Variant report

Variant	esv3337751
Chromosome Location	chrX:110217889-110429181
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	ATF2	chrX:110358073-110358405	GM12878	blood:	n/a	n/a
2	BATF	chrX:110410588-110410857	GM12878	blood:	n/a	n/a
3	BCL11A	chrX:110410596-110410945	GM12878	blood:	n/a	n/a
4	BCL3	chrX:110349210-110349641	GM12878	blood:	n/a	n/a
5	BCL3	chrX:110349264-110349860	GM12878	blood:	n/a	n/a
6	BHLHE40	chrX:110343412-110343498	GM12878	blood:	n/a	n/a
7	BHLHE40	chrX:110413292-110413466	K562	blood:	n/a	n/a
8	BHLHE40	chrX:110367720-110367739	GM12878	blood:	n/a	n/a
9	CEBPB	chrX:110249364-110249723	IMR90	lung:	n/a	n/a
10	CEBPB	chrX:110263567-110263838	H1-hESC	embryonic stem cell:	n/a	chrX:110263706-110263717
11	CEBPB	chrX:110236205-110236508	IMR90	lung:	n/a	chrX:110236366-110236377
12	CEBPB	chrX:110263611-110263895	K562	blood:	n/a	chrX:110263706-110263717
13	CEBPB	chrX:110242389-110242728	A549	lung:	n/a	chrX:110242565-110242574 chrX:110242563-110242576 chrX:110242565-110242576 chrX:110242565-110242574 chrX:110242563-110242574 chrX:110242565-110242574 chrX:110242565-110242574
14	CEBPB	chrX:110353617-110353884	K562	blood:	n/a	chrX:110353752-110353763 chrX:110353821-110353833
15	CEBPB	chrX:110319452-110319799	IMR90	lung:	n/a	chrX:110319615-110319626
16	CEBPB	chrX:110426217-110426526	HepG2	liver:	n/a	chrX:110426379-110426390
17	CEBPB	chrX:110242506-110242605	K562	blood:	n/a	chrX:110242565-110242574 chrX:110242563-110242576 chrX:110242565-110242576 chrX:110242565-110242574 chrX:110242563-110242574 chrX:110242565-110242574 chrX:110242565-110242574
18	CEBPB	chrX:110251285-110251497	IMR90	lung:	n/a	n/a
19	CEBPB	chrX:110353616-110353943	A549	lung:	n/a	chrX:110353752-110353763 chrX:110353821-110353833
20	CEBPB	chrX:110339356-110339399	K562	blood:	n/a	n/a
21	CEBPB	chrX:110249443-110249707	K562	blood:	n/a	n/a
22	CEBPB	chrX:110340170-110340457	IMR90	lung:	n/a	chrX:110340278-110340289 chrX:110340277-110340290 chrX:110340277-110340290
23	CEBPB	chrX:110284224-110284626	IMR90	lung:	n/a	n/a
24	CEBPB	chrX:110340225-110340456	HepG2	liver:	n/a	chrX:110340278-110340289 chrX:110340277-110340290 chrX:110340277-110340290
25	CEBPB	chrX:110290825-110291068	IMR90	lung:	n/a	n/a
26	CEBPB	chrX:110263586-110263791	K562	blood:	n/a	chrX:110263706-110263717
27	CEBPB	chrX:110319444-110319789	HepG2	liver:	n/a	chrX:110319615-110319626
28	CEBPB	chrX:110353589-110353921	IMR90	lung:	n/a	chrX:110353752-110353763 chrX:110353821-110353833
29	CEBPB	chrX:110339200-110339539	IMR90	lung:	n/a	n/a
30	CEBPB	chrX:110249413-110249630	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chrX:110236332-110236495	K562	blood:	n/a	chrX:110236366-110236377
32	CEBPB	chrX:110353583-110353957	HepG2	liver:	n/a	chrX:110353752-110353763 chrX:110353821-110353833
33	CEBPB	chrX:110426193-110426534	H1-hESC	embryonic stem cell:	n/a	chrX:110426379-110426390
34	CEBPB	chrX:110249377-110249708	HepG2	liver:	n/a	n/a
35	CEBPB	chrX:110370366-110370603	IMR90	lung:	n/a	chrX:110370435-110370446
36	CEBPB	chrX:110249394-110249658	A549	lung:	n/a	n/a
37	CEBPB	chrX:110260704-110260939	A549	lung:	n/a	n/a
38	CEBPB	chrX:110344108-110344320	A549	lung:	n/a	n/a
39	CEBPB	chrX:110289642-110289862	A549	lung:	n/a	n/a
40	CEBPB	chrX:110426226-110426546	A549	lung:	n/a	chrX:110426379-110426390
41	CEBPB	chrX:110284262-110284517	HepG2	liver:	n/a	n/a
42	CEBPB	chrX:110339233-110339526	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chrX:110339191-110339529	HepG2	liver:	n/a	n/a
44	CEBPB	chrX:110289617-110289878	IMR90	lung:	n/a	n/a
45	CEBPB	chrX:110340142-110340374	H1-hESC	embryonic stem cell:	n/a	chrX:110340278-110340289 chrX:110340277-110340290 chrX:110340277-110340290
46	CEBPB	chrX:110263531-110263885	IMR90	lung:	n/a	chrX:110263706-110263717
47	CEBPB	chrX:110263532-110263873	A549	lung:	n/a	chrX:110263706-110263717
48	CEBPB	chrX:110242431-110242721	IMR90	lung:	n/a	chrX:110242565-110242574 chrX:110242563-110242576 chrX:110242565-110242576 chrX:110242565-110242574 chrX:110242563-110242574 chrX:110242565-110242574 chrX:110242565-110242574
49	CEBPB	chrX:110284236-110284640	A549	lung:	n/a	n/a
50	CEBPB	chrX:110370377-110370566	A549	lung:	n/a	chrX:110370435-110370446

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:110365847-110365897	HEK293	kidney:	embryo
2	chrX:110339485-110339535	BE2_C	brain:	n/a
3	chrX:110365847-110365897	HEK293	kidney:	embryo
