Variant report

Variant	nsv995120
Chromosome Location	chrX:78528055-78946146
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1390)
CpG islands
(count:429)
Chromatin interactive
region (count:22)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1390 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:78619848-78620082	HepG2	liver:	n/a	n/a
2	ARID3A	chrX:78705812-78706026	K562	blood:	n/a	n/a
3	ARID3A	chrX:78705834-78706050	HepG2	liver:	n/a	n/a
4	BACH1	chrX:78622927-78623123	K562	blood:	n/a	n/a
5	BATF	chrX:78735482-78735650	GM12878	blood:	n/a	n/a
6	BATF	chrX:78885772-78886094	GM12878	blood:	n/a	n/a
7	BATF	chrX:78885743-78886112	GM12878	blood:	n/a	n/a
8	BHLHE40	chrX:78887341-78887467	GM12878	blood:	n/a	n/a
9	BHLHE40	chrX:78622320-78623349	K562	blood:	n/a	n/a
10	BHLHE40	chrX:78622383-78623243	GM12878	blood:	n/a	n/a
11	BHLHE40	chrX:78705870-78705988	GM12878	blood:	n/a	n/a
12	BHLHE40	chrX:78623624-78623797	GM12878	blood:	n/a	n/a
13	BRCA1	chrX:78902429-78902462	GM12878	blood:	n/a	n/a
14	CBX3	chrX:78679880-78680065	K562	blood:	n/a	n/a
15	CBX3	chrX:78679851-78680040	K562	blood:	n/a	n/a
16	CBX3	chrX:78622932-78623236	K562	blood:	n/a	n/a
17	CCNT2	chrX:78622220-78623187	K562	blood:	n/a	chrX:78622571-78622580
18	CEBPB	chrX:78902917-78903215	HepG2	liver:	n/a	chrX:78903096-78903107
19	CEBPB	chrX:78787499-78787686	H1-hESC	embryonic stem cell:	n/a	chrX:78787584-78787595
20	CEBPB	chrX:78902961-78903255	IMR90	lung:	n/a	chrX:78903096-78903107
21	CEBPB	chrX:78622947-78623197	K562	blood:	n/a	n/a
22	CEBPB	chrX:78675590-78675847	K562	blood:	n/a	chrX:78675679-78675690 chrX:78675679-78675688 chrX:78675677-78675688
23	CEBPB	chrX:78787444-78787721	HepG2	liver:	n/a	chrX:78787584-78787595
24	CEBPB	chrX:78675506-78675787	HepG2	liver:	n/a	chrX:78675679-78675690 chrX:78675679-78675688 chrX:78675677-78675688
25	CEBPB	chrX:78611876-78612152	K562	blood:	n/a	n/a
26	CEBPB	chrX:78899061-78899295	A549	lung:	n/a	n/a
27	CEBPB	chrX:78904168-78904463	IMR90	lung:	n/a	chrX:78904306-78904317
28	CEBPB	chrX:78888884-78889153	HepG2	liver:	n/a	chrX:78889057-78889068 chrX:78889043-78889054
29	CEBPB	chrX:78787453-78787776	IMR90	lung:	n/a	chrX:78787584-78787595
30	CEBPB	chrX:78877237-78877446	HepG2	liver:	n/a	chrX:78877347-78877358
31	CEBPB	chrX:78846653-78846908	IMR90	lung:	n/a	n/a
32	CEBPB	chrX:78921262-78921462	IMR90	lung:	n/a	n/a
33	CEBPB	chrX:78781532-78781857	IMR90	lung:	n/a	chrX:78781690-78781701
34	CEBPB	chrX:78918014-78918214	HepG2	liver:	n/a	chrX:78918126-78918137 chrX:78918104-78918115
35	CEBPB	chrX:78787431-78787758	A549	lung:	n/a	chrX:78787584-78787595
36	CEBPB	chrX:78622768-78623232	K562	blood:	n/a	n/a
37	CEBPB	chrX:78904275-78904480	HepG2	liver:	n/a	chrX:78904306-78904317
38	CEBPB	chrX:78675550-78675840	IMR90	lung:	n/a	chrX:78675679-78675690 chrX:78675679-78675688 chrX:78675677-78675688
39	CEBPB	chrX:78704080-78704409	A549	lung:	n/a	chrX:78704261-78704270 chrX:78704261-78704270 chrX:78704259-78704270 chrX:78704261-78704270 chrX:78704261-78704270
40	CEBPB	chrX:78888919-78889149	A549	lung:	n/a	chrX:78889057-78889068 chrX:78889043-78889054
41	CEBPB	chrX:78899082-78899357	IMR90	lung:	n/a	n/a
42	CEBPB	chrX:78619864-78620174	HepG2	liver:	n/a	n/a
43	CEBPB	chrX:78787419-78787664	MCF-7	breast:	n/a	chrX:78787584-78787595
44	CEBPB	chrX:78619906-78620219	K562	blood:	n/a	n/a
45	CEBPB	chrX:78781572-78781859	HepG2	liver:	n/a	chrX:78781690-78781701
46	CEBPB	chrX:78787471-78787718	K562	blood:	n/a	chrX:78787584-78787595
47	CEBPD	chrX:78622834-78623339	K562	blood:	n/a	n/a
48	CEBPD	chrX:78622727-78623240	K562	blood:	n/a	n/a
49	CHD1	chrX:78623554-78623726	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chrX:78622375-78622514	GM12878	blood:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:78624108-78624158	HepG2	liver:	n/a
2	chrX:78623745-78623795	SK-N-SH	brain:	n/a
3	chrX:78624108-78624158	HepG2	liver:	n/a
4	chrX:78623745-78623795	SK-N-SH	brain:	n/a
5	chrX:78622859-78622909	SKMC	muscle:	n/a
6	chrX:78623020-78623070	AG09309	skin:	n/a
7	chrX:78624108-78624158	HUVEC	blood vessel:	n/a
8	chrX:78622682-78622732	HCF	heart:	n/a
9	chrX:78622565-78622615	RPTEC	kidney:	n/a
10	chrX:78622682-78622732	K562	blood:	n/a
