Variant report

Variant	nsv6916
Chromosome Location	chrX:56553895-56598754
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:671)
CpG islands
(count:854)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:56589498-56590094	K562	blood:	n/a	n/a
2	ARID3A	chrX:56593079-56593262	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:56589570-56590129	HepG2	liver:	n/a	n/a
4	BACH1	chrX:56596195-56596448	K562	blood:	n/a	n/a
5	BATF	chrX:56590726-56591085	GM12878	blood:	n/a	n/a
6	BHLHE40	chrX:56589836-56590376	GM12878	blood:	n/a	chrX:56590204-56590220
7	BHLHE40	chrX:56589840-56590285	K562	blood:	n/a	chrX:56590204-56590220
8	BHLHE40	chrX:56595843-56596542	GM12878	blood:	n/a	n/a
9	BHLHE40	chrX:56589233-56589297	GM12878	blood:	n/a	n/a
10	BRCA1	chrX:56589200-56590161	Hela-S3	cervix:	n/a	n/a
11	CBX3	chrX:56571943-56572148	K562	blood:	n/a	n/a
12	CBX3	chrX:56589707-56590153	K562	blood:	n/a	n/a
13	CBX3	chrX:56571886-56572097	K562	blood:	n/a	n/a
14	CCNT2	chrX:56589781-56590490	K562	blood:	n/a	chrX:56589961-56589970 chrX:56589998-56590007 chrX:56589987-56589996
15	CEBPB	chrX:56594271-56594586	A549	lung:	n/a	chrX:56594443-56594454
16	CEBPB	chrX:56581465-56581676	HepG2	liver:	n/a	n/a
17	CEBPB	chrX:56590870-56591234	K562	blood:	n/a	chrX:56591032-56591043
18	CEBPB	chrX:56589668-56591396	Hela-S3	cervix:	n/a	chrX:56591032-56591043
19	CEBPB	chrX:56594280-56594603	IMR90	lung:	n/a	chrX:56594443-56594454
20	CEBPB	chrX:56594294-56594636	K562	blood:	n/a	chrX:56594443-56594454
21	CEBPB	chrX:56590880-56591160	H1-hESC	embryonic stem cell:	n/a	chrX:56591032-56591043
22	CEBPB	chrX:56594295-56594570	HepG2	liver:	n/a	chrX:56594443-56594454
23	CEBPB	chrX:56589688-56589892	A549	lung:	n/a	n/a
24	CEBPB	chrX:56586002-56586071	K562	blood:	n/a	n/a
25	CEBPB	chrX:56590461-56591217	IMR90	lung:	n/a	chrX:56591032-56591043
26	CEBPB	chrX:56590324-56590645	K562	blood:	n/a	n/a
27	CEBPB	chrX:56590892-56591213	A549	lung:	n/a	chrX:56591032-56591043
28	CEBPB	chrX:56590893-56591210	HepG2	liver:	n/a	chrX:56591032-56591043
29	CEBPB	chrX:56590323-56590648	A549	lung:	n/a	n/a
30	CHD1	chrX:56590884-56590906	GM12878	blood:	n/a	n/a
31	CHD1	chrX:56589703-56590509	GM12878	blood:	n/a	chrX:56589962-56589972
32	CHD1	chrX:56590448-56590968	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chrX:56589649-56591260	Hela-S3	cervix:	n/a	chrX:56589962-56589972
34	CHD2	chrX:56589840-56590202	H1-hESC	embryonic stem cell:	n/a	chrX:56589962-56589972
35	CHD2	chrX:56589725-56590530	GM12878	blood:	n/a	chrX:56589962-56589972
36	CHD2	chrX:56589784-56590145	HepG2	liver:	n/a	chrX:56589962-56589972
37	CHD2	chrX:56589725-56590686	K562	blood:	n/a	chrX:56589962-56589972
38	CREB1	chrX:56589655-56590562	GM12878	blood:	n/a	n/a
39	CREB1	chrX:56589717-56590545	HepG2	liver:	n/a	n/a
40	CREB1	chrX:56589757-56590063	A549	lung:	n/a	n/a
41	CREB1	chrX:56589722-56590462	K562	blood:	n/a	n/a
42	CREB1	chrX:56589793-56590450	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chrX:56589756-56590394	A549	lung:	n/a	n/a
44	CREB1	chrX:56595244-56595629	GM12878	blood:	n/a	chrX:56595380-56595393
45	CREB1	chrX:56589662-56590590	K562	blood:	n/a	n/a
46	CREB1	chrX:56589721-56590506	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chrX:56590108-56590114	GM19239	blood:	n/a	n/a
48	CTCF	chrX:56589680-56589830	HFF	foreskin:	n/a	n/a
49	CTCF	chrX:56578224-56578309	GM20000	blood:	n/a	n/a
50	CTCF	chrX:56589738-56589741	LNCaP	prostate:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:56590362-56590412	SAEC	small airway:	n/a
2	chrX:56589768-56589818	HCM	heart:	n/a
3	chrX:56590097-56590147	HIPEpiC	eye:	n/a
4	chrX:56589792-56589842	GM06990	blood:	n/a
5	chrX:56590187-56590237	HMEC	breast:	n/a
6	chrX:56589768-56589818	GM12878	blood:	n/a
7	chrX:56590187-56590237	HCM	heart:	n/a
8	chrX:56589918-56589968	NB4	blood:	n/a
9	chrX:56590386-56590436	AG10803	skin:	n/a
10	chrX:56590386-56590436	IMR90	lung:	fetal
11	chrX:56586577-56586627	GM19239	blood:	n/a
12	chrX:56589768-56589818	Hela-S3	cervix:	n/a
13	chrX:56590113-56590163	HUVEC	blood vessel:	n/a
14	chrX:56590097-56590147	AG10803	skin:	n/a
15	chrX:56590362-56590412	GM12892	blood:	n/a
16	chrX:56589949-56589999	HEK293	kidney:	embryo
17	chrX:56590513-56590563	RPTEC	kidney:	n/a
18	chrX:56586577-56586627	MCF10A-Er-Src	breast:	n/a
19	chrX:56589768-56589818	NHDF-neo	bronchial:	n/a
20	chrX:56589792-56589842	PrEC	prostate:	n/a
21	chrX:56590513-56590563	ECC-1	luminal epithelium:	n/a
22	chrX:56590386-56590436	Hepatocyte	liver:	n/a
23	chrX:56589951-56590001	U87	brain:	n/a
24	chrX:56586577-56586627	CMK	blood:	n/a
25	chrX:56589918-56589968	HMEC	breast:	n/a
26	chrX:56589792-56589842	MCF10A-Er-Src	breast:	n/a
27	chrX:56586577-56586627	GM12891	blood:	n/a
28	chrX:56586577-56586627	Caco-2	colon:	n/a
29	chrX:56589946-56589996	NH-A	brain:	n/a
30	chrX:56590097-56590147	SK-N-SH_RA	brain:	n/a
31	chrX:56589792-56589842	NB4	blood:	n/a
32	chrX:56586577-56586627	AG10803	skin:	n/a
33	chrX:56589792-56589842	HCM	heart:	n/a
34	chrX:56590386-56590436	GM12891	blood:	n/a
35	chrX:56589918-56589968	SK-N-SH_RA	brain:	n/a
36	chrX:56589946-56589996	AG04450	lung:	fetal
37	chrX:56590097-56590147	HPAEpiC	pulmonary alveolar:	n/a
38	chrX:56590537-56590587	Hepatocyte	liver:	n/a
39	chrX:56590362-56590412	PANC-1	pancreas:	n/a
40	chrX:56590097-56590147	ProgFib	skin:	n/a
41	chrX:56590362-56590412	PFSK-1	brain:	n/a
42	chrX:56589949-56589999	HEEpiC	esophagus:	n/a
43	chrX:56590362-56590412	T-47D	breast:	n/a
44	chrX:56590187-56590237	NB4	blood:	n/a
45	chrX:56590187-56590237	HUVEC	blood vessel:	n/a
46	chrX:56589951-56590001	K562	blood:	n/a
47	chrX:56586577-56586627	SK-N-MC	brain:	n/a
48	chrX:56589949-56589999	SK-N-MC	brain:	n/a
49	chrX:56590537-56590587	BE2_C	brain:	n/a
50	chrX:56586577-56586627	AG04449	skin:	fetal

