Variant report

Variant	esv1831010
Chromosome Location	chr10:43674916-43759185
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1929)
CpG islands
(count:1892)
Chromatin interactive
region (count:91)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1929 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:43699491-43699537	K562	blood:	n/a	n/a
2	ARID3A	chr10:43699107-43699244	K562	blood:	n/a	n/a
3	ARID3A	chr10:43697611-43697845	K562	blood:	n/a	n/a
4	ATF3	chr10:43699488-43699780	K562	blood:	n/a	n/a
5	BACH1	chr10:43697668-43698288	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:43698778-43699232	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr10:43700455-43700491	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr10:43725811-43725979	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:43724255-43724899	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr10:43698759-43698935	K562	blood:	n/a	n/a
11	BACH1	chr10:43699552-43699682	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr10:43716663-43717089	H1-hESC	embryonic stem cell:	n/a	chr10:43716761-43716775
13	BATF	chr10:43716620-43716927	GM12878	blood:	n/a	chr10:43716764-43716775
14	BATF	chr10:43716547-43716972	GM12878	blood:	n/a	chr10:43716764-43716775
15	BCL11A	chr10:43716547-43716908	GM12878	blood:	n/a	n/a
16	BHLHE40	chr10:43700495-43700817	K562	blood:	n/a	n/a
17	BHLHE40	chr10:43706244-43706750	K562	blood:	n/a	n/a
18	BHLHE40	chr10:43698653-43699582	K562	blood:	n/a	chr10:43699310-43699326
19	BHLHE40	chr10:43697648-43698011	K562	blood:	n/a	n/a
20	BHLHE40	chr10:43751338-43751539	K562	blood:	n/a	n/a
21	BHLHE40	chr10:43700481-43700677	GM12878	blood:	n/a	n/a
22	BHLHE40	chr10:43751373-43751579	GM12878	blood:	n/a	n/a
23	BHLHE40	chr10:43693561-43693609	HepG2	liver:	n/a	n/a
24	BHLHE40	chr10:43700442-43700768	HepG2	liver:	n/a	n/a
25	BHLHE40	chr10:43697640-43697818	GM12878	blood:	n/a	n/a
26	BHLHE40	chr10:43717038-43717110	K562	blood:	n/a	n/a
27	BRCA1	chr10:43700460-43700570	H1-hESC	embryonic stem cell:	n/a	chr10:43700460-43700467
28	BRCA1	chr10:43700561-43700665	HepG2	liver:	n/a	n/a
29	BRCA1	chr10:43700613-43700784	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr10:43699037-43699881	K562	blood:	n/a	n/a
31	CBX3	chr10:43700471-43700906	K562	blood:	n/a	n/a
32	CBX3	chr10:43697609-43698066	K562	blood:	n/a	n/a
33	CCNT2	chr10:43698852-43699271	K562	blood:	n/a	n/a
34	CCNT2	chr10:43697705-43698509	K562	blood:	n/a	chr10:43698091-43698100 chr10:43698085-43698094
35	CCNT2	chr10:43697137-43697190	K562	blood:	n/a	n/a
36	CCNT2	chr10:43700527-43700727	K562	blood:	n/a	n/a
37	CEBPB	chr10:43700694-43700949	K562	blood:	n/a	n/a
38	CEBPB	chr10:43742253-43742334	K562	blood:	n/a	n/a
39	CEBPB	chr10:43684169-43684459	HepG2	liver:	n/a	chr10:43684300-43684311
40	CEBPB	chr10:43700613-43700990	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr10:43684149-43684496	IMR90	lung:	n/a	chr10:43684300-43684311
42	CEBPB	chr10:43742646-43742953	IMR90	lung:	n/a	chr10:43742769-43742780
43	CEBPB	chr10:43700662-43701007	A549	lung:	n/a	n/a
44	CEBPB	chr10:43742642-43742872	HepG2	liver:	n/a	chr10:43742769-43742780
45	CEBPB	chr10:43700660-43700890	K562	blood:	n/a	n/a
46	CEBPB	chr10:43697770-43697862	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr10:43742639-43742903	K562	blood:	n/a	chr10:43742769-43742780
48	CEBPB	chr10:43700493-43700977	IMR90	lung:	n/a	n/a
49	CEBPB	chr10:43700524-43700969	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr10:43710164-43710668	IMR90	lung:	n/a	n/a

(count:1892 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43697521-43697571	CMK	blood:	n/a
2	chr10:43697521-43697571	CMK	blood:	n/a
3	chr10:43697918-43697968	HPAEpiC	pulmonary alveolar:	n/a
4	chr10:43701731-43701781	BE2_C	brain:	n/a
5	chr10:43728230-43728280	GM12892	blood:	n/a
6	chr10:43746736-43746786	AG09309	skin:	n/a
7	chr10:43698008-43698058	GM12892	blood:	n/a
8	chr10:43691112-43691162	AG04449	skin:	fetal
9	chr10:43691112-43691162	HMEC	breast:	n/a
10	chr10:43721445-43721495	HCM	heart:	n/a
