Variant report

Variant	esv3408138
Chromosome Location	chrX:153664208-153666531
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:264)
CpG islands
(count:553)
Chromatin interactive
region (count:31)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chrX:153665483-153665543	GM12878	blood:	n/a	n/a
2	BHLHE40	chrX:153665481-153665542	K562	blood:	n/a	n/a
3	BRCA1	chrX:153665466-153665727	GM12878	blood:	n/a	n/a
4	CCNT2	chrX:153664814-153665660	K562	blood:	n/a	chrX:153665171-153665180
5	CHD2	chrX:153665261-153665661	K562	blood:	n/a	n/a
6	CHD2	chrX:153665317-153665620	HepG2	liver:	n/a	n/a
7	CHD2	chrX:153664947-153665683	GM12878	blood:	n/a	n/a
8	CHD2	chrX:153665248-153665672	Hela-S3	cervix:	n/a	n/a
9	CHD2	chrX:153665274-153665624	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chrX:153664874-153665135	A549	lung:	n/a	n/a
11	CREB1	chrX:153665402-153665687	H1-hESC	embryonic stem cell:	n/a	n/a
12	CREB1	chrX:153665217-153665664	A549	lung:	n/a	n/a
13	CTCF	chrX:153664890-153664941	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chrX:153665572-153665681	GM19239	blood:	n/a	n/a
15	CTCF	chrX:153664979-153665068	GM19239	blood:	n/a	n/a
16	CTCF	chrX:153665476-153665547	GM19239	blood:	n/a	n/a
17	CTCF	chrX:153664364-153664465	GM10248	blood:	n/a	n/a
18	CUX1	chrX:153664858-153664949	K562	blood:	n/a	n/a
19	E2F4	chrX:153665461-153665600	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F6	chrX:153664781-153665133	K562	blood:	n/a	n/a
21	EGR1	chrX:153665349-153665625	K562	blood:	n/a	n/a
22	EGR1	chrX:153664884-153665161	K562	blood:	n/a	n/a
23	EGR1	chrX:153664908-153665151	K562	blood:	n/a	n/a
24	ELF1	chrX:153665237-153666242	GM12878	blood:	n/a	n/a
25	EP300	chrX:153665390-153665686	H1-hESC	embryonic stem cell:	n/a	n/a
26	EP300	chrX:153665231-153665824	ECC-1	luminal epithelium:	n/a	chrX:153665706-153665715 chrX:153665763-153665772 chrX:153665357-153665373
27	ETS1	chrX:153665390-153665582	K562	blood:	n/a	n/a
28	FOXP2	chrX:153664789-153665166	PFSK-1	brain:	n/a	n/a
29	FOXP2	chrX:153665336-153665662	PFSK-1	brain:	n/a	n/a
30	HCFC1	chrX:153664822-153665087	K562	blood:	n/a	n/a
31	HCFC1	chrX:153665303-153665622	K562	blood:	n/a	n/a
32	HEY1	chrX:153665476-153665756	K562	blood:	n/a	chrX:153665652-153665667
33	HEY1	chrX:153665369-153665673	HepG2	liver:	n/a	chrX:153665652-153665667
34	HMGN3	chrX:153664799-153665161	K562	blood:	n/a	n/a
35	HMGN3	chrX:153665552-153665833	K562	blood:	n/a	n/a
36	IRF1	chrX:153665447-153665529	K562	blood:	n/a	n/a
37	IRF1	chrX:153665347-153665519	K562	blood:	n/a	n/a
38	IRF1	chrX:153665326-153665504	K562	blood:	n/a	n/a
39	JUND	chrX:153665299-153665701	A549	lung:	n/a	n/a
40	JUND	chrX:153664972-153665086	H1-hESC	embryonic stem cell:	n/a	n/a
41	JUND	chrX:153665406-153665555	H1-hESC	embryonic stem cell:	n/a	n/a
42	MAX	chrX:153665304-153665650	K562	blood:	n/a	n/a
43	MAX	chrX:153665217-153665869	A549	lung:	n/a	chrX:153665813-153665822
44	MAX	chrX:153665459-153665629	GM12878	blood:	n/a	n/a
45	MAX	chrX:153664714-153665150	K562	blood:	n/a	n/a
46	MAX	chrX:153665301-153665781	ECC-1	luminal epithelium:	n/a	n/a
47	MAX	chrX:153664705-153665138	H1-hESC	embryonic stem cell:	n/a	n/a
48	MAX	chrX:153664667-153665143	H1-hESC	embryonic stem cell:	n/a	n/a
49	MAX	chrX:153664849-153665170	ECC-1	luminal epithelium:	n/a	n/a
50	MAX	chrX:153665320-153665760	A549	lung:	n/a	n/a

(count:553 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:153665697-153665747	NB4	blood:	n/a
2	chrX:153665714-153665764	HIPEpiC	eye:	n/a
3	chrX:153665103-153665153	HCM	heart:	n/a
4	chrX:153664905-153664955	GM12878	blood:	n/a
5	chrX:153665697-153665747	NB4	blood:	n/a
6	chrX:153665714-153665764	HIPEpiC	eye:	n/a
7	chrX:153665103-153665153	HCM	heart:	n/a
8	chrX:153664905-153664955	GM12878	blood:	n/a
