Variant report

Variant	nsv948447
Chromosome Location	chr5:14771247-14852610
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:14773851-14775004	HepG2	liver:	n/a	n/a
2	ATF1	chr5:14788055-14788067	K562	blood:	n/a	n/a
3	ATF1	chr5:14809675-14810126	K562	blood:	n/a	n/a
4	ATF2	chr5:14809456-14810297	GM12878	blood:	n/a	n/a
5	ATF2	chr5:14809477-14810334	GM12878	blood:	n/a	n/a
6	ATF3	chr5:14826909-14827096	K562	blood:	n/a	n/a
7	ATF3	chr5:14809801-14810101	K562	blood:	n/a	n/a
8	ATF3	chr5:14809781-14809969	HepG2	liver:	n/a	n/a
9	BACH1	chr5:14838695-14838934	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:14778817-14779063	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr5:14809501-14810241	GM12878	blood:	n/a	chr5:14809913-14809924
12	BATF	chr5:14783795-14784174	GM12878	blood:	n/a	chr5:14784003-14784013 chr5:14784002-14784013
13	BATF	chr5:14783822-14784211	GM12878	blood:	n/a	chr5:14784003-14784013 chr5:14784002-14784013
14	BATF	chr5:14809485-14810280	GM12878	blood:	n/a	chr5:14809913-14809924
15	BCL11A	chr5:14809502-14809698	GM12878	blood:	n/a	n/a
16	BCL11A	chr5:14809744-14810217	GM12878	blood:	n/a	n/a
17	BCL11A	chr5:14809442-14810335	GM12878	blood:	n/a	n/a
18	BCL3	chr5:14809750-14810270	GM12878	blood:	n/a	n/a
19	BCL3	chr5:14809730-14810218	GM12878	blood:	n/a	n/a
20	BCLAF1	chr5:14809483-14810322	GM12878	blood:	n/a	n/a
21	BCLAF1	chr5:14809605-14810320	GM12878	blood:	n/a	n/a
22	BHLHE40	chr5:14809510-14810293	GM12878	blood:	n/a	n/a
23	BHLHE40	chr5:14809721-14810169	K562	blood:	n/a	n/a
24	BHLHE40	chr5:14842264-14842576	HepG2	liver:	n/a	n/a
25	CBX3	chr5:14809824-14810095	K562	blood:	n/a	n/a
26	CEBPB	chr5:14782712-14783041	IMR90	lung:	n/a	chr5:14782870-14782881 chr5:14782870-14782883 chr5:14782872-14782881 chr5:14782872-14782881 chr5:14782872-14782881 chr5:14782871-14782882 chr5:14782872-14782881 chr5:14782870-14782883
27	CEBPB	chr5:14817065-14817421	K562	blood:	n/a	chr5:14817209-14817220 chr5:14817236-14817249 chr5:14817237-14817248 chr5:14817236-14817247
28	CEBPB	chr5:14782706-14783061	A549	lung:	n/a	chr5:14782870-14782881 chr5:14782870-14782883 chr5:14782872-14782881 chr5:14782872-14782881 chr5:14782872-14782881 chr5:14782871-14782882 chr5:14782872-14782881 chr5:14782870-14782883
29	CEBPB	chr5:14809653-14810105	IMR90	lung:	n/a	n/a
30	CEBPB	chr5:14782709-14783049	Hela-S3	cervix:	n/a	chr5:14782870-14782881 chr5:14782870-14782883 chr5:14782872-14782881 chr5:14782872-14782881 chr5:14782872-14782881 chr5:14782871-14782882 chr5:14782872-14782881 chr5:14782870-14782883
31	CEBPB	chr5:14809789-14810209	GM12878	blood:	n/a	n/a
32	CEBPB	chr5:14785439-14785550	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr5:14782724-14783052	K562	blood:	n/a	chr5:14782870-14782881 chr5:14782870-14782883 chr5:14782872-14782881 chr5:14782872-14782881 chr5:14782872-14782881 chr5:14782871-14782882 chr5:14782872-14782881 chr5:14782870-14782883
34	CEBPB	chr5:14830069-14830156	K562	blood:	n/a	chr5:14830083-14830094 chr5:14830082-14830093 chr5:14830099-14830110
35	CEBPB	chr5:14817073-14817433	Hela-S3	cervix:	n/a	chr5:14817209-14817220 chr5:14817236-14817249 chr5:14817237-14817248 chr5:14817236-14817247
36	CEBPB	chr5:14843193-14843202	K562	blood:	n/a	n/a
37	CEBPB	chr5:14782728-14783061	MCF-7	breast:	n/a	chr5:14782870-14782881 chr5:14782870-14782883 chr5:14782872-14782881 chr5:14782872-14782881 chr5:14782872-14782881 chr5:14782871-14782882 chr5:14782872-14782881 chr5:14782870-14782883
38	CEBPB	chr5:14809739-14810088	HepG2	liver:	n/a	n/a
39	CEBPB	chr5:14774607-14774922	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:14777243-14777439	A549	lung:	n/a	chr5:14777345-14777356