11	chrX:78623745-78623795	HPAEpiC	pulmonary alveolar:	n/a
12	chrX:78622565-78622615	HPAEpiC	pulmonary alveolar:	n/a
13	chrX:78623745-78623795	AG10803	skin:	n/a
14	chrX:78622565-78622615	GM19239	blood:	n/a
15	chrX:78622859-78622909	SAEC	small airway:	n/a
16	chrX:78622859-78622909	AG09309	skin:	n/a
17	chrX:78623020-78623070	HRCEpiC	kidney:	n/a
18	chrX:78623745-78623795	ovcar-3	ovarian:	n/a
19	chrX:78623956-78624006	NT2-D1	testis:	n/a
20	chrX:78624108-78624158	ProgFib	skin:	n/a
21	chrX:78623745-78623795	ProgFib	skin:	n/a
22	chrX:78623956-78624006	NH-A	brain:	n/a
23	chrX:78623745-78623795	AG09319	gingival:	n/a
24	chrX:78623745-78623795	NT2-D1	testis:	n/a
25	chrX:78623956-78624006	SAEC	small airway:	n/a
26	chrX:78622565-78622615	CMK	blood:	n/a
27	chrX:78623745-78623795	HAEpiC	amniotic membrane:	n/a
28	chrX:78624108-78624158	A549	lung:	n/a
29	chrX:78623956-78624006	HEEpiC	esophagus:	n/a
30	chrX:78623956-78624006	LNCaP	prostate:	n/a
31	chrX:78622565-78622615	GM12891	blood:	n/a
32	chrX:78623745-78623795	PFSK-1	brain:	n/a
33	chrX:78624108-78624158	HEK293	kidney:	embryo
34	chrX:78622682-78622732	ECC-1	luminal epithelium:	n/a
35	chrX:78623020-78623070	Jurkat	blood:	n/a
36	chrX:78622565-78622615	HRCEpiC	kidney:	n/a
37	chrX:78623020-78623070	HCPEpiC	choroid plexus:	n/a
38	chrX:78622859-78622909	H1-hESC	embryonic stem cell:	embryo
39	chrX:78623020-78623070	HIPEpiC	eye:	n/a
40	chrX:78624108-78624158	HAEpiC	amniotic membrane:	n/a
41	chrX:78622859-78622909	ovcar-3	ovarian:	n/a
42	chrX:78622682-78622732	HRPEpiC	eye:	n/a
43	chrX:78623745-78623795	HRPEpiC	eye:	n/a
44	chrX:78622859-78622909	HEEpiC	esophagus:	n/a
45	chrX:78623956-78624006	SK-N-MC	brain:	n/a
46	chrX:78622682-78622732	HRCEpiC	kidney:	n/a
47	chrX:78623020-78623070	HNPCEpiC	eye:	n/a
48	chrX:78624108-78624158	SAEC	small airway:	n/a
49	chrX:78623745-78623795	Jurkat	blood:	n/a
50	chrX:78623020-78623070	PANC-1	pancreas:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chrX:78615570..78618200-chrX:78620529..78622334,2	K562	blood:
2	chrX:78600900..78603777-chrX:78604763..78607370,2	MCF-7	breast:
3	chrX:78611688..78613722-chrX:78621637..78623492,2	K562	blood:
4	chrX:78525004..78527679-chrX:78527827..78529683,2	MCF-7	breast:
5	chr8:55770247..55770767-chrX:78893853..78894478,2	MCF-7	breast:
6	chrX:78600900..78603777-chrX:78604763..78607370,2	MCF-7	breast:
7	chrX:78733188..78733978-chrX:79285640..79286468,2	MCF-7	breast:
8	chrX:78615570..78618200-chrX:78620529..78622334,2	K562	blood:
9	chrX:78623909..78625908-chrX:78627039..78629119,3	K562	blood:
10	chrX:78612180..78614323-chrX:78618566..78621520,2	K562	blood:
11	chr11:118881446..118882428-chrX:78719744..78720315,2	MCF-7	breast:
12	chrX:78884290..78886421-chrX:78889264..78891291,2	K562	blood:
13	chrX:77811500..77813088-chrX:78666250..78667785,2	MCF-7	breast:
14	chr2:219180197..219181031-chrX:78672273..78672996,2	HCT-116	colon:
15	chr8:110352840..110355386-chrX:78849788..78852363,2	MCF-7	breast:
16	chrX:78828818..78830377-chrX:78830400..78832363,2	MCF-7	breast:
17	chrX:78828818..78830377-chrX:78830400..78832363,2	MCF-7	breast:
18	chr15:79105202..79107134-chrX:78755858..78757584,2	MCF-7	breast:
19	chrX:78613371..78615323-chrX:78622479..78624740,2	K562	blood:
20	chrX:78884290..78886421-chrX:78889264..78891291,2	K562	blood:
21	chrX:78615804..78618128-chrX:78622582..78624536,2	K562	blood:
22	chrX:77810661..77811278-chrX:78780189..78780762,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ITM2A-2	chrX:78624861-78625662	NONHSAT137716

No data

Variant related genes	Relation type
KIF4CP	TF binding region
ENSG00000270268	TF binding region
ITM2A	TF binding region
KIF4CP	CpG island
ENSG00000270268	CpG island
ITM2A	CpG island
ENSG00000078596	chromatin interactions
ENSG00000270268	chromatin interactions
ENSG00000186166	chromatin interactions

Extended variants
information (count: 1877 )
Associated
traits (count: 46 )

