Variant report

Variant	nsv521599
Chromosome Location	chrX:77662439-78124078
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1615)
CpG islands
(count:855)
Chromatin interactive
region (count:66)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1615 , 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:77908567-77909461	HepG2	liver:	n/a	n/a
2	ATF2	chrX:77906284-77906758	GM12878	blood:	n/a	n/a
3	ATF2	chrX:77942979-77943482	GM12878	blood:	n/a	n/a
4	ATF2	chrX:77772579-77773090	GM12878	blood:	n/a	n/a
5	ATF2	chrX:77908643-77909099	GM12878	blood:	n/a	n/a
6	ATF2	chrX:77761711-77762194	GM12878	blood:	n/a	n/a
7	ATF2	chrX:77772565-77773116	GM12878	blood:	n/a	n/a
8	ATF2	chrX:77906228-77906839	GM12878	blood:	n/a	n/a
9	ATF2	chrX:78010295-78010918	GM12878	blood:	n/a	n/a
10	BATF	chrX:77908738-77908979	GM12878	blood:	n/a	n/a
11	BATF	chrX:77772620-77773037	GM12878	blood:	n/a	chrX:77772827-77772838 chrX:77772828-77772838
12	BATF	chrX:77761764-77762052	GM12878	blood:	n/a	n/a
13	BATF	chrX:77769389-77769650	GM12878	blood:	n/a	n/a
14	BATF	chrX:77906317-77906637	GM12878	blood:	n/a	n/a
15	BATF	chrX:78087059-78087284	GM12878	blood:	n/a	chrX:78087246-78087256 chrX:78087159-78087169 chrX:78087162-78087173
16	BATF	chrX:77772675-77773046	GM12878	blood:	n/a	chrX:77772827-77772838 chrX:77772828-77772838
17	BATF	chrX:78087034-78087333	GM12878	blood:	n/a	chrX:78087246-78087256 chrX:78087159-78087169 chrX:78087162-78087173
18	BATF	chrX:77908689-77908983	GM12878	blood:	n/a	n/a
19	BATF	chrX:77929215-77929492	GM12878	blood:	n/a	n/a
20	BATF	chrX:77761753-77762099	GM12878	blood:	n/a	n/a
21	BATF	chrX:77906305-77906663	GM12878	blood:	n/a	n/a
22	BATF	chrX:77769473-77769646	GM12878	blood:	n/a	n/a
23	BCL11A	chrX:77906372-77906698	GM12878	blood:	n/a	n/a
24	BCL11A	chrX:77772644-77773045	GM12878	blood:	n/a	chrX:77772827-77772836
25	BCL11A	chrX:77772679-77772971	GM12878	blood:	n/a	chrX:77772827-77772836
26	BCL11A	chrX:77769431-77769752	GM12878	blood:	n/a	n/a
27	BCL11A	chrX:77770214-77770584	H1-hESC	embryonic stem cell:	n/a	n/a
28	BCL11A	chrX:77761815-77762053	GM12878	blood:	n/a	n/a
29	BCL11A	chrX:77769425-77769638	GM12878	blood:	n/a	n/a
30	BCL3	chrX:77761824-77762039	GM12878	blood:	n/a	n/a
31	BCL3	chrX:77772652-77773023	GM12878	blood:	n/a	chrX:77772827-77772836
32	BCLAF1	chrX:77943083-77943431	GM12878	blood:	n/a	n/a
33	BCLAF1	chrX:77810950-77811256	GM12878	blood:	n/a	n/a
34	BCLAF1	chrX:77772542-77772982	GM12878	blood:	n/a	chrX:77772827-77772836
35	BCLAF1	chrX:77906229-77906811	GM12878	blood:	n/a	n/a
36	BCLAF1	chrX:78010291-78010891	GM12878	blood:	n/a	n/a
37	BHLHE40	chrX:77772647-77773002	GM12878	blood:	n/a	n/a
38	BHLHE40	chrX:77906378-77907048	GM12878	blood:	n/a	n/a
39	BRCA1	chrX:77757271-77757283	GM12878	blood:	n/a	n/a
40	CEBPB	chrX:77928768-77929069	HepG2	liver:	n/a	chrX:77928896-77928905 chrX:77928896-77928907 chrX:77928896-77928905 chrX:77928896-77928905 chrX:77928894-77928907 chrX:77928896-77928905 chrX:77928894-77928905 chrX:77928894-77928907
41	CEBPB	chrX:77736595-77736708	A549	lung:	n/a	n/a
42	CEBPB	chrX:77907953-77908218	HepG2	liver:	n/a	chrX:77908089-77908100
43	CEBPB	chrX:77920756-77920940	IMR90	lung:	n/a	n/a
44	CEBPB	chrX:78107898-78108188	HepG2	liver:	n/a	chrX:78108053-78108064
45	CEBPB	chrX:77736528-77736728	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chrX:77957238-77957446	K562	blood:	n/a	chrX:77957375-77957386 chrX:77957375-77957388 chrX:77957375-77957388 chrX:77957376-77957387 chrX:77957377-77957386
47	CEBPB	chrX:77957235-77957487	HepG2	liver:	n/a	chrX:77957375-77957386 chrX:77957375-77957388 chrX:77957375-77957388 chrX:77957376-77957387 chrX:77957377-77957386
48	CEBPB	chrX:78052509-78052828	MCF-7	breast:	n/a	n/a
49	CEBPB	chrX:78052444-78052767	MCF-7	breast:	n/a	n/a
