Variant report

Variant	esv2758874
Chromosome Location	chrX:77226910-77309072
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:703)
CpG islands
(count:122)
Chromatin interactive
region (count:25)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:703 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:77285171-77285468	K562	blood:	n/a	n/a
2	ATF3	chrX:77279939-77280189	K562	blood:	n/a	n/a
3	BACH1	chrX:77256619-77256687	K562	blood:	n/a	n/a
4	BACH1	chrX:77301929-77302210	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chrX:77280257-77280584	GM12878	blood:	n/a	n/a
6	BHLHE40	chrX:77275717-77275853	K562	blood:	n/a	n/a
7	BHLHE40	chrX:77279867-77280560	K562	blood:	n/a	n/a
8	BHLHE40	chrX:77279867-77280571	HepG2	liver:	n/a	n/a
9	BHLHE40	chrX:77285470-77285487	K562	blood:	n/a	n/a
10	BRCA1	chrX:77231298-77231708	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chrX:77280646-77280715	GM12878	blood:	n/a	n/a
12	BRCA1	chrX:77232323-77232379	Hela-S3	cervix:	n/a	n/a
13	CBX3	chrX:77279786-77280190	K562	blood:	n/a	n/a
14	CEBPB	chrX:77305600-77305925	HepG2	liver:	n/a	chrX:77305770-77305781
15	CEBPB	chrX:77231383-77231696	IMR90	lung:	n/a	chrX:77231474-77231487
16	CEBPB	chrX:77305593-77305915	K562	blood:	n/a	chrX:77305770-77305781
17	CEBPB	chrX:77279841-77280497	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chrX:77250973-77251118	K562	blood:	n/a	n/a
19	CEBPB	chrX:77249578-77249744	K562	blood:	n/a	n/a
20	CEBPB	chrX:77232065-77233284	Hela-S3	cervix:	n/a	chrX:77232896-77232907
21	CEBPB	chrX:77277972-77278168	K562	blood:	n/a	n/a
22	CEBPB	chrX:77305586-77305947	IMR90	lung:	n/a	chrX:77305770-77305781
23	CEBPB	chrX:77305604-77305927	A549	lung:	n/a	chrX:77305770-77305781
24	CEBPB	chrX:77231115-77231755	Hela-S3	cervix:	n/a	chrX:77231474-77231487
25	CEBPB	chrX:77303577-77303779	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chrX:77279800-77280541	Hela-S3	cervix:	n/a	n/a
27	CHD2	chrX:77280313-77280484	GM12878	blood:	n/a	n/a
28	CTCF	chrX:77285100-77285250	HAc	cerebellar:	n/a	n/a
29	CTCF	chrX:77285260-77285410	NHEK	skin:	n/a	n/a
30	CTCF	chrX:77280360-77280510	GM12871	blood:	n/a	n/a
31	CTCF	chrX:77280344-77280519	ECC-1	luminal epithelium:	n/a	n/a
32	CTCF	chrX:77285160-77285310	HFF-Myc	foreskin:	n/a	n/a
33	CTCF	chrX:77280320-77280470	AG09319	gingival:	n/a	n/a
34	CTCF	chrX:77284697-77285726	A549	lung:	n/a	n/a
35	CTCF	chrX:77280096-77280163	GM19240	blood:	n/a	n/a
36	CTCF	chrX:77280345-77280546	GM13976	blood:	n/a	n/a
37	CTCF	chrX:77262114-77262215	Pancreas_OC	pancreas:	n/a	n/a
38	CTCF	chrX:77285260-77285410	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chrX:77280340-77280490	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chrX:77280326-77280468	MCF-7	breast:	n/a	n/a
41	CTCF	chrX:77279647-77280813	A549	lung:	n/a	n/a
