Variant report

Variant	nsv895080
Chromosome Location	chr10:43471575-43558757
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:487)
CpG islands
(count:306)
Chromatin interactive
region (count:148)
LncRNA
region (count:9)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:487 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:43474747-43475125	K562	blood:	n/a	n/a
2	ATF1	chr10:43474055-43474377	K562	blood:	n/a	n/a
3	BACH1	chr10:43542430-43542484	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:43521962-43522259	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr10:43508437-43508606	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr10:43484487-43484837	K562	blood:	n/a	n/a
7	BHLHE40	chr10:43476829-43477169	K562	blood:	n/a	chr10:43476970-43476986
8	CBX3	chr10:43528095-43528390	HCT-116	colon:	n/a	n/a
9	CBX3	chr10:43528082-43528334	K562	blood:	n/a	n/a
10	CCNT2	chr10:43476863-43477053	K562	blood:	n/a	n/a
11	CEBPB	chr10:43529212-43529403	IMR90	lung:	n/a	n/a
12	CEBPB	chr10:43474862-43474980	K562	blood:	n/a	n/a
13	CEBPB	chr10:43477134-43477208	K562	blood:	n/a	n/a
14	CEBPB	chr10:43529303-43529336	A549	lung:	n/a	n/a
15	CEBPB	chr10:43528862-43528920	HepG2	liver:	n/a	chr10:43528885-43528896
16	CEBPB	chr10:43528821-43529038	K562	blood:	n/a	chr10:43528885-43528896
17	CEBPB	chr10:43543376-43543576	HepG2	liver:	n/a	chr10:43543414-43543425
18	CHD2	chr10:43542380-43542393	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr10:43522101-43522438	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr10:43538079-43538216	K562	blood:	n/a	chr10:43538131-43538152 chr10:43538138-43538151 chr10:43538136-43538154
21	CTCF	chr10:43470960-43471606	A549	lung:	n/a	chr10:43471275-43471283 chr10:43471268-43471286
22	CTCF	chr10:43521545-43521638	NHEK	skin:	n/a	n/a
23	CTCF	chr10:43538075-43538257	MCF-7	breast:	n/a	chr10:43538131-43538152 chr10:43538138-43538151 chr10:43538136-43538154
24	CTCF	chr10:43514879-43514928	GM13976	blood:	n/a	n/a
25	CTCF	chr10:43538080-43538230	BE2_C	brain:	n/a	chr10:43538131-43538152 chr10:43538138-43538151 chr10:43538136-43538154
26	CTCF	chr10:43538080-43538230	SK-N-SH_RA	brain:	n/a	chr10:43538131-43538152 chr10:43538138-43538151 chr10:43538136-43538154
27	CTCF	chr10:43538067-43538260	MCF-7	breast:	n/a	chr10:43538131-43538152 chr10:43538138-43538151 chr10:43538136-43538154
28	CTCF	chr10:43538080-43538230	GM12875	blood:	n/a	chr10:43538131-43538152 chr10:43538138-43538151 chr10:43538136-43538154
29	CTCF	chr10:43538020-43538170	HL-60	blood:	n/a	chr10:43538131-43538152 chr10:43538138-43538151 chr10:43538136-43538154
30	CTCF	chr10:43537960-43538110	GM12873	blood:	n/a	n/a
31	CTCF	chr10:43537980-43538130	SAEC	small airway:	n/a	n/a
32	CTCF	chr10:43538100-43538209	MCF-7	breast:	n/a	chr10:43538131-43538152 chr10:43538138-43538151 chr10:43538136-43538154
33	CTCF	chr10:43506000-43506150	GM12865	blood:	n/a	n/a
34	CTCF	chr10:43518137-43518139	MCF-7	breast:	n/a	n/a
35	CTCF	chr10:43537980-43538130	NHEK	skin:	n/a	n/a
36	CTCF	chr10:43538060-43538210	GM12873	blood:	n/a	chr10:43538131-43538152 chr10:43538138-43538151 chr10:43538136-43538154
37	CTCF	chr10:43517980-43518130	Caco-2	colon:	n/a	chr10:43518112-43518130 chr10:43518115-43518123 chr10:43518115-43518128
38	CTCF	chr10:43538026-43538283	H1-hESC	embryonic stem cell:	n/a	chr10:43538131-43538152 chr10:43538138-43538151 chr10:43538136-43538154
39	CTCF	chr10:43538043-43538262	NHEK	skin:	n/a	chr10:43538131-43538152 chr10:43538138-43538151 chr10:43538136-43538154
40	CTCF	chr10:43538086-43538219	GM12892	blood:	n/a	chr10:43538131-43538152 chr10:43538138-43538151 chr10:43538136-43538154
41	CTCF	chr10:43537902-43538322	H1-hESC	embryonic stem cell:	n/a	chr10:43538131-43538152 chr10:43538138-43538151 chr10:43538136-43538154
42	CTCF	chr10:43538081-43538212	GM12891	blood:	n/a	chr10:43538131-43538152 chr10:43538138-43538151 chr10:43538136-43538154