9	chrX:153664475-153664525	HNPCEpiC	eye:	n/a
10	chrX:153664905-153664955	PrEC	prostate:	n/a
11	chrX:153665799-153665849	CMK	blood:	n/a
12	chrX:153664862-153664912	U87	brain:	n/a
13	chrX:153665624-153665674	HRPEpiC	eye:	n/a
14	chrX:153665624-153665674	AG04450	lung:	fetal
15	chrX:153665714-153665764	GM12891	blood:	n/a
16	chrX:153664862-153664912	NT2-D1	testis:	n/a
17	chrX:153664905-153664955	SAEC	small airway:	n/a
18	chrX:153665103-153665153	Hepatocyte	liver:	n/a
19	chrX:153665799-153665849	HUVEC	blood vessel:	n/a
20	chrX:153664905-153664955	AG10803	skin:	n/a
21	chrX:153664475-153664525	RPTEC	kidney:	n/a
22	chrX:153665714-153665764	HPAEpiC	pulmonary alveolar:	n/a
23	chrX:153664905-153664955	IMR90	lung:	fetal
24	chrX:153665624-153665674	GM12892	blood:	n/a
25	chrX:153664903-153664953	NH-A	brain:	n/a
26	chrX:153665624-153665674	ovcar-3	ovarian:	n/a
27	chrX:153664475-153664525	IMR90	lung:	fetal
28	chrX:153665103-153665153	HCF	heart:	n/a
29	chrX:153664475-153664525	PrEC	prostate:	n/a
30	chrX:153664905-153664955	HEEpiC	esophagus:	n/a
31	chrX:153664903-153664953	NHDF-neo	bronchial:	n/a
32	chrX:153664905-153664955	SKMC	muscle:	n/a
33	chrX:153664903-153664953	H1-hESC	embryonic stem cell:	embryo
34	chrX:153665714-153665764	SK-N-SH	brain:	n/a
35	chrX:153665624-153665674	SK-N-SH	brain:	n/a
36	chrX:153664905-153664955	Hela-S3	cervix:	n/a
37	chrX:153664905-153664955	PFSK-1	brain:	n/a
38	chrX:153664475-153664525	BJ	skin:	n/a
39	chrX:153665624-153665674	AoSMC	blood vessel:	n/a
40	chrX:153664903-153664953	SK-N-MC	brain:	n/a
41	chrX:153664475-153664525	U87	brain:	n/a
42	chrX:153664903-153664953	IMR90	lung:	fetal
43	chrX:153665103-153665153	SKMC	muscle:	n/a
44	chrX:153664905-153664955	HCF	heart:	n/a
45	chrX:153664903-153664953	BJ	skin:	n/a
46	chrX:153665624-153665674	HEK293	kidney:	embryo
47	chrX:153665624-153665674	AG09309	skin:	n/a
48	chrX:153665624-153665674	PANC-1	pancreas:	n/a
49	chrX:153664903-153664953	SKMC	muscle:	n/a
50	chrX:153664905-153664955	HPAEpiC	pulmonary alveolar:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chrX:153601346..153604087-chrX:153662858..153664785,2	MCF-7	breast:
2	chrX:153665329..153668066-chrX:153774780..153776926,2	MCF-7	breast:
3	X:153657611-153671976..X:153701576-153715648	Hela-S3	cervix:
4	X:153657611-153671976..X:153755323-153771683	Hela-S3	cervix:
5	chrX:153664219..153666172-chrX:153706574..153708655,2	MCF-7	breast:
6	chrX:153595338..153600468-chrX:153664217..153668349,5	K562	blood:
7	chrX:153663553..153666950-chrX:153742012..153745567,3	MCF-7	breast:
8	chrX:153596589..153600122-chrX:153663177..153666593,6	K562	blood:
9	chrX:153666530..153668825-chrX:153707267..153708924,2	MCF-7	breast:
10	X:153657611-153671976..X:153736289-153755323	Hela-S3	cervix:
11	X:153214268-153230257..X:153657611-153671976	H1-hESC	embryonic stem cell:	embryo
12	chrX:153625525..153632382-chrX:153663983..153668753,13	K562	blood:
13	X:153187063-153190397..X:153657611-153671976	H1-hESC	embryonic stem cell:	embryo
14	chrX:153664786..153666596-chrX:153718680..153720601,2	MCF-7	breast:
15	X:153657611-153671976..X:153681712-153701576	Hela-S3	cervix:
16	X:153657611-153671976..X:153967468-153979902	H1-hESC	embryonic stem cell:	embryo
17	X:153657611-153671976..X:154015910-154019964	Hela-S3	cervix:
18	chrX:153665315..153667101-chrX:153706247..153709053,2	K562	blood:
19	chrX:153597446..153602147-chrX:153663095..153667390,6	MCF-7	breast:
20	chrX:153638347..153641309-chrX:153665287..153666936,2	K562	blood:
21	chrX:153636168..153639473-chrX:153663428..153667737,8	MCF-7	breast:
22	X:153586280-153597086..X:153657611-153671976	H1-hESC	embryonic stem cell:	embryo
23	X:153198557-153214268..X:153657611-153671976	Hela-S3	cervix:
24	X:153625659-153635385..X:153657611-153671976	H1-hESC	embryonic stem cell:	embryo
