Variant report

Variant	nsv533955
Chromosome Location	chrY:20826207-21640200
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1471)
CpG islands
(count:855)
Chromatin interactive
region (count:0)
LncRNA
region (count:67)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1471 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrY:21516142-21516326	HepG2	liver:	n/a	n/a
2	ATF2	chrY:21153407-21155092	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chrY:21152512-21152927	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chrY:21515962-21516342	A549	lung:	n/a	n/a
5	BCL3	chrY:21516007-21516319	A549	lung:	n/a	n/a
6	CEBPB	chrY:21034657-21034881	A549	lung:	n/a	n/a
7	CEBPB	chrY:21256729-21257036	A549	lung:	n/a	n/a
8	CEBPB	chrY:21237640-21237887	A549	lung:	n/a	n/a
9	CEBPB	chrY:21624082-21624365	A549	lung:	n/a	chrY:21624203-21624214
10	CEBPB	chrY:21257430-21257724	A549	lung:	n/a	chrY:21257507-21257518 chrY:21257547-21257558
11	CEBPB	chrY:21049354-21049508	HepG2	liver:	n/a	chrY:21049408-21049419
12	CEBPB	chrY:21257362-21257702	HepG2	liver:	n/a	chrY:21257507-21257518 chrY:21257547-21257558
13	CEBPB	chrY:21257358-21257675	A549	lung:	n/a	chrY:21257507-21257518 chrY:21257547-21257558
14	CEBPB	chrY:21430214-21430427	A549	lung:	n/a	n/a
15	CEBPB	chrY:21094299-21094464	A549	lung:	n/a	n/a
16	CEBPB	chrY:21624055-21624378	HepG2	liver:	n/a	chrY:21624203-21624214
17	CEBPB	chrY:21261554-21261779	HepG2	liver:	n/a	chrY:21261694-21261705
18	CEBPB	chrY:21178972-21179257	HepG2	liver:	n/a	chrY:21179111-21179122
19	CHD2	chrY:21154716-21154916	HepG2	liver:	n/a	n/a
20	CREB1	chrY:21154439-21155132	H1-hESC	embryonic stem cell:	n/a	n/a
21	CREB1	chrY:21237760-21238097	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chrY:21154468-21154977	A549	lung:	n/a	n/a
23	CTCF	chrY:21114000-21114150	BJ	skin:	n/a	n/a
24	CTCF	chrY:21154700-21154850	RPTEC	kidney:	n/a	n/a
25	CTCF	chrY:20926251-20926315	GM10266	blood:	n/a	n/a
26	CTCF	chrY:20831784-20831973	ProgFib	skin:	n/a	n/a
27	CTCF	chrY:21427740-21427890	GM12872	blood:	n/a	n/a
28	CTCF	chrY:21595080-21595230	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chrY:21154720-21154870	Caco-2	colon:	n/a	n/a
30	CTCF	chrY:21021610-21021791	ProgFib	skin:	n/a	n/a
31	CTCF	chrY:21154700-21154850	HMEC	breast:	n/a	n/a
32	CTCF	chrY:20952383-20952519	GM10266	blood:	n/a	n/a
33	CTCF	chrY:21159660-21159810	NHLF	lung:	n/a	n/a
34	CTCF	chrY:20943259-20943260	GM10248	blood:	n/a	n/a
35	CTCF	chrY:20872695-20872710	GM19239	blood:	n/a	n/a
36	CTCF	chrY:21154655-21154857	HepG2	liver:	n/a	n/a
37	CTCF	chrY:21045468-21045543	GM20000	blood:	n/a	n/a
38	CTCF	chrY:21114160-21114310	A549	lung:	n/a	n/a
39	CTCF	chrY:21154660-21154810	GM12864	blood:	n/a	n/a
40	CTCF	chrY:21114063-21114188	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chrY:20831126-20831188	GM20000	blood:	n/a	n/a
42	CTCF	chrY:21177860-21178010	GM12872	blood:	n/a	n/a
43	CTCF	chrY:21177831-21178063	GM19239	blood:	n/a	n/a
44	CTCF	chrY:21595040-21595190	AG04449	skin:	n/a	n/a
45	CTCF	chrY:21427780-21427930	GM12871	blood:	n/a	n/a
46	CTCF	chrY:20998716-20998801	GM20000	blood:	n/a	n/a
47	CTCF	chrY:20873972-20873981	ProgFib	skin:	n/a	n/a
48	CTCF	chrY:20937689-20937746	ProgFib	skin:	n/a	n/a
49	CTCF	chrY:21154720-21154870	HEK293	kidney:	n/a	n/a
50	CTCF	chrY:21154860-21155010	RPTEC	kidney:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrY:21155270-21155320	HEEpiC	esophagus:	n/a
2	chrY:21155270-21155320	HEEpiC	esophagus:	n/a
3	chrY:21239461-21239511	GM19239	blood:	n/a
4	chrY:21239607-21239657	HCT-116	colon:	n/a
5	chrY:21239348-21239398	ECC-1	luminal epithelium:	n/a
6	chrY:21155270-21155320	SK-N-MC	brain:	n/a
7	chrY:21100472-21100522	MCF10A-Er-Src	breast:	n/a
8	chrY:21239219-21239269	GM12878	blood:	n/a
9	chrY:21239607-21239657	HMEC	breast:	n/a
10	chrY:21238886-21238936	BE2_C	brain:	n/a
11	chrY:21238472-21238522	Hepatocyte	liver:	n/a
12	chrY:21239332-21239382	HNPCEpiC	eye:	n/a
13	chrY:21239348-21239398	ProgFib	skin:	n/a
14	chrY:21240004-21240054	HepG2	liver:	n/a
15	chrY:21239461-21239511	CMK	blood:	n/a
16	chrY:21239607-21239657	MCF10A-Er-Src	breast:	n/a
17	chrY:21238886-21238936	MCF-7	breast:	n/a
18	chrY:21100472-21100522	PANC-1	pancreas:	n/a
19	chrY:21238886-21238936	GM19239	blood:	n/a
20	chrY:21036986-21037036	HEK293	kidney:	embryo
21	chrY:21239607-21239657	HNPCEpiC	eye:	n/a
22	chrY:21239332-21239382	A549	lung:	n/a
