Variant report

Variant	nsv437200
Chromosome Location	chr1:10366487-10387704
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:107)
CpG islands
(count:489)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:107 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:10380482-10380682	K562	blood:	n/a	n/a
2	BACH1	chr1:10380446-10380697	K562	blood:	n/a	n/a
3	BACH1	chr1:10380469-10380692	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr1:10378295-10378488	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr1:10380375-10380575	K562	blood:	n/a	n/a
6	CEBPB	chr1:10386383-10386600	HepG2	liver:	n/a	chr1:10386478-10386489 chr1:10386480-10386491 chr1:10386478-10386491
7	CEBPB	chr1:10383519-10383776	A549	lung:	n/a	chr1:10383630-10383641
8	CEBPB	chr1:10382890-10383082	Hela-S3	cervix:	n/a	chr1:10382929-10382942 chr1:10382929-10382940 chr1:10382929-10382942 chr1:10382930-10382941
9	CEBPB	chr1:10383497-10383695	HepG2	liver:	n/a	chr1:10383630-10383641
10	CEBPB	chr1:10387479-10387658	K562	blood:	n/a	n/a
11	CEBPB	chr1:10378740-10378791	K562	blood:	n/a	n/a
12	CEBPB	chr1:10376225-10376499	HepG2	liver:	n/a	chr1:10376337-10376348
13	CEBPB	chr1:10382876-10383076	H1-hESC	embryonic stem cell:	n/a	chr1:10382929-10382942 chr1:10382929-10382940 chr1:10382929-10382942 chr1:10382930-10382941
14	CEBPB	chr1:10382798-10383196	K562	blood:	n/a	chr1:10382929-10382942 chr1:10382929-10382940 chr1:10382929-10382942 chr1:10382930-10382941
15	CEBPB	chr1:10383561-10383760	H1-hESC	embryonic stem cell:	n/a	chr1:10383630-10383641
16	CEBPB	chr1:10382872-10383022	HepG2	liver:	n/a	chr1:10382929-10382942 chr1:10382929-10382940 chr1:10382929-10382942 chr1:10382930-10382941
17	CEBPB	chr1:10378633-10378791	HepG2	liver:	n/a	chr1:10378727-10378738
18	CEBPB	chr1:10383499-10383806	IMR90	lung:	n/a	chr1:10383630-10383641
19	CEBPB	chr1:10383512-10383795	K562	blood:	n/a	chr1:10383630-10383641
20	CTCF	chr1:10383031-10383104	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr1:10383039-10383118	GM12892	blood:	n/a	n/a
22	CTCF	chr1:10382996-10383120	K562	blood:	n/a	n/a
23	CTCF	chr1:10383026-10383118	A549	lung:	n/a	n/a
24	CTCF	chr1:10382960-10383110	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr1:10383065-10383094	NHEK	skin:	n/a	n/a
26	CTCF	chr1:10382940-10383090	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr1:10383029-10383055	Medullo	brain:	n/a	n/a
28	CTCF	chr1:10383033-10383125	MCF-7	breast:	n/a	n/a
29	CTCF	chr1:10383039-10383108	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:10382968-10383174	K562	blood:	n/a	n/a
31	CTCF	chr1:10383047-10383052	K562	blood:	n/a	n/a
32	CTCF	chr1:10383040-10383190	HepG2	liver:	n/a	n/a
33	CTCF	chr1:10382967-10383300	K562	blood:	n/a	n/a
34	CTCF	chr1:10383043-10383113	GM19239	blood:	n/a	n/a
35	CTCF	chr1:10383042-10383111	GM19238	blood:	n/a	n/a
36	CTCF	chr1:10383060-10383210	AG09319	gingival:	n/a	n/a
37	CTCF	chr1:10383058-10383097	K562	blood:	n/a	n/a
38	CTCF	chr1:10383035-10383129	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr1:10382940-10383090	HMF	breast:	n/a	n/a
40	CUX1	chr1:10380168-10380521	K562	blood:	n/a	n/a
41	EP300	chr1:10380151-10380608	K562	blood:	n/a	n/a
42	EP300	chr1:10380320-10380405	GM12878	blood:	n/a	n/a
43	EP300	chr1:10369887-10370020	GM12878	blood:	n/a	n/a
44	EP300	chr1:10378167-10378456	H1-hESC	embryonic stem cell:	n/a	n/a
45	FOS	chr1:10383627-10383740	MCF10A-Er-Src	breast:	n/a	n/a
46	GATA2	chr1:10370512-10370729	SH-SY5Y	brain:	n/a	n/a
47	GATA3	chr1:10368072-10368187	SH-SY5Y	brain:	n/a	n/a
48	GATA3	chr1:10370523-10370838	SH-SY5Y	brain:	n/a	n/a
49	HDAC2	chr1:10378145-10378521	H1-hESC	embryonic stem cell:	n/a	n/a
50	IRF1	chr1:10384824-10384992	K562	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10386389-10386439	HIPEpiC	eye:	n/a
2	chr1:10386389-10386439	HIPEpiC	eye:	n/a
3	chr1:10386247-10386297	Hepatocyte	liver:	n/a
4	chr1:10386247-10386297	AoSMC	blood vessel:	n/a
5	chr1:10370540-10370590	ProgFib	skin:	n/a
6	chr1:10370540-10370590	HNPCEpiC	eye:	n/a
7	chr1:10384888-10384938	HepG2	liver:	n/a
8	chr1:10370540-10370590	T-47D	breast:	n/a
9	chr1:10370540-10370590	HCPEpiC	choroid plexus:	n/a
10	chr1:10386331-10386381	HUVEC	blood vessel:	n/a
11	chr1:10386331-10386381	HNPCEpiC	eye:	n/a
12	chr1:10384888-10384938	PANC-1	pancreas:	n/a
13	chr1:10384888-10384938	GM12892	blood:	n/a
14	chr1:10386268-10386318	SK-N-SH	brain:	n/a
15	chr1:10370540-10370590	HCM	heart:	n/a
16	chr1:10368286-10368336	GM06990	blood:	n/a
17	chr1:10384888-10384938	HPAEpiC	pulmonary alveolar:	n/a
18	chr1:10386331-10386381	AG04449	skin:	fetal
19	chr1:10384888-10384938	SKMC	muscle:	n/a
20	chr1:10386247-10386297	BE2_C	brain:	n/a
21	chr1:10386268-10386318	AG04449	skin:	fetal
22	chr1:10386247-10386297	SK-N-SH	brain:	n/a
23	chr1:10386247-10386297	HCT-116	colon:	n/a
24	chr1:10386268-10386318	H1-hESC	embryonic stem cell:	embryo
25	chr1:10386247-10386297	NB4	blood:	n/a
26	chr1:10386331-10386381	HCM	heart:	n/a
27	chr1:10386331-10386381	Jurkat	blood:	n/a
28	chr1:10384888-10384938	ovcar-3	ovarian:	n/a
29	chr1:10386268-10386318	PANC-1	pancreas:	n/a
30	chr1:10386268-10386318	K562	blood:	n/a
31	chr1:10368286-10368336	H1-hESC	embryonic stem cell:	embryo
32	chr1:10386389-10386439	U87	brain:	n/a
33	chr1:10384888-10384938	AG10803	skin:	n/a
