Variant report

Variant	nsv930979
Chromosome Location	chrY:22515425-23165096
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:779)
CpG islands
(count:1893)
Chromatin interactive
region (count:0)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:779 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrY:23159252-23159761	HepG2	liver:	n/a	n/a
2	ARID3A	chrY:22737425-22738037	HepG2	liver:	n/a	n/a
3	ARID3A	chrY:22677946-22678147	HepG2	liver:	n/a	n/a
4	ATF3	chrY:22737440-22737716	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chrY:22737471-22737700	HepG2	liver:	n/a	n/a
6	ATF3	chrY:22737389-22737845	HepG2	liver:	n/a	n/a
7	ATF3	chrY:22737445-22737814	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chrY:22737462-22737688	HepG2	liver:	n/a	n/a
9	CEBPB	chrY:22990567-22991072	HepG2	liver:	n/a	chrY:22990725-22990736
10	CEBPB	chrY:22964434-22964681	HepG2	liver:	n/a	chrY:22964540-22964551
11	CEBPB	chrY:22937887-22938160	HepG2	liver:	n/a	chrY:22937975-22937986
12	CEBPB	chrY:22922767-22923012	HepG2	liver:	n/a	chrY:22922931-22922942
13	CEBPB	chrY:22724095-22724459	HepG2	liver:	n/a	chrY:22724271-22724282
14	CEBPB	chrY:22990566-22990914	A549	lung:	n/a	chrY:22990725-22990736
15	CEBPB	chrY:22682089-22682443	HepG2	liver:	n/a	chrY:22682245-22682256
16	CEBPB	chrY:23159051-23160062	HepG2	liver:	n/a	n/a
17	CEBPB	chrY:22888682-22888905	A549	lung:	n/a	chrY:22888758-22888769
18	CEBPB	chrY:22813416-22813802	HepG2	liver:	n/a	chrY:22813627-22813638
19	CEBPB	chrY:23113667-23113988	HepG2	liver:	n/a	chrY:23113828-23113839
20	CEBPB	chrY:23149207-23150143	HepG2	liver:	n/a	n/a
21	CEBPB	chrY:23159288-23159455	HepG2	liver:	n/a	n/a
22	CEBPB	chrY:22751277-22751566	A549	lung:	n/a	n/a
23	CEBPB	chrY:22724089-22724456	A549	lung:	n/a	chrY:22724271-22724282
24	CEBPB	chrY:23113701-23113956	A549	lung:	n/a	chrY:23113828-23113839
25	CEBPB	chrY:23163500-23164313	HepG2	liver:	n/a	chrY:23163716-23163727
26	CEBPB	chrY:22711218-22711562	HepG2	liver:	n/a	chrY:22711389-22711400
27	CEBPB	chrY:23159376-23159999	A549	lung:	n/a	n/a
28	CEBPB	chrY:23158094-23158301	A549	lung:	n/a	chrY:23158190-23158201
29	CEBPB	chrY:22682135-22682390	A549	lung:	n/a	chrY:22682245-22682256
30	CEBPB	chrY:22990621-22990897	A549	lung:	n/a	chrY:22990725-22990736
31	CEBPB	chrY:22888703-22888903	HepG2	liver:	n/a	chrY:22888758-22888769
32	CEBPB	chrY:23163543-23164257	A549	lung:	n/a	chrY:23163716-23163727
33	CEBPB	chrY:22990461-22990956	A549	lung:	n/a	chrY:22990725-22990736
34	CEBPB	chrY:23157938-23158380	HepG2	liver:	n/a	chrY:23158190-23158201
35	CEBPB	chrY:22917369-22917612	A549	lung:	n/a	n/a
36	CREB1	chrY:22737365-22737872	A549	lung:	n/a	n/a
37	CREB1	chrY:22737405-22737894	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chrY:22737244-22738018	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chrY:22737211-22738110	HepG2	liver:	n/a	n/a
40	CREB1	chrY:22737303-22738141	HepG2	liver:	n/a	n/a
41	CREB1	chrY:22737366-22737799	A549	lung:	n/a	n/a
42	CREB1	chrY:22960201-22960415	A549	lung:	n/a	n/a
43	CTCF	chrY:22737577-22737610	HepG2	liver:	n/a	n/a
44	CTCF	chrY:22920437-22920568	HepG2	liver:	n/a	n/a
45	CTCF	chrY:22720580-22720730	HCM	heart:	n/a	n/a
46	CTCF	chrY:22920440-22920590	GM12864	blood:	n/a	n/a
47	CTCF	chrY:22890260-22890328	Medullo	brain:	n/a	n/a
48	CTCF	chrY:23106059-23106127	Medullo	brain:	n/a	n/a
49	CTCF	chrY:22810420-22810570	HFF	foreskin:	n/a	n/a
50	CTCF	chrY:22738500-22738650	HVMF	connective:	n/a	n/a