50	CEBPB	chrX:78048049-78048358	IMR90	lung:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:78003113-78003163	RPTEC	kidney:	n/a
2	chrX:78003113-78003163	RPTEC	kidney:	n/a
3	chrX:77914115-77914165	GM12891	blood:	n/a
4	chrX:77914115-77914165	HNPCEpiC	eye:	n/a
5	chrX:78001744-78001794	HepG2	liver:	n/a
6	chrX:77914054-77914104	HCPEpiC	choroid plexus:	n/a
7	chrX:77914149-77914199	HRE	kidney:	n/a
8	chrX:78003205-78003255	ECC-1	luminal epithelium:	n/a
9	chrX:77912297-77912347	AoSMC	blood vessel:	n/a
10	chrX:78002454-78002504	U87	brain:	n/a
11	chrX:78010565-78010615	CMK	blood:	n/a
12	chrX:77914054-77914104	NH-A	brain:	n/a
13	chrX:77912605-77912655	HRCEpiC	kidney:	n/a
14	chrX:78003113-78003163	AoSMC	blood vessel:	n/a
15	chrX:78002454-78002504	HNPCEpiC	eye:	n/a
16	chrX:77914149-77914199	Jurkat	blood:	n/a
17	chrX:78003113-78003163	HepG2	liver:	n/a
18	chrX:78002454-78002504	HCT-116	colon:	n/a
19	chrX:78003113-78003163	BE2_C	brain:	n/a
20	chrX:78012038-78012088	HEK293	kidney:	embryo
21	chrX:77914115-77914165	NB4	blood:	n/a
22	chrX:78010565-78010615	Jurkat	blood:	n/a
23	chrX:78003346-78003396	Hela-S3	cervix:	n/a
24	chrX:77912297-77912347	HRE	kidney:	n/a
25	chrX:77914054-77914104	MCF-7	breast:	n/a
26	chrX:77914115-77914165	AoSMC	blood vessel:	n/a
27	chrX:77912297-77912347	AG10803	skin:	n/a
28	chrX:77914149-77914199	PANC-1	pancreas:	n/a
29	chrX:78001744-78001794	BJ	skin:	n/a
30	chrX:77912605-77912655	MCF10A-Er-Src	breast:	n/a
31	chrX:77915772-77915822	HEK293	kidney:	embryo
32	chrX:77915772-77915822	NHDF-neo	bronchial:	n/a
33	chrX:78001744-78001794	HRPEpiC	eye:	n/a
34	chrX:78012038-78012088	NHBE	bronchial:	n/a
35	chrX:78012038-78012088	MCF10A-Er-Src	breast:	n/a
36	chrX:78010565-78010615	PANC-1	pancreas:	n/a
37	chrX:78003205-78003255	NH-A	brain:	n/a
38	chrX:78003346-78003396	PrEC	prostate:	n/a
39	chrX:78003091-78003141	ECC-1	luminal epithelium:	n/a
40	chrX:77915772-77915822	SK-N-SH	brain:	n/a
41	chrX:78003346-78003396	Hepatocyte	liver:	n/a
42	chrX:77912605-77912655	Caco-2	colon:	n/a
43	chrX:77914149-77914199	HCPEpiC	choroid plexus:	n/a
44	chrX:78003205-78003255	U87	brain:	n/a
45	chrX:77912605-77912655	NT2-D1	testis:	n/a
46	chrX:78003205-78003255	GM12892	blood:	n/a
47	chrX:78010565-78010615	BE2_C	brain:	n/a
48	chrX:78003091-78003141	PANC-1	pancreas:	n/a
49	chrX:78001744-78001794	HEK293	kidney:	embryo
50	chrX:78003091-78003141	SKMC	muscle:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chrX:78093876..78095834-chrX:78097029..78098923,2	MCF-7	breast:
2	chr6:142366297..142366801-chrX:77931321..77931822,2	MCF-7	breast:
3	chrX:77956386..77958471-chrX:77962322..77965270,2	MCF-7	breast:
4	chrX:77707988..77710201-chrX:77716605..77718523,2	MCF-7	breast:
5	chr3:73159068..73162072-chrX:77930319..77931843,8	K562	blood:
6	chr11:62607637..62609222-chrX:77930319..77931823,3	K562	blood:
7	chr6:26285173..26286112-chrX:77845459..77845980,2	Hela-S3	cervix:
8	chr11:62607628..62609202-chrX:77930320..77933340,4	MCF-7	breast:
9	chrX:77956386..77958471-chrX:77962322..77965270,2	MCF-7	breast:
10	chr20:51476079..51476599-chrX:77931319..77931843,2	HCT-116	colon:
11	chr4:163161292..163161812-chrX:77845459..77845979,2	Hela-S3	cervix:
12	chrX:78093876..78095834-chrX:78097029..78098923,2	MCF-7	breast:
13	chrX:77910506..77913354-chrX:77917540..77919275,2	MCF-7	breast:
14	chrX:77830536..77833521-chrX:77844830..77846659,2	MCF-7	breast:
15	chr19:49942464..49943982-chrX:77930320..77931841,2	K562	blood:
16	chr17:41398809..41403842-chrX:77930319..77933342,10	MCF-7	breast:
17	chrX:78001590..78003904-chrX:78007428..78009145,2	MCF-7	breast:
18	chrX:78094327..78097258-chrX:78335741..78337438,2	MCF-7	breast:
19	chr17:41380127..41383707-chrX:77930323..77933342,7	K562	blood:
20	chr11:62608629..62609217-chrX:77931319..77931841,2	NB4	blood:
