Variant report

Variant	esv3494957
Chromosome Location	chrX:55328700-55585199
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1618)
CpG islands
(count:1345)
Chromatin interactive
region (count:18)
LncRNA
region (count:4)
Mature miRNA
region (count: 4)
miRNA target
sites (count:0)

(count:1618 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:55506933-55507364	K562	blood:	n/a	n/a
2	ATF1	chrX:55506954-55507404	K562	blood:	n/a	n/a
3	ATF1	chrX:55353407-55353649	K562	blood:	n/a	n/a
4	BACH1	chrX:55516407-55516607	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chrX:55478411-55478700	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chrX:55517421-55517768	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chrX:55482404-55482614	GM12878	blood:	n/a	n/a
8	BATF	chrX:55491525-55491918	GM12878	blood:	n/a	n/a
9	BATF	chrX:55543404-55543649	GM12878	blood:	n/a	n/a
10	BATF	chrX:55490910-55491095	GM12878	blood:	n/a	n/a
11	BATF	chrX:55534117-55534510	GM12878	blood:	n/a	n/a
12	BATF	chrX:55534938-55535123	GM12878	blood:	n/a	n/a
13	BATF	chrX:55482384-55482629	GM12878	blood:	n/a	n/a
14	BATF	chrX:55543419-55543629	GM12878	blood:	n/a	n/a
15	BCL3	chrX:55360146-55360356	GM12878	blood:	n/a	n/a
16	BHLHE40	chrX:55507203-55507460	K562	blood:	n/a	n/a
17	BHLHE40	chrX:55478482-55478800	K562	blood:	n/a	n/a
18	BHLHE40	chrX:55515573-55516240	GM12878	blood:	n/a	n/a
19	BHLHE40	chrX:55515858-55516304	K562	blood:	n/a	n/a
20	BHLHE40	chrX:55369623-55369757	K562	blood:	n/a	n/a
21	BRCA1	chrX:55516007-55516048	GM12878	blood:	n/a	n/a
22	CBX3	chrX:55478345-55478660	K562	blood:	n/a	n/a
23	CCNT2	chrX:55507150-55507397	K562	blood:	n/a	chrX:55507307-55507327
24	CCNT2	chrX:55514995-55516347	K562	blood:	n/a	chrX:55516326-55516335 chrX:55515661-55515670
25	CEBPB	chrX:55441143-55441278	A549	lung:	n/a	n/a
26	CEBPB	chrX:55507237-55507439	K562	blood:	n/a	n/a
27	CEBPB	chrX:55472006-55472217	IMR90	lung:	n/a	chrX:55472028-55472039
28	CEBPB	chrX:55506570-55506795	K562	blood:	n/a	n/a
29	CEBPB	chrX:55441069-55441359	IMR90	lung:	n/a	chrX:55441139-55441152 chrX:55441141-55441150
30	CEBPB	chrX:55396797-55397250	IMR90	lung:	n/a	n/a
31	CEBPB	chrX:55412611-55412849	A549	lung:	n/a	n/a
32	CEBPB	chrX:55365362-55365675	IMR90	lung:	n/a	chrX:55365525-55365536
33	CEBPB	chrX:55365397-55365653	A549	lung:	n/a	chrX:55365525-55365536
34	CEBPB	chrX:55365436-55365636	HepG2	liver:	n/a	chrX:55365525-55365536
35	CEBPB	chrX:55366047-55366244	K562	blood:	n/a	chrX:55366125-55366136
36	CEBPB	chrX:55432928-55433200	IMR90	lung:	n/a	n/a
37	CEBPB	chrX:55365479-55365697	K562	blood:	n/a	chrX:55365525-55365536
38	CEBPB	chrX:55406772-55407008	IMR90	lung:	n/a	n/a
39	CEBPB	chrX:55365982-55366294	HepG2	liver:	n/a	chrX:55366125-55366136
40	CEBPB	chrX:55412619-55412835	IMR90	lung:	n/a	n/a
41	CEBPB	chrX:55432947-55433155	K562	blood:	n/a	n/a
42	CEBPB	chrX:55472004-55472211	HepG2	liver:	n/a	chrX:55472028-55472039
43	CEBPB	chrX:55514343-55514601	K562	blood:	n/a	n/a
44	CEBPD	chrX:55507118-55507575	K562	blood:	n/a	n/a
45	CEBPD	chrX:55507154-55507481	K562	blood:	n/a	n/a
46	CHD1	chrX:55515264-55515417	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chrX:55515733-55515968	GM12878	blood:	n/a	n/a
48	CHD1	chrX:55515703-55516071	H1-hESC	embryonic stem cell:	n/a	chrX:55515715-55515722
49	CHD2	chrX:55478405-55478743	K562	blood:	n/a	n/a
50	CHD2	chrX:55515354-55515800	K562	blood:	n/a	chrX:55515715-55515722