4	chrX:110339485-110339535	BE2_C	brain:	n/a
5	chrX:110365767-110365817	SK-N-MC	brain:	n/a
6	chrX:110339372-110339422	ProgFib	skin:	n/a
7	chrX:110339485-110339535	LNCaP	prostate:	n/a
8	chrX:110335660-110335710	HNPCEpiC	eye:	n/a
9	chrX:110365847-110365897	GM06990	blood:	n/a
10	chrX:110339837-110339887	A549	lung:	n/a
11	chrX:110339365-110339415	HIPEpiC	eye:	n/a
12	chrX:110365603-110365653	HAEpiC	amniotic membrane:	n/a
13	chrX:110398983-110399033	GM06990	blood:	n/a
14	chrX:110339051-110339101	HRPEpiC	eye:	n/a
15	chrX:110339313-110339363	HMEC	breast:	n/a
16	chrX:110339654-110339704	HEK293	kidney:	embryo
17	chrX:110339485-110339535	K562	blood:	n/a
18	chrX:110339365-110339415	HepG2	liver:	n/a
19	chrX:110339862-110339912	MCF10A-Er-Src	breast:	n/a
20	chrX:110339365-110339415	CMK	blood:	n/a
21	chrX:110342214-110342264	GM12892	blood:	n/a
22	chrX:110365767-110365817	NT2-D1	testis:	n/a
23	chrX:110339837-110339887	GM19239	blood:	n/a
24	chrX:110339654-110339704	HUVEC	blood vessel:	n/a
25	chrX:110339862-110339912	HEEpiC	esophagus:	n/a
26	chrX:110339654-110339704	ProgFib	skin:	n/a
27	chrX:110365767-110365817	Hepatocyte	liver:	n/a
28	chrX:110339372-110339422	H1-hESC	embryonic stem cell:	embryo
29	chrX:110339654-110339704	HCF	heart:	n/a
30	chrX:110339654-110339704	AoSMC	blood vessel:	n/a
31	chrX:110365767-110365817	HCPEpiC	choroid plexus:	n/a
32	chrX:110339005-110339055	NHBE	bronchial:	n/a
33	chrX:110365767-110365817	Caco-2	colon:	n/a
34	chrX:110339313-110339363	HAEpiC	amniotic membrane:	n/a
35	chrX:110339005-110339055	U87	brain:	n/a
36	chrX:110339485-110339535	HRPEpiC	eye:	n/a
37	chrX:110339837-110339887	SK-N-SH	brain:	n/a
38	chrX:110365767-110365817	GM06990	blood:	n/a
39	chrX:110339051-110339101	HL-60	blood:	n/a
40	chrX:110339313-110339363	GM19239	blood:	n/a
41	chrX:110339485-110339535	NHBE	bronchial:	n/a
42	chrX:110365603-110365653	AoSMC	blood vessel:	n/a
43	chrX:110339032-110339082	IMR90	lung:	fetal
44	chrX:110366476-110366526	CMK	blood:	n/a
45	chrX:110365767-110365817	GM12891	blood:	n/a
46	chrX:110342214-110342264	BJ	skin:	n/a
47	chrX:110366476-110366526	MCF10A-Er-Src	breast:	n/a
48	chrX:110339051-110339101	LNCaP	prostate:	n/a
49	chrX:110339051-110339101	NHBE	bronchial:	n/a
50	chrX:110339837-110339887	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chrX:110407872..110408407-chrX:110687695..110688340,2	MCF-7	breast:
2	chrX:110407993..110408709-chrX:110487120..110487699,2	MCF-7	breast:
3	chrX:110349889..110351867-chrX:110354398..110356796,2	MCF-7	breast:
4	chrX:110368396..110371071-chrX:110375207..110377505,2	K562	blood:
5	chrX:110249821..110252396-chrX:110256754..110259778,3	K562	blood:
6	chrX:110407677..110408191-chrX:110688626..110689442,2	MCF-7	breast:
7	chrX:110096476..110097281-chrX:110343043..110343676,2	MCF-7	breast:
8	chrX:110411443..110412188-chrX:110688239..110689107,2	MCF-7	breast:
9	chrX:110326362..110328069-chrX:110331254..110332905,2	K562	blood:
10	chrX:110407226..110408219-chrX:110690311..110690819,2	MCF-7	breast:
11	chrX:110249821..110252612-chrX:110256754..110259778,3	K562	blood:
12	chrX:110411337..110412053-chrX:110690623..110691185,2	MCF-7	breast:
13	chrX:110368396..110371071-chrX:110375207..110377505,2	K562	blood:
14	chrX:110342959..110344460-chrX:110514484..110517120,2	K562	blood:
15	chrX:110326362..110328069-chrX:110331254..110332905,2	K562	blood:
16	chrX:110411370..110412231-chrX:110487261..110487854,2	MCF-7	breast:
17	chrX:110249821..110252612-chrX:110256754..110259778,3	K562	blood:
18	chrX:110349889..110351867-chrX:110354398..110356796,2	MCF-7	breast:
19	chrX:110235520..110236090-chrX:110690097..110690889,2	MCF-7	breast:
20	chrX:110249821..110252396-chrX:110256754..110259778,3	K562	blood:
21	chrX:110096399..110097420-chrX:110342866..110344069,8	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG13-8	chrX:110339771-110339965	NONHSAT138173
2	lnc-RGAG1-4	chrX:110228634-110230907	NONHSAT138172
3	lnc-RGAG1-5	chrX:110254149-110259085	ucscGeneNc_uc004epb_2
4	lnc-ALG13-8	chrX:110341768-110342014	NONHSAT138173
5	lnc-ALG13-8	chrX:110340618-110340684	NONHSAT138173
6	lnc-ALG13-7	chrX:110367493-110372431	NONHSAT138174
7	lnc-ALG13-8	chrX:110339553-110339643	NONHSAT138173
8	lnc-ALG13-8	chrX:110340803-110340912	NONHSAT138173

Variant related genes	Relation type
PAK3	TF binding region
FCF1P4	TF binding region
PAK3	CpG island
FCF1P4	CpG island

Extended variants