(count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrY:22737556-22737606	NB4	blood:	n/a
2	chrY:22737505-22737555	AG09319	gingival:	n/a
3	chrY:22737556-22737606	NB4	blood:	n/a
4	chrY:22737505-22737555	AG09319	gingival:	n/a
5	chrY:22917937-22917987	IMR90	lung:	fetal
6	chrY:22917937-22917987	PrEC	prostate:	n/a
7	chrY:22917782-22917832	K562	blood:	n/a
8	chrY:22917087-22917137	Jurkat	blood:	n/a
9	chrY:22737556-22737606	HPAEpiC	pulmonary alveolar:	n/a
10	chrY:22738029-22738079	RPTEC	kidney:	n/a
11	chrY:22736584-22736634	NH-A	brain:	n/a
12	chrY:22681436-22681486	SK-N-MC	brain:	n/a
13	chrY:22917894-22917944	SAEC	small airway:	n/a
14	chrY:22737969-22738019	ECC-1	luminal epithelium:	n/a
15	chrY:22682393-22682443	Jurkat	blood:	n/a
16	chrY:22737424-22737474	HRPEpiC	eye:	n/a
17	chrY:22737896-22737946	PrEC	prostate:	n/a
18	chrY:22736584-22736634	PANC-1	pancreas:	n/a
19	chrY:22741795-22741845	AG04450	lung:	fetal
20	chrY:22917913-22917963	Caco-2	colon:	n/a
21	chrY:22737505-22737555	SK-N-MC	brain:	n/a
22	chrY:22736528-22736578	LNCaP	prostate:	n/a
23	chrY:22735320-22735370	AG09319	gingival:	n/a
24	chrY:22917087-22917137	NHDF-neo	bronchial:	n/a
25	chrY:22917937-22917987	ProgFib	skin:	n/a
26	chrY:22741795-22741845	ProgFib	skin:	n/a
27	chrY:22738771-22738821	LNCaP	prostate:	n/a
28	chrY:22737896-22737946	GM12878	blood:	n/a
29	chrY:22736528-22736578	GM12892	blood:	n/a
30	chrY:22737591-22737641	NHDF-neo	bronchial:	n/a
31	chrY:22917782-22917832	H1-hESC	embryonic stem cell:	embryo
32	chrY:22737391-22737441	HNPCEpiC	eye:	n/a
33	chrY:22917913-22917963	RPTEC	kidney:	n/a
34	chrY:22917937-22917987	PANC-1	pancreas:	n/a
35	chrY:22735320-22735370	HCM	heart:	n/a
36	chrY:22737424-22737474	GM19239	blood:	n/a
37	chrY:22917942-22917992	K562	blood:	n/a
38	chrY:22738029-22738079	IMR90	lung:	fetal
39	chrY:22736528-22736578	HIPEpiC	eye:	n/a
40	chrY:22680010-22680060	CMK	blood:	n/a
41	chrY:22735320-22735370	Jurkat	blood:	n/a
42	chrY:22736833-22736883	NHDF-neo	bronchial:	n/a
43	chrY:22736833-22736883	AG04450	lung:	fetal
44	chrY:22737896-22737946	BE2_C	brain:	n/a
45	chrY:22737556-22737606	NHBE	bronchial:	n/a
46	chrY:22737424-22737474	HEEpiC	esophagus:	n/a
47	chrY:22754881-22754931	HCM	heart:	n/a
48	chrY:22917913-22917963	HUVEC	blood vessel:	n/a
49	chrY:22917937-22917987	GM12891	blood:	n/a
50	chrY:22918038-22918088	PrEC	prostate:	n/a

