Variant report

Variant	nsv524075
Chromosome Location	chr5:36156782-36158394
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:36)
CpG islands
(count:62)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:36 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:36156729-36156961	HepG2	liver:	n/a	n/a
2	EP300	chr5:36157701-36158776	SK-N-SH_RA	brain:	n/a	chr5:36158707-36158720 chr5:36158685-36158699
3	EP300	chr5:36158018-36158825	SK-N-SH_RA	brain:	n/a	chr5:36158707-36158720 chr5:36158685-36158699
4	EP300	chr5:36158010-36158824	SK-N-SH	brain:	n/a	chr5:36158707-36158720 chr5:36158685-36158699
5	EP300	chr5:36155969-36159687	SK-N-SH	brain:	n/a	chr5:36157593-36157603 chr5:36158707-36158720 chr5:36158685-36158699
6	FOXP2	chr5:36158288-36158704	SK-N-MC	brain:	n/a	n/a
7	GATA2	chr5:36158000-36159146	SH-SY5Y	brain:	n/a	chr5:36158899-36158910
8	GATA3	chr5:36158062-36158875	SK-N-SH	brain:	n/a	n/a
9	GATA3	chr5:36157753-36158830	SK-N-SH	brain:	n/a	n/a
10	MAFF	chr5:36156830-36157178	HepG2	liver:	n/a	n/a
11	MAFK	chr5:36156831-36157151	HepG2	liver:	n/a	n/a
12	MAFK	chr5:36156867-36157179	Hela-S3	cervix:	n/a	n/a
13	MAFK	chr5:36156508-36157230	IMR90	lung:	n/a	n/a
14	MAFK	chr5:36156825-36157233	HepG2	liver:	n/a	n/a
15	NFIC	chr5:36158104-36158867	SK-N-SH	brain:	n/a	n/a
16	PBX3	chr5:36158160-36158834	SK-N-SH	brain:	n/a	chr5:36158725-36158736
17	PBX3	chr5:36158089-36158812	SK-N-SH	brain:	n/a	chr5:36158725-36158736
18	POLR2A	chr5:36157607-36157662	HUVEC	blood vessel:	n/a	n/a
19	POLR2A	chr5:36158282-36158700	SK-N-SH	brain:	n/a	n/a
20	POLR2A	chr5:36156770-36156796	K562	blood:	n/a	n/a
21	POLR2A	chr5:36158103-36158777	SK-N-SH	brain:	n/a	n/a
22	RAD21	chr5:36158133-36158743	SK-N-SH_RA	brain:	n/a	chr5:36158501-36158515
23	RAD21	chr5:36158063-36158742	SK-N-SH_RA	brain:	n/a	chr5:36158501-36158515
24	REST	chr5:36158313-36158615	SK-N-SH	brain:	n/a	chr5:36158514-36158523 chr5:36158510-36158523
25	REST	chr5:36158174-36158616	SK-N-SH	brain:	n/a	chr5:36158514-36158523 chr5:36158510-36158523
26	SIN3AK20	chr5:36158073-36158661	SK-N-SH	brain:	n/a	n/a
27	SPI1	chr5:36157548-36157874	HL-60	blood:	n/a	chr5:36157637-36157644
28	TBL1XR1	chr5:36157515-36157545	K562	blood:	n/a	n/a
29	TCF12	chr5:36158010-36158797	SK-N-SH	brain:	n/a	n/a
30	TCF12	chr5:36157874-36158878	SK-N-SH	brain:	n/a	n/a
31	TEAD4	chr5:36158131-36158767	SK-N-SH	brain:	n/a	n/a
32	TEAD4	chr5:36157986-36158737	SK-N-SH	brain:	n/a	n/a
33	USF1	chr5:36158388-36158688	SK-N-SH_RA	brain:	n/a	n/a
34	USF1	chr5:36158305-36158702	SK-N-SH_RA	brain:	n/a	n/a
35	YY1	chr5:36158077-36158737	SK-N-SH_RA	brain:	n/a	n/a
36	YY1	chr5:36158070-36158747	SK-N-SH_RA	brain:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:36157329-36157379	HNPCEpiC	eye:	n/a
2	chr5:36157329-36157379	HNPCEpiC	eye:	n/a
3	chr5:36157329-36157379	PFSK-1	brain:	n/a
4	chr5:36157329-36157379	Caco-2	colon:	n/a
5	chr5:36157329-36157379	HIPEpiC	eye:	n/a
6	chr5:36157329-36157379	AG09319	gingival:	n/a
7	chr5:36157329-36157379	RPTEC	kidney:	n/a
8	chr5:36157329-36157379	NB4	blood:	n/a
9	chr5:36157329-36157379	HRCEpiC	kidney:	n/a
10	chr5:36157329-36157379	HPAEpiC	pulmonary alveolar:	n/a
11	chr5:36157329-36157379	BE2_C	brain:	n/a
12	chr5:36157329-36157379	H1-hESC	embryonic stem cell:	embryo
13	chr5:36157329-36157379	HCF	heart:	n/a
14	chr5:36157329-36157379	AG04450	lung:	fetal
15	chr5:36157329-36157379	GM12878	blood:	n/a
16	chr5:36157329-36157379	GM12891	blood:	n/a
17	chr5:36157329-36157379	NHBE	bronchial:	n/a
18	chr5:36157329-36157379	GM19239	blood:	n/a
19	chr5:36157329-36157379	GM12892	blood:	n/a
20	chr5:36157329-36157379	HAEpiC	amniotic membrane:	n/a
21	chr5:36157329-36157379	NHDF-neo	bronchial:	n/a
22	chr5:36157329-36157379	T-47D	breast:	n/a
23	chr5:36157329-36157379	ECC-1	luminal epithelium:	n/a
24	chr5:36157329-36157379	HEEpiC	esophagus:	n/a
25	chr5:36157329-36157379	CMK	blood:	n/a
26	chr5:36157329-36157379	MCF10A-Er-Src	breast:	n/a
27	chr5:36157329-36157379	SK-N-SH_RA	brain:	n/a
28	chr5:36157329-36157379	HRPEpiC	eye:	n/a
29	chr5:36157329-36157379	K562	blood:	n/a
30	chr5:36157329-36157379	HCPEpiC	choroid plexus:	n/a
31	chr5:36157329-36157379	Hepatocyte	liver:	n/a
32	chr5:36157329-36157379	AoSMC	blood vessel:	n/a
33	chr5:36157329-36157379	PrEC	prostate:	n/a
34	chr5:36157329-36157379	AG10803	skin:	n/a
35	chr5:36157329-36157379	Jurkat	blood:	n/a
36	chr5:36157329-36157379	SK-N-MC	brain:	n/a
37	chr5:36157329-36157379	SKMC	muscle:	n/a
38	chr5:36157329-36157379	HepG2	liver:	n/a
39	chr5:36157329-36157379	AG04449	skin:	fetal
40	chr5:36157329-36157379	HMEC	breast:	n/a
41	chr5:36157329-36157379	LNCaP	prostate:	n/a
