Variant report

Variant	nsv1030370
Chromosome Location	chr5:180080795-180216254
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1149)
CpG islands
(count:1466)
Chromatin interactive
region (count:60)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1149 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:180144959-180145359	GM12878	blood:	n/a	n/a
2	ATF2	chr5:180212679-180213244	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr5:180212570-180213141	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr5:180145061-180145379	GM12878	blood:	n/a	chr5:180145207-180145218
5	BATF	chr5:180097198-180097443	GM12878	blood:	n/a	n/a
6	BATF	chr5:180145040-180145312	GM12878	blood:	n/a	chr5:180145207-180145218
7	BATF	chr5:180169789-180169977	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:180145100-180145299	GM12878	blood:	n/a	chr5:180145235-180145244
9	BCL11A	chr5:180145000-180145348	GM12878	blood:	n/a	chr5:180145235-180145244
10	BCL11A	chr5:180085399-180085773	GM12878	blood:	n/a	n/a
11	BCL3	chr5:180097085-180097491	GM12878	blood:	n/a	n/a
12	CBX3	chr5:180208858-180209504	K562	blood:	n/a	n/a
13	CBX3	chr5:180198844-180199194	K562	blood:	n/a	n/a
14	CBX3	chr5:180127492-180127736	K562	blood:	n/a	n/a
15	CBX3	chr5:180198766-180199290	K562	blood:	n/a	n/a
16	CBX3	chr5:180208965-180209392	K562	blood:	n/a	n/a
17	CBX3	chr5:180215613-180215981	K562	blood:	n/a	n/a
18	CEBPB	chr5:180131341-180131657	K562	blood:	n/a	n/a
19	CEBPB	chr5:180208882-180209430	K562	blood:	n/a	n/a
20	CEBPB	chr5:180209005-180209250	K562	blood:	n/a	n/a
21	CEBPD	chr5:180208780-180209396	K562	blood:	n/a	n/a
22	CEBPD	chr5:180208777-180209303	K562	blood:	n/a	n/a
23	CEBPD	chr5:180131384-180131803	K562	blood:	n/a	n/a
24	CREB1	chr5:180144836-180145451	GM12878	blood:	n/a	n/a
25	CREB1	chr5:180144917-180145413	GM12878	blood:	n/a	n/a
26	CTCF	chr5:180097640-180097790	GM12865	blood:	n/a	chr5:180097737-180097755 chr5:180097732-180097753
27	CTCF	chr5:180211620-180211770	Hela-S3	cervix:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
28	CTCF	chr5:180097652-180097839	SK-N-SH_RA	brain:	n/a	chr5:180097737-180097755 chr5:180097732-180097753
29	CTCF	chr5:180097700-180097850	HPAF	blood vessel:	n/a	chr5:180097737-180097755 chr5:180097732-180097753
30	CTCF	chr5:180211565-180211811	GM19239	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
31	CTCF	chr5:180211528-180211985	SK-N-SH	brain:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
32	CTCF	chr5:180146180-180146330	HRE	kidney:	n/a	n/a
33	CTCF	chr5:180145792-180146035	HepG2	liver:	n/a	n/a
34	CTCF	chr5:180211620-180211770	HMEC	breast:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
35	CTCF	chr5:180145796-180146008	HepG2	liver:	n/a	n/a
36	CTCF	chr5:180145843-180146006	A549	lung:	n/a	n/a
37	CTCF	chr5:180145800-180145950	GM12878	blood:	n/a	n/a
38	CTCF	chr5:180211620-180211770	AG09319	gingival:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
39	CTCF	chr5:180211547-180211829	Spleen_OC	spleen:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
40	CTCF	chr5:180097660-180097810	GM12866	blood:	n/a	chr5:180097737-180097755 chr5:180097732-180097753
41	CTCF	chr5:180145666-180146117	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:180097640-180097790	HEK293	kidney:	n/a	chr5:180097737-180097755 chr5:180097732-180097753
43	CTCF	chr5:180100392-180100524	GM12891	blood:	n/a	chr5:180100461-180100470 chr5:180100458-180100476 chr5:180100461-180100474
44	CTCF	chr5:180211620-180211770	AoAF	blood vessel:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
45	CTCF	chr5:180211620-180211770	GM12871	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
46	CTCF	chr5:180100353-180100538	Hela-S3	cervix:	n/a	chr5:180100461-180100470 chr5:180100458-180100476 chr5:180100461-180100474
47	CTCF	chr5:180097660-180097810	HCT-116	colon:	n/a	chr5:180097737-180097755 chr5:180097732-180097753
48	CTCF	chr5:180145840-180145990	AG09319	gingival:	n/a	n/a
49	CTCF	chr5:180211556-180211829	HepG2	liver:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