No data

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF1AY-3	chrY:22558157-22558682	NONHSAT139633
2	lnc-EIF1AY-3	chrY:22551937-22551996	NONHSAT139633
3	lnc-KDM5D-3	chrY:22680157-22681114	ENSG00000229236
4	lnc-KDM5D-3	chrY:22669140-22669342	ENSG00000229236
5	lnc-KDM5D-3	chrY:22628314-22628553	ENSG00000229236
6	lnc-EIF1AY-1	chrY:22658375-22665078	NONHSAT139636
7	lnc-CYorf17-6	chrY:23069230-23069448	NONHSAT139644
8	lnc-CYorf17-8	chrY:22970662-22971351	NONHSAT139642
9	lnc-KDM5D-3	chrY:22631758-22631867	ENSG00000229236
10	lnc-EIF1AY-2	chrY:22632803-22633080	NONHSAT139634
11	lnc-CYorf17-8	chrY:22973205-22973695	NONHSAT139642
12	lnc-EIF1AY-2	chrY:22619300-22619584	NONHSAT139634
13	lnc-KDM5D-3	chrY:22630075-22630134	ENSG00000229236
14	lnc-KDM5D-3	chrY:22680157-22680293	ENSG00000229236
15	lnc-KDM5D-4	chrY:22681834-22683186	XLOC_008328
16	lnc-KDM5D-3	chrY:22669238-22669342	ENSG00000229236
17	lnc-EIF1AY-3	chrY:22557394-22557905	NONHSAT139633
18	lnc-KDM5D-3	chrY:22627554-22627708	ENSG00000229236
19	lnc-KDM5D-4	chrY:22686154-22686319	XLOC_008328

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	EIF1AY	hsa-miR-26b-5p	chrY:22754614-22754636

Variant related genes	Relation type
ZNF885P	TF binding region
GAPDHP17	TF binding region
EIF1AY	TF binding region
HSFY4P	TF binding region
TBL1YP1	TF binding region
RPS4Y2	TF binding region
TMEM167AP1	TF binding region
ENSG00000216844	TF binding region
TTTY10	TF binding region
ZNF885P	CpG island
GAPDHP17	CpG island
EIF1AY	CpG island
HSFY4P	CpG island
TBL1YP1	CpG island
RPS4Y2	CpG island
TMEM167AP1	CpG island
ENSG00000216844	CpG island
TTTY10	CpG island

Extended variants
information (count: 1077 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1077 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556907386	chrY:22529878-22529879	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs200429325	chrY:22529949-22529950	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs373588782	chrY:22530148-22530149	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs369443952	chrY:22530185-22530186	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs539514470	chrY:22547875-22547876	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs111583430	chrY:22547919-22547920	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs112831628	chrY:22547922-22547923	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs78343276	chrY:22548038-22548039	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs79279955	chrY:22548041-22548042	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs77474341	chrY:22548249-22548250	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs34146869	chrY:22548545-22548546	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs531155682	chrY:22557810-22557811	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs550859215	chrY:22558300-22558301	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs373116404	chrY:22558351-22558352	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs374283433	chrY:22560672-22560673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs199543781	chrY:22560797-22560798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs370386020	chrY:22561115-22561116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs11799103	chrY:22582201-22582202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375982250	chrY:22582305-22582306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370629524	chrY:22582439-22582440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs373116908	chrY:22583507-22583508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs201605160	chrY:22584021-22584022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575936549	chrY:22584200-22584201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112043973	chrY:22584390-22584391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs367615464	chrY:22595505-22595506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561766719	chrY:22595951-22595952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113739844	chrY:22596423-22596424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376398720	chrY:22596622-22596623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372155056	chrY:22596715-22596716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs13303754	chrY:22597106-22597107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560621875	chrY:22597231-22597232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371196599	chrY:22597322-22597323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374959059	chrY:22597915-22597916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377613848	chrY:22598262-22598263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs562938375	chrY:22599009-22599010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369701162	chrY:22599195-22599196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9785928	chrY:22601068-22601069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34768548	chrY:22601441-22601442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576958260	chrY:22601453-22601454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548536866	chrY:22602411-22602412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567456291	chrY:22602532-22602533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112183066	chrY:22602612-22602613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376015318	chrY:22602719-22602720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs72615019	chrY:22603043-22603044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546433356	chrY:22603294-22603295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566317456	chrY:22603469-22603470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112943866	chrY:22604140-22604141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs35089536	chrY:22604379-22604380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533038220	chrY:22605080-22605081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373332437	chrY:22605163-22605164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Mental retardation	17901693	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
XY gonadal dysgenesis	20685758	CNVD

