Variant report

Variant	nsv895097
Chromosome Location	chr10:44876586-44888130
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	ARID3A	chr10:44882107-44882307	HepG2	liver:	n/a	n/a
2	ATF3	chr10:44882112-44882269	K562	blood:	n/a	n/a
3	BACH1	chr10:44882052-44882506	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:44879399-44880089	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr10:44881774-44881807	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:44880796-44881429	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr10:44881995-44882274	GM12878	blood:	n/a	n/a
8	BHLHE40	chr10:44882094-44882278	K562	blood:	n/a	chr10:44882150-44882166
9	BRCA1	chr10:44882054-44882214	HepG2	liver:	n/a	n/a
10	CCNT2	chr10:44882111-44882345	K562	blood:	n/a	n/a
11	CEBPB	chr10:44886015-44886389	HepG2	liver:	n/a	chr10:44886190-44886201
12	CEBPB	chr10:44886070-44886276	HepG2	liver:	n/a	chr10:44886190-44886201
13	CEBPB	chr10:44882134-44882409	K562	blood:	n/a	n/a
14	CEBPB	chr10:44882112-44882349	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr10:44886029-44886357	A549	lung:	n/a	chr10:44886190-44886201
16	CEBPB	chr10:44886057-44886288	HepG2	liver:	n/a	chr10:44886190-44886201
17	CEBPB	chr10:44882081-44882254	HepG2	liver:	n/a	n/a
18	CEBPB	chr10:44886067-44886325	K562	blood:	n/a	chr10:44886190-44886201
19	CEBPB	chr10:44882105-44882260	HepG2	liver:	n/a	n/a
20	CEBPB	chr10:44886019-44886366	IMR90	lung:	n/a	chr10:44886190-44886201
21	CHD2	chr10:44882077-44882239	HepG2	liver:	n/a	n/a
22	CREB1	chr10:44879975-44880721	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTBP2	chr10:44882086-44882642	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTBP2	chr10:44877649-44880413	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr10:44882060-44882210	A549	lung:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
26	CTCF	chr10:44882461-44882584	GM20000	blood:	n/a	n/a
27	CTCF	chr10:44877840-44877990	AG09319	gingival:	n/a	n/a
28	CTCF	chr10:44882140-44882290	GM06990	blood:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
29	CTCF	chr10:44882140-44882290	HFF-Myc	foreskin:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
30	CTCF	chr10:44881920-44882070	GM12870	blood:	n/a	n/a
31	CTCF	chr10:44882120-44882270	GM12864	blood:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
32	CTCF	chr10:44882160-44882310	BJ	skin:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
33	CTCF	chr10:44882059-44882327	SK-N-SH_RA	brain:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
34	CTCF	chr10:44882120-44882270	AG04449	skin:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
35	CTCF	chr10:44882120-44882270	AG09309	skin:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
36	CTCF	chr10:44879580-44879730	HCM	heart:	n/a	n/a
37	CTCF	chr10:44882048-44882330	A549	lung:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
38	CTCF	chr10:44882160-44882310	HCFaa	heart:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
39	CTCF	chr10:44882100-44882250	HCM	heart:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
40	CTCF	chr10:44882050-44882367	MCF-7	breast:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
41	CTCF	chr10:44882160-44882310	GM12869	blood:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
42	CTCF	chr10:44882120-44882270	GM12874	blood:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
43	CTCF	chr10:44882440-44882590	Caco-2	colon:	n/a	n/a
44	CTCF	chr10:44879740-44879816	MCF-7	breast:	n/a	n/a
45	CTCF	chr10:44882160-44882310	HBMEC	blood vessel:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
46	CTCF	chr10:44882580-44882730	AG04450	lung:	n/a	n/a
47	CTCF	chr10:44880229-44880313	MCF-7	breast:	n/a	n/a
48	CTCF	chr10:44882100-44882250	GM12866	blood:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
49	CTCF	chr10:44882080-44882230	HRPEpiC	eye:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190
50	CTCF	chr10:44882140-44882290	AG09319	gingival:	n/a	chr10:44882177-44882190 chr10:44882177-44882190 chr10:44882176-44882192 chr10:44882175-44882193 chr10:44882178-44882188 chr10:44882170-44882191 chr10:44882181-44882190