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:56560010..56562165-chrX:56589519..56591706,2	K562	blood:
2	chrX:56581297..56583296-chrX:56585127..56587340,2	K562	blood:
3	chr11:93474405..93474909-chrX:56589618..56590518,2	Hela-S3	cervix:
4	chrX:56589521..56592004-chrX:56754888..56757482,3	MCF-7	breast:
5	chr14:91976352..91977083-chrX:56590252..56590789,2	Hela-S3	cervix:
6	chrX:56593306..56595130-chrX:56601752..56604305,2	K562	blood:
7	chr9:128508522..128509472-chrX:56589807..56590542,2	Hela-S3	cervix:
8	chrX:56583895..56586731-chrX:56587526..56591392,3	K562	blood:
9	chrX:55743259..55745403-chrX:56589658..56591573,2	MCF-7	breast:
10	chr15:59664953..59665488-chrX:56589789..56590649,2	Hela-S3	cervix:
11	chrX:56581288..56583917-chrX:56588931..56591229,2	MCF-7	breast:
12	chrX:56580407..56582140-chrX:56590600..56592126,2	K562	blood:
13	chrX:56581292..56583296-chrX:56585105..56587340,2	K562	blood:
14	chrX:56580407..56582140-chrX:56590600..56592126,2	K562	blood:
15	chrX:56582792..56586142-chrX:56588656..56592207,5	MCF-7	breast:
16	chrX:56592338..56594016-chrX:56602006..56603920,2	MCF-7	breast:
17	chrX:56581297..56583296-chrX:56585127..56587340,2	K562	blood:
18	chrX:56595142..56598529-chrX:56599430..56604121,4	K562	blood:
19	chr16:3313684..3314490-chrX:56589920..56590436,2	Hela-S3	cervix:
20	chrX:56595436..56598724-chrX:56598981..56601324,4	K562	blood:
21	chrX:56583300..56586802-chrX:56587902..56592521,5	K562	blood:
22	chrX:56581292..56583296-chrX:56585105..56587340,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	UBQLN2	hsa-miR-155-5p	chrX:56593322-56593344
2	UBQLN2	hsa-miR-155-5p	chrX:56593242-56593263