11	chr10:43704423-43704473	LNCaP	prostate:	n/a
12	chr10:43725376-43725426	SAEC	small airway:	n/a
13	chr10:43697521-43697571	GM12878	blood:	n/a
14	chr10:43701731-43701781	HCPEpiC	choroid plexus:	n/a
15	chr10:43725376-43725426	ProgFib	skin:	n/a
16	chr10:43697521-43697571	NH-A	brain:	n/a
17	chr10:43698931-43698981	NT2-D1	testis:	n/a
18	chr10:43698931-43698981	PrEC	prostate:	n/a
19	chr10:43723859-43723909	BJ	skin:	n/a
20	chr10:43697918-43697968	Hepatocyte	liver:	n/a
21	chr10:43680087-43680137	GM12878	blood:	n/a
22	chr10:43728230-43728280	Jurkat	blood:	n/a
23	chr10:43728230-43728280	ECC-1	luminal epithelium:	n/a
24	chr10:43694587-43694637	ProgFib	skin:	n/a
25	chr10:43725612-43725662	HMEC	breast:	n/a
26	chr10:43694587-43694637	HRPEpiC	eye:	n/a
27	chr10:43725612-43725662	SK-N-MC	brain:	n/a
28	chr10:43680087-43680137	HRCEpiC	kidney:	n/a
29	chr10:43701941-43701991	HNPCEpiC	eye:	n/a
30	chr10:43697849-43697899	GM12892	blood:	n/a
31	chr10:43698008-43698058	BJ	skin:	n/a
32	chr10:43694587-43694637	HNPCEpiC	eye:	n/a
33	chr10:43697918-43697968	GM12891	blood:	n/a
34	chr10:43691112-43691162	HEEpiC	esophagus:	n/a
35	chr10:43725376-43725426	Hela-S3	cervix:	n/a
36	chr10:43725277-43725327	HepG2	liver:	n/a
37	chr10:43691112-43691162	HRE	kidney:	n/a
38	chr10:43691112-43691162	U87	brain:	n/a
39	chr10:43725275-43725325	SAEC	small airway:	n/a
40	chr10:43701690-43701740	Caco-2	colon:	n/a
41	chr10:43728230-43728280	SAEC	small airway:	n/a
42	chr10:43711423-43711473	HNPCEpiC	eye:	n/a
43	chr10:43701941-43701991	SKMC	muscle:	n/a
44	chr10:43725411-43725461	MCF-7	breast:	n/a
45	chr10:43697521-43697571	RPTEC	kidney:	n/a
46	chr10:43723859-43723909	SAEC	small airway:	n/a
47	chr10:43698008-43698058	IMR90	lung:	fetal
48	chr10:43698834-43698884	NHDF-neo	bronchial:	n/a
49	chr10:43721445-43721495	NHBE	bronchial:	n/a
50	chr10:43704423-43704473	AG04449	skin:	fetal

(count:91 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:43689923..43692438-chr10:43693060..43695471,2	MCF-7	breast:
2	chr10:43726760..43729695-chr10:43750265..43752104,2	MCF-7	breast:
3	chr10:43684501..43692416-chr10:43693896..43701465,17	K562	blood:
4	chr10:43715924..43718494-chr10:43721120..43724521,4	K562	blood:
5	chr10:43748329..43751092-chr10:43758387..43762104,3	MCF-7	breast:
6	chr10:43741068..43743342-chr10:43744213..43745801,2	K562	blood:
7	chr10:43633034..43634988-chr10:43692928..43695424,2	K562	blood:
8	chr10:43682496..43684417-chr10:43696461..43698091,2	K562	blood:
9	chr10:43700022..43701253-chr10:43750988..43751917,9	MCF-7	breast:
10	chr10:43697811..43700668-chr10:43716914..43719743,2	K562	blood:
11	chr10:43698957..43702295-chr10:43702554..43706038,5	K562	blood:
12	chr10:43709038..43711304-chr10:43890579..43893237,2	K562	blood:
13	chr10:43699342..43701842-chr10:43722370..43724384,2	K562	blood:
14	chr10:43749564..43751225-chr10:43756675..43758831,2	K562	blood:
15	chr10:43729621..43731654-chr10:43739921..43741494,2	MCF-7	breast:
16	chr10:43750362..43752659-chr10:43753450..43755922,3	K562	blood:
17	chr10:43705914..43707657-chr10:43711294..43713443,2	MCF-7	breast:
18	chr10:43749536..43751095-chr10:43809193..43811814,2	K562	blood:
19	chr10:43623236..43626129-chr10:43750680..43753451,2	K562	blood:
20	chr10:43682668..43685704-chr10:43685961..43688550,3	MCF-7	breast:
21	chr10:43699342..43701842-chr10:43722370..43724384,2	K562	blood:
22	chr10:43724977..43726823-chr10:43731228..43733575,2	MCF-7	breast:
23	chr10:43753888..43756103-chr10:43898148..43900430,2	K562	blood:
24	chr10:43600712..43601532-chr10:43751532..43752231,2	K562	blood:
25	chr10:43741068..43743342-chr10:43744213..43745801,2	K562	blood:
26	chr10:43745055..43746859-chr10:43757087..43758973,2	MCF-7	breast:
27	chr10:43704701..43705317-chr10:43751108..43751738,2	MCF-7	breast:
28	chr10:43665667..43666593-chr10:43751227..43751730,2	K562	blood:
29	chr10:43629065..43631893-chr10:43754557..43757372,3	MCF-7	breast:
30	chr10:43679135..43682088-chr10:43694226..43696696,2	MCF-7	breast:
31	chr10:43716710..43720339-chr10:43755141..43758566,3	K562	blood:
32	chr10:43700322..43701097-chr10:43750638..43751735,4	MCF-7	breast:
33	chr10:43746978..43749423-chr10:43756169..43758679,2	K562	blood:
34	chr10:43746969..43750119-chr10:43752543..43755778,3	K562	blood:
35	chr10:43746978..43749423-chr10:43756169..43758679,2	K562	blood:
36	chr10:43682668..43685704-chr10:43685961..43688550,3	MCF-7	breast:
37	chr10:43632694..43635237-chr10:43697053..43700182,3	MCF-7	breast:
38	chr10:43749564..43751225-chr10:43756675..43758831,2	K562	blood:
39	chr10:43720076..43721666-chr10:43723376..43725809,2	K562	blood:
40	chr10:43705495..43708277-chr10:43710722..43714581,3	K562	blood:
41	chr10:43745055..43746859-chr10:43757087..43758973,2	MCF-7	breast:
42	chr10:43689923..43692438-chr10:43693060..43695471,2	MCF-7	breast:
43	chr10:43696064..43699246-chr10:43901638..43904576,3	K562	blood:
44	chr10:43692631..43693170-chr10:43957145..43957979,2	K562	blood:
45	chr10:43721241..43722992-chr10:43727167..43730117,3	MCF-7	breast:
46	chr10:43700322..43701097-chr10:43750638..43751735,4	MCF-7	breast:
47	chr10:43705829..43707653-chr10:43720065..43721565,2	K562	blood:
48	chr10:43700767..43702295-chr10:43702554..43705359,2	K562	blood:
49	chr10:43692827..43695385-chr10:43696281..43699647,3	K562	blood:
50	chr10:43716710..43720339-chr10:43755141..43758566,3	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSGALNACT2-2	chr10:43724848-43725231	l_304_chr10:43724730-43729936_testes
2	lnc-HNRNPF-3	chr10:43727747-43727780	NONHSAT012945
3	lnc-CSGALNACT2-2	chr10:43724731-43724847	l_304_chr10:43724730-43729936_testes
4	lnc-HNRNPF-2	chr10:43729604-43729960	NONHSAT012947
5	lnc-HNRNPF-2	chr10:43729353-43729460	NONHSAT012947
6	lnc-CSGALNACT2-2	chr10:43729213-43729690	NONHSAT012946
7	lnc-CSGALNACT2-1	chr10:43682611-43682793	NONHSAT012944
8	lnc-CSGALNACT2-2	chr10:43758646-43758735	NONHSAT012948
9	lnc-CSGALNACT2-1	chr10:43674865-43675814	NONHSAT012944
10	lnc-HNRNPF-3	chr10:43727747-43727797	l_303_chr10:43716824-43727797_testes
11	lnc-CSGALNACT2-2	chr10:43729213-43729936	l_304_chr10:43724730-43729936_testes
12	lnc-HNRNPF-3	chr10:43718876-43719043	l_303_chr10:43716824-43727797_testes
13	lnc-HNRNPF-3	chr10:43716819-43717277	NONHSAT012945
14	lnc-HNRNPF-3	chr10:43716825-43717277	l_303_chr10:43716824-43727797_testes
15	lnc-CSGALNACT2-1	chr10:43710319-43710887	NONHSAT012944
16	lnc-CSGALNACT2-1	chr10:43689644-43689866	NONHSAT012944
17	lnc-CSGALNACT2-2	chr10:43727898-43727932	NONHSAT012946
18	lnc-CSGALNACT2-1	chr10:43677333-43677381	NONHSAT012944
19	lnc-CSGALNACT2-2	chr10:43756176-43756431	NONHSAT012948
20	lnc-CSGALNACT2-2	chr10:43727803-43727932	l_304_chr10:43724730-43729936_testes
21	lnc-CSGALNACT2-2	chr10:43758646-43758735	l_304_chr10:43724730-43729936_testes
22	lnc-CSGALNACT2-2	chr10:43754457-43755996	NONHSAT012948

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CSGALNACT2	hsa-miR-192-5p	chr10:43680213-43680232
2	CSGALNACT2	hsa-miR-215-5p	chr10:43680213-43680232

Variant related genes	Relation type
RASGEF1A	TF binding region
RASGEF1A	CpG island
ENSG00000273008	chromatin interactions
ENSG00000169826	chromatin interactions
ENSG00000169813	chromatin interactions
ENSG00000198915	chromatin interactions

Extended variants
information (count: 3394 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:3394 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145220461	chr10:43674933-43674934	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs574962971	chr10:43674967-43674968	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs542450998	chr10:43674977-43674978	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs560742685	chr10:43674980-43674981	Weak transcription ZNF genes & repeats Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs528436112	chr10:43675017-43675018	Weak transcription ZNF genes & repeats Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs540161624	chr10:43675074-43675075	Weak transcription ZNF genes & repeats Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs137863082	chr10:43675087-43675088	Weak transcription ZNF genes & repeats Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs190168658	chr10:43675091-43675092	Weak transcription ZNF genes & repeats Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs35577875	chr10:43675212-43675213	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