(count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:55478180-55478230	AoSMC	blood vessel:	n/a
2	chrX:55479357-55479407	SK-N-SH	brain:	n/a
3	chrX:55478610-55478660	GM12878	blood:	n/a
4	chrX:55478180-55478230	AoSMC	blood vessel:	n/a
5	chrX:55479357-55479407	SK-N-SH	brain:	n/a
6	chrX:55478610-55478660	GM12878	blood:	n/a
7	chrX:55479202-55479252	HepG2	liver:	n/a
8	chrX:55513504-55513554	HUVEC	blood vessel:	n/a
9	chrX:55478814-55478864	SKMC	muscle:	n/a
10	chrX:55519357-55519407	HEEpiC	esophagus:	n/a
11	chrX:55479357-55479407	HNPCEpiC	eye:	n/a
12	chrX:55478329-55478379	Hepatocyte	liver:	n/a
13	chrX:55478610-55478660	HEEpiC	esophagus:	n/a
14	chrX:55479616-55479666	A549	lung:	n/a
15	chrX:55477154-55477204	HCM	heart:	n/a
16	chrX:55479616-55479666	BE2_C	brain:	n/a
17	chrX:55513079-55513129	K562	blood:	n/a
18	chrX:55478610-55478660	PFSK-1	brain:	n/a
19	chrX:55513079-55513129	HNPCEpiC	eye:	n/a
20	chrX:55477154-55477204	GM19239	blood:	n/a
21	chrX:55478814-55478864	GM06990	blood:	n/a
22	chrX:55479616-55479666	PFSK-1	brain:	n/a
23	chrX:55519357-55519407	NHBE	bronchial:	n/a
24	chrX:55478180-55478230	GM12892	blood:	n/a
25	chrX:55515315-55515365	HCM	heart:	n/a
26	chrX:55479357-55479407	K562	blood:	n/a
27	chrX:55477154-55477204	HAEpiC	amniotic membrane:	n/a
28	chrX:55515952-55516002	HUVEC	blood vessel:	n/a
29	chrX:55478814-55478864	HRPEpiC	eye:	n/a
30	chrX:55478180-55478230	NHDF-neo	bronchial:	n/a
31	chrX:55479616-55479666	HCPEpiC	choroid plexus:	n/a
32	chrX:55478814-55478864	RPTEC	kidney:	n/a
33	chrX:55515952-55516002	AG09309	skin:	n/a
34	chrX:55513504-55513554	HCM	heart:	n/a
35	chrX:55477154-55477204	AG04450	lung:	fetal
36	chrX:55519357-55519407	HEK293	kidney:	embryo
37	chrX:55515614-55515664	A549	lung:	n/a
38	chrX:55513504-55513554	Caco-2	colon:	n/a
39	chrX:55515614-55515664	HCPEpiC	choroid plexus:	n/a
40	chrX:55478329-55478379	SK-N-SH	brain:	n/a
41	chrX:55478329-55478379	PrEC	prostate:	n/a
42	chrX:55513079-55513129	HL-60	blood:	n/a
43	chrX:55515315-55515365	LNCaP	prostate:	n/a
44	chrX:55516236-55516286	NT2-D1	testis:	n/a
45	chrX:55513504-55513554	HL-60	blood:	n/a
46	chrX:55516236-55516286	GM06990	blood:	n/a
47	chrX:55515952-55516002	NHBE	bronchial:	n/a
48	chrX:55516224-55516274	RPTEC	kidney:	n/a
49	chrX:55515483-55515533	NHDF-neo	bronchial:	n/a
50	chrX:55479616-55479666	AoSMC	blood vessel:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:55161366..55162313-chrX:55339201..55340117,3	MCF-7	breast:
2	chrX:55459913..55461518-chrX:55462425..55464666,2	K562	blood:
3	chrX:55564880..55567793-chrX:55576082..55578141,2	K562	blood:
4	chrX:55352524..55354094-chrX:55354666..55357445,2	MCF-7	breast:
5	chrX:55507203..55510619-chrX:55512765..55519080,7	K562	blood:
6	chr4:129731682..129733884-chrX:55516164..55517683,2	K562	blood:
7	chrX:55379431..55381921-chrX:55391030..55393821,2	K562	blood:
8	chrX:55459913..55461518-chrX:55462425..55464666,2	K562	blood:
9	chrX:55478272..55480275-chrX:55742945..55745674,2	MCF-7	breast:
10	chrX:55339432..55341262-chrX:55355594..55357140,2	K562	blood:
11	chrX:55161709..55162983-chrX:55369213..55369929,3	MCF-7	breast:
12	chrX:55339432..55341262-chrX:55355594..55357140,2	K562	blood:
13	chrX:55379431..55381921-chrX:55391030..55393821,2	K562	blood:
14	chrX:55564880..55567793-chrX:55576082..55578141,2	K562	blood:
15	chrX:55352524..55354094-chrX:55354666..55357445,2	MCF-7	breast:
16	chr3:145877632..145880246-chrX:55477813..55479806,2	MCF-7	breast:
17	chrX:55515441..55517417-chrX:55743446..55745792,2	MCF-7	breast:
18	chrX:55477578..55479496-chrX:55512126..55514643,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USP51-2	chrX:55515669-55515798	NONHSAT137252
2	lnc-USP51-2	chrX:55516209-55516513	NONHSAT137252
3	lnc-USP51-1	chrX:55515603-55515641	NONHSAT137251
4	lnc-USP51-1	chrX:55514448-55515421	NONHSAT137251