34	chr1:10386331-10386381	U87	brain:	n/a
35	chr1:10368286-10368336	MCF10A-Er-Src	breast:	n/a
36	chr1:10386331-10386381	GM12892	blood:	n/a
37	chr1:10386247-10386297	AG04449	skin:	fetal
38	chr1:10386331-10386381	HPAEpiC	pulmonary alveolar:	n/a
39	chr1:10384888-10384938	H1-hESC	embryonic stem cell:	embryo
40	chr1:10368286-10368336	HepG2	liver:	n/a
41	chr1:10386268-10386318	HEEpiC	esophagus:	n/a
42	chr1:10386268-10386318	CMK	blood:	n/a
43	chr1:10386389-10386439	HPAEpiC	pulmonary alveolar:	n/a
44	chr1:10370540-10370590	PANC-1	pancreas:	n/a
45	chr1:10368286-10368336	HUVEC	blood vessel:	n/a
46	chr1:10383706-10383756	AoSMC	blood vessel:	n/a
47	chr1:10370540-10370590	NHBE	bronchial:	n/a
48	chr1:10386247-10386297	T-47D	breast:	n/a
49	chr1:10383706-10383756	HMEC	breast:	n/a
50	chr1:10386331-10386381	NT2-D1	testis:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:10364625..10366634-chr1:10534316..10536742,2	K562	blood:
2	chr1:10381461..10384413-chr1:10458819..10461275,2	K562	blood:
3	chr1:10382484..10384507-chr1:10403370..10405612,2	K562	blood:
4	chr1:10362813..10365795-chr1:10373892..10375674,2	K562	blood:
5	chr1:10363969..10365666-chr1:10368809..10370955,2	MCF-7	breast:
6	chr1:10366942..10370900-chr1:10370974..10374307,3	K562	blood:
7	chr1:10366942..10370900-chr1:10370974..10374307,3	K562	blood:
8	chr1:10386481..10388666-chr1:10391684..10394464,2	K562	blood:
9	chr1:10380885..10383260-chr1:10390219..10391956,2	K562	blood:
10	chr1:10382347..10384488-chr1:10398364..10401134,2	K562	blood:
11	chr1:10362138..10364567-chr1:10385021..10386678,2	K562	blood:
12	chr1:10380119..10382361-chr1:10412218..10415075,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PGD-4	chr1:10366523-10366813	NONHSAT000844

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	KIF1B	hsa-miR-124-3p	chr1:10368174-10368194
2	KIF1B	hsa-miR-9-5p	chr1:10367933-10367939
3	KIF1B	hsa-miR-9-5p	chr1:10367916-10367940
4	KIF1B	hsa-miR-124-3p	chr1:10368212-10368218
5	KIF1B	hsa-miR-9-5p	chr1:10367079-10367085

Variant related genes	Relation type
RN7SL731P	TF binding region
RN7SL731P	CpG island
ENSG00000054523	chromatin interactions
ENSG00000142655	chromatin interactions
ENSG00000142657	chromatin interactions

Extended variants
information (count: 769 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:769 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8019	chr1:10366487-10366488	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565643539	chr1:10366491-10366492	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs12141319	chr1:10366502-10366503	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs12141352	chr1:10366601-10366602	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs4623	chr1:10366692-10366693	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs569309633	chr1:10366741-10366742	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
7	rs56164683	chr1:10366765-10366766	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs187140427	chr1:10366768-10366769	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
9	rs572063663	chr1:10366776-10366777	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
10	rs376684894	chr1:10366816-10366817	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs78995041	chr1:10366820-10366821	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs76604610	chr1:10366821-10366822	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs199974119	chr1:10366885-10366886	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191433724	chr1:10366967-10366968	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183625005	chr1:10367027-10367028	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571525585	chr1:10367057-10367058	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs41274464	chr1:10367058-10367059	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs564393204	chr1:10367240-10367241	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187945386	chr1:10367244-10367245	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369415150	chr1:10367279-10367280	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555047774	chr1:10367293-10367294	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536985817	chr1:10367307-10367308	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142468272	chr1:10367350-10367351	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544161583	chr1:10367378-10367379	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2004034	chr1:10367424-10367425	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs145733356	chr1:10367443-10367444	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541274721	chr1:10367538-10367539	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs559888050	chr1:10367548-10367549	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs41274466	chr1:10367570-10367571	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs143823495	chr1:10367579-10367580	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562980434	chr1:10367588-10367589	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs1065828	chr1:10367591-10367592	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs79405882	chr1:10367604-10367605	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs193222943	chr1:10367633-10367634	