50	CTCF	chr5:180097620-180097770	Hela-S3	cervix:	n/a	chr5:180097737-180097755 chr5:180097732-180097753

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:180167724-180167774	AG04450	lung:	fetal
2	chr5:180085924-180085974	HRE	kidney:	n/a
3	chr5:180167724-180167774	AG04450	lung:	fetal
4	chr5:180085924-180085974	HRE	kidney:	n/a
5	chr5:180085446-180085496	SK-N-SH_RA	brain:	n/a
6	chr5:180116385-180116435	AG09309	skin:	n/a
7	chr5:180101143-180101193	HNPCEpiC	eye:	n/a
8	chr5:180167132-180167182	Hepatocyte	liver:	n/a
9	chr5:180166492-180166542	K562	blood:	n/a
10	chr5:180166492-180166542	LNCaP	prostate:	n/a
11	chr5:180103241-180103291	BE2_C	brain:	n/a
12	chr5:180103241-180103291	HUVEC	blood vessel:	n/a
13	chr5:180113361-180113411	GM12892	blood:	n/a
14	chr5:180100963-180101013	PANC-1	pancreas:	n/a
15	chr5:180112929-180112979	MCF-7	breast:	n/a
16	chr5:180111966-180112016	AG04449	skin:	fetal
17	chr5:180097910-180097960	A549	lung:	n/a
18	chr5:180097910-180097960	ECC-1	luminal epithelium:	n/a
19	chr5:180100963-180101013	LNCaP	prostate:	n/a
20	chr5:180112929-180112979	ProgFib	skin:	n/a
21	chr5:180112929-180112979	HRCEpiC	kidney:	n/a
22	chr5:180113357-180113407	H1-hESC	embryonic stem cell:	embryo
23	chr5:180103241-180103291	PFSK-1	brain:	n/a
24	chr5:180099956-180100006	AG09319	gingival:	n/a
25	chr5:180111800-180111850	HepG2	liver:	n/a
26	chr5:180097910-180097960	GM12891	blood:	n/a
27	chr5:180167965-180168015	AG09319	gingival:	n/a
28	chr5:180111966-180112016	NB4	blood:	n/a
29	chr5:180101143-180101193	MCF10A-Er-Src	breast:	n/a
30	chr5:180112929-180112979	HIPEpiC	eye:	n/a
31	chr5:180111800-180111850	AG10803	skin:	n/a
32	chr5:180100701-180100751	HCM	heart:	n/a
33	chr5:180111800-180111850	A549	lung:	n/a
34	chr5:180111966-180112016	HCF	heart:	n/a
35	chr5:180111800-180111850	BJ	skin:	n/a
36	chr5:180103241-180103291	ECC-1	luminal epithelium:	n/a
37	chr5:180166492-180166542	GM06990	blood:	n/a
38	chr5:180103241-180103291	U87	brain:	n/a
39	chr5:180111800-180111850	T-47D	breast:	n/a
40	chr5:180086260-180086310	SK-N-MC	brain:	n/a
41	chr5:180116385-180116435	MCF-7	breast:	n/a
42	chr5:180111966-180112016	MCF10A-Er-Src	breast:	n/a
43	chr5:180167132-180167182	AG10803	skin:	n/a
44	chr5:180100963-180101013	BE2_C	brain:	n/a
45	chr5:180085924-180085974	PrEC	prostate:	n/a
46	chr5:180085446-180085496	IMR90	lung:	fetal
47	chr5:180100963-180101013	Hepatocyte	liver:	n/a
48	chr5:180166694-180166744	NHBE	bronchial:	n/a
49	chr5:180166492-180166542	GM12878	blood:	n/a
50	chr5:180101143-180101193	HRPEpiC	eye:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:180048663..180050730-chr5:180113911..180116171,2	K562	blood:
2	chr5:180146148..180147851-chr5:180235768..180238086,2	K562	blood:
3	chr5:180208714..180211702-chr5:180212096..180213803,2	K562	blood:
4	chr5:180171538..180174150-chr5:180179388..180180987,2	K562	blood:
5	chr5:180208714..180211260-chr5:180212096..180214924,3	K562	blood:
6	chr5:180168390..180170515-chr5:180204872..180207367,2	K562	blood:
7	chr5:180114639..180117305-chr5:180118582..180121501,2	MCF-7	breast:
8	chr5:180143140..180144948-chr5:180229622..180231793,2	K562	blood:
9	chr5:180092442..180094516-chr5:180097000..180098654,2	K562	blood:
10	chr5:180207628..180210924-chr5:180228309..180230947,5	MCF-7	breast:
11	chr5:180170663..180173512-chr5:180175093..180176860,2	K562	blood:
12	chr5:180212092..180214294-chr5:180453988..180456472,2	K562	blood:
13	chr5:180037911..180038640-chr5:180145288..180145999,2	MCF-7	breast:
14	chr5:180211375..180212214-chr5:180226180..180226854,2	MCF-7	breast:
15	chr5:180113673..180116367-chr5:180119581..180121156,3	K562	blood:
16	chr5:180091768..180093922-chr5:180095583..180097208,2	K562	blood:
17	chr5:180158275..180159905-chr5:180163258..180165205,2	K562	blood:
18	chr5:179919075..179921338-chr5:180210769..180213087,2	MCF-7	breast:
19	chr5:180032730..180033573-chr5:180097208..180098138,2	MCF-7	breast:
20	chr3:18286488..18287319-chr5:180097543..180098157,2	MCF-7	breast:
21	chr5:180168390..180170515-chr5:180204872..180207367,2	K562	blood:
22	chr5:180094037..180096535-chr5:180099976..180102790,2	K562	blood:
23	chr5:180158275..180159905-chr5:180163258..180165205,2	K562	blood:
24	chr5:180130605..180132994-chr5:180134010..180136773,2	MCF-7	breast:
25	chr5:180136617..180138276-chr5:180153652..180155749,2	K562	blood:
26	chr5:180083705..180084315-chr6:10033064..10033612,2	MCF-7	breast:
27	chr5:180092442..180094516-chr5:180097000..180098654,2	K562	blood:
28	chr5:180202321..180205166-chr5:180643152..180645917,2	K562	blood:
29	chr5:180202113..180204208-chr5:180208493..180210882,2	K562	blood:
30	chr5:180076787..180079357-chr5:180092252..180095157,2	K562	blood:
31	chr5:179553744..179554692-chr5:180097393..180098230,2	MCF-7	breast:
32	chr5:180208930..180211085-chr5:180226767..180229407,2	K562	blood:
33	chr5:180208714..180211702-chr5:180212096..180213803,2	K562	blood:
34	chr5:180211640..180213961-chr5:180214094..180219248,5	K562	blood:
35	chr5:180038293..180038846-chr5:180097248..180097778,2	K562	blood:
36	chr5:180211185..180212156-chr5:180225940..180226892,9	MCF-7	breast:
37	chr5:180097643..180098351-chr5:180145367..180146387,3	MCF-7	breast:
38	chr5:180168086..180169925-chr5:180190599..180192805,2	K562	blood:
39	chr5:180097643..180098351-chr5:180145367..180146387,3	MCF-7	breast:
40	chr5:180130605..180132994-chr5:180134010..180136773,2	MCF-7	breast:
41	chr5:180171538..180174150-chr5:180179388..180180987,2	K562	blood:
42	chr5:180022631..180025317-chr5:180096101..180098291,2	MCF-7	breast:
43	chr5:180210430..180214631-chr5:180286463..180290673,6	MCF-7	breast:
44	chr5:180091768..180093922-chr5:180095583..180097208,2	K562	blood:
45	chr5:180094037..180096535-chr5:180099976..180102790,2	K562	blood:
46	chr5:180170663..180173512-chr5:180175093..180176860,2	K562	blood:
47	chr5:179720167..179721132-chr5:180096980..180097838,2	K562	blood:
48	chr5:180210073..180212750-chr5:180649135..180651698,2	MCF-7	breast:
49	chr5:180209019..180210957-chr5:180453882..180456380,2	K562	blood:
50	chr5:180154735..180156600-chr5:180159240..180161653,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTNL8-8	chr5:180190563-180190835	ucscGeneNc_uc003mmk_2
2	lnc-OR2Y1-1	chr5:180155280-180155484	expReg_chr5_11028_-
3	lnc-OR2Y1-2	chr5:180189565-180191201	ucscGeneNc_uc003mmj_1
4	lnc-BTNL8-8	chr5:180193918-180195284	ucscGeneNc_uc003mmk_2
5	lnc-CNOT6-3	chr5:180111766-180111906	XLOC_004682
6	lnc-CNOT6-3	chr5:180111765-180111906	NONHSAT105706
7	lnc-CNOT6-3	chr5:180112648-180113546	NONHSAT105706
8	lnc-FLT4-1	chr5:180098892-180099598	NONHSAT105695
9	lnc-BTNL8-8	chr5:180192279-180192466	ucscGeneNc_uc003mmk_2
10	lnc-CNOT6-3	chr5:180112649-180113546	XLOC_004682

No data

Variant related genes	Relation type
RNU1-17P	TF binding region
ENSG00000260841	TF binding region
ENSG00000248717	TF binding region
OR2Y1	TF binding region
FLT4	TF binding region
OR2AI1P	TF binding region
ENSG00000251352	TF binding region
RNU1-17P	CpG island
ENSG00000260841	CpG island
ENSG00000248717	CpG island
OR2Y1	CpG island
FLT4	CpG island
OR2AI1P	CpG island
ENSG00000251352	CpG island
ENSG00000196670	chromatin interactions
ENSG00000199892	chromatin interactions
ENSG00000131446	chromatin interactions
ENSG00000260841	chromatin interactions
ENSG00000146063	chromatin interactions
ENSG00000037280	chromatin interactions
ENSG00000236791	chromatin interactions
ENSG00000264732	chromatin interactions
ENSG00000248367	chromatin interactions

Extended variants
information (count: 3684 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:3684 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372137452	chr5:180085605-180085606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs113675834	chr5:180085618-180085619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149414228	chr5:180085621-180085622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs372646960	chr5:180085629-180085630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113223352	chr5:180085636-180085637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs376409470	chr5:180085637-180085638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs369935850	