42	CTCF	chrX:77280862-77280872	GM10266	blood:	n/a	n/a
43	CTCF	chrX:77280320-77280470	AG09309	skin:	n/a	n/a
44	CTCF	chrX:77280263-77280518	A549	lung:	n/a	n/a
45	CTCF	chrX:77280380-77280530	HCM	heart:	n/a	n/a
46	CTCF	chrX:77285280-77285430	AoAF	blood vessel:	n/a	n/a
47	CTCF	chrX:77280319-77280525	LNCaP	prostate:	n/a	n/a
48	CTCF	chrX:77285260-77285410	A549	lung:	n/a	n/a
49	CTCF	chrX:77280060-77280210	GM12866	blood:	n/a	n/a
50	CTCF	chrX:77280460-77280610	WI-38	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:77239706-77239756	AoSMC	blood vessel:	n/a
2	chrX:77239706-77239756	ProgFib	skin:	n/a
3	chrX:77303876-77303926	GM19239	blood:	n/a
4	chrX:77303876-77303926	HepG2	liver:	n/a
5	chrX:77239706-77239756	HPAEpiC	pulmonary alveolar:	n/a
6	chrX:77303876-77303926	HCPEpiC	choroid plexus:	n/a
7	chrX:77303876-77303926	MCF10A-Er-Src	breast:	n/a
8	chrX:77303876-77303926	RPTEC	kidney:	n/a
9	chrX:77303876-77303926	ECC-1	luminal epithelium:	n/a
10	chrX:77239706-77239756	MCF-7	breast:	n/a
11	chrX:77303876-77303926	GM06990	blood:	n/a
12	chrX:77239706-77239756	MCF10A-Er-Src	breast:	n/a
13	chrX:77239706-77239756	AG04450	lung:	fetal
14	chrX:77303876-77303926	HRE	kidney:	n/a
15	chrX:77303876-77303926	HCF	heart:	n/a
16	chrX:77303876-77303926	HPAEpiC	pulmonary alveolar:	n/a
17	chrX:77303876-77303926	CMK	blood:	n/a
18	chrX:77239706-77239756	HRPEpiC	eye:	n/a
19	chrX:77239706-77239756	AG09319	gingival:	n/a
20	chrX:77303876-77303926	HCM	heart:	n/a
21	chrX:77303876-77303926	K562	blood:	n/a
22	chrX:77303876-77303926	SK-N-SH_RA	brain:	n/a
23	chrX:77239706-77239756	NH-A	brain:	n/a
24	chrX:77239706-77239756	PrEC	prostate:	n/a
25	chrX:77239706-77239756	SK-N-SH	brain:	n/a
26	chrX:77303876-77303926	Caco-2	colon:	n/a
27	chrX:77239706-77239756	HAEpiC	amniotic membrane:	n/a
28	chrX:77239706-77239756	SK-N-MC	brain:	n/a
29	chrX:77303876-77303926	SK-N-MC	brain:	n/a
30	chrX:77239706-77239756	ovcar-3	ovarian:	n/a
31	chrX:77239706-77239756	BE2_C	brain:	n/a
32	chrX:77239706-77239756	GM06990	blood:	n/a
33	chrX:77239706-77239756	HIPEpiC	eye:	n/a
34	chrX:77239706-77239756	Hepatocyte	liver:	n/a
35	chrX:77239706-77239756	NT2-D1	testis:	n/a
36	chrX:77239706-77239756	U87	brain:	n/a
37	chrX:77239706-77239756	HepG2	liver:	n/a
38	chrX:77239706-77239756	HUVEC	blood vessel:	n/a
39	chrX:77239706-77239756	NB4	blood:	n/a
40	chrX:77239706-77239756	AG10803	skin:	n/a
41	chrX:77303876-77303926	PANC-1	pancreas:	n/a
42	chrX:77303876-77303926	LNCaP	prostate:	n/a
43	chrX:77239706-77239756	HCF	heart:	n/a
44	chrX:77239706-77239756	HMEC	breast:	n/a
45	chrX:77303876-77303926	H1-hESC	embryonic stem cell:	embryo
46	chrX:77303876-77303926	A549	lung:	n/a
47	chrX:77239706-77239756	GM12891	blood:	n/a
48	chrX:77239706-77239756	HCM	heart:	n/a
49	chrX:77239706-77239756	AG04449	skin:	fetal
50	chrX:77239706-77239756	IMR90	lung:	fetal