43	CTCF	chr10:43475360-43475510	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr10:43538114-43538170	GM12878	blood:	n/a	chr10:43538131-43538152 chr10:43538138-43538151 chr10:43538136-43538154
45	CTCF	chr10:43538147-43538190	Fibrobl	skin:	n/a	n/a
46	CTCF	chr10:43542066-43542292	K562	blood:	n/a	n/a
47	CTCF	chr10:43524160-43524310	NHEK	skin:	n/a	n/a
48	CTCF	chr10:43538103-43538183	GM19240	blood:	n/a	chr10:43538131-43538152 chr10:43538138-43538151 chr10:43538136-43538154
49	CTCF	chr10:43542150-43542223	GM12892	blood:	n/a	n/a
50	CTCF	chr10:43475300-43475530	BE2_C	brain:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43507407-43507457	SKMC	muscle:	n/a
2	chr10:43507407-43507457	SKMC	muscle:	n/a
3	chr10:43507407-43507457	HNPCEpiC	eye:	n/a
4	chr10:43522190-43522240	IMR90	lung:	fetal
5	chr10:43522190-43522240	HRE	kidney:	n/a
6	chr10:43539572-43539622	ProgFib	skin:	n/a
7	chr10:43522143-43522193	HIPEpiC	eye:	n/a
8	chr10:43539572-43539622	K562	blood:	n/a
9	chr10:43522143-43522193	PrEC	prostate:	n/a
10	chr10:43507407-43507457	GM12891	blood:	n/a
11	chr10:43522143-43522193	HCM	heart:	n/a
12	chr10:43507407-43507457	PANC-1	pancreas:	n/a
13	chr10:43522343-43522393	HPAEpiC	pulmonary alveolar:	n/a
14	chr10:43539572-43539622	GM12892	blood:	n/a
15	chr10:43522190-43522240	SKMC	muscle:	n/a
16	chr10:43522143-43522193	HNPCEpiC	eye:	n/a
17	chr10:43522343-43522393	GM19239	blood:	n/a
18	chr10:43522143-43522193	NHDF-neo	bronchial:	n/a
19	chr10:43522190-43522240	GM12878	blood:	n/a
20	chr10:43522190-43522240	AG04450	lung:	fetal
21	chr10:43522143-43522193	SK-N-SH_RA	brain:	n/a
22	chr10:43539572-43539622	HCPEpiC	choroid plexus:	n/a
23	chr10:43522143-43522193	NT2-D1	testis:	n/a
24	chr10:43522143-43522193	NH-A	brain:	n/a
25	chr10:43522343-43522393	NH-A	brain:	n/a
26	chr10:43522143-43522193	CMK	blood:	n/a
27	chr10:43539572-43539622	HIPEpiC	eye:	n/a
28	chr10:43522343-43522393	HRE	kidney:	n/a
29	chr10:43522343-43522393	HCM	heart:	n/a
30	chr10:43539572-43539622	HCT-116	colon:	n/a
31	chr10:43507407-43507457	AG09319	gingival:	n/a
32	chr10:43522143-43522193	AG04450	lung:	fetal
33	chr10:43522343-43522393	HL-60	blood:	n/a
34	chr10:43522190-43522240	A549	lung:	n/a
35	chr10:43539572-43539622	Jurkat	blood:	n/a
36	chr10:43539572-43539622	HAEpiC	amniotic membrane:	n/a
37	chr10:43522343-43522393	SKMC	muscle:	n/a
38	chr10:43522190-43522240	HNPCEpiC	eye:	n/a
39	chr10:43539572-43539622	IMR90	lung:	fetal
40	chr10:43522143-43522193	HPAEpiC	pulmonary alveolar:	n/a
41	chr10:43539572-43539622	H1-hESC	embryonic stem cell:	embryo
42	chr10:43507407-43507457	SK-N-SH	brain:	n/a
43	chr10:43522190-43522240	HEEpiC	esophagus:	n/a
44	chr10:43522190-43522240	Hepatocyte	liver:	n/a
45	chr10:43522343-43522393	HAEpiC	amniotic membrane:	n/a
46	chr10:43522190-43522240	HCM	heart:	n/a
47	chr10:43507407-43507457	GM12892	blood:	n/a
48	chr10:43539572-43539622	HEK293	kidney:	embryo
49	chr10:43539572-43539622	NB4	blood:	n/a
50	chr10:43522190-43522240	HMEC	breast:	n/a

(count:148 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr10:43494122..43496846-chr10:43520768..43523139,2	MCF-7	breast:
2	chr10:43511982..43514503-chr10:43520094..43521790,2	MCF-7	breast:
3	chr10:43521831..43522342-chr10:43536915..43537421,2	MCF-7	breast:
4	chr10:43521899..43522422-chr10:43563847..43564568,2	MCF-7	breast:
5	chr10:43533868..43538087-chr10:43571876..43574676,3	MCF-7	breast:
6	chr10:43540640..43543554-chr10:43558547..43560903,3	MCF-7	breast:
7	chr10:43521831..43522342-chr10:43536915..43537421,2	MCF-7	breast:
8	chr10:43521470..43522630-chr10:43533126..43534089,18	MCF-7	breast:
9	chr10:43539137..43541120-chr10:43541349..43544216,2	K562	blood:
10	chr10:43471160..43472154-chr11:102217419..102218246,2	NB4	blood:
11	chr10:43469169..43471779-chr10:43471792..43473949,2	K562	blood:
12	chr10:43476360..43477929-chr10:43521585..43522547,22	MCF-7	breast:
13	chr10:43542939..43545690-chr10:43632908..43635258,2	MCF-7	breast:
14	chr10:43472744..43475645-chr10:43482853..43485433,2	K562	blood:
15	chr10:43474227..43476529-chr10:43479652..43481353,2	MCF-7	breast:
16	chr10:43544147..43547451-chr10:43554029..43556833,3	MCF-7	breast:
17	chr10:43521597..43522422-chr10:43563847..43564424,2	MCF-7	breast:
18	chr10:43365868..43366659-chr10:43470638..43471752,5	MCF-7	breast:
19	chr10:43494122..43496846-chr10:43520768..43523139,2	MCF-7	breast:
20	chr10:43474536..43476774-chr10:43520389..43522895,3	MCF-7	breast:
21	chr10:43531494..43533212-chr10:43549327..43551773,2	MCF-7	breast:
22	chr10:43521503..43524600-chr10:43558785..43561738,3	MCF-7	breast:
23	chr10:43450408..43453024-chr10:43497080..43499917,2	K562	blood:
24	chr10:43537183..43538884-chr10:43539008..43541736,2	MCF-7	breast:
25	chr10:43471183..43472148-chr4:106629910..106630418,2	NB4	blood:
26	chr10:43535157..43537866-chr10:43555666..43557650,2	K562	blood:
27	chr10:43476496..43477680-chr10:43521631..43522494,5	MCF-7	breast:
28	chr10:43540474..43542331-chr10:43555929..43558160,2	MCF-7	breast:
29	chr10:43476360..43477727-chr10:43521597..43522461,10	MCF-7	breast:
30	chr10:43471330..43471857-chr3:38035458..38036022,2	NB4	blood:
31	chr10:43481086..43483555-chr10:43520776..43523098,2	MCF-7	breast:
32	chr10:43365921..43366623-chr10:43521643..43522303,3	MCF-7	breast:
33	chr10:43533165..43534049-chr10:43605965..43606922,5	MCF-7	breast:
34	chr10:43521844..43522463-chr10:43539904..43540728,3	MCF-7	breast:
35	chr10:43521937..43524113-chr10:43534529..43536882,2	MCF-7	breast:
36	chr10:43539819..43542010-chr10:43547836..43549508,2	MCF-7	breast:
37	chr10:43526502..43530077-chr10:43530668..43533866,3	K562	blood:
38	chr10:43522082..43523941-chr10:43632029..43633686,2	MCF-7	breast:
39	chr10:43521855..43522376-chr10:43577254..43578134,2	MCF-7	breast:
40	chr10:43472378..43475581-chr10:43520718..43522410,3	MCF-7	breast:
41	chr10:43517249..43519024-chr10:43519060..43521993,5	MCF-7	breast:
42	chr10:43469610..43472857-chr10:43520371..43524809,5	MCF-7	breast:
43	chr10:43495233..43497382-chr10:43502437..43504369,2	MCF-7	breast:
44	chr10:43521853..43522545-chr10:43539851..43540728,3	MCF-7	breast:
45	chr10:43361871..43362799-chr10:43470867..43471733,6	MCF-7	breast:
46	chr10:43533504..43534088-chr10:43577355..43578166,2	MCF-7	breast:
47	chr10:43521554..43522492-chr10:43543717..43544592,2	MCF-7	breast:
48	chr10:43487519..43490099-chr10:43491819..43493663,2	MCF-7	breast:
49	chr10:43521578..43522089-chr10:51547030..51547754,2	MCF-7	breast:
50	chr10:43509037..43511424-chr10:43519957..43522490,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASGEF1A-1	chr10:43474465-43474547	XLOC_008790
2	lnc-RET-3	chr10:43487172-43487532	ucscGeneNc_uc001jba_2
3	lnc-RET-3	chr10:43487762-43487899	ucscGeneNc_uc001jba_2
4	lnc-RET-3	chr10:43489288-43490153	ucscGeneNc_uc001jba_2
5	lnc-RASGEF1A-1	chr10:43476816-43476955	XLOC_008790
6	lnc-RET-2	chr10:43482124-43482459	NONHSAT012938
7	lnc-RASGEF1A-1	chr10:43475731-43476007	XLOC_008790
8	lnc-RET-2	chr10:43481122-43481247	NONHSAT012938
9	lnc-RET-3	chr10:43486575-43486975	ucscGeneNc_uc001jba_2

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5100	chr10:43493078-43493099	MIMAT0022259

No data

Variant related genes	Relation type
MIR5100	TF binding region
ENSG00000229630	TF binding region
MIR5100	CpG island
ENSG00000229630	CpG island
ENSG00000169826	chromatin interactions
ENSG00000273008	chromatin interactions
ENSG00000110330	chromatin interactions
ENSG00000138785	chromatin interactions
ENSG00000229630	chromatin interactions
ENSG00000234944	chromatin interactions
ENSG00000165731	chromatin interactions
ENSG00000138780	chromatin interactions
ENSG00000263795	chromatin interactions
ENSG00000136059	chromatin interactions

Extended variants
information (count: 3591 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3591 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10900290	chr10:43471575-43471576	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	mRNA abundance