chr5:180085645-180085646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200897302	chr5:180085653-180085654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs201490362	chr5:180085658-180085659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377366783	chr5:180085661-180085662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566488153	chr5:180085662-180085663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs199892579	chr5:180085669-180085670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs200970404	chr5:180085693-180085694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs201820941	chr5:180085698-180085699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs377603473	chr5:180085701-180085702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370258424	chr5:180085709-180085710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374973766	chr5:180085722-180085723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs368468004	chr5:180085725-180085726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372860988	chr5:180085733-180085734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538639730	chr5:180085741-180085742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374178884	chr5:180085743-180085744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368489091	chr5:180085749-180085750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113258998	chr5:180085759-180085760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372138774	chr5:180085765-180085766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs201070502	chr5:180085770-180085771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376099397	chr5:180085773-180085774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113950347	chr5:180085778-180085779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369337359	chr5:180085781-180085782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs202154870	chr5:180085786-180085787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112015421	chr5:180085789-180085790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73349225	chr5:180085817-180085818	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs369741585	chr5:180085839-180085840	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
33	rs569314711	chr5:180085843-180085844	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
34	rs200944537	chr5:180085854-180085855	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
35	rs71577415	chr5:180085862-180085863	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
36	rs11746155	chr5:180085863-180085864	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs190304555	chr5:180085874-180085875	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
38	rs66807875	chr5:180085875-180085876	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs554493733	chr5:180085924-180085925	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
40	rs182572959	chr5:180085951-180085952	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
41	rs544997003	chr5:180085975-180085976	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
42	rs564863475	chr5:180085997-180085998	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
43	rs530594051	chr5:180085998-180085999	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
44	rs144783176	chr5:180085999-180086000	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
45	rs561091167	chr5:180086027-180086028	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
46	rs529948314	chr5:180086050-180086051	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
47	rs373253496	chr5:180086068-180086069	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
48	rs546531375	chr5:180086069-180086070	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
49	rs574105592	chr5:180086098-180086099	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
50	rs139880636	chr5:180086160-180086161	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	17440070	CNVD