Chromatin state (count:890 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrY:22529800-22530200	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chrY:22529800-22530200	Active TSS	H9 Cell Line	embryonic stem cell
3	chrY:22529800-22530200	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chrY:22560600-22561200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chrY:22580600-22584800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chrY:22581800-22582400	Enhancers	Psoas Muscle	Psoas
7	chrY:22584800-22585000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chrY:22595000-22596800	Weak transcription	Left Ventricle	heart
9	chrY:22595200-22596800	Enhancers	Dnd41	blood
10	chrY:22595200-22599400	Weak transcription	Right Ventricle	heart
11	chrY:22595200-22615800	Weak transcription	Aorta	Aorta
12	chrY:22595400-22597000	Weak transcription	Spleen	Spleen
13	chrY:22595400-22598200	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chrY:22595600-22597200	Weak transcription	Pancreas	Pancrea
15	chrY:22596400-22598600	Weak transcription	Gastric	stomach
16	chrY:22596600-22597000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chrY:22596800-22597600	Strong transcription	Left Ventricle	heart
18	chrY:22597000-22597600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
19	chrY:22597000-22597600	Strong transcription	Spleen	Spleen
20	chrY:22597200-22597800	Strong transcription	Pancreas	Pancrea
21	chrY:22597600-22597800	Active TSS	Spleen	Spleen
22	chrY:22597600-22599000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chrY:22597600-22605800	Weak transcription	Left Ventricle	heart
24	chrY:22597800-22604000	Weak transcription	Pancreas	Pancrea
25	chrY:22604800-22605800	Enhancers	Dnd41	blood
26	chrY:22605800-22606000	Enhancers	Left Ventricle	heart
27	chrY:22605800-22606400	Flanking Active TSS	Dnd41	blood
28	chrY:22606000-22611400	Weak transcription	Left Ventricle	heart
29	chrY:22606400-22610800	Enhancers	Dnd41	blood
30	chrY:22609000-22609200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chrY:22609200-22609800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chrY:22609200-22610600	Enhancers	HSMMtube	muscle
33	chrY:22609800-22610000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chrY:22610000-22610400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chrY:22610400-22616200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chrY:22610800-22611200	ZNF genes & repeats	Dnd41	blood
37	chrY:22611400-22611800	ZNF genes & repeats	Left Ventricle	heart
38	chrY:22611800-22628800	Weak transcription	Left Ventricle	heart
39	chrY:22616600-22618200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chrY:22625400-22626400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chrY:22626400-22628000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chrY:22628000-22638400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chrY:22628800-22629000	Enhancers	Left Ventricle	heart
44	chrY:22637800-22640200	Weak transcription	Brain Hippocampus Middle	brain
45	chrY:22638400-22639800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chrY:22648800-22649600	Enhancers	Thymus	Thymus
47	chrY:22652000-22653800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chrY:22652600-22680000	Weak transcription	Left Ventricle	heart
49	chrY:22653800-22654400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chrY:22654400-22672200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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