Variant report

Variant	nsv869394
Chromosome Location	chrY:16699218-17364088
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:860)
CpG islands
(count:552)
Chromatin interactive
region (count:0)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:860 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrY:16740017-16740510	HepG2	liver:	n/a	n/a
2	ARID3A	chrY:16746925-16747352	HepG2	liver:	n/a	n/a
3	ARID3A	chrY:16874744-16875075	HepG2	liver:	n/a	n/a
4	BHLHE40	chrY:16740192-16740477	HepG2	liver:	n/a	n/a
5	BHLHE40	chrY:16930420-16930717	HepG2	liver:	n/a	n/a
6	BHLHE40	chrY:17276454-17276645	HepG2	liver:	n/a	n/a
7	CEBPB	chrY:16962658-16962903	HepG2	liver:	n/a	chrY:16962800-16962811 chrY:16962824-16962835 chrY:16962776-16962787
8	CEBPB	chrY:17109074-17109334	HepG2	liver:	n/a	chrY:17109216-17109227
9	CEBPB	chrY:17319131-17319410	HepG2	liver:	n/a	n/a
10	CEBPB	chrY:16740105-16740477	HepG2	liver:	n/a	chrY:16740278-16740289
11	CEBPB	chrY:16962622-16962983	A549	lung:	n/a	chrY:16962800-16962811 chrY:16962824-16962835 chrY:16962776-16962787
12	CEBPB	chrY:17289471-17289739	A549	lung:	n/a	chrY:17289579-17289590
13	CEBPB	chrY:17289403-17289768	HepG2	liver:	n/a	chrY:17289579-17289590
14	CEBPB	chrY:16962606-16963005	HepG2	liver:	n/a	chrY:16962800-16962811 chrY:16962824-16962835 chrY:16962776-16962787
15	CEBPB	chrY:16875570-16875697	HepG2	liver:	n/a	chrY:16875638-16875649
16	CEBPB	chrY:17020597-17020723	A549	lung:	n/a	n/a
17	CEBPB	chrY:16740169-16740386	HepG2	liver:	n/a	chrY:16740278-16740289
18	CEBPB	chrY:16836849-16837101	HepG2	liver:	n/a	chrY:16836977-16836988
19	CEBPB	chrY:16962694-16962903	HepG2	liver:	n/a	chrY:16962800-16962811 chrY:16962824-16962835 chrY:16962776-16962787
20	CEBPB	chrY:17076523-17076720	A549	lung:	n/a	n/a
21	CEBPB	chrY:16962655-16962931	A549	lung:	n/a	chrY:16962800-16962811 chrY:16962824-16962835 chrY:16962776-16962787
22	CEBPB	chrY:16973035-16973306	HepG2	liver:	n/a	n/a
23	CEBPB	chrY:16875508-16876477	HepG2	liver:	n/a	chrY:16875638-16875649
24	CEBPB	chrY:16962578-16962961	A549	lung:	n/a	chrY:16962800-16962811 chrY:16962824-16962835 chrY:16962776-16962787
25	CEBPB	chrY:16817174-16817348	A549	lung:	n/a	n/a
26	CEBPD	chrY:16962642-16962877	HepG2	liver:	n/a	n/a
27	CREB1	chrY:16740117-16740570	HepG2	liver:	n/a	n/a
28	CTCF	chrY:16750980-16751043	LNCaP	prostate:	n/a	n/a
29	CTCF	chrY:16722515-16722619	LNCaP	prostate:	n/a	n/a
30	CTCF	chrY:16713441-16713515	A549	lung:	n/a	n/a
31	CTCF	chrY:17341083-17341207	Medullo	brain:	n/a	n/a
32	CTCF	chrY:16734065-16734144	GM20000	blood:	n/a	n/a
33	CTCF	chrY:16730400-16730550	HFF-Myc	foreskin:	n/a	n/a
34	CTCF	chrY:16861180-16861330	RPTEC	kidney:	n/a	n/a
35	CTCF	chrY:16730560-16730710	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chrY:17341020-17341170	AG04450	lung:	n/a	n/a
37	CTCF	chrY:16730505-16730654	HepG2	liver:	n/a	n/a
38	CTCF	chrY:16909246-16909289	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chrY:16811227-16811389	LNCaP	prostate:	n/a	n/a
40	CTCF	chrY:16886064-16886112	Medullo	brain:	n/a	n/a
41	CTCF	chrY:16713320-16713470	HepG2	liver:	n/a	n/a
42	CTCF	chrY:17027567-17027686	GM10248	blood:	n/a	n/a
43	CTCF	chrY:17320346-17320370	GM10266	blood:	n/a	n/a
44	CTCF	chrY:17203530-17203623	GM10248	blood:	n/a	n/a
45	CTCF	chrY:17138031-17138130	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chrY:16917374-16917450	GM20000	blood:	n/a	n/a
47	CTCF	chrY:16787235-16787258	LNCaP	prostate:	n/a	n/a
48	CTCF	chrY:17330819-17330829	GM10248	blood:	n/a	n/a
49	CTCF	chrY:17341120-17341270	AG10803	skin:	n/a	n/a
50	CTCF	chrY:16729680-16729830	GM12874	blood:	n/a	n/a