Variant related genes	Relation type
UBQLN2	TF binding region
UBQLN2	CpG island
ENSG00000157483	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000204272	chromatin interactions
ENSG00000006194	chromatin interactions
ENSG00000229582	chromatin interactions
ENSG00000188021	chromatin interactions
ENSG00000083750	chromatin interactions
ENSG00000157470	chromatin interactions
ENSG00000100796	chromatin interactions
ENSG00000166012	chromatin interactions

Extended variants
information (count: 310 )
Associated
traits (count: 41 )

Variant overlapped rSNPs/rCNVs (count:310 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191761815	chrX:56556422-56556423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs181555351	chrX:56556478-56556479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553171943	chrX:56556541-56556542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185826524	chrX:56556595-56556596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190153223	chrX:56556633-56556634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs370878528	chrX:56556637-56556638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182367572	chrX:56556639-56556640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552931522	chrX:56556767-56556768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373885056	chrX:56556778-56556779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187483099	chrX:56556827-56556828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146781767	chrX:56556909-56556910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs377146379	chrX:56556941-56556942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140427586	chrX:56556981-56556982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192329695	chrX:56556987-56556988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs151049005	chrX:56560155-56560156	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs190966864	chrX:56560159-56560160	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs1889850	chrX:56560214-56560215	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs182770643	chrX:56560246-56560247	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs73626204	chrX:56560251-56560252	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs190787601	chrX:56560350-56560351	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs5914700	chrX:56560352-56560353	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs147645808	chrX:56560353-56560354	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs182944697	chrX:56560385-56560386	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs142141685	chrX:56560472-56560473	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs145966403	chrX:56560492-56560493	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs187243445	chrX:56560545-56560546	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs191703670	chrX:56560647-56560648	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs183227447	chrX:56560710-56560711	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs138702190	chrX:56560795-56560796	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs545003204	chrX:56561141-56561142	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs374814777	chrX:56561399-56561400	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs188213156	chrX:56561410-56561411	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs192447051	chrX:56561412-56561413	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs34715679	chrX:56561461-56561462	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs190466825	chrX:56561478-56561479	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs192401622	chrX:56561495-56561496	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs7066052	chrX:56561517-56561518	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs184564190	chrX:56561593-56561594	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs188883934	chrX:56561668-56561669	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs181589584	chrX:56561691-56561692	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs186495857	chrX:56561840-56561841	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs4826476	chrX:56561873-56561874	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs189761078	chrX:56561883-56561884	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs180960358	chrX:56561996-56561997	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs372100882	chrX:56562017-56562018	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs185949988	chrX:56580856-56580857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs144239913	chrX:56580949-56580950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188724993	chrX:56581019-56581020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs369370169	chrX:56581063-56581064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs148058224	chrX:56581178-56581179	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:41)