23	chrY:21239348-21239398	AG09319	gingival:	n/a
24	chrY:21236229-21236279	HRCEpiC	kidney:	n/a
25	chrY:21239461-21239511	BJ	skin:	n/a
26	chrY:21100472-21100522	RPTEC	kidney:	n/a
27	chrY:21239332-21239382	HEEpiC	esophagus:	n/a
28	chrY:21238472-21238522	T-47D	breast:	n/a
29	chrY:21239219-21239269	BJ	skin:	n/a
30	chrY:21100472-21100522	GM19239	blood:	n/a
31	chrY:21239219-21239269	PrEC	prostate:	n/a
32	chrY:21100472-21100522	HPAEpiC	pulmonary alveolar:	n/a
33	chrY:21041339-21041389	HCPEpiC	choroid plexus:	n/a
34	chrY:21041339-21041389	SAEC	small airway:	n/a
35	chrY:21240004-21240054	Hela-S3	cervix:	n/a
36	chrY:21238886-21238936	NHBE	bronchial:	n/a
37	chrY:21100472-21100522	AG04450	lung:	fetal
38	chrY:21238472-21238522	ECC-1	luminal epithelium:	n/a
39	chrY:21036986-21037036	ECC-1	luminal epithelium:	n/a
40	chrY:21239461-21239511	T-47D	breast:	n/a
41	chrY:21239348-21239398	GM19239	blood:	n/a
42	chrY:21239461-21239511	ovcar-3	ovarian:	n/a
43	chrY:21240004-21240054	HMEC	breast:	n/a
44	chrY:21239348-21239398	AG09309	skin:	n/a
45	chrY:21036986-21037036	AG09309	skin:	n/a
46	chrY:21036986-21037036	BJ	skin:	n/a
47	chrY:21239461-21239511	NH-A	brain:	n/a
48	chrY:21236229-21236279	GM12892	blood:	n/a
49	chrY:21239332-21239382	LNCaP	prostate:	n/a
50	chrY:21236229-21236279	GM12878	blood:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KDM5D-8	chrY:21573858-21574142	FPKM1_group_35560_transcript_1
2	lnc-HSFY1-2	chrY:20894741-20894877	ENSG00000131009.4
3	lnc-HSFY2-3	chrY:21038954-21039091	NONHSAT139607
4	lnc-HSFY2-5	chrY:20938165-20938289	NONHSAT139595
5	lnc-HSFY1-2	chrY:20899941-20901083	NONHSAT139592
6	lnc-HSFY1-12	chrY:21024221-21024338	NONHSAT139602
7	lnc-HSFY1-2	chrY:20894045-20894158	ENSG00000131009.4
8	lnc-HSFY1-12	chrY:21026120-21026187	NONHSAT139602
9	lnc-HSFY2-3	chrY:21038954-21040114	ENSG00000176728.3
10	lnc-HSFY2-5	chrY:20941185-20941313	NONHSAT139595
11	lnc-HSFY1-12	chrY:21011415-21011615	NONHSAT139602
12	lnc-HSFY2-3	chrY:21237827-21237882	ENSG00000176728.3
13	lnc-HSFY1-10	chrY:20949636-20949966	NONHSAT139596
14	lnc-HSFY2-10	chrY:21154353-21154595	NONHSAT139611
15	lnc-HSFY1-12	chrY:21013835-21013899	NONHSAT139602
16	lnc-HSFY2-3	chrY:21040091-21040254	NONHSAT139607
17	lnc-HSFY2-6	chrY:20973224-20973715	NONHSAT139598
18	lnc-HSFY2-3	chrY:21078626-21078730	ucscGeneNc_uc004fuj_1
19	lnc-HSFY1-12	chrY:21013987-21014016	NONHSAT139602
20	lnc-HSFY2-3	chrY:21034400-21034720	XLOC_008326
21	lnc-HSFY1-2	chrY:20893583-20893683	ENSG00000131009.4
22	lnc-HSFY1-12	chrY:21010150-21010221	NONHSAT139602
23	lnc-KDM5D-8	chrY:21573858-21574142	NONHSAT139618
24	lnc-HSFY2-7	chrY:20995937-20996093	NONHSAT139600
25	lnc-HSFY2-3	chrY:21206428-21206581	ENSG00000176728.3
26	lnc-HSFY1-12	chrY:21027300-21027399	NONHSAT139602
27	lnc-HSFY1-12	chrY:21018720-21018835	NONHSAT139602
28	lnc-HSFY2-7	chrY:21001068-21001199	NONHSAT139600
29	lnc-HSFY2-3	chrY:21038954-21039091	ENSG00000176728.3
30	lnc-HSFY2-3	chrY:21238931-21239004	ENSG00000176728.3
31	lnc-HSFY2-3	chrY:21034411-21034720	NONHSAT139607
32	lnc-HSFY1-12	chrY:21029026-21029166	NONHSAT139602
33	lnc-HSFY2-7	chrY:20995360-20995534	NONHSAT139600
34	lnc-KDM5D-8	chrY:21589418-21589465	NONHSAT139618
35	lnc-HSFY2-3	chrY:21038954-21040114	XLOC_008326
36	lnc-HSFY1-11	chrY:20991185-20991373	NONHSAT139599
37	lnc-HSFY2-3	chrY:21038954-21039091	XLOC_008326
38	lnc-HSFY2-7	chrY:20995776-20995804	NONHSAT139600
39	lnc-HSFY2-3	chrY:21034389-21034720	ENSG00000176728.3
40	lnc-HSFY2-3	chrY:21037702-21037941	ucscGeneNc_uc004fuj_1
41	lnc-HSFY2-3	chrY:21207128-21207177	ENSG00000176728.3
42	lnc-HSFY1-11	chrY:20987993-20988213	NONHSAT139599
43	lnc-HSFY2-3	chrY:21034388-21034720	XLOC_008326
44	lnc-HSFY1-12	chrY:21018235-21018371	NONHSAT139602
45	lnc-HSFY2-3	chrY:21041146-21041255	ucscGeneNc_uc004fuj_1
46	lnc-HSFY2-3	chrY:21230610-21230684	ENSG00000176728.3
47	lnc-HSFY2-3	chrY:21074254-21074294	XLOC_008326
48	lnc-HSFY1-13	chrY:21147061-21147740	NONHSAT139610
49	lnc-HSFY1-11	chrY:20989185-20989278	NONHSAT139599
50	lnc-HSFY2-3	chrY:21034387-21034720	ENSG00000176728.3

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CD24	hsa-miR-373-3p	chrY:21153845-21153868

Variant related genes	Relation type
OFD1P6Y	TF binding region
ZNF839P1	TF binding region
USP9YP10	TF binding region
RNU6-255P	TF binding region
USP9YP2	TF binding region
GAPDHP19	TF binding region