25	chrX:153664924..153665561-chrX:153718679..153719442,2	MCF-7	breast:
26	chrX:153661692..153667668-chrX:153711020..153716574,8	MCF-7	breast:
27	X:153574513-153584637..X:153657611-153671976	H1-hESC	embryonic stem cell:	embryo
28	chrX:153639669..153642525-chrX:153662814..153665264,2	K562	blood:
29	chrX:153662094..153664647-chrX:153718535..153720101,2	MCF-7	breast:
30	chrX:153625254..153633054-chrX:153663966..153667311,10	MCF-7	breast:
31	chrX:153661960..153666485-chrX:153685751..153689252,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GDI1-1	chrX:153664502-153664773	NONHSAT139174

No data

Variant related genes	Relation type
GDI1	TF binding region
GDI1	CpG island
ENSG00000160219	chromatin interactions
ENSG00000196924	chromatin interactions
ENSG00000071889	chromatin interactions
ENSG00000261773	chromatin interactions
ENSG00000073009	chromatin interactions
ENSG00000102032	chromatin interactions
ENSG00000102178	chromatin interactions
ENSG00000196976	chromatin interactions
ENSG00000147403	chromatin interactions
ENSG00000102125	chromatin interactions
ENSG00000130830	chromatin interactions
ENSG00000126903	chromatin interactions
ENSG00000207165	chromatin interactions
ENSG00000013563	chromatin interactions
ENSG00000089820	chromatin interactions
ENSG00000130827	chromatin interactions
ENSG00000160211	chromatin interactions
ENSG00000172534	chromatin interactions
ENSG00000102030	chromatin interactions

Extended variants
information (count: 37 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:37 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199817275	chrX:153664249-153664250	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
2	rs112489029	chrX:153664255-153664256	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
3	rs374907857	chrX:153664256-153664257	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
4	rs201951115	chrX:153664279-153664280	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
5	rs8425	chrX:153664332-153664333	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
6	rs8689	chrX:153664498-153664499	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
7	rs185605730	chrX:153664522-153664523	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	Overlapped CNVs	n/a
8	rs190656483	chrX:153664629-153664630	Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region lncRNA	20 gene(s)	Overlapped CNVs	n/a
9	rs10140	chrX:153664644-153664645	Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region lncRNA	20 gene(s)	Overlapped CNVs	n/a
10	rs369345078	chrX:153664669-153664670	Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region lncRNA	19 gene(s)	Overlapped CNVs	n/a
11	rs6727	chrX:153664698-153664699	Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region lncRNA	19 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs14662	chrX:153664728-153664729	Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region lncRNA	19 gene(s)	Overlapped CNVs	n/a
13	rs181478584	chrX:153664744-153664745	Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region lncRNA	19 gene(s)	Overlapped CNVs	n/a
14	rs12496	chrX:153664779-153664780	Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
15	rs1043623	chrX:153664789-153664790	Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
16	rs186922842	chrX:153664997-153664998	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
17	rs368904774	chrX:153665084-153665085	Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
18	rs377749920	chrX:153665100-153665101	Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
19	rs192115845	chrX:153665539-153665540	Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
20	rs377447247	chrX:153665555-153665556	Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