2	rs533936593	chr10:43471586-43471587	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs370571523	chr10:43471587-43471588	Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs140267879	chr10:43471590-43471591	Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs577185071	chr10:43471604-43471605	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs372194053	chr10:43471605-43471606	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs55923201	chr10:43471623-43471624	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs574771689	chr10:43471624-43471625	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs541997703	chr10:43471634-43471635	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs183104774	chr10:43471636-43471637	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs572308544	chr10:43471640-43471641	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs72779317	chr10:43471672-43471673	Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs564456079	chr10:43471700-43471701	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs375148766	chr10:43471715-43471716	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs531916393	chr10:43471716-43471717	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs116184424	chr10:43471731-43471732	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs78855838	chr10:43471732-43471733	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs544272373	chr10:43471733-43471734	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs547992151	chr10:43471736-43471737	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs186793310	chr10:43471786-43471787	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs527507709	chr10:43471795-43471796	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs116145359	chr10:43471828-43471829	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs190653060	chr10:43471887-43471888	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs538187248	chr10:43471915-43471916	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs150982722	chr10:43471920-43471921	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs373639826	chr10:43471935-43471936	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs114160804	chr10:43471940-43471941	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs11818789	chr10:43471943-43471944	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs140898278	chr10:43471959-43471960	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs546690439	chr10:43471962-43471963	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs114148518	chr10:43471963-43471964	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs572173181	chr10:43471980-43471981	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs546063164	chr10:43472020-43472021	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs61845273	chr10:43472037-43472038	Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs150162749	chr10:43472038-43472039	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs576227427	chr10:43472047-43472048	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs183218449	chr10:43472066-43472067	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs74135435	chr10:43472086-43472087	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs548754475	chr10:43472101-43472102	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs543803873	chr10:43472117-43472118	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs138625337	chr10:43472134-43472135	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs568854473	chr10:43472139-43472140	Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs541784051	chr10:43472166-43472167	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs146378511	chr10:43472179-43472180	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs75986480	chr10:43472181-43472182	