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185481776	chr1:10367643-10367644	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141358777	chr1:10367686-10367687	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529603522	chr1:10367700-10367701	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs568242121	chr1:10367712-10367713	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190384993	chr1:10367782-10367783	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34480927	chr1:10367788-10367789	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs368966853	chr1:10367808-10367809	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs145128126	chr1:10367818-10367819	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576570168	chr1:10367829-10367830	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537445846	chr1:10367884-10367885	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs375721546	chr1:10367902-10367903	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558871810	chr1:10367908-10367909	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577509475	chr1:10367959-10367960	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs142832592	chr1:10368084-10368085	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs17401588	chr1:10368099-10368100	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs556515444	chr1:10368107-10368108	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	20406844	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	20164919	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:695 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10272600-10368200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:10315400-10373400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr1:10316800-10380200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr1:10318400-10367600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr1:10331600-10368000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr1:10347800-10366800	Strong transcription	HSMM	muscle
7	chr1:10348200-10367600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr1:10349800-10369400	Weak transcription	Right Atrium	heart
9	chr1:10352000-10366800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:10352600-10381800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr1:10353200-10381800	Weak transcription	Primary hematopoietic stem cells	blood
12	chr1:10356600-10368000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr1:10356800-10367800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr1:10356800-10368000	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr1:10357200-10368000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr1:10357400-10385600	Weak transcription	Small Intestine	intestine
17	chr1:10357600-10397000	Weak transcription	Fetal Thymus	thymus
18	chr1:10358000-10367000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr1:10358000-10367800	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr1:10358000-10381800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr1:10358200-10367000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr1:10358400-10369400	Weak transcription	Psoas Muscle	Psoas
23	chr1:10358600-10381800	Weak transcription	Primary T cells from cord blood	blood
24	chr1:10358800-10407000	Weak transcription	Primary B cells from cord blood	blood
25	chr1:10360000-10370200	Weak transcription	GM12878-XiMat	blood
26	chr1:10361800-10366600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr1:10361800-10370800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr1:10362000-10366800	Strong transcription	Rectal Mucosa Donor 29	rectum
29	chr1:10362400-10366800	Strong transcription	Duodenum Mucosa	Duodenum
30	chr1:10362600-10366800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr1:10362600-10366800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr1:10362600-10366800	Strong transcription	Fetal Intestine Large	intestine
33	chr1:10362600-10366800	Strong transcription	Fetal Muscle Leg	muscle
34	chr1:10362600-10367400	Strong transcription	Fetal Muscle Trunk	muscle
35	chr1:10362600-10367400	Strong transcription	Osteobl	bone
36	chr1:10362800-10366600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
37	chr1:10363000-10373200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr1:10363000-10379800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr1:10363200-10366600	Strong transcription	Skeletal Muscle Male	skeletal muscle
40	chr1:10363400-10366800	Strong transcription	Fetal Brain Male	brain
41	chr1:10363600-10366800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr1:10363600-10373400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr1:10363800-10380000	Weak transcription	A549	lung
44	chr1:10364200-10368600	Weak transcription	K562	blood
45	chr1:10364200-10381800	Weak transcription	Gastric	stomach
46	chr1:10364200-10394600	Weak transcription	Dnd41	blood
47	chr1:10364400-10366600	Weak transcription	Thymus	Thymus
48	chr1:10364400-10367200	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr1:10364400-10367800	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr1:10364400-10380000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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