Variant overlapped rSNPs/rCNVs (count:1877 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138425719	chrX:78528155-78528156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs4240016	chrX:78528194-78528195	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs185152924	chrX:78528233-78528234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190084132	chrX:78528274-78528275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs34219226	chrX:78528330-78528331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs193209980	chrX:78528340-78528341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201739928	chrX:78528416-78528417	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7890114	chrX:78528585-78528586	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184740108	chrX:78528603-78528604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188118254	chrX:78528684-78528685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181019575	chrX:78528751-78528752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs367744628	chrX:78528814-78528815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7892183	chrX:78528827-78528828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371186243	chrX:78528845-78528846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183905012	chrX:78528887-78528888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs149326146	chrX:78528920-78528921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7878964	chrX:78529007-78529008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189703298	chrX:78529029-78529030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181349248	chrX:78529088-78529089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186778408	chrX:78529117-78529118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139116696	chrX:78529193-78529194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191606343	chrX:78529202-78529203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143969616	chrX:78529211-78529212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181890755	chrX:78529295-78529296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186581446	chrX:78529348-78529349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189753751	chrX:78529719-78529720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182425286	chrX:78529762-78529763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186862462	chrX:78529794-78529795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191322086	chrX:78529870-78529871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183024593	chrX:78529888-78529889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188501434	chrX:78529916-78529917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7061393	chrX:78530055-78530056	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
33	rs192985047	chrX:78530156-78530157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375293325	chrX:78530186-78530187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs578217813	chrX:78530566-78530567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184699768	chrX:78530592-78530593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374769231	chrX:78530618-78530619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192558835	chrX:78530716-78530717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs148644793	chrX:78530798-78530799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142111445	chrX:78530838-78530839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546240350	chrX:78530885-78530886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183523637	chrX:78530962-78530963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201337160	chrX:78530997-78530998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199622363	chrX:78530998-78530999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34009778	chrX:78531008-78531009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564753750	chrX:78531009-78531010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531017146	chrX:78531178-78531179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189184130	chrX:78531232-78531233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181120564	chrX:78531251-78531252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs5912855	chrX:78531291-78531292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:46)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	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