TCEB1P14	TF binding region
MTCYBP2	TF binding region
RNU1-41P	TF binding region
XKRYP2	TF binding region
PRYP6	TF binding region
USP9YP28	TF binding region
CD24P4	TF binding region
TTTY14	TF binding region
OFD1P7Y	TF binding region
HSFY2	TF binding region
GPM6BP2	TF binding region
OFD1P6Y	CpG island
ZNF839P1	CpG island
USP9YP10	CpG island
RNU6-255P	CpG island
USP9YP2	CpG island
GAPDHP19	CpG island
TCEB1P14	CpG island
MTCYBP2	CpG island
RNU1-41P	CpG island
XKRYP2	CpG island
PRYP6	CpG island
USP9YP28	CpG island
CD24P4	CpG island
TTTY14	CpG island
OFD1P7Y	CpG island
HSFY2	CpG island
GPM6BP2	CpG island

Extended variants
information (count: 1167 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1167 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376484921	chrY:20826983-20826984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs34760176	chrY:20827177-20827178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374240543	chrY:20827796-20827797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76389735	chrY:20828172-20828173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs368408685	chrY:20828486-20828487	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs372214569	chrY:20828549-20828550	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs9786501	chrY:20828795-20828796	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs35125699	chrY:20831549-20831550	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs13303953	chrY:20832009-20832010	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs13304468	chrY:20832033-20832034	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs13304003	chrY:20832034-20832035	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs13304438	chrY:20832062-20832063	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs13304954	chrY:20832066-20832067	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs13304582	chrY:20832076-20832077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs13305244	chrY:20832084-20832085	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs13304603	chrY:20832092-20832093	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs13305335	chrY:20832125-20832126	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs13304693	chrY:20832126-20832127	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs13305363	chrY:20832136-20832137	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs13304715	chrY:20832137-20832138	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs112428276	chrY:20957936-20957937	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs369049970	chrY:21031817-21031818	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs112457592	chrY:21033095-21033096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376034331	chrY:21033470-21033471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374019343	chrY:21033479-21033480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376360268	chrY:21033485-21033486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372657465	chrY:21033566-21033567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377064977	chrY:21033747-21033748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371858633	chrY:21033798-21033799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374608777	chrY:21034194-21034195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113616577	chrY:21034710-21034711	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs534100104	chrY:21035372-21035373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537839449	chrY:21035766-21035767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368691327	chrY:21036619-21036620	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs36049573	chrY:21038122-21038123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370384082	chrY:21038589-21038590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34090559	chrY:21039520-21039521	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs372971842	chrY:21040649-21040650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112916107	chrY:21040853-21040854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370768334	chrY:21041376-21041377	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs375382194	chrY:21042525-21042526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs207481424	chrY:21043028-21043029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113271534	