Variant report

Variant	nsv1044043
Chromosome Location	chr10:89678935-89701069
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:334)
CpG islands
(count:122)
Chromatin interactive
region (count:21)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:89691648-89691960	K562	blood:	n/a	n/a
2	ATF1	chr10:89691662-89691909	K562	blood:	n/a	n/a
3	ATF2	chr10:89689222-89689710	GM12878	blood:	n/a	n/a
4	ATF2	chr10:89690977-89691901	GM12878	blood:	n/a	n/a
5	ATF2	chr10:89690821-89691719	GM12878	blood:	n/a	n/a
6	ATF3	chr10:89699280-89699454	K562	blood:	n/a	n/a
7	BATF	chr10:89691207-89691590	GM12878	blood:	n/a	n/a
8	BATF	chr10:89691222-89691524	GM12878	blood:	n/a	n/a
9	BCL3	chr10:89691208-89691611	GM12878	blood:	n/a	n/a
10	BHLHE40	chr10:89688678-89689119	GM12878	blood:	n/a	n/a
11	BRCA1	chr10:89683710-89683778	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr10:89681545-89682122	K562	blood:	n/a	n/a
13	CEBPB	chr10:89692598-89692923	K562	blood:	n/a	chr10:89692767-89692778 chr10:89692620-89692633
14	CEBPB	chr10:89696721-89696941	K562	blood:	n/a	chr10:89696790-89696801 chr10:89696789-89696802
15	CEBPB	chr10:89690795-89691224	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr10:89692759-89692786	HepG2	liver:	n/a	chr10:89692767-89692778
17	CEBPB	chr10:89696622-89696957	IMR90	lung:	n/a	chr10:89696790-89696801 chr10:89696789-89696802
18	CEBPB	chr10:89696611-89696969	HepG2	liver:	n/a	chr10:89696790-89696801 chr10:89696789-89696802
19	CEBPB	chr10:89696655-89696952	Hela-S3	cervix:	n/a	chr10:89696790-89696801 chr10:89696789-89696802
20	CEBPB	chr10:89696650-89696923	A549	lung:	n/a	chr10:89696790-89696801 chr10:89696789-89696802
21	CEBPB	chr10:89695592-89695831	Hela-S3	cervix:	n/a	chr10:89695662-89695673
22	CEBPB	chr10:89692303-89692476	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr10:89685373-89685685	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr10:89692215-89692929	IMR90	lung:	n/a	chr10:89692767-89692778 chr10:89692620-89692633
25	CEBPB	chr10:89695689-89695731	HepG2	liver:	n/a	n/a
26	CEBPB	chr10:89692736-89692937	A549	lung:	n/a	chr10:89692767-89692778
27	CHD1	chr10:89688881-89689025	GM12878	blood:	n/a	n/a
28	CTCF	chr10:89680473-89680558	ProgFib	skin:	n/a	n/a
29	CTCF	chr10:89699259-89699298	Lung_OC	lung:	n/a	n/a
30	CTCF	chr10:89700640-89700790	HPF	lung:	n/a	n/a
31	CTCF	chr10:89680464-89680546	Fibrobl	skin:	n/a	n/a
32	CUX1	chr10:89691714-89691926	K562	blood:	n/a	n/a
33	CUX1	chr10:89693333-89693489	GM12878	blood:	n/a	n/a
34	CUX1	chr10:89691102-89691952	GM12878	blood:	n/a	n/a
35	CUX1	chr10:89689536-89689657	GM12878	blood:	n/a	n/a
36	EBF1	chr10:89691259-89691576	GM12878	blood:	n/a	n/a
37	EBF1	chr10:89689444-89689656	GM12878	blood:	n/a	n/a
38	EBF1	chr10:89691075-89691895	GM12878	blood:	n/a	n/a
39	EGR1	chr10:89699287-89699511	K562	blood:	n/a	n/a
40	EGR1	chr10:89699296-89699436	K562	blood:	n/a	n/a
41	EP300	chr10:89691115-89691932	GM12878	blood:	n/a	n/a
42	EP300	chr10:89691690-89691903	Hela-S3	cervix:	n/a	n/a
43	EP300	chr10:89691412-89692181	SK-N-SH	brain:	n/a	n/a
44	EP300	chr10:89685339-89685656	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr10:89691323-89692498	SK-N-SH	brain:	n/a	chr10:89692373-89692387
46	EP300	chr10:89691353-89692221	SK-N-SH	brain:	n/a	n/a
47	EP300	chr10:89689324-89689601	GM12878	blood:	n/a	n/a
48	EP300	chr10:89691507-89692052	SK-N-SH_RA	brain:	n/a	n/a
49	EP300	chr10:89691524-89691874	K562	blood:	n/a	n/a
50	EP300	chr10:89688874-89689074	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:89696774-89696824	NB4	blood:	n/a
2	chr10:89690234-89690284	ProgFib	skin:	n/a
3	chr10:89690234-89690284	AoSMC	blood vessel:	n/a
4	chr10:89696774-89696824	HUVEC	blood vessel:	n/a
5	chr10:89696774-89696824	RPTEC	kidney:	n/a
6	chr10:89690234-89690284	AG04450	lung:	fetal
7	chr10:89690234-89690284	HepG2	liver:	n/a
8	chr10:89690234-89690284	LNCaP	prostate:	n/a
9	chr10:89696774-89696824	HCT-116	colon:	n/a
10	chr10:89696774-89696824	K562	blood:	n/a
11	chr10:89690234-89690284	T-47D	breast:	n/a
12	chr10:89690234-89690284	IMR90	lung:	fetal
13	chr10:89696774-89696824	HRE	kidney:	n/a
14	chr10:89696774-89696824	HL-60	blood:	n/a
15	chr10:89690234-89690284	HCT-116	colon:	n/a
16	chr10:89696774-89696824	Jurkat	blood:	n/a
17	chr10:89696774-89696824	SK-N-MC	brain:	n/a
18	chr10:89696774-89696824	HIPEpiC	eye:	n/a
