
Ewing''s sarcoma	21437220	CNVD
infertility	21210740	CNVD
Klinefelter syndrome	17968468	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
infertility	20668881	CNVD
Klinefelter syndrome	20603808	CNVD
Meiotic abnormalities	17428878	CNVD
Oligozoospermia	20576090	CNVD
Azoospermia	16445861	CNVD
Cryptorchidism	16988323	CNVD
Non-syndromic sensorineural hearing loss	17409464	CNVD
infertile	20603812	CNVD
infertile	22120929	CNVD
infertile	19369647	CNVD
severe oligozoospermia and azoospermia	21887237	CNVD
spermatozoa with elongated heads	17208942	CNVD
Azoospermia	17187159	CNVD
Oligozoospermia	17187159	CNVD
infertile	19440834	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
infertility	21340528	CNVD
Klinefelter syndrome	16612480	CNVD
infertile	16612480	CNVD
Infertility	16469004	CNVD
Recurrent pregnancy loss	20943704	CNVD
infertile	16469004	CNVD
infertility	18832950	CNVD
Maturation arrest	22820855	CNVD
Azoospermia	16709604	CNVD
Astheno-teratozoospermia syndrome	22371775	CNVD
Asthenozoospermia	22371775	CNVD
Azoospermia	22371775	CNVD
Oligoasthenoteratozoospermia	22371775	CNVD
Oligoasthenozoospermia	22371775	CNVD
Oligoteratozoospermia	22371775	CNVD
Teratozoospermia	22371775	CNVD
infertile	17554051	CNVD
Klinefelter syndrome	20805717	CNVD
subfertile	22371775	CNVD
infertile	19966830	CNVD
Azoospermia	20823911	CNVD
Non-syndromic sensorineural hearing loss	18200580	CNVD
infertile oligozoospermic	17712493	CNVD
Hereditary coagulopathy	21993689	CNVD
Honadal dysgenesis	21048976	CNVD
Breast cancer	21045282	CNVD
Chordoma	18071362	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrY:20104200-20104400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chrY:20807200-20807600	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chrY:20811000-20811400	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chrY:20815600-20816600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chrY:20826600-20826800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chrY:20826800-20828200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chrY:20828200-20828800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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