Variant report

Variant	nsv895073
Chromosome Location	chr10:42884169-43066505
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:993)
CpG islands
(count:2441)
Chromatin interactive
region (count:21)
LncRNA
region (count:74)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:993 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:43048312-43048668	K562	blood:	n/a	n/a
2	ARID3A	chr10:43048220-43048891	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:43052572-43052664	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:43039486-43039576	K562	blood:	n/a	n/a
5	ATF1	chr10:43039443-43039723	K562	blood:	n/a	n/a
6	ATF1	chr10:43048147-43048550	K562	blood:	n/a	n/a
7	ATF3	chr10:43048166-43048482	K562	blood:	n/a	n/a
8	BATF	chr10:42986683-42986872	GM12878	blood:	n/a	n/a
9	BCLAF1	chr10:43048079-43048628	GM12878	blood:	n/a	n/a
10	BCLAF1	chr10:43048131-43048562	GM12878	blood:	n/a	n/a
11	BHLHE40	chr10:43039540-43039783	K562	blood:	n/a	n/a
12	BHLHE40	chr10:43039480-43039805	HepG2	liver:	n/a	n/a
13	BHLHE40	chr10:43047425-43048669	GM12878	blood:	n/a	n/a
14	BHLHE40	chr10:43048282-43048608	K562	blood:	n/a	n/a
15	BHLHE40	chr10:43047423-43047809	K562	blood:	n/a	n/a
16	CBX3	chr10:43040372-43040751	K562	blood:	n/a	n/a
17	CBX3	chr10:43047484-43047987	K562	blood:	n/a	n/a
18	CBX3	chr10:43015266-43015902	K562	blood:	n/a	n/a
19	CBX3	chr10:43047384-43048810	K562	blood:	n/a	n/a
20	CBX3	chr10:43015181-43016130	K562	blood:	n/a	n/a
21	CBX3	chr10:43048210-43048732	K562	blood:	n/a	n/a
22	CCNT2	chr10:43048115-43048301	K562	blood:	n/a	n/a
23	CCNT2	chr10:43039415-43039525	K562	blood:	n/a	n/a
24	CEBPB	chr10:43018576-43018909	IMR90	lung:	n/a	chr10:43018759-43018770
25	CEBPB	chr10:43045379-43045476	IMR90	lung:	n/a	n/a
26	CEBPB	chr10:43045338-43045634	HepG2	liver:	n/a	n/a
27	CEBPB	chr10:42926554-42927004	A549	lung:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
28	CEBPB	chr10:42926575-42926908	IMR90	lung:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
29	CEBPB	chr10:43051301-43051501	HepG2	liver:	n/a	n/a
30	CEBPB	chr10:42903832-42903893	IMR90	lung:	n/a	chr10:42903853-42903864
31	CEBPB	chr10:43018597-43018904	K562	blood:	n/a	chr10:43018759-43018770
32	CEBPB	chr10:42926615-42926811	HepG2	liver:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
33	CEBPB	chr10:42886922-42886990	HepG2	liver:	n/a	chr10:42886933-42886944
34	CEBPB	chr10:42940311-42940534	HepG2	liver:	n/a	chr10:42940438-42940451 chr10:42940432-42940441 chr10:42940430-42940443 chr10:42940432-42940441 chr10:42940440-42940451 chr10:42940432-42940441 chr10:42940430-42940443 chr10:42940440-42940451 chr10:42940430-42940441 chr10:42940432-42940443 chr10:42940432-42940441
35	CEBPB	chr10:42926569-42926928	HepG2	liver:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
36	CEBPB	chr10:43048102-43048620	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr10:43018579-43018913	HepG2	liver:	n/a	chr10:43018759-43018770
38	CEBPB	chr10:43018635-43018900	Hela-S3	cervix:	n/a	chr10:43018759-43018770
39	CEBPB	chr10:42926541-42926950	ECC-1	luminal epithelium:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
40	CEBPB	chr10:42926626-42926861	HepG2	liver:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
41	CEBPB	chr10:42903805-42903926	HepG2	liver:	n/a	chr10:42903853-42903864
42	CEBPB	chr10:42926578-42926926	A549	lung:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
43	CEBPB	chr10:42926636-42926923	MCF-7	breast:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
44	CEBPB	chr10:42940373-42940490	IMR90	lung:	n/a	chr10:42940438-42940451 chr10:42940432-42940441 chr10:42940430-42940443 chr10:42940432-42940441 chr10:42940440-42940451 chr10:42940432-42940441 chr10:42940430-42940443 chr10:42940440-42940451 chr10:42940430-42940441 chr10:42940432-42940443 chr10:42940432-42940441
45	CEBPB	chr10:42926607-42926907	Hela-S3	cervix:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
46	CEBPB	chr10:42926578-42926940	MCF-7	breast:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