Disease	PMID	Source
Cancer	21637783	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Cancer	16751803	CNVD
Intellectual disability	23615299	CNVD
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Astrocytoma	17387387	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	21979893	CNVD
Schizophrenia	23904455	CNVD
Olfactory neuroblastoma	18408657	CNVD
infertile	22614455	CNVD
Acute myeloid leukemia	20729466	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	22286061	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Cancer	20164919	CNVD
Premature ovarian failure	20952765	CNVD
Thyroid cancer	19087340	CNVD
lymphocytic leukemia	21291569	CNVD
Cervical cancer	21062161	CNVD
Follicular lymphoma	20505157	CNVD
primary effusion lymphomas	17116491	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	19835627	CNVD
Mental retardation	21735175	CNVD

Chromatin state (count:605 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:56556400-56557200	Enhancers	Liver	Liver
2	chrX:56580800-56582000	Enhancers	Liver	Liver
3	chrX:56581200-56581800	Enhancers	HepG2	liver
4	chrX:56581200-56582000	Enhancers	Rectal Mucosa Donor 31	rectum
5	chrX:56587400-56587600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chrX:56587600-56588800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chrX:56587600-56589200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chrX:56588000-56589200	Enhancers	Dnd41	blood
9	chrX:56588600-56589000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chrX:56588600-56589000	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chrX:56588600-56589200	Enhancers	Primary hematopoietic stem cells	blood
12	chrX:56588600-56589200	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chrX:56588600-56589400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chrX:56588800-56589200	Enhancers	Primary T cells from cord blood	blood
15	chrX:56588800-56589200	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chrX:56588800-56589200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chrX:56588800-56593400	Bivalent/Poised TSS	Fetal Brain Female	brain
18	chrX:56589000-56589200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chrX:56589000-56589200	Enhancers	NH-A	brain
20	chrX:56589000-56589400	Enhancers	Primary B cells from cord blood	blood
21	chrX:56589000-56593800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chrX:56589200-56589400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chrX:56589200-56589400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chrX:56589200-56589400	Enhancers	Primary monocytes fromperipheralblood	blood
25	chrX:56589200-56589400	Flanking Active TSS	Primary T cells from cord blood	blood
26	chrX:56589200-56589400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
27	chrX:56589200-56589400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chrX:56589200-56589400	Enhancers	Adipose Nuclei	Adipose
29	chrX:56589200-56589600	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chrX:56589200-56589600	Enhancers	Primary B cells from peripheral blood	blood
31	chrX:56589200-56589600	Flanking Active TSS	Primary hematopoietic stem cells	blood
32	chrX:56589200-56589600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chrX:56589200-56589600	Enhancers	Fetal Intestine Small	intestine
34	chrX:56589200-56589600	Active TSS	Fetal Muscle Leg	muscle
35	chrX:56589200-56589600	Flanking Active TSS	NH-A	brain
36	chrX:56589200-56589800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
37	chrX:56589200-56589800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chrX:56589200-56590600	Active TSS	Dnd41	blood
39	chrX:56589200-56590800	Active TSS	K562	blood
40	chrX:56589200-56591200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chrX:56589200-56591200	Active TSS	Hela-S3	cervix
42	chrX:56589200-56591400	Active TSS	HUVEC	blood vessel
43	chrX:56589200-56592200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chrX:56589200-56592600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
45	chrX:56589200-56592600	Active TSS	HSMM	muscle
46	chrX:56589200-56593000	Active TSS	Fetal Brain Male	brain
47	chrX:56589200-56593200	Active TSS	Primary hematopoietic stem cells short term culture	blood
48	chrX:56589200-56593200	Active TSS	Cortex derived primary cultured neurospheres	brain
49	chrX:56589200-56593200	Active TSS	HSMMtube	muscle
50	chrX:56589200-56593200	Active TSS	Osteobl	bone

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