19	chr10:89690234-89690284	Jurkat	blood:	n/a
20	chr10:89690234-89690284	SKMC	muscle:	n/a
21	chr10:89690234-89690284	A549	lung:	n/a
22	chr10:89696774-89696824	SAEC	small airway:	n/a
23	chr10:89696774-89696824	GM12891	blood:	n/a
24	chr10:89696774-89696824	HCF	heart:	n/a
25	chr10:89696774-89696824	GM12878	blood:	n/a
26	chr10:89696774-89696824	AoSMC	blood vessel:	n/a
27	chr10:89690234-89690284	NB4	blood:	n/a
28	chr10:89690234-89690284	HL-60	blood:	n/a
29	chr10:89696774-89696824	PrEC	prostate:	n/a
30	chr10:89696774-89696824	NHBE	bronchial:	n/a
31	chr10:89690234-89690284	GM06990	blood:	n/a
32	chr10:89696774-89696824	GM06990	blood:	n/a
33	chr10:89690234-89690284	RPTEC	kidney:	n/a
34	chr10:89696774-89696824	MCF10A-Er-Src	breast:	n/a
35	chr10:89696774-89696824	AG10803	skin:	n/a
36	chr10:89690234-89690284	H1-hESC	embryonic stem cell:	embryo
37	chr10:89696774-89696824	NT2-D1	testis:	n/a
38	chr10:89696774-89696824	BJ	skin:	n/a
39	chr10:89696774-89696824	HNPCEpiC	eye:	n/a
40	chr10:89690234-89690284	HRE	kidney:	n/a
41	chr10:89690234-89690284	K562	blood:	n/a
42	chr10:89690234-89690284	BJ	skin:	n/a
43	chr10:89690234-89690284	HPAEpiC	pulmonary alveolar:	n/a
44	chr10:89690234-89690284	HCPEpiC	choroid plexus:	n/a
45	chr10:89690234-89690284	BE2_C	brain:	n/a
46	chr10:89690234-89690284	HRCEpiC	kidney:	n/a
47	chr10:89696774-89696824	Caco-2	colon:	n/a
48	chr10:89696774-89696824	ECC-1	luminal epithelium:	n/a
49	chr10:89696774-89696824	NHDF-neo	bronchial:	n/a
50	chr10:89690234-89690284	HCF	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:89683604..89685198-chr10:89700673..89703491,2	K562	blood:
2	chr10:89696435..89697962-chr10:89699594..89701674,2	MCF-7	breast:
3	chr10:89679106..89681199-chr10:89681260..89684202,3	K562	blood:
4	chr10:89673644..89678140-chr10:89679296..89683460,5	K562	blood:
5	chr10:89686969..89688514-chr10:89688807..89691753,2	K562	blood:
6	chr10:89622549..89624064-chr10:89699463..89701923,2	MCF-7	breast:
7	chr10:89688499..89690095-chr10:89694777..89697091,2	MCF-7	breast:
8	chr10:89620410..89622010-chr10:89680788..89683163,3	MCF-7	breast:
9	chr10:89686969..89688514-chr10:89688807..89691753,2	K562	blood:
10	chr10:89639384..89642070-chr10:89695863..89697662,2	K562	blood:
11	chr10:89688499..89690095-chr10:89694777..89697091,2	MCF-7	breast:
12	chr10:89692563..89694138-chr10:89862900..89864985,2	MCF-7	breast:
13	chr10:89683604..89685198-chr10:89700673..89703491,2	K562	blood:
14	chr10:89685840..89688439-chr10:89700788..89703474,2	MCF-7	breast:
15	chr10:89620590..89623557-chr10:89689802..89694135,6	MCF-7	breast:
16	chr10:89671146..89673722-chr10:89679466..89681540,2	MCF-7	breast:
17	chr10:89621607..89624056-chr10:89678567..89681006,2	MCF-7	breast:
18	chr10:89696435..89697962-chr10:89699594..89701674,2	MCF-7	breast:
19	chr10:89685265..89687757-chr10:89688407..89691640,3	MCF-7	breast:
20	chr10:89679106..89681199-chr10:89681260..89684202,3	K562	blood:
21	chr10:89685840..89688439-chr10:89700788..89703474,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAPSS2-9	chr10:89696356-89696835	expReg_chr10_5676_+
2	lnc-PAPSS2-7	chr10:89685390-89685627	expReg_chr10_5653_+
3	lnc-KLLN-1	chr10:89698640-89699108	ENSG00000245981

No data

Variant related genes	Relation type
ENSG00000213613	TF binding region
PTEN	TF binding region
ENSG00000213613	CpG island
PTEN	CpG island
ENSG00000171862	chromatin interactions
ENSG00000227268	chromatin interactions
NR2C2AP	miRNA target sites

Extended variants
information (count: 766 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:766 , 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	rs183011978	chr10:89678967-89678968	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs17106914	chr10:89679020-89679021	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs143876952	chr10:89679069-89679070	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs141458806	chr10:89679087-89679088	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs541087455	chr10:89679139-89679140	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs576663979	chr10:89679154-89679155	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs574546932	chr10:89679169-89679170	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs200727253	chr10:89679285-89679286	