10	rs550966426	chr10:43675319-43675320	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
11	rs569402780	chr10:43675379-43675380	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
12	rs530201919	chr10:43675402-43675403	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
13	rs182349185	chr10:43675410-43675411	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
14	rs7903283	chr10:43675418-43675419	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs142477705	chr10:43675426-43675427	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
16	rs371494394	chr10:43675427-43675428	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
17	rs374583498	chr10:43675432-43675433	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
18	rs558993812	chr10:43675437-43675438	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
19	rs145955862	chr10:43675456-43675457	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
20	rs374953543	chr10:43675481-43675482	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
21	rs139925537	chr10:43675527-43675528	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
22	rs374564597	chr10:43675553-43675554	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
23	rs534240965	chr10:43675583-43675584	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
24	rs542313984	chr10:43675586-43675587	Weak transcription Strong transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
25	rs186092940	chr10:43675615-43675616	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs554198541	chr10:43675628-43675629	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs2435383	chr10:43675671-43675672	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs2503841	chr10:43675721-43675722	Weak transcription Strong transcription ZNF genes & repeats Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs554326073	chr10:43675836-43675837	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190901388	chr10:43675842-43675843	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569745089	chr10:43675847-43675848	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs75842659	chr10:43675887-43675888	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577045367	chr10:43675893-43675894	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544652671	chr10:43675934-43675935	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs144651857	chr10:43675935-43675936	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530264115	chr10:43675938-43675939	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs148476145	chr10:43675939-43675940	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs374555918	chr10:43675971-43675972	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560591972	chr10:43675977-43675978	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372566940	chr10:43676001-43676002	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs373851668	chr10:43676094-43676095	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs377001903	chr10:43676095-43676096	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs567527653	chr10:43676111-43676112	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs74650392	chr10:43676200-43676201	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs142291947	chr10:43676254-43676255	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs111683217	chr10:43676281-43676282	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs35040097	chr10:43676282-43676283	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538142395	chr10:43676309-43676310	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs147881170	chr10:43676350-43676351	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs568518489	chr10:43676354-43676355	Weak transcription Strong transcription Enhancers	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