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:44880559-44880609	Hepatocyte	liver:	n/a
2	chr10:44880559-44880609	Hepatocyte	liver:	n/a
3	chr10:44882135-44882185	IMR90	lung:	fetal
4	chr10:44880562-44880612	MCF-7	breast:	n/a
5	chr10:44878373-44878423	ECC-1	luminal epithelium:	n/a
6	chr10:44885910-44885960	GM12878	blood:	n/a
7	chr10:44881934-44881984	NT2-D1	testis:	n/a
8	chr10:44881054-44881104	Jurkat	blood:	n/a
9	chr10:44879465-44879515	RPTEC	kidney:	n/a
10	chr10:44881551-44881601	SKMC	muscle:	n/a
11	chr10:44881934-44881984	Hepatocyte	liver:	n/a
12	chr10:44880559-44880609	GM19239	blood:	n/a
13	chr10:44880559-44880609	RPTEC	kidney:	n/a
14	chr10:44880236-44880286	AoSMC	blood vessel:	n/a
15	chr10:44880708-44880758	HCT-116	colon:	n/a
16	chr10:44882135-44882185	SK-N-MC	brain:	n/a
17	chr10:44880236-44880286	PrEC	prostate:	n/a
18	chr10:44880236-44880286	AG04450	lung:	fetal
19	chr10:44881750-44881800	HRPEpiC	eye:	n/a
20	chr10:44880545-44880595	HAEpiC	amniotic membrane:	n/a
21	chr10:44880236-44880286	NH-A	brain:	n/a
22	chr10:44880128-44880178	HepG2	liver:	n/a
23	chr10:44882599-44882649	SAEC	small airway:	n/a
24	chr10:44881934-44881984	HCT-116	colon:	n/a
25	chr10:44880545-44880595	NHDF-neo	bronchial:	n/a
26	chr10:44881934-44881984	AoSMC	blood vessel:	n/a
27	chr10:44880128-44880178	HEEpiC	esophagus:	n/a
28	chr10:44880730-44880780	AG09309	skin:	n/a
29	chr10:44881934-44881984	HEEpiC	esophagus:	n/a
30	chr10:44879465-44879515	NT2-D1	testis:	n/a
31	chr10:44880819-44880869	AG04449	skin:	fetal
32	chr10:44880562-44880612	SK-N-SH	brain:	n/a
33	chr10:44880236-44880286	NT2-D1	testis:	n/a
34	chr10:44878373-44878423	CMK	blood:	n/a
35	chr10:44880542-44880592	NH-A	brain:	n/a
36	chr10:44880559-44880609	LNCaP	prostate:	n/a
37	chr10:44881054-44881104	Caco-2	colon:	n/a
38	chr10:44880545-44880595	ProgFib	skin:	n/a
39	chr10:44879465-44879515	HCM	heart:	n/a
40	chr10:44878373-44878423	Jurkat	blood:	n/a
41	chr10:44882340-44882390	HCPEpiC	choroid plexus:	n/a
42	chr10:44880708-44880758	PrEC	prostate:	n/a
43	chr10:44880545-44880595	HEK293	kidney:	embryo
44	chr10:44880128-44880178	ProgFib	skin:	n/a
45	chr10:44880708-44880758	ECC-1	luminal epithelium:	n/a
46	chr10:44881551-44881601	NB4	blood:	n/a
47	chr10:44881054-44881104	HCT-116	colon:	n/a
48	chr10:44882599-44882649	PrEC	prostate:	n/a
49	chr10:44882599-44882649	AG04449	skin:	fetal
50	chr10:44885910-44885960	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:44874626..44876126-chr10:44876143..44877664,2	MCF-7	breast:
2	chr10:44166808..44167608-chr10:44882043..44882606,2	MCF-7	breast:
3	chr10:44779480..44780239-chr10:44881943..44882604,2	K562	blood:
4	chr10:44879083..44880666-chr10:44886270..44889199,2	MCF-7	breast:
5	chr10:44882608..44885734-chr10:44887032..44891125,3	MCF-7	breast:
6	chr10:44882608..44885734-chr10:44887032..44891125,3	MCF-7	breast:

Variant related genes	Relation type
CXCL12	TF binding region
CXCL12	CpG island
ENSG00000107562	chromatin interactions