41	CEBPB	chr5:14817070-14817416	A549	lung:	n/a	chr5:14817209-14817220 chr5:14817236-14817249 chr5:14817237-14817248 chr5:14817236-14817247
42	CEBPB	chr5:14817041-14817475	IMR90	lung:	n/a	chr5:14817209-14817220 chr5:14817236-14817249 chr5:14817237-14817248 chr5:14817236-14817247
43	CEBPB	chr5:14777297-14777434	HepG2	liver:	n/a	chr5:14777345-14777356
44	CEBPB	chr5:14809503-14810362	GM12878	blood:	n/a	n/a
45	CEBPB	chr5:14816969-14817538	A549	lung:	n/a	chr5:14817209-14817220 chr5:14817236-14817249 chr5:14817237-14817248 chr5:14817236-14817247
46	CEBPB	chr5:14812445-14812544	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr5:14817041-14817435	MCF-7	breast:	n/a	chr5:14817209-14817220 chr5:14817236-14817249 chr5:14817237-14817248 chr5:14817236-14817247
48	CEBPB	chr5:14782717-14783066	HepG2	liver:	n/a	chr5:14782870-14782881 chr5:14782870-14782883 chr5:14782872-14782881 chr5:14782872-14782881 chr5:14782872-14782881 chr5:14782871-14782882 chr5:14782872-14782881 chr5:14782870-14782883
49	CEBPB	chr5:14817034-14817407	A549	lung:	n/a	chr5:14817209-14817220 chr5:14817236-14817249 chr5:14817237-14817248 chr5:14817236-14817247
50	CEBPB	chr5:14809610-14810328	HCT-116	colon:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:14772977-14773027	HCF	heart:	n/a
2	chr5:14849935-14849985	HEK293	kidney:	embryo
3	chr5:14810180-14810230	HIPEpiC	eye:	n/a
4	chr5:14849935-14849985	HL-60	blood:	n/a
5	chr5:14848690-14848740	Caco-2	colon:	n/a
6	chr5:14848690-14848740	BJ	skin:	n/a
7	chr5:14779011-14779061	SK-N-SH	brain:	n/a
8	chr5:14810180-14810230	LNCaP	prostate:	n/a
9	chr5:14779011-14779061	Caco-2	colon:	n/a
10	chr5:14848758-14848808	HRCEpiC	kidney:	n/a
11	chr5:14848690-14848740	GM06990	blood:	n/a
12	chr5:14772977-14773027	Hela-S3	cervix:	n/a
13	chr5:14779011-14779061	GM12892	blood:	n/a
14	chr5:14848690-14848740	AG10803	skin:	n/a
15	chr5:14772977-14773027	AoSMC	blood vessel:	n/a
16	chr5:14848690-14848740	CMK	blood:	n/a
17	chr5:14772977-14773027	HepG2	liver:	n/a
18	chr5:14779011-14779061	HRPEpiC	eye:	n/a
19	chr5:14810180-14810230	MCF10A-Er-Src	breast:	n/a
20	chr5:14848758-14848808	HAEpiC	amniotic membrane:	n/a
21	chr5:14849935-14849985	BJ	skin:	n/a
22	chr5:14848690-14848740	GM12892	blood:	n/a
23	chr5:14779011-14779061	AG09309	skin:	n/a
24	chr5:14848690-14848740	A549	lung:	n/a
25	chr5:14816929-14816979	SK-N-MC	brain:	n/a
26	chr5:14848690-14848740	PANC-1	pancreas:	n/a
27	chr5:14849935-14849985	Caco-2	colon:	n/a
28	chr5:14848758-14848808	HEK293	kidney:	embryo
29	chr5:14816929-14816979	AG09319	gingival:	n/a
30	chr5:14849935-14849985	HRPEpiC	eye:	n/a
31	chr5:14772977-14773027	SK-N-MC	brain:	n/a
32	chr5:14849935-14849985	AoSMC	blood vessel:	n/a
33	chr5:14816929-14816979	A549	lung:	n/a
34	chr5:14848758-14848808	GM19239	blood:	n/a
35	chr5:14779011-14779061	Jurkat	blood:	n/a
36	chr5:14849935-14849985	SK-N-SH_RA	brain:	n/a
37	chr5:14772977-14773027	AG04450	lung:	fetal
38	chr5:14772977-14773027	HAEpiC	amniotic membrane:	n/a
39	chr5:14816929-14816979	HUVEC	blood vessel:	n/a
40	chr5:14772977-14773027	K562	blood:	n/a
41	chr5:14848758-14848808	AG04449	skin:	fetal
42	chr5:14848758-14848808	Jurkat	blood:	n/a
43	chr5:14816929-14816979	SKMC	muscle:	n/a
44	chr5:14810180-14810230	Caco-2	colon:	n/a
45	chr5:14816929-14816979	Jurkat	blood:	n/a
46	chr5:14772977-14773027	ECC-1	luminal epithelium:	n/a
47	chr5:14810180-14810230	HRE	kidney:	n/a
48	chr5:14848690-14848740	Hepatocyte	liver:	n/a
49	chr5:14779011-14779061	ProgFib	skin:	n/a