Autism	22495311	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Follicular lymphoma	20505157	CNVD
primary effusion lymphomas	17116491	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	22429812	CNVD
Cancer	16751803	CNVD
Premature ovarian failure	20952765	CNVD
Astrocytoma	22246337	CNVD
Mental retardation	17339581	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Alcoholism	21790672	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:78522200-78528800	Enhancers	Primary T helper cells fromperipheralblood	blood
2	chrX:78522200-78529200	Enhancers	Primary T helper cells PMA-I stimulated	--
3	chrX:78522600-78528600	Enhancers	Primary T cells from cord blood	blood
4	chrX:78522800-78528200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chrX:78523000-78542200	Weak transcription	Thymus	Thymus
6	chrX:78525000-78529200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chrX:78526800-78529200	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chrX:78527000-78528200	Weak transcription	Primary B cells from peripheral blood	blood
9	chrX:78527200-78528200	Weak transcription	Dnd41	blood
10	chrX:78527400-78528200	Enhancers	Primary B cells from cord blood	blood
11	chrX:78527400-78528600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chrX:78527400-78528800	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chrX:78527800-78528600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
14	chrX:78528200-78528400	Enhancers	Dnd41	blood
15	chrX:78528200-78529400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chrX:78528400-78528600	Enhancers	Primary B cells from peripheral blood	blood
17	chrX:78529400-78529600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chrX:78542200-78542400	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chrX:78542200-78542400	Enhancers	Fetal Thymus	thymus
20	chrX:78542200-78542600	Enhancers	Thymus	Thymus
21	chrX:78542200-78542800	Enhancers	Primary T cells from cord blood	blood
22	chrX:78542200-78547800	Enhancers	Dnd41	blood
23	chrX:78542400-78542600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
24	chrX:78542400-78545800	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chrX:78542600-78543600	Weak transcription	Fetal Thymus	thymus
26	chrX:78542600-78543600	Weak transcription	Thymus	Thymus
27	chrX:78542600-78543800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chrX:78542800-78543200	Active TSS	Primary T cells from cord blood	blood
29	chrX:78543200-78543600	Flanking Active TSS	Primary T cells from cord blood	blood
30	chrX:78543600-78544600	Enhancers	Primary T cells from cord blood	blood
31	chrX:78543600-78544600	Enhancers	Primary T cells fromperipheralblood	blood
32	chrX:78543600-78544600	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chrX:78543600-78547400	Enhancers	Thymus	Thymus
34	chrX:78543600-78547800	Enhancers	Fetal Thymus	thymus
35	chrX:78543800-78545000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chrX:78544200-78544800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chrX:78544400-78544800	Enhancers	H1 Cell Line	embryonic stem cell
38	chrX:78544600-78545600	Weak transcription	Primary T cells from cord blood	blood
39	chrX:78544600-78546200	Weak transcription	Primary T cells fromperipheralblood	blood
40	chrX:78545000-78545400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chrX:78545400-78546600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chrX:78545600-78547600	Enhancers	Primary T cells from cord blood	blood
43	chrX:78545800-78546200	Enhancers	Primary T helper cells fromperipheralblood	blood
44	chrX:78545800-78547400	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chrX:78546000-78546200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chrX:78546000-78547600	Enhancers	Primary hematopoietic stem cells	blood
47	chrX:78546200-78546800	Enhancers	Primary T cells fromperipheralblood	blood
48	chrX:78546200-78547600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chrX:78546800-78547400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chrX:78549000-78549600	Enhancers	HUES6 Cell Line	embryonic stem cell

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