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs560308666	chr10:43472222-43472223	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs527407311	chr10:43472276-43472277	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs571878733	chr10:43472278-43472279	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs564189687	chr10:43472309-43472310	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs552296753	chr10:43472314-43472315	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:444 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43470200-43471600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:43471000-43474800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:43471200-43474800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr10:43471600-43474600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr10:43474000-43474200	Bivalent/Poised TSS	Fetal Lung	lung
6	chr10:43474200-43474400	Bivalent Enhancer	Fetal Brain Male	brain
7	chr10:43474200-43474600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr10:43474200-43474600	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr10:43474200-43475000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr10:43474400-43475000	Enhancers	Fetal Brain Male	brain
11	chr10:43474600-43474800	Enhancers	Gastric	stomach
12	chr10:43474600-43475000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr10:43474600-43475400	Enhancers	Brain Germinal Matrix	brain
14	chr10:43474800-43475000	Enhancers	K562	blood
15	chr10:43474800-43475200	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr10:43474800-43475200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr10:43474800-43475200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr10:43474800-43475400	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr10:43474800-43475400	Weak transcription	Gastric	stomach
20	chr10:43474800-43476000	Enhancers	Pancreas	Pancrea
21	chr10:43475000-43475200	Enhancers	Stomach Mucosa	stomach
22	chr10:43475000-43477200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr10:43475200-43475600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr10:43475200-43475600	Enhancers	Dnd41	blood
25	chr10:43475400-43475600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr10:43475400-43475600	Bivalent Enhancer	Fetal Stomach	stomach
27	chr10:43475400-43476600	Weak transcription	Stomach Mucosa	stomach
28	chr10:43475400-43477600	Enhancers	Gastric	stomach
29	chr10:43475600-43477800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr10:43476000-43476200	Weak transcription	Pancreas	Pancrea
31	chr10:43476000-43476200	Active TSS	Spleen	Spleen
32	chr10:43476000-43479000	Enhancers	Fetal Intestine Small	intestine
33	chr10:43476200-43477200	Enhancers	Pancreas	Pancrea
34	chr10:43476200-43482600	Weak transcription	Spleen	Spleen
35	chr10:43476400-43479800	Enhancers	Fetal Intestine Large	intestine
36	chr10:43476600-43477800	Enhancers	Stomach Mucosa	stomach
37	chr10:43476800-43477400	Enhancers	Left Ventricle	heart
38	chr10:43477200-43477600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr10:43477200-43477600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr10:43477200-43477600	Enhancers	Esophagus	oesophagus
41	chr10:43477200-43478000	Enhancers	Duodenum Mucosa	Duodenum
42	chr10:43477600-43478800	Weak transcription	Gastric	stomach
43	chr10:43477600-43479000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr10:43477600-43482600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr10:43478000-43478600	Weak transcription	Duodenum Mucosa	Duodenum
46	chr10:43478400-43479400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
47	chr10:43478600-43478800	Enhancers	Duodenum Mucosa	Duodenum
48	chr10:43478800-43479000	Enhancers	Gastric	stomach
49	chr10:43479000-43479200	Enhancers	Fetal Muscle Leg	muscle
50	chr10:43479000-43479400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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