50	chr5:14848690-14848740	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:14783436..14785006-chr5:14787434..14790380,2	K562	blood:
2	chr5:14762511..14765018-chr5:14793298..14795761,2	K562	blood:
3	chr5:14807445..14808156-chr5:14864155..14865031,3	MCF-7	breast:
4	chr5:14727546..14728089-chr5:14778195..14778972,2	MCF-7	breast:
5	chr5:14774249..14779166-chr5:14785300..14788951,5	MCF-7	breast:
6	chr5:14796002..14798417-chr5:14798624..14800724,2	MCF-7	breast:
7	chr5:14815464..14817984-chr5:14822641..14824319,2	K562	blood:
8	chr5:14815464..14817984-chr5:14822641..14824319,2	K562	blood:
9	chr5:14796002..14798417-chr5:14798624..14800724,2	MCF-7	breast:
10	chr5:14851792..14853991-chr5:14869985..14871997,2	MCF-7	breast:
11	chr5:14788291..14790064-chr5:14792077..14794888,2	MCF-7	breast:
12	chr5:14850589..14853387-chr5:14861534..14863865,2	MCF-7	breast:
13	chr5:14803203..14805368-chr5:14807741..14809611,2	MCF-7	breast:
14	chr5:14768806..14770667-chr5:14771716..14774525,2	MCF-7	breast:
15	chr5:14826927..14829271-chr5:14829445..14831346,2	K562	blood:
16	chr5:14814901..14816441-chr5:14887392..14889230,2	K562	blood:
17	chr5:14807486..14808341-chr5:14864093..14865028,3	MCF-7	breast:
18	chr5:14803203..14805368-chr5:14807741..14809611,2	MCF-7	breast:
19	chr5:14809897..14811757-chr5:14812423..14814739,2	K562	blood:
20	chr5:14766810..14770157-chr5:14772222..14775732,5	K562	blood:
21	chr5:14727245..14728077-chr5:14778558..14779280,2	MCF-7	breast:
22	chr5:14789541..14791953-chr5:14870274..14872270,2	MCF-7	breast:
23	chr5:14809897..14811757-chr5:14812423..14814739,2	K562	blood:
24	chr5:14824343..14826536-chr5:14829301..14831889,2	MCF-7	breast:
25	chr5:14826927..14829271-chr5:14829445..14831346,2	K562	blood:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4637	chr5:14826041-14826062	MIMAT0019694

Variant related genes	Relation type
RBBP4P1	TF binding region
ANKH	TF binding region
MIR4637	TF binding region
RBBP4P1	CpG island
ANKH	CpG island
MIR4637	CpG island
ENSG00000154122	chromatin interactions
ENSG00000264792	chromatin interactions

Extended variants
information (count: 3037 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:3037 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17317417	chr5:14771247-14771248	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs139800096	chr5:14771289-14771290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575633391	chr5:14771358-14771359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs79555669	chr5:14771376-14771377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189565930	chr5:14771386-14771387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540147928	chr5:14771399-14771400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560917162	chr5:14771419-14771420	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs79449893	chr5:14771434-14771435	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546843768	chr5:14771516-14771517	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565235426	chr5:14771545-14771546	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543159479	chr5:14771561-14771562	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs376387620	chr5:14771585-14771586	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532882297	chr5:14771612-14771613	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550879393	chr5:14771620-14771621	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569465500	chr5:14771631-14771632	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182739424	chr5:14771641-14771642	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548323675	chr5:14771676-14771677	