Variant report

Variant	nsv531129
Chromosome Location	chrX:76703995-77038914
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1427)
CpG islands
(count:489)
Chromatin interactive
region (count:61)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1427 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:76859117-76859830	HepG2	liver:	n/a	n/a
2	BATF	chrX:76896223-76896405	GM12878	blood:	n/a	chrX:76896340-76896351
3	BATF	chrX:76896163-76896505	GM12878	blood:	n/a	chrX:76896340-76896351
4	BCL3	chrX:76757473-76757813	GM12878	blood:	n/a	n/a
5	BHLHE40	chrX:76783204-76783727	K562	blood:	n/a	n/a
6	BHLHE40	chrX:76861103-76861111	GM12878	blood:	n/a	n/a
7	BRCA1	chrX:76820559-76820598	Hela-S3	cervix:	n/a	n/a
8	CBX3	chrX:76783099-76783483	K562	blood:	n/a	n/a
9	CBX3	chrX:76783571-76783845	K562	blood:	n/a	n/a
10	CBX3	chrX:76786757-76787011	K562	blood:	n/a	n/a
11	CCNT2	chrX:76783174-76783715	K562	blood:	n/a	n/a
12	CCNT2	chrX:76711851-76712122	K562	blood:	n/a	n/a
13	CEBPB	chrX:76782752-76783080	Hela-S3	cervix:	n/a	chrX:76782904-76782915
14	CEBPB	chrX:76762644-76762935	IMR90	lung:	n/a	chrX:76762780-76762791
15	CEBPB	chrX:76996006-76996321	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chrX:76822354-76822684	IMR90	lung:	n/a	chrX:76822527-76822538
17	CEBPB	chrX:76888331-76888578	HepG2	liver:	n/a	chrX:76888331-76888348 chrX:76888415-76888426
18	CEBPB	chrX:76790904-76791369	Hela-S3	cervix:	n/a	chrX:76790907-76790920
19	CEBPB	chrX:76762653-76762919	A549	lung:	n/a	chrX:76762780-76762791
20	CEBPB	chrX:76822378-76822660	A549	lung:	n/a	chrX:76822527-76822538
21	CEBPB	chrX:76715767-76716057	A549	lung:	n/a	n/a
22	CEBPB	chrX:76782215-76783425	K562	blood:	n/a	chrX:76782904-76782915 chrX:76782272-76782285 chrX:76782383-76782396
23	CEBPB	chrX:76852179-76853000	IMR90	lung:	n/a	n/a
24	CEBPB	chrX:76822460-76822695	K562	blood:	n/a	chrX:76822527-76822538
25	CEBPB	chrX:76782758-76783048	K562	blood:	n/a	chrX:76782904-76782915
26	CEBPB	chrX:76715738-76716032	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chrX:77005207-77005606	IMR90	lung:	n/a	n/a
28	CEBPB	chrX:76760734-76761087	IMR90	lung:	n/a	n/a
29	CEBPB	chrX:76924438-76924808	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chrX:76857453-76857668	HepG2	liver:	n/a	chrX:76857528-76857539
31	CEBPB	chrX:76924466-76924781	K562	blood:	n/a	n/a
32	CEBPB	chrX:76762700-76762920	HepG2	liver:	n/a	chrX:76762780-76762791
33	CEBPB	chrX:77005177-77005630	A549	lung:	n/a	n/a
34	CEBPB	chrX:76782216-76783050	A549	lung:	n/a	chrX:76782904-76782915 chrX:76782272-76782285 chrX:76782383-76782396
35	CEBPB	chrX:76822417-76822632	H1-hESC	embryonic stem cell:	n/a	chrX:76822527-76822538
36	CEBPB	chrX:76924457-76924769	IMR90	lung:	n/a	n/a
37	CEBPB	chrX:76822382-76822673	HepG2	liver:	n/a	chrX:76822527-76822538
38	CEBPB	chrX:76759163-76759200	A549	lung:	n/a	n/a
39	CEBPB	chrX:76852201-76852999	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chrX:77005233-77005612	A549	lung:	n/a	n/a
41	CEBPB	chrX:76924422-76924728	K562	blood:	n/a	n/a
42	CEBPB	chrX:76910983-76911274	IMR90	lung:	n/a	n/a
43	CEBPB	chrX:77005268-77005612	A549	lung:	n/a	n/a
44	CEBPB	chrX:76852730-76852876	A549	lung:	n/a	n/a
45	CEBPB	chrX:76786910-76786960	K562	blood:	n/a	n/a
46	CEBPB	chrX:76959119-76959392	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chrX:76782236-76783063	HepG2	liver:	n/a	chrX:76782904-76782915 chrX:76782272-76782285 chrX:76782383-76782396
48	CEBPB	chrX:76782744-76783031	H1-hESC	embryonic stem cell:	n/a	chrX:76782904-76782915
49	CEBPB	chrX:76762638-76762900	K562	blood:	n/a	chrX:76762780-76762791
50	CEBPB	chrX:76857403-76857655	IMR90	lung:	n/a	chrX:76857528-76857539

