Variant report

Variant	nsv432352
Chromosome Location	chrX:104346855-104831855
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chrX:104465503-104465543	K562	blood:	n/a	n/a
2	CEBPB	chrX:104745813-104746070	HepG2	liver:	n/a	chrX:104745966-104745977
3	CEBPB	chrX:104708657-104709000	IMR90	lung:	n/a	chrX:104708827-104708838
4	CEBPB	chrX:104484452-104484671	IMR90	lung:	n/a	n/a
5	CEBPB	chrX:104494193-104494491	A549	lung:	n/a	chrX:104494341-104494352
6	CEBPB	chrX:104573501-104573850	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chrX:104473363-104473509	HepG2	liver:	n/a	chrX:104473428-104473439
8	CEBPB	chrX:104374282-104374584	A549	lung:	n/a	chrX:104374412-104374423
9	CEBPB	chrX:104747173-104747745	MCF-7	breast:	n/a	chrX:104747378-104747391 chrX:104747380-104747389
10	CEBPB	chrX:104437731-104437894	K562	blood:	n/a	chrX:104437816-104437829 chrX:104437816-104437827 chrX:104437815-104437832 chrX:104437816-104437829 chrX:104437816-104437829 chrX:104437817-104437828 chrX:104437816-104437827
11	CEBPB	chrX:104707615-104707887	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chrX:104714821-104715113	IMR90	lung:	n/a	chrX:104714968-104714979
13	CEBPB	chrX:104440347-104440598	A549	lung:	n/a	chrX:104440450-104440461 chrX:104440448-104440459 chrX:104440448-104440461
14	CEBPB	chrX:104440305-104440595	HepG2	liver:	n/a	chrX:104440450-104440461 chrX:104440448-104440459 chrX:104440448-104440461
15	CEBPB	chrX:104558226-104558799	Hela-S3	cervix:	n/a	chrX:104558362-104558373
16	CEBPB	chrX:104620445-104620631	HepG2	liver:	n/a	n/a
17	CEBPB	chrX:104526302-104526502	IMR90	lung:	n/a	n/a
18	CEBPB	chrX:104559084-104559614	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chrX:104747223-104747624	MCF-7	breast:	n/a	chrX:104747378-104747391 chrX:104747380-104747389
20	CEBPB	chrX:104437751-104437855	HepG2	liver:	n/a	chrX:104437816-104437829 chrX:104437816-104437827 chrX:104437815-104437832 chrX:104437816-104437829 chrX:104437816-104437829 chrX:104437817-104437828 chrX:104437816-104437827
21	CEBPB	chrX:104568463-104569104	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chrX:104424389-104424698	A549	lung:	n/a	chrX:104424514-104424525
23	CEBPB	chrX:104374245-104374566	HepG2	liver:	n/a	chrX:104374412-104374423
24	CEBPB	chrX:104796373-104796720	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chrX:104552449-104552697	Hela-S3	cervix:	n/a	chrX:104552572-104552583
26	CEBPB	chrX:104552457-104552705	HepG2	liver:	n/a	chrX:104552572-104552583
27	CEBPB	chrX:104424342-104424701	IMR90	lung:	n/a	chrX:104424514-104424525
28	CEBPB	chrX:104714935-104715135	A549	lung:	n/a	chrX:104714968-104714979
29	CEBPB	chrX:104552430-104552754	IMR90	lung:	n/a	chrX:104552572-104552583
30	CEBPB	chrX:104714904-104715104	HepG2	liver:	n/a	chrX:104714968-104714979
31	CEBPB	chrX:104559983-104560311	IMR90	lung:	n/a	n/a
32	CEBPB	chrX:104494164-104494527	IMR90	lung:	n/a	chrX:104494341-104494352
33	CEBPB	chrX:104485832-104486032	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chrX:104745949-104746070	A549	lung:	n/a	chrX:104745966-104745977
35	CEBPB	chrX:104424404-104424677	H1-hESC	embryonic stem cell:	n/a	chrX:104424514-104424525
36	CEBPB	chrX:104573542-104573889	MCF-7	breast:	n/a	n/a
37	CEBPB	chrX:104440315-104440601	IMR90	lung:	n/a	chrX:104440450-104440461 chrX:104440448-104440459 chrX:104440448-104440461
38	CEBPB	chrX:104424375-104424630	Hela-S3	cervix:	n/a	chrX:104424514-104424525
39	CEBPB	chrX:104558261-104558398	HepG2	liver:	n/a	chrX:104558362-104558373
40	CEBPB	chrX:104424359-104424651	K562	blood:	n/a	chrX:104424514-104424525
41	CEBPB	chrX:104424396-104424690	HepG2	liver:	n/a	chrX:104424514-104424525
42	CEBPB	chrX:104494237-104494437	K562	blood:	n/a	chrX:104494341-104494352
43	CEBPB	chrX:104573473-104573880	MCF-7	breast:	n/a	n/a
44	CEBPB	chrX:104708662-104709007	Hela-S3	cervix:	n/a	chrX:104708827-104708838
45	CEBPB	chrX:104559872-104560361	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chrX:104541827-104542057	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chrX:104374274-104374592	IMR90	lung:	n/a	chrX:104374412-104374423
48	CEBPB	chrX:104708682-104708963	A549	lung:	n/a	chrX:104708827-104708838
49	CEBPB	chrX:104649475-104649615	IMR90	lung:	n/a	n/a
50	CEBPB	chrX:104706034-104706556	Hela-S3	cervix:	n/a	chrX:104706244-104706257