21	rs201463367	chrX:153665571-153665572	Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
22	rs183953177	chrX:153665579-153665580	Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
23	rs373598827	chrX:153665588-153665589	Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
24	rs200645358	chrX:153665589-153665590	Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
25	rs368181402	chrX:153665658-153665659	Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
26	rs370426944	chrX:153665672-153665673	Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
27	rs187704798	chrX:153665789-153665790	Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
28	rs189578067	chrX:153665794-153665795	Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
29	rs200697643	chrX:153665846-153665847	Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
30	rs182606975	chrX:153665860-153665861	Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
31	rs369912312	chrX:153665953-153665954	Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
32	rs186835302	chrX:153666022-153666023	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
33	rs111924714	chrX:153666043-153666044	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
34	rs192129807	chrX:153666065-153666066	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
35	rs185359167	chrX:153666125-153666126	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
36	rs377615342	chrX:153666333-153666334	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
37	rs370753683	chrX:153666335-153666336	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Astrocytoma	17387387	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	21979893	CNVD
Schizophrenia	23904455	CNVD
Olfactory neuroblastoma	18408657	CNVD
infertile	22614455	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 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
Cancer	16751803	CNVD
small cell lung cancer	20016488	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
abnormal development	18461090	CNVD
Multiple myeloma	17550852	CNVD
Premature ovarian failure	20952765	CNVD
Abnormal corpus callosum	21572526	CNVD
Breast cancer	21364760	CNVD
Astrocytoma	22246337	CNVD
Cerebellar atrophy	21569638	CNVD
periventricular nodular heterotopia	21572526	CNVD
Cerebellar hypoplasia	21569638	CNVD
Hoyeraal-Hreidarsson syndrome	21569638	CNVD
Oto-palato-digital type II	21569638	CNVD
incontinentia pigmenti anhidrotic ectodermal dysplasia with immunodeficiency	18350553	CNVD
Aqueductal stenosis	21572526	CNVD
Hirschsprung''s Disease	21712996	CNVD
Vermis hypoplasia	21569638	CNVD
X-linked hydrocephalus	21569638	CNVD
Rett syndrome	21569638	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	20970697	CNVD
Epilepsy	20970697	CNVD
Hemophilia A	17823971	CNVD
Rett syndrome	18923514	CNVD
Rett syndrome	22241247	CNVD
Intellectual disability	21984752	CNVD
Mental retardation	19951919	CNVD
Hypotonia	17088400	CNVD
Intellectual disability	22511893	CNVD
Mental retardation	17088400	CNVD
Mental retardation	21119712	CNVD
Neurodevelopmental disorder	19324899	CNVD
Recurrent Infections	17088400	CNVD
Rett syndrome	22283845	CNVD
Rett syndrome	21383316	CNVD
Cryptorchidism	21048976	CNVD
Disorders of sex development	21048976	CNVD
Cervical cancer	21062161	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
Hemophilia A	18787571	CNVD
Hunters syndrom	18787571	CNVD
Prader-willi syndrome	20588305	CNVD
Mental retardation	19057379	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
abortions and stillbirths	19751515	CNVD
Hereditary coagulopathy	21993689	CNVD
Intellectual disability	23615299	CNVD
Mental retardation	17621639	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:153656400-153665000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