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrY:16733442-16733492	HL-60	blood:	n/a
2	chrY:16942154-16942204	HNPCEpiC	eye:	n/a
3	chrY:16733930-16733980	MCF10A-Er-Src	breast:	n/a
4	chrY:16733442-16733492	HL-60	blood:	n/a
5	chrY:16942154-16942204	HNPCEpiC	eye:	n/a
6	chrY:16733930-16733980	MCF10A-Er-Src	breast:	n/a
7	chrY:16924422-16924472	IMR90	lung:	fetal
8	chrY:16942232-16942282	K562	blood:	n/a
9	chrY:16924422-16924472	HNPCEpiC	eye:	n/a
10	chrY:16924422-16924472	HEEpiC	esophagus:	n/a
11	chrY:16924422-16924472	HRE	kidney:	n/a
12	chrY:16733251-16733301	HepG2	liver:	n/a
13	chrY:16733442-16733492	SAEC	small airway:	n/a
14	chrY:16733930-16733980	NB4	blood:	n/a
15	chrY:16945913-16945963	AG09319	gingival:	n/a
16	chrY:16941591-16941641	HCM	heart:	n/a
17	chrY:16733930-16733980	GM19239	blood:	n/a
18	chrY:16939383-16939433	SK-N-SH	brain:	n/a
19	chrY:16939383-16939433	PrEC	prostate:	n/a
20	chrY:16942232-16942282	PFSK-1	brain:	n/a
21	chrY:16942154-16942204	Jurkat	blood:	n/a
22	chrY:16733442-16733492	ovcar-3	ovarian:	n/a
23	chrY:16733930-16733980	HCT-116	colon:	n/a
24	chrY:16924422-16924472	HCPEpiC	choroid plexus:	n/a
25	chrY:16939383-16939433	HCT-116	colon:	n/a
26	chrY:16942154-16942204	BJ	skin:	n/a
27	chrY:16942154-16942204	SK-N-SH	brain:	n/a
28	chrY:16942232-16942282	HCF	heart:	n/a
29	chrY:16945913-16945963	MCF10A-Er-Src	breast:	n/a
30	chrY:16945913-16945963	HUVEC	blood vessel:	n/a
31	chrY:16939383-16939433	ECC-1	luminal epithelium:	n/a
32	chrY:16942154-16942204	HEEpiC	esophagus:	n/a
33	chrY:16941591-16941641	NHDF-neo	bronchial:	n/a
34	chrY:16941591-16941641	PANC-1	pancreas:	n/a
35	chrY:16733442-16733492	SKMC	muscle:	n/a
36	chrY:16733442-16733492	RPTEC	kidney:	n/a
37	chrY:16941591-16941641	HAEpiC	amniotic membrane:	n/a
38	chrY:16924422-16924472	NT2-D1	testis:	n/a
39	chrY:16939383-16939433	NT2-D1	testis:	n/a
40	chrY:16941591-16941641	AG04449	skin:	fetal
41	chrY:16924422-16924472	HRPEpiC	eye:	n/a
42	chrY:16942154-16942204	SKMC	muscle:	n/a
43	chrY:16939383-16939433	HMEC	breast:	n/a
44	chrY:16924422-16924472	LNCaP	prostate:	n/a
45	chrY:16942232-16942282	HRE	kidney:	n/a
46	chrY:16945913-16945963	HCPEpiC	choroid plexus:	n/a
47	chrY:16945913-16945963	HMEC	breast:	n/a
48	chrY:16733251-16733301	NB4	blood:	n/a
49	chrY:16733442-16733492	A549	lung:	n/a
50	chrY:16733442-16733492	HPAEpiC	pulmonary alveolar:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VCY1B-2	chrY:16915885-16915913	ENSG00000228787.1
2	lnc-VCY1B-2	chrY:16905522-16905867	ENSG00000228787.1
3	lnc-VCY1B-2	chrY:16913156-16913224	ENSG00000228787.1
4	lnc-VCY1B-2	chrY:16910502-16910589	ENSG00000228787.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	NLGN4Y	hsa-miR-124-3p	chrY:16955740-16955746