21	chr17:41463853..41465371-chrX:77930319..77931842,2	K562	blood:
22	chr11:62608635..62609203-chrX:77931321..77931843,3	MCF-7	breast:
23	chr13:90583692..90586688-chrX:77930321..77933319,2	K562	blood:
24	chrX:78094539..78095931-chrX:78127975..78128803,4	MCF-7	breast:
25	chr17:54134584..54136104-chrX:77931820..77933340,2	K562	blood:
26	chr14:44978638..44981619-chrX:77931842..77933343,2	K562	blood:
27	chrX:77951016..77952967-chrX:77953012..77954872,2	K562	blood:
28	chr4:103260693..103262212-chrX:77930319..77931843,2	K562	blood:
29	chr17:41463645..41464360-chrX:77931822..77932340,2	Hela-S3	cervix:
30	chrX:77910506..77913354-chrX:77917540..77919275,2	MCF-7	breast:
31	chr17:41463347..41466392-chrX:77930320..77931839,3	MCF-7	breast:
32	chrX:78106489..78109093-chrX:78124500..78126136,2	MCF-7	breast:
33	chr17:41380127..41383584-chrX:77930339..77933342,6	K562	blood:
34	chr11:62607618..62609220-chrX:77930319..77931843,4	MCF-7	breast:
35	chrX:78089294..78090982-chrX:78092265..78094385,2	MCF-7	breast:
36	chrX:77830536..77833521-chrX:77844830..77846659,2	MCF-7	breast:
37	chr11:62608638..62609150-chrX:77931319..77931823,3	HCT-116	colon:
38	chrX:78094432..78096189-chrX:78129912..78132270,2	MCF-7	breast:
39	chr17:41466185..41468150-chrX:77930341..77933340,3	K562	blood:
40	chr19:49943464..49943984-chrX:77931321..77931843,3	Hela-S3	cervix:
41	chrX:78089294..78090982-chrX:78092265..78094385,2	MCF-7	breast:
42	chr3:73158602..73162090-chrX:77930319..77931843,9	K562	blood:
43	chr6:142366316..142367825-chrX:77930343..77931843,2	K562	blood:
44	chr5:133457468..133458993-chrX:77930323..77931842,3	K562	blood:
45	chr6:142364797..142367795-chrX:77930320..77931841,2	K562	blood:
46	chr17:41463457..41467189-chrX:77930321..77933342,6	MCF-7	breast:
47	chrX:77951016..77952967-chrX:77953012..77954872,2	K562	blood:
48	chrX:77811500..77813088-chrX:78666250..78667785,2	MCF-7	breast:
49	chrX:78094332..78095123-chrX:78156592..78157249,2	MCF-7	breast:
50	chrX:77810661..77811278-chrX:78780189..78780762,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPAR4-1	chrX:78018723-78019396	NONHSAT137709
2	lnc-ZCCHC5-3	chrX:77775090-77775280	NONHSAT137705
3	lnc-P2RY10-1	chrX:78005671-78005720	ENSG00000250534.1
4	lnc-P2RY10-1	chrX:78003228-78003531	ENSG00000250534.1
5	lnc-P2RY10-1	chrX:78006707-78006808	ENSG00000250534.1
6	lnc-ZCCHC5-1	chrX:77954881-77955388	NONHSAT137707
7	lnc-ZCCHC5-3	chrX:77775585-77775683	NONHSAT137705
8	lnc-ZCCHC5-2	chrX:77809909-77810248	NONHSAT137706
9	lnc-P2RY10-1	chrX:78010288-78010503	ENSG00000250534.1

No data

Variant related genes	Relation type
PPATP2	TF binding region
UBE2V1P7	TF binding region
LPAR4	TF binding region
HMGN1P34	TF binding region
RPL7P54	TF binding region
ZCCHC5	TF binding region
PPATP2	CpG island
UBE2V1P7	CpG island
LPAR4	CpG island
HMGN1P34	CpG island
RPL7P54	CpG island
ZCCHC5	CpG island
ENSG00000188825	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000006451	chromatin interactions
ENSG00000067596	chromatin interactions
ENSG00000158406	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000147145	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 2197 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:2197 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192944687	chrX:77708208-77708209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs558677631	chrX:77708330-77708331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184110823	chrX:77708396-77708397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149966003	chrX:77708452-77708453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs1600070	chrX:77708474-77708475	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs374178774	chrX:77708510-77708511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188852284	