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs541636788	chr10:89679291-89679292	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs7917883	chr10:89679312-89679313	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs574773845	chr10:89679368-89679369	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs188233293	chr10:89679482-89679483	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs11202599	chr10:89679489-89679490	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs528111718	chr10:89679491-89679492	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs144540067	chr10:89679493-89679494	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs568141534	chr10:89679494-89679495	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs59795104	chr10:89679513-89679514	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs12765500	chr10:89679580-89679581	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs12765661	chr10:89679611-89679612	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs12765675	chr10:89679641-89679642	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs557453090	chr10:89679665-89679666	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs192802557	chr10:89679749-89679750	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs184276879	chr10:89679757-89679758	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs541599127	chr10:89679763-89679764	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs544141582	chr10:89679808-89679809	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs558834624	chr10:89679840-89679841	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs564695554	chr10:89680045-89680046	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs36069123	chr10:89680062-89680063	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs12255199	chr10:89680123-89680124	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs550338253	chr10:89680138-89680139	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs374514976	chr10:89680158-89680159	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs189227608	chr10:89680182-89680183	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs78652303	chr10:89680218-89680219	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs542347311	chr10:89680231-89680232	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs556871829	chr10:89680272-89680273	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs529289499	chr10:89680274-89680275	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs575397642	chr10:89680313-89680314	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs548155592	chr10:89680325-89680326	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs564396789	chr10:89680361-89680362	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs528425873	chr10:89680362-89680363	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs568357641	chr10:89680367-89680368	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs561709082	chr10:89680401-89680402	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs562351831	chr10:89680427-89680428	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs192417185	chr10:89680430-89680431	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs71487194	chr10:89680491-89680492	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs200042219	chr10:89680572-89680573	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs74940511	chr10:89680583-89680584	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs113820650	chr10:89680584-89680585	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs78310943	chr10:89680585-89680586	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs371932748	chr10:89680586-89680587	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:122)

Disease	PMID	Source
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
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	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
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21569311	CNVD
Cancer	20164919	CNVD
Melanoma	17363583	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Glioblastoma multiforme	19115005	CNVD
Prostate cancer	21147910	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	20020426	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	22065749	CNVD