Schizophrenia	21346763	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:960 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:180085600-180085800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:180085800-180086000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr5:180085800-180086000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:180085800-180086000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
5	chr5:180085800-180086000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr5:180085800-180086000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr5:180085800-180086000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr5:180085800-180086000	Bivalent Enhancer	Brain Germinal Matrix	brain
9	chr5:180085800-180086000	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
10	chr5:180085800-180086000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
11	chr5:180085800-180086000	Bivalent Enhancer	Fetal Brain Male	brain
12	chr5:180085800-180086000	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
13	chr5:180085800-180086000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
14	chr5:180085800-180086200	Active TSS	H9 Cell Line	embryonic stem cell
15	chr5:180085800-180086200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
16	chr5:180085800-180086200	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr5:180085800-180086200	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr5:180085800-180086200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr5:180085800-180086200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
20	chr5:180085800-180086200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
21	chr5:180085800-180086200	Bivalent/Poised TSS	Primary T cells from cord blood	blood
22	chr5:180085800-180086200	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr5:180085800-180086200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
24	chr5:180085800-180086200	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
25	chr5:180085800-180086200	Bivalent Enhancer	Spleen	Spleen
26	chr5:180085800-180086600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
27	chr5:180085800-180086600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
28	chr5:180085800-180086600	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr5:180085800-180086600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
30	chr5:180085800-180086600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
31	chr5:180085800-180086600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
32	chr5:180085800-180086600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
33	chr5:180086000-180086200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr5:180086000-180086200	Bivalent/Poised TSS	Brain Germinal Matrix	brain
35	chr5:180086000-180086200	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
36	chr5:180086000-180086400	Bivalent/Poised TSS	HSMM	muscle
37	chr5:180086200-180086600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr5:180086200-180086600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr5:180086200-180086800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
40	chr5:180086200-180100400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr5:180086400-180086600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
42	chr5:180086400-180086600	Bivalent Enhancer	Fetal Thymus	thymus
43	chr5:180086600-180086800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr5:180086600-180086800	Bivalent Enhancer	Brain Hippocampus Middle	brain
45	chr5:180086600-180091800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr5:180091000-180091800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr5:180091800-180092000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr5:180091800-180092000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr5:180092000-180095800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr5:180092000-180097200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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