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:77285841..77288705-chrX:77290926..77293069,3	MCF-7	breast:
2	chrX:77231965..77235028-chrX:77236693..77239954,3	K562	blood:
3	chrX:77263570..77265987-chrX:77271725..77274130,2	K562	blood:
4	chrX:77231280..77233851-chrX:77237053..77239063,3	K562	blood:
5	chrX:77040121..77042552-chrX:77285390..77286999,2	MCF-7	breast:
6	chrX:77228292..77229799-chrX:77231409..77232965,2	MCF-7	breast:
7	chrX:77231280..77233851-chrX:77237053..77239063,3	K562	blood:
8	chrX:77262120..77263891-chrX:77267020..77269535,2	K562	blood:
9	chrX:77165649..77166434-chrX:77279943..77280808,5	MCF-7	breast:
10	chr10:11799709..11800460-chrX:77279944..77280508,2	K562	blood:
11	chrX:77164463..77167095-chrX:77284287..77285862,2	MCF-7	breast:
12	chrX:77263570..77265987-chrX:77271725..77274130,2	K562	blood:
13	chrX:77262120..77263891-chrX:77267020..77269535,2	K562	blood:
14	chrX:77150766..77152768-chrX:77280557..77283082,2	MCF-7	breast:
15	chrX:77154804..77156498-chrX:77275417..77277236,2	MCF-7	breast:
16	chrX:77153329..77155413-chrX:77248472..77249987,2	K562	blood:
17	chrX:77231965..77235028-chrX:77236693..77239954,3	K562	blood:
18	chrX:77165056..77166786-chrX:77252829..77255558,2	K562	blood:
19	chrX:77163838..77167539-chrX:77275299..77277613,3	MCF-7	breast:
20	chrX:77300334..77302047-chrX:77359005..77361971,2	K562	blood:
21	chrX:77165450..77167011-chrX:77279937..77280889,12	MCF-7	breast:
22	chrX:77153159..77156073-chrX:77281305..77283544,2	MCF-7	breast:
23	chrX:75499119..75500013-chrX:77279958..77280736,2	K562	blood:
24	chrX:77285841..77288705-chrX:77290926..77293069,3	MCF-7	breast:
25	chrX:77228292..77229799-chrX:77231409..77232965,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PGK1-2	chrX:77263703-77263995	expReg_chrX_4934_+
2	lnc-PGK1-3	chrX:77261614-77261936	expReg_chrX_4933_+