Extended variants
information (count: 448 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199671734	chr10:44876586-44876587	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs577734754	chr10:44876636-44876637	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533604989	chr10:44876721-44876722	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556483342	chr10:44876744-44876745	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545305191	chr10:44876762-44876763	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563397234	chr10:44876763-44876764	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113367315	chr10:44876768-44876769	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs17883700	chr10:44876837-44876838	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs11239026	chr10:44876838-44876839	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs538648057	chr10:44876865-44876866	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs552410795	chr10:44876874-44876875	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs548616325	chr10:44876879-44876880	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs560539442	chr10:44876894-44876895	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs76816127	chr10:44877005-44877006	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs546358787	chr10:44877040-44877041	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs193149605	chr10:44877070-44877071	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs538819915	chr10:44877096-44877097	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs115754241	chr10:44877138-44877139	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs535194327	chr10:44877163-44877164	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs569524057	chr10:44877168-44877169	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs536942210	chr10:44877211-44877212	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs555042550	chr10:44877389-44877390	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs573258986	chr10:44877440-44877441	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs372618731	chr10:44877463-44877464	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs11592974	chr10:44877501-44877502	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs558747904	chr10:44877508-44877509	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs577777653	chr10:44877511-44877512	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs544830734	chr10:44877526-44877527	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs2760669	chr10:44877651-44877652	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs17881591	chr10:44877675-44877676	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs370007394	chr10:44877677-44877678	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs575191579	chr10:44877685-44877686	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs536788117	chr10:44877721-44877722	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs556993461	chr10:44877740-44877741	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs576862537	chr10:44877790-44877791	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs545829637	chr10:44877808-44877809	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs560581179	chr10:44877896-44877897	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs528052150	chr10:44877944-44877945	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs376676340	chr10:44877946-44877947	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs112970552	chr10:44877950-44877951	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs540336279	chr10:44877963-44877964	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs564784951	chr10:44878010-44878011	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs184754513	chr10:44878036-44878037	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs188296320	chr10:44878045-44878046	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs550938688	chr10:44878051-44878052	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs17886196	chr10:44878064-44878065	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs17879548	chr10:44878114-44878115	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs541990773	chr10:44878123-44878124	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs548878663	chr10:44878137-44878138	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs149407406	chr10:44878140-44878141	Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:648 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44850600-44877600	Weak transcription	Duodenum Mucosa	Duodenum
2	chr10:44860000-44879000	Weak transcription	Gastric	stomach
3	chr10:44864600-44876800	Strong transcription	Fetal Stomach	stomach
4	chr10:44864800-44877800	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr10:44865600-44878000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr10:44866000-44877600	Weak transcription	Fetal Brain Female	brain
7	chr10:44866400-44878600	Weak transcription	Liver	Liver
8	chr10:44866600-44877600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr10:44867000-44878200	Weak transcription	Brain Hippocampus Middle	brain
10	chr10:44867400-44878000	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr10:44867600-44878600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr10:44869600-44878200	Weak transcription	Brain Substantia Nigra	brain
13	chr10:44870200-44877600	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr10:44871000-44877600	Weak transcription	Rectal Smooth Muscle	rectum
15	chr10:44871600-44877000	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr10:44871800-44877000	Weak transcription	Stomach Smooth Muscle	stomach
17	chr10:44872400-44877400	Weak transcription	Fetal Kidney	kidney
18	chr10:44873200-44877600	Weak transcription	Lung	lung
19	chr10:44873600-44876600	Strong transcription	Fetal Lung	lung
20	chr10:44874400-44877800	Weak transcription	Right Ventricle	heart
21	chr10:44874600-44876600	Genic enhancers	Fetal Muscle Leg	muscle
22	chr10:44874600-44877800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr10:44874600-44877800	Enhancers	Psoas Muscle	Psoas
24	chr10:44874800-44877800	Weak transcription	Spleen	Spleen
25	chr10:44874800-44879200	Weak transcription	Aorta	Aorta
26	chr10:44875200-44877600	Weak transcription	Ovary	ovary
27	chr10:44875200-44877800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr10:44875200-44878000	Weak transcription	NH-A	brain
29	chr10:44875400-44876600	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr10:44875600-44876600	Transcr. at gene 5' and 3'	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr10:44875600-44876600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
32	chr10:44875600-44877400	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr10:44875800-44876600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr10:44875800-44877600	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr10:44875800-44878000	Weak transcription	NHLF	lung
36	chr10:44876000-44877000	Genic enhancers	Osteobl	bone
37	chr10:44876000-44877600	Weak transcription	Colon Smooth Muscle	Colon
38	chr10:44876000-44878000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr10:44876000-44878600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr10:44876200-44876600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr10:44876200-44876600	Enhancers	Brain Anterior Caudate	brain
42	chr10:44876200-44876600	Genic enhancers	Left Ventricle	heart
43	chr10:44876200-44876600	Enhancers	Right Atrium	heart
44	chr10:44876200-44877000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr10:44876200-44877400	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr10:44876200-44877600	Enhancers	H9 Cell Line	embryonic stem cell
47	chr10:44876200-44877600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr10:44876200-44877800	Enhancers	Brain Germinal Matrix	brain
49	chr10:44876200-44878400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr10:44876400-44876600	Genic enhancers	Fetal Muscle Trunk	muscle

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