2	chrX:153658000-153664400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chrX:153658000-153664600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chrX:153658200-153664400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chrX:153658200-153664400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chrX:153658200-153664400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chrX:153658200-153664800	Weak transcription	Rectal Smooth Muscle	rectum
8	chrX:153658200-153664800	Weak transcription	HMEC	breast
9	chrX:153658200-153665200	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chrX:153658400-153664600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chrX:153658400-153664600	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chrX:153658400-153664600	Weak transcription	Muscle Satellite Cultured Cells	--
13	chrX:153658400-153664600	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chrX:153658400-153664800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chrX:153658400-153664800	Weak transcription	Psoas Muscle	Psoas
16	chrX:153658400-153665600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chrX:153658600-153664600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chrX:153658600-153665000	ZNF genes & repeats	Fetal Stomach	stomach
19	chrX:153658800-153664600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chrX:153659000-153664400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chrX:153659200-153664400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chrX:153659200-153664800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chrX:153659200-153665000	ZNF genes & repeats	Fetal Brain Female	brain
24	chrX:153659400-153664400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chrX:153659400-153664400	Weak transcription	Fetal Heart	heart
26	chrX:153659400-153664400	Strong transcription	Skeletal Muscle Female	skeletal muscle
27	chrX:153659400-153664800	Weak transcription	Fetal Kidney	kidney
28	chrX:153659400-153664800	Weak transcription	Right Atrium	heart
29	chrX:153659400-153665000	Weak transcription	Hela-S3	cervix
30	chrX:153659400-153665000	Weak transcription	HepG2	liver
31	chrX:153659600-153664400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chrX:153659600-153664600	Weak transcription	Brain Angular Gyrus	brain
33	chrX:153659600-153664600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
34	chrX:153659600-153666000	Weak transcription	Stomach Mucosa	stomach
35	chrX:153659800-153664400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chrX:153659800-153664400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chrX:153659800-153664400	Strong transcription	Fetal Thymus	thymus
38	chrX:153659800-153664600	Weak transcription	GM12878-XiMat	blood
39	chrX:153659800-153664600	Weak transcription	HUVEC	blood vessel
40	chrX:153660000-153664400	Strong transcription	Primary T helper cells fromperipheralblood	blood
41	chrX:153660000-153664400	Strong transcription	Adipose Nuclei	Adipose
42	chrX:153660000-153664400	Strong transcription	Brain Hippocampus Middle	brain
43	chrX:153660000-153664400	Strong transcription	Left Ventricle	heart
44	chrX:153660000-153664400	Strong transcription	Pancreas	Pancrea
45	chrX:153660000-153664400	Strong transcription	Right Ventricle	heart
46	chrX:153660000-153664600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chrX:153660000-153664600	Strong transcription	Fetal Intestine Small	intestine
48	chrX:153660200-153664400	Strong transcription	Liver	Liver
49	chrX:153660200-153664400	Strong transcription	Brain Inferior Temporal Lobe	brain
50	chrX:153660200-153664400	Strong transcription	Duodenum Mucosa	Duodenum

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