information (count: 2578 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:2578 , 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	rs566466234	chrX:110222856-110222857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186293922	chrX:110223246-110223247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140631940	chrX:110223514-110223515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs376719376	chrX:110223525-110223526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190734328	chrX:110223667-110223668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181529223	chrX:110223886-110223887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187100752	chrX:110223941-110223942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79474778	chrX:110223949-110223950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371613652	chrX:110224047-110224048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs145198804	chrX:110224227-110224228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs149126359	chrX:110224241-110224242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374524394	chrX:110224480-110224481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191081210	chrX:110224503-110224504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs367776899	chrX:110224544-110224545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182693792	chrX:110224546-110224547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185034774	chrX:110224575-110224576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35923790	chrX:110224771-110224772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs200341090	chrX:110224772-110224773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371391586	chrX:110224793-110224794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs3033534	chrX:110224796-110224797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs397896815	chrX:110224797-110224798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113137971	chrX:110224844-110224845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369189644	chrX:110224879-110224880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12836972	chrX:110224883-110224884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189552931	chrX:110225019-110225020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182209927	chrX:110225091-110225092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551959664	chrX:110225174-110225175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145829272	chrX:110225478-110225479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138395049	chrX:110225602-110225603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs371704854	chrX:110225627-110225628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188663967	chrX:110225684-110225685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368003576	chrX:110225735-110225736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558512753	chrX:110225740-110225741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370048189	chrX:110225799-110225800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368663694	chrX:110225848-110225849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374042132	chrX:110225985-110225986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192357809	chrX:110226322-110226323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150258433	chrX:110226489-110226490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138941825	chrX:110226572-110226573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183340898	chrX:110226583-110226584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79401221	chrX:110226704-110226705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34616270	chrX:110226708-110226709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs57629808	chrX:110226720-110226721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201968065	chrX:110226721-110226722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs200267819	chrX:110226722-110226723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372672428	chrX:110226723-110226724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200062259	chrX:110226750-110226751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376905488	chrX:110226754-110226755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371203251	chrX:110226755-110226756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201440744	chrX:110226756-110226757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:48)