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	ATP7A	hsa-miR-9-5p	chrX:77304997-77305003
2	ATP7A	hsa-miR-148b-3p	chrX:77302103-77302110
3	ATP7A	hsa-miR-148b-3p	chrX:77302089-77302110
4	ATP7A	hsa-miR-320a	chrX:77302588-77302611

Variant related genes	Relation type
PGAM4	TF binding region
PGAM4	CpG island
ENSG00000248503	chromatin interactions
ENSG00000131174	chromatin interactions
ENSG00000085224	chromatin interactions
ENSG00000102144	chromatin interactions
ENSG00000102158	chromatin interactions
ENSG00000165240	chromatin interactions

Extended variants
information (count: 979 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374368574	chrX:77226986-77226987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145406974	chrX:77227195-77227196	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs376662883	chrX:77227273-77227274	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs200365512	chrX:77227301-77227302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139196328	chrX:77227452-77227453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113665704	chrX:77227586-77227587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184412702	chrX:77227620-77227621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371378425	chrX:77227806-77227807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539447719	chrX:77227942-77227943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538873356	chrX:77227943-77227944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147642975	chrX:77228199-77228200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140270766	chrX:77228450-77228451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187551287	chrX:77228660-77228661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs207478435	chrX:77228999-77229000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs193009346	chrX:77229223-77229224	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185678470	chrX:77229233-77229234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190552021	chrX:77229263-77229264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557564137	chrX:77229271-77229272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576242175	chrX:77229306-77229307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs180837193	chrX:77229310-77229311	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs74605876	chrX:77229347-77229348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs207478436	chrX:77229553-77229554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183719086	chrX:77229560-77229561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573845239	chrX:77229561-77229562	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35353275	chrX:77229652-77229653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541135244	chrX:77229717-77229718	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs148857351	chrX:77229951-77229952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181246931	chrX:77229986-77229987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374783104	chrX:77230193-77230194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200458835	chrX:77230387-77230388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368552817	chrX:77230407-77230408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs5902756	chrX:77230470-77230471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11381696	chrX:77230471-77230472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368239691	chrX:77230689-77230690	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs371982320	chrX:77230747-77230748	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185705395	chrX:77230930-77230931	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs5902757	chrX:77230978-77230979	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs200260360	chrX:77231004-77231005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs150524278	chrX:77231006-77231007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs5913629	chrX:77231171-77231172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191861088	chrX:77231229-77231230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559135768	chrX:77231233-77231234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375243655	chrX:77231278-77231279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs34715153	chrX:77231279-77231280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35963092	chrX:77231286-77231287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs143338812	chrX:77231297-77231298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs10521358	chrX:77231335-77231336	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs181891686	chrX:77231340-77231341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187341244	chrX:77231447-77231448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs5959962	chrX:77231618-77231619	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:43)

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
Breast cancer	21611746	CNVD
Premature ovarian failure	20952765	CNVD
Astrocytoma	22246337	CNVD
Mental retardation	17339581	CNVD
Breast cancer	21364760	CNVD
Alcoholism	21790672	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:77169200-77228200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chrX:77209200-77229400	Weak transcription	Ovary	ovary
3	chrX:77209800-77236400	Weak transcription	Primary hematopoietic stem cells	blood
4	chrX:77216600-77228600	Weak transcription	Dnd41	blood
5	chrX:77217200-77230600	Weak transcription	Hela-S3	cervix
6	chrX:77217400-77240200	Weak transcription	Primary B cells from peripheral blood	blood
7	chrX:77218000-77253800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chrX:77218200-77227800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chrX:77218200-77240400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chrX:77218200-77289000	Weak transcription	Primary T cells fromperipheralblood	blood
11	chrX:77219000-77228400	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chrX:77220400-77228000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chrX:77220400-77230800	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chrX:77220400-77232800	Weak transcription	Primary B cells from cord blood	blood
15	chrX:77220400-77237400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chrX:77223600-77238800	Weak transcription	Fetal Intestine Small	intestine
17	chrX:77224000-77268200	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chrX:77228200-77231000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chrX:77228400-77229200	Strong transcription	Primary T helper cells PMA-I stimulated	--
20	chrX:77228800-77231400	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chrX:77228800-77231400	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chrX:77228800-77231600	Weak transcription	Stomach Smooth Muscle	stomach
23	chrX:77229200-77302200	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chrX:77230600-77233800	Enhancers	Hela-S3	cervix
25	chrX:77231000-77232200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chrX:77231600-77232600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chrX:77231600-77233200	Enhancers	NHDF-Ad	bronchial
28	chrX:77232200-77232400	Enhancers	Fetal Kidney	kidney
29	chrX:77232200-77233600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chrX:77232400-77248000	Weak transcription	Fetal Kidney	kidney
31	chrX:77232600-77233200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chrX:77233200-77233400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chrX:77233600-77252200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chrX:77237800-77244800	Weak transcription	Primary T cells from cord blood	blood
35	chrX:77240200-77240400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chrX:77240200-77240800	Enhancers	Primary B cells from peripheral blood	blood
37	chrX:77240400-77240800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chrX:77240400-77251200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chrX:77240800-77244200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chrX:77242000-77253600	Weak transcription	Primary neutrophils fromperipheralblood	blood
41	chrX:77242400-77300600	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chrX:77242800-77245000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chrX:77243000-77244800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chrX:77243200-77245600	Weak transcription	Esophagus	oesophagus
45	chrX:77243800-77244000	Enhancers	Gastric	stomach
46	chrX:77243800-77246200	Weak transcription	Psoas Muscle	Psoas
47	chrX:77244000-77245800	Weak transcription	Gastric	stomach
48	chrX:77244200-77245400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chrX:77244800-77245400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chrX:77244800-77245600	Strong transcription	Primary T cells from cord blood	blood

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