47	CEBPB	chr10:42940399-42940458	K562	blood:	n/a	chr10:42940438-42940451 chr10:42940432-42940441 chr10:42940430-42940443 chr10:42940432-42940441 chr10:42940440-42940451 chr10:42940432-42940441 chr10:42940430-42940443 chr10:42940440-42940451 chr10:42940430-42940441 chr10:42940432-42940443 chr10:42940432-42940441
48	CEBPB	chr10:42926558-42926930	K562	blood:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
49	CEBPB	chr10:42926584-42926914	K562	blood:	n/a	chr10:42926737-42926750 chr10:42926737-42926748 chr10:42926738-42926749
50	CEBPB	chr10:42984929-42984953	HepG2	liver:	n/a	chr10:42984939-42984950

(count:2441 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43048298-43048348	IMR90	lung:	fetal
2	chr10:43048298-43048348	IMR90	lung:	fetal
3	chr10:42970842-42970892	HEK293	kidney:	embryo
4	chr10:42971575-42971625	HMEC	breast:	n/a
5	chr10:43050941-43050991	PrEC	prostate:	n/a
6	chr10:42971011-42971061	H1-hESC	embryonic stem cell:	embryo
7	chr10:42970618-42970668	SK-N-SH_RA	brain:	n/a
8	chr10:42972782-42972832	PANC-1	pancreas:	n/a
9	chr10:43048342-43048392	AG04449	skin:	fetal
10	chr10:43048734-43048784	HUVEC	blood vessel:	n/a
11	chr10:43047371-43047421	BJ	skin:	n/a
12	chr10:42970785-42970835	NHDF-neo	bronchial:	n/a
13	chr10:43048696-43048746	GM12891	blood:	n/a
14	chr10:42970923-42970973	CMK	blood:	n/a
15	chr10:43047784-43047834	Hepatocyte	liver:	n/a
16	chr10:43050881-43050931	NH-A	brain:	n/a
17	chr10:42971732-42971782	SK-N-SH_RA	brain:	n/a
18	chr10:42971575-42971625	HL-60	blood:	n/a
19	chr10:42971209-42971259	HIPEpiC	eye:	n/a
20	chr10:43048471-43048521	ProgFib	skin:	n/a
21	chr10:42975642-42975692	SK-N-MC	brain:	n/a
22	chr10:42931123-42931173	GM12878	blood:	n/a
23	chr10:43047134-43047184	AG09319	gingival:	n/a
24	chr10:43047893-43047943	HMEC	breast:	n/a
25	chr10:43047255-43047305	HEK293	kidney:	embryo
26	chr10:43048298-43048348	AG09309	skin:	n/a
27	chr10:42975642-42975692	HCM	heart:	n/a
28	chr10:43047784-43047834	PANC-1	pancreas:	n/a
29	chr10:43047893-43047943	SKMC	muscle:	n/a
30	chr10:43047180-43047230	Jurkat	blood:	n/a
31	chr10:42971251-42971301	ovcar-3	ovarian:	n/a
32	chr10:43048294-43048344	A549	lung:	n/a
33	chr10:42970351-42970401	BJ	skin:	n/a
34	chr10:42970351-42970401	AG10803	skin:	n/a
35	chr10:43047255-43047305	IMR90	lung:	fetal
36	chr10:43047180-43047230	HUVEC	blood vessel:	n/a
37	chr10:43048294-43048344	HPAEpiC	pulmonary alveolar:	n/a
38	chr10:42972753-42972803	PrEC	prostate:	n/a
39	chr10:43048206-43048256	GM06990	blood:	n/a
40	chr10:42970625-42970675	NHDF-neo	bronchial:	n/a
41	chr10:43047180-43047230	SK-N-SH_RA	brain:	n/a
42	chr10:43048734-43048784	SK-N-SH_RA	brain:	n/a
43	chr10:42970618-42970668	ECC-1	luminal epithelium:	n/a
44	chr10:43047180-43047230	AG10803	skin:	n/a
45	chr10:42970147-42970197	NB4	blood:	n/a
46	chr10:43048206-43048256	AG04449	skin:	fetal
47	chr10:43047134-43047184	GM12891	blood:	n/a
48	chr10:42970923-42970973	ProgFib	skin:	n/a
49	chr10:43047180-43047230	HL-60	blood:	n/a
50	chr10:43047784-43047834	AoSMC	blood vessel:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:43048254..43049868-chr10:43050241..43052640,2	K562	blood:
2	chr10:43046301..43049301-chr10:43278095..43279962,3	K562	blood:
3	chr10:42939273..42941878-chr10:42945639..42947236,2	K562	blood:
4	chr10:42939273..42941878-chr10:42945639..42947236,2	K562	blood:
5	chr10:43007068..43009795-chr10:43011451..43013885,2	K562	blood:
6	chr10:43007068..43009795-chr10:43011451..43013885,2	K562	blood:
7	chr10:43005354..43008168-chr10:43008561..43011194,2	K562	blood:
8	chr10:43046145..43048386-chr10:43132522..43135382,4	MCF-7	breast:
9	chr10:43006886..43009795-chr10:43011451..43013119,2	K562	blood:
10	chr10:43039662..43041965-chr10:43046880..43049075,3	K562	blood:
11	chr10:43048254..43049868-chr10:43050241..43052640,2	K562	blood:
12	chr10:43037621..43040787-chr10:43042829..43044959,3	K562	blood:
13	chr10:42969759..42972522-chr10:42973543..42976083,2	K562	blood:
14	chr10:42965526..42968231-chr10:42980133..42982358,2	MCF-7	breast:
15	chr10:43037621..43040787-chr10:43042829..43044959,3	K562	blood:
16	chr10:43005354..43008168-chr10:43008561..43011194,2	K562	blood:
17	chr10:43006886..43009795-chr10:43011451..43013119,2	K562	blood:
18	chr10:42969759..42973137-chr10:42973543..42977083,4	K562	blood:
19	chr10:43038071..43041790-chr10:43046782..43049075,3	K562	blood:
20	chr10:43043951..43049889-chr10:43132519..43135803,5	K562	blood:
21	chr10:42969989..42972327-chr10:43278200..43280239,2	K562	blood:

(count:74 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF33B-4	chr10:43047021-43048044	NONHSAT012901
2	lnc-ZNF33B-4	chr10:43018630-43018753	NONHSAT012887
3	lnc-BMS1-3	chr10:42987524-42987790	NONHSAT012885
4	lnc-ZNF33B-4	chr10:43046005-43046063	NONHSAT012894
5	lnc-ZNF33B-4	chr10:43018630-43018753	NONHSAT012896
6	lnc-BMS1-3	chr10:42972709-42972890	NONHSAT012880
7	lnc-ZNF33B-4	chr10:43047438-43047728	NONHSAT012887
8	lnc-ZNF33B-4	chr10:43018658-43018772	NONHSAT012892
9	lnc-ZNF33B-4	chr10:43019060-43019186	NONHSAT012891
10	lnc-ZNF33B-4	chr10:43046005-43046266	NONHSAT012897
11	lnc-BMS1-3	chr10:42982427-42982574	NONHSAT012879
12	lnc-ZNF33B-4	chr10:43047025-43047306	NONHSAT012896
13	lnc-ZNF33B-4	chr10:43008961-43016575	NONHSAT012887
14	lnc-ZNF33B-4	chr10:43046005-43046063	NONHSAT012893
15	lnc-ZNF33B-4	chr10:43018630-43018772	NONHSAT012895
16	lnc-ZNF33B-4	chr10:43047025-43047262	NONHSAT012892
17	lnc-ZNF33B-4	chr10:43019060-43019186	NONHSAT012897
18	lnc-ZNF33B-4	chr10:43048040-43048250	NONHSAT012899
19	lnc-ZNF33B-4	chr10:43018630-43018753	NONHSAT012891
20	lnc-ZNF33B-4	chr10:43019060-43019186	NONHSAT012893
21	lnc-ZNF33B-4	chr10:43016235-43016575	NONHSAT012891
22	lnc-ZNF33B-4	chr10:43046005-43046063	NONHSAT012895
23	lnc-ZNF33B-4	chr10:43016388-43016575	NONHSAT012893
24	lnc-BMS1-3	chr10:42971373-42971412	NONHSAT012879
25	lnc-BMS1-3	chr10:42989463-42989826	NONHSAT012880
26	lnc-ZNF33B-4	chr10:43019060-43019186	NONHSAT012887
27	lnc-ZNF33B-4	chr10:43019060-43019186	NONHSAT012896
28	lnc-ZNF33B-4	chr10:43047021-43047262	NONHSAT012887
29	lnc-BMS1-3	chr10:42989463-42990585	NONHSAT012885
30	lnc-BMS1-3	chr10:42972709-42972890	NONHSAT012881
31	lnc-BMS1-3	chr10:42987528-42987790	NONHSAT012882
32	lnc-ZNF33B-4	chr10:43048018-43048236	NONHSAT012895
33	lnc-BMS1-3	chr10:42971951-42971978	NONHSAT012881
34	lnc-ZNF33B-4	chr10:43047025-43048236	NONHSAT012894
35	lnc-ZNF33B-4	chr10:43016388-43016575	NONHSAT012892
36	lnc-ZNF33B-4	chr10:43015143-43016494	NONHSAT012890
37	lnc-ZNF33B-4	chr10:43046005-43046063	NONHSAT012896
38	lnc-ZNF33B-4	chr10:43047438-43047899	NONHSAT012895
39	lnc-BMS1-3	chr10:42982427-42982574	NONHSAT012881
40	lnc-ZNF33B-4	chr10:43046005-43046063	NONHSAT012887
41	lnc-ZNF33B-4	chr10:43018631-43018753	NONHSAT012897
42	lnc-ZNF33B-4	chr10:43047438-43047550	NONHSAT012902
43	lnc-BMS1-3	chr10:42982427-42982574	NONHSAT012882
44	lnc-ZNF33B-4	chr10:43046005-43046063	NONHSAT012899
45	lnc-BMS1-3	chr10:42987528-42987779	NONHSAT012880
46	lnc-BMS1-3	chr10:42971380-42971412	NONHSAT012880
47	lnc-ZNF33B-4	chr10:43047438-43047739	NONHSAT012892
48	lnc-ZNF33B-4	chr10:43047836-43047990	NONHSAT012887
49	lnc-ZNF33B-4	chr10:43019060-43019186	NONHSAT012899
50	lnc-ZNF33B-4	chr10:43048247-43048270	NONHSAT012891

No data

Variant related genes	Relation type
EIF3LP2	TF binding region
LINC00839	TF binding region
ZNF37BP	TF binding region
FXYD6P1	TF binding region
CCNYL2	TF binding region
EIF3LP2	CpG island
LINC00839	CpG island
ZNF37BP	CpG island
FXYD6P1	CpG island
CCNYL2	CpG island
ENSG00000272373	chromatin interactions
ENSG00000196693	chromatin interactions
ENSG00000182632	chromatin interactions
ENSG00000234420	chromatin interactions
ENSG00000165733	chromatin interactions
ENSG00000270762	chromatin interactions
ENSG00000185904	chromatin interactions

Extended variants