chrX:77708652-77708653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181690806	chrX:77708699-77708700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs1600069	chrX:77708727-77708728	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs143166092	chrX:77708746-77708747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1600068	chrX:77708834-77708835	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs186217069	chrX:77708862-77708863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190664930	chrX:77709008-77709009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542178441	chrX:77709222-77709223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs180676515	chrX:77709260-77709261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560469154	chrX:77709397-77709398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs17174124	chrX:77709463-77709464	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs186160262	chrX:77709483-77709484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191034204	chrX:77709513-77709514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs59090331	chrX:77709549-77709550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1979379	chrX:77709594-77709595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182604787	chrX:77709689-77709690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185896340	chrX:77709698-77709699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190606700	chrX:77709710-77709711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183073622	chrX:77709784-77709785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140596540	chrX:77709853-77709854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188594006	chrX:77709886-77709887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs1477918	chrX:77709891-77709892	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs138145492	chrX:77710005-77710006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374648575	chrX:77710022-77710023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs5913723	chrX:77710039-77710040	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs553757964	chrX:77710078-77710079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs193276498	chrX:77710216-77710217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs35756747	chrX:77710222-77710223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs367569242	chrX:77710248-77710249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182435483	chrX:77710283-77710284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371407141	chrX:77710311-77710312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs13440647	chrX:77710345-77710346	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs60534787	chrX:77710486-77710487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187808325	chrX:77710544-77710545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2126727	chrX:77710553-77710554	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs13440824	chrX:77710561-77710562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191390606	chrX:77710579-77710580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs13441057	chrX:77710663-77710664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs13440725	chrX:77710681-77710682	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs141784333	chrX:77710777-77710778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1979378	chrX:77710872-77710873	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs370421392	chrX:77710877-77710878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs3943322	chrX:77711036-77711037	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs68019538	chrX:77711049-77711050	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