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4536-3p	chrX:55477995-55478015	MIMAT0020959
hsa-miR-4536-5p	chrX:55477929-55477949	MIMAT0019078
hsa-miR-4536-3p	chrX:55477928-55477948	MIMAT0020959_1
hsa-miR-4536-5p	chrX:55477994-55478014	MIMAT0019078_1

No data

Variant related genes	Relation type
ENSG00000266328	TF binding region
USP51	TF binding region
MAGEH1	TF binding region
ENSG00000266328	CpG island
USP51	CpG island
MAGEH1	CpG island
ENSG00000266328	chromatin interactions
ENSG00000077684	chromatin interactions
ENSG00000083750	chromatin interactions
ENSG00000187601	chromatin interactions
ENSG00000152952	chromatin interactions
ENSG00000247746	chromatin interactions

Extended variants
information (count: 630 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:630 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528915211	chrX:55339522-55339523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs374049281	chrX:55339583-55339584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181986826	chrX:55339585-55339586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186715285	chrX:55339692-55339693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190421498	chrX:55339844-55339845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145346799	chrX:55349627-55349628	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs183391213	chrX:55349631-55349632	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs555880375	chrX:55349713-55349714	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs147669965	chrX:55349734-55349735	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs187391731	chrX:55349824-55349825	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs192221161	chrX:55349836-55349837	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs184054820	chrX:55349841-55349842	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs1927296	chrX:55353419-55353420	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs190828638	chrX:55353434-55353435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146148755	chrX:55353507-55353508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368244981	chrX:55353568-55353569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183265805	chrX:55353609-55353610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187982604	chrX:55353717-55353718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs140017918	chrX:55353740-55353741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs149403735	chrX:55353772-55353773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192607631	chrX:55353850-55353851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372272044	chrX:55353905-55353906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572335839	chrX:55354019-55354020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs5914314	chrX:55354043-55354044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs148523550	chrX:55354049-55354050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182983465	chrX:55354165-55354166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs73214695	chrX:55354229-55354230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188531980	chrX:55354240-55354241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565817675	chrX:55354245-55354246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184590161	chrX:55354830-55354831	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs144652245	chrX:55354936-55354937	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs151004086	chrX:55354955-55354956	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs373436885	chrX:55354994-55354995	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs140907080	chrX:55355003-55355004	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs375194155	chrX:55355151-55355152	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs189230817	chrX:55355178-55355179	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs148374459	chrX:55356605-55356606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553138722	chrX:55356697-55356698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs72620373	chrX:55356780-55356781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs141580980	chrX:55356893-55356894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375246678	chrX:55356904-55356905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs150866191	chrX:55356909-55356910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138494028	chrX:55357029-55357030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs376523083	chrX:55357054-55357055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs12396664	chrX:55357094-55357095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190923661	chrX:55357152-55357153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs180786840	chrX:55357175-55357176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs185452364	chrX:55357219-55357220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs11798822	chrX:55357354-55357355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs147268823	chrX:55357379-55357380	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