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:76711903-76711953	HIPEpiC	eye:	n/a
2	chrX:76711903-76711953	HIPEpiC	eye:	n/a
3	chrX:76709434-76709484	ProgFib	skin:	n/a
4	chrX:76708880-76708930	Jurkat	blood:	n/a
5	chrX:76709731-76709781	NHBE	bronchial:	n/a
6	chrX:76709434-76709484	SK-N-MC	brain:	n/a
7	chrX:76711903-76711953	T-47D	breast:	n/a
8	chrX:76709731-76709781	U87	brain:	n/a
9	chrX:76709434-76709484	Jurkat	blood:	n/a
10	chrX:76709434-76709484	Caco-2	colon:	n/a
11	chrX:76709238-76709288	GM06990	blood:	n/a
12	chrX:76709731-76709781	ProgFib	skin:	n/a
13	chrX:76832207-76832257	CMK	blood:	n/a
14	chrX:77037960-77038010	NT2-D1	testis:	n/a
15	chrX:76709434-76709484	HRE	kidney:	n/a
16	chrX:76709434-76709484	HCPEpiC	choroid plexus:	n/a
17	chrX:76709500-76709550	AG04450	lung:	fetal
18	chrX:77037960-77038010	A549	lung:	n/a
19	chrX:76832207-76832257	U87	brain:	n/a
20	chrX:76709434-76709484	Hepatocyte	liver:	n/a
21	chrX:76709731-76709781	HCF	heart:	n/a
22	chrX:76832207-76832257	HPAEpiC	pulmonary alveolar:	n/a
23	chrX:76709238-76709288	HMEC	breast:	n/a
24	chrX:76711903-76711953	Caco-2	colon:	n/a
25	chrX:77037960-77038010	SK-N-SH_RA	brain:	n/a
26	chrX:76709434-76709484	PANC-1	pancreas:	n/a
27	chrX:76709238-76709288	SK-N-SH_RA	brain:	n/a
28	chrX:76709500-76709550	ProgFib	skin:	n/a
29	chrX:77037960-77038010	BJ	skin:	n/a
30	chrX:76709731-76709781	HRPEpiC	eye:	n/a
31	chrX:76708880-76708930	RPTEC	kidney:	n/a
32	chrX:76709731-76709781	ECC-1	luminal epithelium:	n/a
33	chrX:76709434-76709484	SK-N-SH_RA	brain:	n/a
34	chrX:76709731-76709781	PANC-1	pancreas:	n/a
35	chrX:76709731-76709781	AG09309	skin:	n/a
36	chrX:76709731-76709781	T-47D	breast:	n/a
37	chrX:76708880-76708930	NH-A	brain:	n/a
38	chrX:76709434-76709484	H1-hESC	embryonic stem cell:	embryo
39	chrX:77037960-77038010	PFSK-1	brain:	n/a
40	chrX:76709500-76709550	Hela-S3	cervix:	n/a
41	chrX:76709731-76709781	HIPEpiC	eye:	n/a
42	chrX:76709238-76709288	Caco-2	colon:	n/a
43	chrX:76711903-76711953	H1-hESC	embryonic stem cell:	embryo
44	chrX:77037960-77038010	IMR90	lung:	fetal
45	chrX:76832207-76832257	HepG2	liver:	n/a
46	chrX:76709731-76709781	GM19239	blood:	n/a
47	chrX:76709434-76709484	MCF10A-Er-Src	breast:	n/a
48	chrX:76709731-76709781	GM12891	blood:	n/a
49	chrX:76711903-76711953	PANC-1	pancreas:	n/a
50	chrX:76708880-76708930	NT2-D1	testis:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chrX:76926746..76928859-chrX:76931303..76934886,3	K562	blood:
2	chrX:76883999..76886686-chrX:76887036..76889742,2	K562	blood:
3	chrX:76993528..76995377-chrX:76996626..76999172,2	MCF-7	breast:
4	chrX:76848785..76850331-chrX:76854737..76856395,2	K562	blood:
5	chrX:76800591..76802545-chrX:76807334..76809410,2	MCF-7	breast:
6	chrX:76749546..76752499-chrX:76758608..76760224,2	K562	blood:
7	chrX:76761448..76764250-chrX:76766493..76768451,2	MCF-7	breast:
8	chrX:77014212..77016135-chrX:77018406..77021296,2	K562	blood:
9	chrX:76749546..76752499-chrX:76758608..76760224,2	K562	blood:
10	chrX:76777436..76779959-chrX:76781784..76783298,2	K562	blood:
11	chr2:9877832..9879411-chrX:76718203..76719726,2	K562	blood:
12	chrX:76893077..76895046-chrX:77147729..77150138,2	MCF-7	breast:
13	chrX:76927289..76929660-chrX:76931892..76933429,2	MCF-7	breast:
14	chrX:76884700..76887437-chrX:76888624..76890232,2	K562	blood:
15	chrX:76853327..76855673-chrX:76856891..76859601,2	MCF-7	breast:
16	chrX:76912843..76915064-chrX:76919242..76920879,2	K562	blood:
17	chrX:76889584..76891766-chrX:76894639..76897322,2	K562	blood:
18	chrX:76916841..76919206-chrX:76922058..76924326,2	MCF-7	breast:
19	chrX:76883532..76887606-chrX:77150415..77153534,3	MCF-7	breast:
20	chrX:77026149..77028968-chrX:77037279..77039869,2	K562	blood:
21	chrX:77023181..77025657-chrX:77041110..77043745,2	MCF-7	breast:
22	chrX:77034724..77036644-chrX:77040474..77043894,3	K562	blood:
23	chrX:77034133..77037506-chrX:77038826..77043053,5	MCF-7	breast:
24	chrX:76891482..76894301-chrX:76899024..76901296,2	MCF-7	breast:
25	chrX:76922852..76925730-chrX:76926707..76929215,2	K562	blood:
26	chrX:76926746..76928859-chrX:76931303..76934886,3	K562	blood:
27	chrX:76777436..76780005-chrX:76781673..76783298,3	K562	blood:
28	chrX:76884700..76887437-chrX:76888624..76890232,2	K562	blood:
29	chrX:76800591..76802545-chrX:76807334..76809410,2	MCF-7	breast:
30	chrX:76912843..76915064-chrX:76919242..76920879,2	K562	blood:
31	chrX:76883999..76886686-chrX:76887036..76889742,2	K562	blood:
32	chrX:76890266..76892127-chrX:76895822..76897834,2	K562	blood:
33	chrX:76950089..76952987-chrX:76954385..76957043,2	MCF-7	breast:
34	chrX:77014212..77016135-chrX:77018406..77021296,2	K562	blood:
35	chrX:76927289..76929660-chrX:76931892..76933429,2	MCF-7	breast:
36	chrX:76964747..76966310-chrX:76968662..76971050,2	MCF-7	breast:
37	chrX:77038474..77040783-chrX:77043178..77044820,2	MCF-7	breast:
38	chrX:76996384..76998942-chrX:77041132..77042972,2	MCF-7	breast:
39	chrX:76942261..76943831-chrX:76947036..76949639,2	MCF-7	breast:
40	chrX:77038824..77040402-chrX:77040852..77043710,2	MCF-7	breast:
41	chrX:77033474..77036528-chrX:77040329..77042995,4	MCF-7	breast:
42	chrX:76900558..76902843-chrX:76905942..76907892,2	MCF-7	breast:
43	chrX:76964747..76966310-chrX:76968662..76971050,2	MCF-7	breast:
44	chrX:77038723..77041459-chrX:77150362..77152719,2	MCF-7	breast:
45	chrX:76900558..76902843-chrX:76905942..76907892,2	MCF-7	breast:
46	chrX:76853327..76855673-chrX:76856891..76859601,2	MCF-7	breast:
47	chrX:76704759..76707077-chrX:76710548..76712188,2	MCF-7	breast:
48	chr12:90582805..90583489-chrX:76978499..76979499,2	MCF-7	breast:
49	chrX:76942261..76943831-chrX:76947036..76949639,2	MCF-7	breast:
50	chrX:76922852..76925730-chrX:76926707..76929215,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COX7B-5	chrX:76983344-76983557	NONHSAT137691