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:104465526-104465576	Hela-S3	cervix:	n/a
2	chrX:104465196-104465246	GM06990	blood:	n/a
3	chrX:104464033-104464083	H1-hESC	embryonic stem cell:	embryo
4	chrX:104465196-104465246	HCM	heart:	n/a
5	chrX:104464033-104464083	PANC-1	pancreas:	n/a
6	chrX:104465219-104465269	IMR90	lung:	fetal
7	chrX:104465219-104465269	ProgFib	skin:	n/a
8	chrX:104465395-104465445	HEK293	kidney:	embryo
9	chrX:104464033-104464083	NT2-D1	testis:	n/a
10	chrX:104465398-104465448	ovcar-3	ovarian:	n/a
11	chrX:104463622-104463672	MCF10A-Er-Src	breast:	n/a
12	chrX:104465219-104465269	K562	blood:	n/a
13	chrX:104465196-104465246	NHDF-neo	bronchial:	n/a
14	chrX:104465395-104465445	IMR90	lung:	fetal
15	chrX:104465526-104465576	RPTEC	kidney:	n/a
16	chrX:104463622-104463672	GM19239	blood:	n/a
17	chrX:104464033-104464083	HIPEpiC	eye:	n/a
18	chrX:104465395-104465445	RPTEC	kidney:	n/a
19	chrX:104465788-104465838	NH-A	brain:	n/a
20	chrX:104465219-104465269	GM12878	blood:	n/a
21	chrX:104465196-104465246	PANC-1	pancreas:	n/a
22	chrX:104465219-104465269	AG09309	skin:	n/a
23	chrX:104465526-104465576	ECC-1	luminal epithelium:	n/a
24	chrX:104464033-104464083	PrEC	prostate:	n/a
25	chrX:104465788-104465838	AG04449	skin:	fetal
26	chrX:104466053-104466103	CMK	blood:	n/a
27	chrX:104466053-104466103	ovcar-3	ovarian:	n/a
28	chrX:104465219-104465269	Hela-S3	cervix:	n/a
29	chrX:104466053-104466103	HepG2	liver:	n/a
30	chrX:104465395-104465445	ECC-1	luminal epithelium:	n/a
31	chrX:104464033-104464083	NHBE	bronchial:	n/a
32	chrX:104465788-104465838	Jurkat	blood:	n/a
33	chrX:104463622-104463672	HCF	heart:	n/a
34	chrX:104465196-104465246	HAEpiC	amniotic membrane:	n/a
35	chrX:104465788-104465838	SK-N-MC	brain:	n/a
36	chrX:104465788-104465838	SK-N-SH	brain:	n/a
37	chrX:104465395-104465445	Caco-2	colon:	n/a
38	chrX:104465526-104465576	HEEpiC	esophagus:	n/a
39	chrX:104465398-104465448	K562	blood:	n/a
40	chrX:104465196-104465246	AoSMC	blood vessel:	n/a
41	chrX:104464033-104464083	HRPEpiC	eye:	n/a
42	chrX:104463622-104463672	SK-N-MC	brain:	n/a