chrY:21043055-21043056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35766733	chrY:21043105-21043106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541528057	chrY:21043448-21043449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368725889	chrY:21043748-21043749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112835254	chrY:21044132-21044133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112563800	chrY:21044471-21044472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371613454	chrY:21044962-21044963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13305251	chrY:21045242-21045243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Mental retardation	17901693	CNVD

Chromatin state (count:1288 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrY:20826600-20826800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chrY:20826800-20828200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chrY:20828200-20828800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chrY:21032600-21040800	Weak transcription	Fetal Intestine Large	intestine
5	chrY:21034600-21034800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chrY:21036600-21037000	Active TSS	Primary neutrophils fromperipheralblood	blood
7	chrY:21036800-21043600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chrY:21037000-21053400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chrY:21037600-21040200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chrY:21040200-21040800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chrY:21040600-21043200	Weak transcription	Psoas Muscle	Psoas
12	chrY:21040800-21054800	Weak transcription	HSMMtube	muscle
13	chrY:21042200-21042400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
14	chrY:21042400-21046800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chrY:21042800-21045000	Weak transcription	Primary hematopoietic stem cells	blood
16	chrY:21046400-21047400	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chrY:21046800-21047000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chrY:21047400-21055200	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chrY:21055200-21055400	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chrY:21055400-21056000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
21	chrY:21056000-21065200	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chrY:21063400-21064000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chrY:21063800-21064000	Enhancers	Left Ventricle	heart
24	chrY:21064000-21067400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chrY:21064000-21092200	Weak transcription	Left Ventricle	heart
26	chrY:21065000-21066200	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chrY:21065200-21065400	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chrY:21066000-21066200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chrY:21066200-21071200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chrY:21066200-21089000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chrY:21067400-21067800	Enhancers	HSMM	muscle
32	chrY:21067400-21068000	Enhancers	HSMMtube	muscle
33	chrY:21067400-21068600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chrY:21067800-21071400	Weak transcription	HSMM	muscle
35	chrY:21068000-21071000	Weak transcription	HSMMtube	muscle
36	chrY:21068200-21068400	Enhancers	Right Atrium	heart
37	chrY:21068600-21069200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chrY:21069200-21069400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chrY:21069200-21069400	Enhancers	NH-A	brain
40	chrY:21069400-21071400	Weak transcription	NH-A	brain
41	chrY:21071200-21071400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chrY:21071400-21071800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chrY:21071400-21071800	Enhancers	NH-A	brain
44	chrY:21071400-21072400	Enhancers	HSMM	muscle
45	chrY:21071800-21072200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chrY:21072200-21072600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chrY:21072400-21085200	Weak transcription	HSMM	muscle
48	chrY:21072800-21085000	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chrY:21083200-21083800	Enhancers	Thymus	Thymus
50	chrY:21084800-21085600	Enhancers	HSMMtube	muscle

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