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
Ovarian clear cell carcinoma	21343371	CNVD
Astrocytoma	22246337	CNVD
Hirschsprung''s Disease	21712996	CNVD
X-linked lissencephaly	21572526	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Oligozoospermia	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:845 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:110222800-110227200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chrX:110227200-110229200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chrX:110227400-110227600	Enhancers	H9 Cell Line	embryonic stem cell
4	chrX:110227400-110228000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chrX:110227600-110227800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
6	chrX:110227600-110227800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chrX:110227600-110227800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
8	chrX:110227600-110230200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chrX:110227800-110228600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chrX:110228000-110228400	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chrX:110228200-110229000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
12	chrX:110228400-110229200	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chrX:110228600-110228800	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chrX:110228600-110229000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
15	chrX:110228600-110229200	Enhancers	Stomach Mucosa	stomach
16	chrX:110228800-110230400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chrX:110229000-110229400	Enhancers	HMEC	breast
18	chrX:110229200-110229400	Enhancers	Brain Germinal Matrix	brain
19	chrX:110229400-110230000	Weak transcription	Brain Germinal Matrix	brain
20	chrX:110230000-110230200	Enhancers	Brain Germinal Matrix	brain
21	chrX:110230200-110230400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
22	chrX:110230200-110230600	Enhancers	H9 Cell Line	embryonic stem cell
23	chrX:110230200-110248800	Weak transcription	Brain Germinal Matrix	brain
24	chrX:110230400-110230600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
25	chrX:110230400-110230600	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chrX:110232200-110232400	Bivalent Enhancer	Fetal Kidney	kidney
27	chrX:110232800-110233000	Enhancers	Rectal Mucosa Donor 31	rectum
28	chrX:110233000-110233200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
29	chrX:110235800-110236000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
30	chrX:110235800-110236000	Enhancers	Pancreas	Pancrea
31	chrX:110236000-110266000	Weak transcription	Pancreas	Pancrea
32	chrX:110242200-110242400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
33	chrX:110242400-110242600	Bivalent Enhancer	Lung	lung
34	chrX:110244000-110244200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chrX:110244000-110244400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
36	chrX:110246600-110246800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
37	chrX:110246600-110247600	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chrX:110246800-110247400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chrX:110247200-110249000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chrX:110247400-110247600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chrX:110247400-110249000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chrX:110247400-110249200	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chrX:110247600-110247800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chrX:110247600-110248800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
45	chrX:110247600-110249000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chrX:110247800-110248200	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chrX:110248000-110248800	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chrX:110248000-110249200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chrX:110248200-110248600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
50	chrX:110248200-110254200	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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