information (count: 3736 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3736 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564933993	chr10:42918235-42918236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs12765826	chr10:42918251-42918252	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs184151846	chr10:42918268-42918269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560744034	chr10:42918272-42918273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187323703	chr10:42918275-42918276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs371124311	chr10:42918344-42918345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143786399	chr10:42918410-42918411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189653773	chr10:42918413-42918414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569340597	chr10:42918438-42918439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538392970	chr10:42918442-42918443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182338634	chr10:42918446-42918447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187010741	chr10:42918460-42918461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545073582	chr10:42918500-42918501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191714502	chr10:42918529-42918530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529657559	chr10:42918534-42918535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553736853	chr10:42918535-42918536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs116349021	chr10:42918579-42918580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs542556937	chr10:42918593-42918594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556281398	chr10:42939209-42939210	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs372196718	chr10:42939210-42939211	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs202065748	chr10:42939241-42939242	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs200389372	chr10:42939246-42939247	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs185130942	chr10:42939282-42939283	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs567725237	chr10:42939316-42939317	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs530491005	chr10:42939322-42939323	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs550228828	chr10:42939328-42939329	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs570305019	chr10:42939364-42939365	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs386743112	chr10:42939368-42939369	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs113909182	chr10:42939369-42939370	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs35350909	chr10:42939405-42939406	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs182459274	chr10:42939441-42939442	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs35548310	chr10:42939446-42939447	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs74135581	chr10:42939454-42939455	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs553744730	chr10:42939465-42939466	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs2154316	chr10:42939466-42939467	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs35981740	chr10:42939469-42939470	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs545691318	chr10:42939543-42939544	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs188408991	chr10:42939551-42939552	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs543778596	chr10:42939588-42939589	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs564745925	chr10:42939616-42939617	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs373142144	chr10:42939617-42939618	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs117267867	chr10:42939635-42939636	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs112187522	chr10:42939649-42939650	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs140471986	chr10:42939714-42939715	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs191552193	chr10:42939739-42939740	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs528229433	chr10:42939795-42939796	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs73250242	chr10:42939809-42939810	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs75125072	chr10:42939815-42939816	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs200578360	chr10:42939819-42939820	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs74135582	chr10:42939845-42939846	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:69)

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