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1973 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43635600-43689000	Weak transcription	Esophagus	oesophagus
2	chr10:43652600-43697200	Weak transcription	Pancreas	Pancrea
3	chr10:43654600-43678000	Weak transcription	Hela-S3	cervix
4	chr10:43655000-43680600	Weak transcription	Colonic Mucosa	Colon
5	chr10:43658800-43690600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr10:43660400-43687400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr10:43662000-43677000	Strong transcription	Osteobl	bone
8	chr10:43662200-43684400	Strong transcription	Primary T helper cells fromperipheralblood	blood
9	chr10:43662200-43697600	Weak transcription	NHEK	skin
10	chr10:43662600-43690000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr10:43662800-43681600	Weak transcription	HMEC	breast
12	chr10:43663000-43678000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr10:43663600-43679800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr10:43663600-43683800	Strong transcription	Fetal Thymus	thymus
15	chr10:43664000-43679600	Strong transcription	Fetal Muscle Trunk	muscle
16	chr10:43664000-43680400	Strong transcription	Dnd41	blood
17	chr10:43664200-43676800	Strong transcription	HSMMtube	muscle
18	chr10:43664400-43675600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr10:43664800-43675000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr10:43665200-43680000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr10:43665400-43679400	Strong transcription	Thymus	Thymus
22	chr10:43665400-43679800	Strong transcription	Adipose Nuclei	Adipose
23	chr10:43667400-43679400	Strong transcription	Stomach Smooth Muscle	stomach
24	chr10:43667600-43675000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr10:43667600-43679200	Strong transcription	Muscle Satellite Cultured Cells	--
26	chr10:43667800-43685200	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr10:43667800-43692800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr10:43668000-43685200	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr10:43668200-43694000	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr10:43668600-43675000	Weak transcription	Brain Substantia Nigra	brain
31	chr10:43668600-43683800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr10:43668600-43683800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr10:43668800-43680200	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr10:43668800-43684400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr10:43669000-43677400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr10:43669000-43677600	Weak transcription	Brain Anterior Caudate	brain
37	chr10:43669000-43684200	Strong transcription	Primary neutrophils fromperipheralblood	blood
38	chr10:43669200-43678800	Weak transcription	HepG2	liver
39	chr10:43669400-43677000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr10:43669600-43676400	Strong transcription	Cortex derived primary cultured neurospheres	brain
41	chr10:43669600-43679000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr10:43669600-43689400	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr10:43669800-43683000	Strong transcription	Fetal Brain Female	brain
44	chr10:43670000-43680000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr10:43670400-43676400	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr10:43670800-43676800	Strong transcription	Ovary	ovary
47	chr10:43670800-43679400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr10:43671000-43689800	Weak transcription	Gastric	stomach
49	chr10:43671200-43676200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr10:43671200-43678200	Weak transcription	Fetal Heart	heart

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