Cancer	22000013	CNVD
Colon cancer	22065749	CNVD
Endometrial cancer	22065749	CNVD
Lung cancer	20668451	CNVD
Breast cancer	17634833	CNVD
Cancer	20215515	CNVD
Glioblastoma multiforme	21727940	CNVD
Prostate cancer	19363497	CNVD
Prostate cancer	17700571	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Ovarian cancer	21781307	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20964600	CNVD
Endometrial cancer	19261849	CNVD
Central neurocytomas	17123091	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung adenocarcinoma	17982442	CNVD
Bannayan-Riley-Ruvalcaba syndrome	20848651	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:1042 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:89647000-89711200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr10:89648000-89683000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr10:89663600-89686400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr10:89663600-89687400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr10:89663800-89725400	Weak transcription	Colonic Mucosa	Colon
6	chr10:89664000-89681800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr10:89666000-89712400	Weak transcription	Fetal Brain Male	brain
8	chr10:89666600-89682800	Weak transcription	Placenta	Placenta
9	chr10:89671600-89682800	Weak transcription	Spleen	Spleen
10	chr10:89672000-89681600	Weak transcription	Aorta	Aorta
11	chr10:89673400-89679800	Genic enhancers	Dnd41	blood
12	chr10:89673600-89679400	Weak transcription	Brain Hippocampus Middle	brain
13	chr10:89673600-89726000	Weak transcription	Brain Substantia Nigra	brain
14	chr10:89674000-89685600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr10:89674200-89695200	Weak transcription	Brain Cingulate Gyrus	brain
16	chr10:89674200-89711000	Weak transcription	HepG2	liver
17	chr10:89674600-89682600	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr10:89674600-89684400	Weak transcription	Fetal Kidney	kidney
19	chr10:89674600-89686400	Weak transcription	HSMMtube	muscle
20	chr10:89674600-89687000	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr10:89674600-89689800	Weak transcription	Fetal Lung	lung
22	chr10:89674600-89695600	Weak transcription	Fetal Muscle Trunk	muscle
23	chr10:89674800-89682200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr10:89674800-89724400	Weak transcription	Fetal Brain Female	brain
25	chr10:89675000-89679000	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr10:89675000-89679800	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr10:89675200-89679000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
28	chr10:89675200-89679800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr10:89675400-89679000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr10:89675400-89679600	Enhancers	Primary T cells from cord blood	blood
31	chr10:89675400-89681200	Weak transcription	Lung	lung
32	chr10:89675400-89681600	Weak transcription	Ovary	ovary
33	chr10:89675400-89686400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr10:89675400-89726000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr10:89675600-89680200	Weak transcription	Fetal Intestine Small	intestine
36	chr10:89675600-89680400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr10:89675600-89681600	Weak transcription	Right Ventricle	heart
38	chr10:89675600-89681600	Weak transcription	HSMM	muscle
39	chr10:89675600-89681800	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr10:89675600-89682800	Weak transcription	Pancreas	Pancrea
41	chr10:89675600-89682800	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr10:89675600-89683800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr10:89675600-89685400	Weak transcription	Duodenum Mucosa	Duodenum
44	chr10:89675600-89686200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr10:89675600-89687200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr10:89675600-89705000	Weak transcription	Fetal Stomach	stomach
47	chr10:89675600-89705200	Weak transcription	Esophagus	oesophagus
48	chr10:89675800-89679400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
49	chr10:89675800-89682000	Weak transcription	Colon Smooth Muscle	Colon
50	chr10:89676000-89681400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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