Breast cancer	21509527	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
Obesity	20622171	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
Lung cancer	21569311	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Autism	20531469	CNVD
small cell lung cancer	20016488	CNVD
Cancer	17440070	CNVD
Melanoma	20877625	CNVD
Hirschsprung''s Disease	19925665	CNVD
Hirschsprung''s Disease	20456320	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1271 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:42918200-42918600	Enhancers	Left Ventricle	heart
2	chr10:42939200-42940000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr10:42948200-42948800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr10:42949600-42949800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr10:42949600-42950200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr10:42961800-42962000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr10:42970000-42970600	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr10:42970600-42970800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr10:42970600-42970800	Enhancers	Aorta	Aorta
10	chr10:42970600-42970800	Enhancers	HMEC	breast
11	chr10:42970600-42971400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
12	chr10:42970600-42971400	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
13	chr10:42970600-42971800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr10:42970600-42972000	Active TSS	Brain Cingulate Gyrus	brain
15	chr10:42970600-42972600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr10:42970800-42971000	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
17	chr10:42970800-42971000	Weak transcription	Aorta	Aorta
18	chr10:42970800-42971000	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
19	chr10:42970800-42971000	Active TSS	Stomach Smooth Muscle	stomach
20	chr10:42970800-42971200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr10:42970800-42971200	Flanking Active TSS	HMEC	breast
22	chr10:42970800-42971400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr10:42970800-42971800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr10:42970800-42972000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr10:42970800-42972000	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
26	chr10:42970800-42972000	Bivalent/Poised TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr10:42970800-42972000	Active TSS	Brain Angular Gyrus	brain
28	chr10:42970800-42972000	Active TSS	Brain Anterior Caudate	brain
29	chr10:42970800-42972000	ZNF genes & repeats	Fetal Stomach	stomach
30	chr10:42970800-42972200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr10:42970800-42972200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr10:42970800-42972200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr10:42970800-42972200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr10:42970800-42972200	ZNF genes & repeats	Fetal Brain Female	brain
35	chr10:42970800-42972600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr10:42970800-42972600	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr10:42971000-42971200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr10:42971000-42971200	Flanking Active TSS	Esophagus	oesophagus
39	chr10:42971000-42971200	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
40	chr10:42971000-42971200	Bivalent Enhancer	Left Ventricle	heart
41	chr10:42971000-42971200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
42	chr10:42971000-42971400	Active TSS	Duodenum Mucosa	Duodenum
43	chr10:42971000-42971400	Active TSS	Fetal Kidney	kidney
44	chr10:42971000-42971400	Flanking Bivalent TSS/Enh	Lung	lung
45	chr10:42971000-42971600	Bivalent/Poised TSS	Adipose Nuclei	Adipose
46	chr10:42971000-42971600	Bivalent Enhancer	Placenta	Placenta
47	chr10:42971000-42971600	Active TSS	NHDF-Ad	bronchial
48	chr10:42971000-42971800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
49	chr10:42971000-42971800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr10:42971000-42971800	Active TSS	Colon Smooth Muscle	Colon

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