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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:745 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:77708200-77708600	Enhancers	Muscle Satellite Cultured Cells	--
2	chrX:77708200-77708600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chrX:77708200-77708600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chrX:77708600-77711400	Weak transcription	Muscle Satellite Cultured Cells	--
5	chrX:77709800-77710400	Enhancers	Rectal Smooth Muscle	rectum
6	chrX:77711400-77712000	Enhancers	Muscle Satellite Cultured Cells	--
7	chrX:77711400-77712000	Enhancers	HSMM	muscle
8	chrX:77727600-77728600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
9	chrX:77727800-77728200	Active TSS	A549	lung
10	chrX:77747400-77748200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chrX:77748000-77748600	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chrX:77748200-77748600	Enhancers	Primary T cells from cord blood	blood
13	chrX:77748200-77749200	Enhancers	Dnd41	blood
14	chrX:77762800-77763400	Enhancers	Dnd41	blood
15	chrX:77762800-77763600	Enhancers	Fetal Thymus	thymus
16	chrX:77769000-77769400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
17	chrX:77769000-77770200	Enhancers	Muscle Satellite Cultured Cells	--
18	chrX:77769000-77771200	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chrX:77769200-77772000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chrX:77769400-77769600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chrX:77769400-77769800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chrX:77769400-77770200	Enhancers	H1 Cell Line	embryonic stem cell
23	chrX:77769400-77770200	Enhancers	H9 Cell Line	embryonic stem cell
24	chrX:77769400-77770600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chrX:77769600-77770800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chrX:77769600-77771800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chrX:77769800-77770200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
28	chrX:77769800-77770200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chrX:77769800-77770200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chrX:77769800-77770800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chrX:77769800-77771400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chrX:77769800-77773000	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chrX:77769800-77775000	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chrX:77770000-77770800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chrX:77770000-77771200	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chrX:77770000-77773800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chrX:77770000-77773800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
38	chrX:77770000-77774000	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chrX:77770200-77770600	Weak transcription	H9 Cell Line	embryonic stem cell
40	chrX:77770200-77770800	Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chrX:77770200-77770800	Weak transcription	H1 Cell Line	embryonic stem cell
42	chrX:77770200-77773800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chrX:77770400-77771600	Enhancers	Primary T cells fromperipheralblood	blood
44	chrX:77770400-77774200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chrX:77770600-77771400	Enhancers	H9 Cell Line	embryonic stem cell
46	chrX:77770800-77771000	Enhancers	H1 Cell Line	embryonic stem cell
47	chrX:77770800-77771200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chrX:77770800-77771200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chrX:77770800-77771200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chrX:77770800-77771200	Enhancers	GM12878-XiMat	blood

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