Variant related genes	Relation type
CYCSP46	TF binding region
AGKP1	TF binding region
NLGN4Y	TF binding region
ENSG00000224518	TF binding region
MED13P1	TF binding region
NLGN4Y-AS1	TF binding region
CYCSP46	CpG island
AGKP1	CpG island
NLGN4Y	CpG island
ENSG00000224518	CpG island
MED13P1	CpG island
NLGN4Y-AS1	CpG island

Extended variants
information (count: 850 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:850 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs36097043	chrY:16699228-16699229	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs17222244	chrY:16699334-16699335	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573862565	chrY:16700571-16700572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369458131	chrY:16700625-16700626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111641065	chrY:16701159-16701160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376432375	chrY:16701321-16701322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530086101	chrY:16701365-16701366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199974114	chrY:16701526-16701527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373634884	chrY:16701659-16701660	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73621793	chrY:16701905-16701906	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs374377127	chrY:16701969-16701970	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs377192441	chrY:16701993-16701994	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs112505390	chrY:16702056-16702057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559560200	chrY:16702393-16702394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528197261	chrY:16702473-16702474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112333552	chrY:16702587-16702588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545083903	chrY:16702868-16702869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200959984	chrY:16703492-16703493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369686515	chrY:16703945-16703946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376832760	chrY:16704181-16704182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34176065	chrY:16704306-16704307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371456515	chrY:16704666-16704667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374579396	chrY:16704675-16704676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564983692	chrY:16704749-16704750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368891399	chrY:16704849-16704850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377355671	chrY:16704916-16704917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370326187	chrY:16704973-16704974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530471274	chrY:16705083-16705084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550530018	chrY:16705411-16705412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375049705	chrY:16705480-16705481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs367995942	chrY:16705851-16705852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370621727	chrY:16705969-16705970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373011285	chrY:16706776-16706777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375109860	chrY:16706857-16706858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375102498	chrY:16707074-16707075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs34533890	chrY:16707366-16707367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9699384	chrY:16707631-16707632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530297856	chrY:16707964-16707965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201960905	chrY:16708324-16708325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs368434890	chrY:16708498-16708499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs370714127	chrY:16708524-16708525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111868713	chrY:16708681-16708682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113246742	chrY:16708921-16708922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372135854	chrY:16708943-16708944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546814946	chrY:16709304-16709305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375462348	chrY:16709306-16709307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs367577483	chrY:16709332-16709333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545807085	chrY:16709417-16709418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566680886	chrY:16709464-16709465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372395075	chrY:16709509-16709510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:50)

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
Breast cancer	21045282	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

Chromatin state (count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrY:16652800-16724800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chrY:16672800-16718000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chrY:16688000-16706000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chrY:16688800-16699600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chrY:16689000-16699400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chrY:16691400-16725400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chrY:16694800-16724400	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chrY:16697600-16700000	Enhancers	HUVEC	blood vessel
9	chrY:16698000-16700000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chrY:16698800-16701200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chrY:16698800-16724600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chrY:16699400-16700400	Strong transcription	H1 Cell Line	embryonic stem cell
13	chrY:16699600-16702000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chrY:16699800-16724800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chrY:16700000-16700600	Weak transcription	HUVEC	blood vessel
16	chrY:16700000-16710200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chrY:16700400-16738000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chrY:16701200-16729000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chrY:16701600-16702400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chrY:16702000-16711000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chrY:16710000-16710600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chrY:16711000-16711800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chrY:16711800-16733200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chrY:16713800-16714400	Enhancers	HUVEC	blood vessel
25	chrY:16717600-16718600	Enhancers	Brain Hippocampus Middle	brain
26	chrY:16718000-16719000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chrY:16719000-16734000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chrY:16722600-16724800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chrY:16724400-16725800	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chrY:16724600-16725600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chrY:16724800-16725400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chrY:16724800-16725600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chrY:16724800-16725800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chrY:16725400-16726400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chrY:16725400-16738200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chrY:16725600-16733800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chrY:16725600-16738200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chrY:16725800-16734000	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chrY:16725800-16738000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chrY:16726400-16735200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chrY:16727000-16727800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chrY:16727800-16729000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chrY:16729000-16729600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chrY:16729200-16729400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chrY:16729400-16729600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chrY:16729400-16729600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chrY:16729600-16730600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chrY:16729600-16759400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chrY:16730000-16740800	Weak transcription	Aorta	Aorta
50	chrY:16730200-16738400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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