43	chrX:104464033-104464083	HUVEC	blood vessel:	n/a
44	chrX:104465219-104465269	HAEpiC	amniotic membrane:	n/a
45	chrX:104466053-104466103	PANC-1	pancreas:	n/a
46	chrX:104465526-104465576	HRCEpiC	kidney:	n/a
47	chrX:104463622-104463672	Jurkat	blood:	n/a
48	chrX:104466053-104466103	NB4	blood:	n/a
49	chrX:104465526-104465576	U87	brain:	n/a
50	chrX:104466053-104466103	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chrX:104695087..104696676-chrX:104697612..104699703,2	MCF-7	breast:
2	chrX:104381527..104384030-chrX:104399783..104402502,2	MCF-7	breast:
3	chrX:104600822..104602584-chrX:104652742..104654935,2	K562	blood:
4	chrX:104615663..104618237-chrX:104623681..104625989,2	MCF-7	breast:
5	chrX:104442154..104443725-chrX:104444147..104445757,2	K562	blood:
6	chrX:104600822..104602584-chrX:104652742..104654935,2	K562	blood:
7	chrX:104695776..104698042-chrX:104700975..104702588,2	MCF-7	breast:
8	chrX:104157994..104158575-chrX:104434799..104435541,2	MCF-7	breast:
9	chrX:104166569..104167244-chrX:104434712..104435505,3	MCF-7	breast:
10	chrX:104217213..104218153-chrX:104434855..104435519,2	MCF-7	breast:
11	chrX:104695087..104696676-chrX:104697612..104699703,2	MCF-7	breast:
12	chrX:104648472..104650735-chrX:104652409..104654061,2	K562	blood:
13	chr17:41398721..41401059-chrX:104396318..104397818,2	K562	blood:
14	chrX:103913621..103914287-chrX:104434797..104435572,2	MCF-7	breast:
15	chrX:104442154..104443725-chrX:104444147..104445757,2	K562	blood:
16	chrX:104695776..104698042-chrX:104700975..104702588,2	MCF-7	breast:
17	chrX:104678068..104682056-chrX:104682586..104684264,3	MCF-7	breast:
18	chrX:104381527..104384030-chrX:104399783..104402502,2	MCF-7	breast:
19	chrX:104714816..104716970-chrX:104717696..104719801,2	MCF-7	breast:
20	chrX:104615663..104618237-chrX:104623681..104625989,2	MCF-7	breast:
21	chrX:104331567..104334480-chrX:104412138..104414483,2	MCF-7	breast:
22	chrX:104714816..104716970-chrX:104717696..104719801,2	MCF-7	breast:
23	chr6:158452948..158455282-chrX:104716070..104718223,2	MCF-7	breast:
24	chrX:104678068..104682056-chrX:104682586..104684264,3	MCF-7	breast:

Variant related genes	Relation type
KCTD9P2	TF binding region
TEX13A	TF binding region
KCTD9P2	CpG island
TEX13A	CpG island
ENSG00000078269	chromatin interactions
ENSG00000181819	chromatin interactions

Extended variants
information (count: 2576 )
Associated
traits (count: 47 )

Variant overlapped rSNPs/rCNVs (count:2576 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146662110	chrX:104354504-104354505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs191002903	chrX:104354556-104354557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs139762517	chrX:104354574-104354575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181953723	chrX:104354599-104354600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185127334	chrX:104354626-104354627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113372770	chrX:104354675-104354676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189946944	chrX:104354776-104354777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs151094603	chrX:104354807-104354808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73527993	chrX:104354920-104354921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150240312	chrX:104355203-104355204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs375942364	chrX:104364234-104364235	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs182427948	chrX:104364252-104364253	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs201723817	chrX:104364301-104364302	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs200350882	chrX:104364306-104364307	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs72616887	chrX:104364312-104364313	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs560138287	chrX:104366036-104366037	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs185257031	chrX:104366038-104366039	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs375830166	chrX:104366060-104366061	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs137963104	chrX:104366159-104366160	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs186383660	chrX:104376261-104376262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191137032	chrX:104376324-104376325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138934934	chrX:104376340-104376341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs180877860	chrX:104376366-104376367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114171268	chrX:104376389-104376390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186110782	chrX:104376454-104376455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191261483	chrX:104376540-104376541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs116332636	chrX:104376546-104376547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144782266	chrX:104376600-104376601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs207478707	chrX:104376605-104376606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs5916869	chrX:104376962-104376963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs190561934	chrX:104377081-104377082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148537175	chrX:104377098-104377099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2009995	chrX:104377178-104377179	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs4644396	chrX:104377301-104377302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528438580	chrX:104377354-104377355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545092612	chrX:104377414-104377415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183008970	chrX:104377432-104377433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187683947	chrX:104377433-104377434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs74449825	chrX:104377457-104377458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs193151847	chrX:104377510-104377511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564369264	chrX:104377642-104377643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533089488	chrX:104377741-104377742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182817811	chrX:104377753-104377754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs5916725	chrX:104377812-104377813	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs187636441	chrX:104377921-104377922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192825616	chrX:104377942-104377943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184221380	chrX:104378006-104378007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369945265	chrX:104378085-104378086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201714057	chrX:104378154-104378155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115122737	chrX:104378242-104378243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:47)

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
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
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
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Multiple myeloma	17550852	CNVD
Cerebellar hypoplasia	21569638	CNVD
X-linked lissencephaly	21569638	CNVD
Pelizaeus-Merzbacher disease	18923514	CNVD
Pelizaeus-Merzbacher disease	22241247	CNVD
Cervical cancer	21062161	CNVD
Myxofibrosarcoma	16751306	CNVD
Pelizaeus-Merzbacher disease	22470819	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Astrocytoma	22246337	CNVD
Hirschsprung''s Disease	21712996	CNVD
X-linked lissencephaly	21572526	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:104354400-104355200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chrX:104354600-104355200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
3	chrX:104354600-104355200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chrX:104354800-104355400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chrX:104364200-104364400	Bivalent Enhancer	Fetal Kidney	kidney
6	chrX:104366000-104366200	Bivalent Enhancer	Fetal Kidney	kidney
7	chrX:104376200-104376800	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chrX:104376200-104377000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chrX:104376400-104377200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chrX:104376400-104377400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chrX:104377400-104378400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chrX:104378400-104378600	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chrX:104380600-104382200	Enhancers	HMEC	breast
14	chrX:104381400-104382400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chrX:104394800-104395000	Bivalent Enhancer	Fetal Kidney	kidney
16	chrX:104394800-104395200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chrX:104398000-104398800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chrX:104398000-104399200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chrX:104398200-104398800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chrX:104398200-104399600	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chrX:104398400-104399000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chrX:104398400-104399200	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chrX:104398800-104399200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chrX:104399000-104399200	Flanking Bivalent TSS/Enh	Fetal Kidney	kidney
25	chrX:104399200-104399400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chrX:104399200-104400200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chrX:104399400-104400800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chrX:104400400-104400600	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chrX:104400800-104401200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chrX:104401000-104401200	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chrX:104412600-104413400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chrX:104412600-104413600	Enhancers	HMEC	breast
33	chrX:104412800-104413400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chrX:104428000-104428600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chrX:104434600-104435000	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chrX:104435000-104436200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chrX:104436400-104436600	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chrX:104469600-104469800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chrX:104469800-104472200	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chrX:104470600-104471600	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chrX:104470800-104471600	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chrX:104470800-104471600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chrX:104470800-104472800	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chrX:104471400-104473200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chrX:104471600-104473600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chrX:104472200-104473000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chrX:104472600-104474400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chrX:104472800-104473600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chrX:104473400-104473800	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chrX:104473400-104474400	Enhancers	Liver	Liver

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