42	chr5:36157329-36157379	HUVEC	blood vessel:	n/a
43	chr5:36157329-36157379	SK-N-SH	brain:	n/a
44	chr5:36157329-36157379	NH-A	brain:	n/a
45	chr5:36157329-36157379	SAEC	small airway:	n/a
46	chr5:36157329-36157379	HCT-116	colon:	n/a
47	chr5:36157329-36157379	MCF-7	breast:	n/a
48	chr5:36157329-36157379	HEK293	kidney:	embryo
49	chr5:36157329-36157379	BJ	skin:	n/a
50	chr5:36157329-36157379	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:36149758..36152986-chr5:36154099..36157491,3	MCF-7	breast:
2	chr5:36150277..36153703-chr5:36154371..36162094,13	K562	blood:
3	chr5:36151610..36154488-chr5:36157527..36159493,2	MCF-7	breast:

No data

Variant related genes	Relation type
LMBRD2	TF binding region
LMBRD2	CpG island
ENSG00000164187	chromatin interactions
ENSG00000145604	chromatin interactions

Extended variants
information (count: 53 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:53 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3804446	chr5:36156782-36156783	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560754799	chr5:36156798-36156799	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs113699621	chr5:36156803-36156804	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs549529224	chr5:36156860-36156861	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs559424582	chr5:36156864-36156865	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs569262388	chr5:36156895-36156896	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs527881957	chr5:36156916-36156917	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs538285410	chr5:36156957-36156958	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs185200465	chr5:36156964-36156965	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs375321473	chr5:36157003-36157004	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs561524146	chr5:36157027-36157028	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs145392984	chr5:36157074-36157075	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs534101518	chr5:36157124-36157125	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs543809369	chr5:36157167-36157168	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs369602857	chr5:36157179-36157180	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs530420915	chr5:36157203-36157204	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs550119545	chr5:36157237-36157238	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs5867305	chr5:36157262-36157263	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs67655181	chr5:36157263-36157264	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs573800579	chr5:36157288-36157289	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs4440390	chr5:36157330-36157331	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs148293648	chr5:36157334-36157335	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs575621778	chr5:36157344-36157345	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs544651330	chr5:36157397-36157398	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs79332724	chr5:36157488-36157489	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs79615338	chr5:36157490-36157491	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs35440361	chr5:36157523-36157524	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs541512455	chr5:36157548-36157549	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs386687209	chr5:36157599-36157600	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs113013822	chr5:36157600-36157601	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs464812	chr5:36157601-36157602	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs555284130	chr5:36157640-36157641	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs540945326	chr5:36157641-36157642	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs76812715	chr5:36157697-36157698	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs554349527	chr5:36157730-36157731	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs3804445	chr5:36157737-36157738	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs3804444	chr5:36157742-36157743	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs3804443	chr5:36157812-36157813	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs33678	chr5:36157815-36157816	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs33679	chr5:36157963-36157964	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs377593873	chr5:36157976-36157977	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs141433621	chr5:36157990-36157991	