Autism	22495311	CNVD
Glioblastoma multiforme	22286061	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Mental retardation	20877625	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:766 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:55339200-55340000	Enhancers	HMEC	breast
2	chrX:55349600-55350000	ZNF genes & repeats	Lung	lung
3	chrX:55353400-55354400	Enhancers	Rectal Mucosa Donor 31	rectum
4	chrX:55354800-55355200	Bivalent Enhancer	Adipose Nuclei	Adipose
5	chrX:55356600-55357400	Enhancers	Spleen	Spleen
6	chrX:55361000-55361400	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chrX:55361000-55361800	Enhancers	Primary T cells fromperipheralblood	blood
8	chrX:55361000-55361800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chrX:55361200-55362000	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chrX:55361800-55362000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chrX:55361800-55368200	Weak transcription	Primary T cells fromperipheralblood	blood
12	chrX:55362000-55362800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chrX:55362000-55369200	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chrX:55362800-55363000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chrX:55363000-55367000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chrX:55364400-55368200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chrX:55367000-55368200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chrX:55367000-55368400	Enhancers	NHEK	skin
19	chrX:55367200-55368400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chrX:55367400-55367800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chrX:55367600-55368200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chrX:55367600-55368400	Enhancers	Left Ventricle	heart
23	chrX:55367600-55369600	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chrX:55368000-55368600	Enhancers	Fetal Intestine Small	intestine
25	chrX:55368000-55369200	Enhancers	Fetal Intestine Large	intestine
26	chrX:55368200-55368400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chrX:55368200-55368400	Enhancers	Primary T cells fromperipheralblood	blood
28	chrX:55368200-55368400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chrX:55368200-55368400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chrX:55368200-55368400	Flanking Active TSS	Lung	lung
31	chrX:55368200-55369200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chrX:55368200-55369800	Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chrX:55368400-55369200	Weak transcription	Primary T cells fromperipheralblood	blood
34	chrX:55368400-55369200	Weak transcription	Left Ventricle	heart
35	chrX:55368400-55369400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chrX:55368400-55369600	Active TSS	ES-I3 Cell Line	embryonic stem cell
37	chrX:55368400-55369600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chrX:55368600-55369600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chrX:55368800-55369000	Enhancers	Primary hematopoietic stem cells	blood
40	chrX:55368800-55369200	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chrX:55368800-55369800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
42	chrX:55368800-55370400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chrX:55369200-55369400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
44	chrX:55369200-55369600	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chrX:55369200-55369800	Enhancers	Left Ventricle	heart
46	chrX:55369200-55370600	Enhancers	Primary T cells fromperipheralblood	blood
47	chrX:55369200-55370600	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chrX:55369400-55370000	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chrX:55369600-55370000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chrX:55369600-55370200	Enhancers	Primary T helper cells fromperipheralblood	blood

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