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ATRX	hsa-miR-30a-5p	chrX:76762578-76762600

Variant related genes	Relation type
ATRX	TF binding region
FGF16	TF binding region
FABP5P15	TF binding region
ATRX	CpG island
FGF16	CpG island
FABP5P15	CpG island
ENSG00000102158	chromatin interactions
ENSG00000085224	chromatin interactions

Extended variants
information (count: 3665 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:3665 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182831779	chrX:76704066-76704067	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs186570800	chrX:76704318-76704319	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs191078931	chrX:76704493-76704494	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs28510987	chrX:76704513-76704514	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs368778546	chrX:76704537-76704538	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs183228681	chrX:76704589-76704590	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs375621016	chrX:76704924-76704925	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs371435941	chrX:76704957-76704958	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs187600003	chrX:76704999-76705000	Weak transcription Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs193043230	chrX:76705003-76705004	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs183140506	chrX:76705248-76705249	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs202168631	chrX:76705267-76705268	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs140573148	chrX:76705273-76705274	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs534665643	chrX:76705403-76705404	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs28756066	chrX:76705428-76705429	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs145735876	chrX:76705480-76705481	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs188182161	chrX:76705538-76705539	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs192513351	chrX:76705666-76705667	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs183645728	chrX:76705921-76705922	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs187959830	chrX:76706120-76706121	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs553022230	chrX:76706163-76706164	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs142597272	chrX:76706184-76706185	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs34854374	chrX:76706415-76706416	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs560179684	chrX:76706426-76706427	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs192590507	chrX:76706462-76706463	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs527300905	chrX:76706771-76706772	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs150144352	chrX:76706876-76706877	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs184571464	chrX:76706997-76706998	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs199652643	chrX:76707013-76707014	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs376916807	chrX:76707015-76707016	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs190114513	chrX:76707484-76707485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138629085	chrX:76707598-76707599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs35714861	chrX:76707673-76707674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs28513868	chrX:76707750-76707751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs28602939	chrX:76707794-76707795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs181707281	chrX:76707817-76707818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373443955	chrX:76707858-76707859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186521603	chrX:76708163-76708164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189799910	chrX:76708221-76708222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs551710847	chrX:76708405-76708406	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs139494920	chrX:76708439-76708440	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs181123131	chrX:76708442-76708443	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs185331289	chrX:76708458-76708459	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs189747544	chrX:76708588-76708589	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs28690770	chrX:76708694-76708695	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs147173358	chrX:76708711-76708712	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs183452839	chrX:76708809-76708810	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs186390924	chrX:76709073-76709074	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs57828703	chrX:76709128-76709129	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs376449088	chrX:76709220-76709221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:45)

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
Glioblastoma multiforme	22286061	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
small cell lung cancer	20016488	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
Pancreatic cancer	17952125	CNVD
Alcoholism	21790672	CNVD
Mental retardation	22129561	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:3747 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:76703600-76704000	Active TSS	iPS-15b Cell Line	embryonic stem cell
2	chrX:76703600-76704000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
3	chrX:76703600-76704200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
4	chrX:76703600-76704400	Active TSS	H9 Cell Line	embryonic stem cell
5	chrX:76703600-76704400	Active TSS	Primary hematopoietic stem cells short term culture	blood
6	chrX:76703600-76705400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chrX:76703800-76704000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
8	chrX:76703800-76704000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
9	chrX:76703800-76704000	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
10	chrX:76703800-76704000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
11	chrX:76703800-76704000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
12	chrX:76703800-76704000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
13	chrX:76703800-76704000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
14	chrX:76703800-76704000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chrX:76703800-76704000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
16	chrX:76703800-76704200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
17	chrX:76703800-76704200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
18	chrX:76703800-76704200	Flanking Active TSS	Primary hematopoietic stem cells	blood
19	chrX:76703800-76704200	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
20	chrX:76703800-76704200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
21	chrX:76703800-76704400	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
22	chrX:76703800-76704600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chrX:76703800-76704600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
24	chrX:76703800-76704600	Enhancers	Right Ventricle	heart
25	chrX:76703800-76704800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
26	chrX:76703800-76704800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
27	chrX:76703800-76704800	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chrX:76703800-76705400	Flanking Active TSS	HUVEC	blood vessel
29	chrX:76703800-76706200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chrX:76704000-76704200	Flanking Bivalent TSS/Enh	ES-WA7 Cell Line	embryonic stem cell
31	chrX:76704000-76704200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chrX:76704000-76704400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
33	chrX:76704000-76704400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
34	chrX:76704000-76704600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chrX:76704000-76704800	Enhancers	Left Ventricle	heart
36	chrX:76704000-76705000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
37	chrX:76704200-76704400	Bivalent Enhancer	Adipose Nuclei	Adipose
38	chrX:76704200-76704600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
39	chrX:76704200-76704600	Active TSS	Primary hematopoietic stem cells	blood
40	chrX:76704200-76705000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
41	chrX:76704200-76705600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chrX:76704200-76705800	Active TSS	Fetal Muscle Trunk	muscle
43	chrX:76704400-76704600	Active TSS	iPS-15b Cell Line	embryonic stem cell
44	chrX:76704400-76704600	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
45	chrX:76704400-76704800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
46	chrX:76704400-76705000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
47	chrX:76704400-76705200	Enhancers	Fetal Heart	heart
48	chrX:76704600-76704800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chrX:76704600-76704800	Flanking Active TSS	Primary hematopoietic stem cells	blood
50	chrX:76704600-76704800	Enhancers	Right Atrium	heart

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