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs146270029	chr5:36158032-36158033	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs150787655	chr5:36158082-36158083	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs528380310	chr5:36158153-36158154	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs567331732	chr5:36158187-36158188	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs536081519	chr5:36158191-36158192	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs189605880	chr5:36158218-36158219	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs575685351	chr5:36158228-36158229	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs139459338	chr5:36158280-36158281	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	21147910	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36153200-36157400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr5:36153200-36157600	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr5:36153200-36158000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:36153200-36160800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:36153200-36164000	Weak transcription	Colonic Mucosa	Colon
6	chr5:36153400-36156800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr5:36153400-36156800	Transcr. at gene 5' and 3'	Fetal Muscle Trunk	muscle
8	chr5:36153600-36157400	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr5:36153600-36159000	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:36153800-36158400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr5:36153800-36159000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr5:36153800-36160800	Weak transcription	Gastric	stomach
13	chr5:36153800-36162600	Strong transcription	H9 Cell Line	embryonic stem cell
14	chr5:36153800-36164000	Weak transcription	Pancreas	Pancrea
15	chr5:36153800-36184400	Strong transcription	HUES64 Cell Line	embryonic stem cell
16	chr5:36154000-36156800	Genic enhancers	Fetal Intestine Small	intestine
17	chr5:36154000-36158000	Strong transcription	Brain Inferior Temporal Lobe	brain
18	chr5:36154000-36158400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr5:36154000-36159600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr5:36154000-36160600	Weak transcription	Stomach Mucosa	stomach
21	chr5:36154000-36162000	Genic enhancers	HepG2	liver
22	chr5:36154000-36162600	Genic enhancers	Fetal Intestine Large	intestine
23	chr5:36154000-36168200	Strong transcription	Primary T cells from cord blood	blood
24	chr5:36154000-36168200	Weak transcription	Rectal Smooth Muscle	rectum
25	chr5:36154000-36175400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
26	chr5:36154000-36175600	Strong transcription	H1 Cell Line	embryonic stem cell
27	chr5:36154000-36175600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:36154000-36184200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr5:36154200-36156800	Strong transcription	Primary hematopoietic stem cells	blood
30	chr5:36154200-36157200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr5:36154200-36158800	Weak transcription	Duodenum Mucosa	Duodenum
32	chr5:36154200-36168400	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr5:36154200-36179000	Strong transcription	A549	lung
34	chr5:36154200-36184400	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr5:36154200-36184400	Strong transcription	Fetal Thymus	thymus
36	chr5:36154400-36157200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr5:36154400-36157400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr5:36154400-36157400	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr5:36154400-36157600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr5:36154400-36158800	Genic enhancers	Muscle Satellite Cultured Cells	--
41	chr5:36154400-36159000	Genic enhancers	Fetal Brain Female	brain
42	chr5:36154400-36159200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr5:36154400-36162400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr5:36154400-36164800	Strong transcription	Cortex derived primary cultured neurospheres	brain
45	chr5:36154400-36175000	Strong transcription	Primary B cells from peripheral blood	blood
46	chr5:36154400-36175200	Strong transcription	Thymus	Thymus
47	chr5:36154400-36184400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
48	chr5:36154400-36210800	Weak transcription	Small Intestine	intestine
49	chr5:36154600-36157400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr5:36154600-36157800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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