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566436387	chr5:14771686-14771687	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370413737	chr5:14771699-14771700	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs533771984	chr5:14771726-14771727	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143199357	chr5:14771757-14771758	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188259965	chr5:14771758-14771759	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192763967	chr5:14771808-14771809	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185227371	chr5:14771836-14771837	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs55791375	chr5:14771845-14771846	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs532273825	chr5:14771855-14771856	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576508193	chr5:14771866-14771867	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543887687	chr5:14771877-14771878	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377201660	chr5:14771922-14771923	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139420956	chr5:14771940-14771941	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565179593	chr5:14772020-14772021	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs139376697	chr5:14772030-14772031	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs547529021	chr5:14772039-14772040	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs201524735	chr5:14772040-14772041	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs200132168	chr5:14772041-14772042	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs565742888	chr5:14772043-14772044	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs58228373	chr5:14772044-14772045	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs28386788	chr5:14772045-14772046	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs377017231	chr5:14772046-14772047	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs113966843	chr5:14772048-14772049	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs28446763	chr5:14772052-14772053	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs375769817	chr5:14772053-14772054	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs377342657	chr5:14772055-14772056	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs200023808	chr5:14772056-14772057	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs55670675	chr5:14772057-14772058	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs28642095	chr5:14772058-14772059	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs2441202	chr5:14772062-14772063	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs28490001	chr5:14772064-14772065	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs187403857	chr5:14772076-14772077	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs56164585	chr5:14772133-14772134	Weak transcription Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	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
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	17643093	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	18940311	CNVD
Central neurocytomas	17123091	CNVD
Mental retardation	17847001	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	19546859	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Williams Syndrome	20824207	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Gastric cancer	17229543	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:2006 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14729200-14791000	Weak transcription	Small Intestine	intestine
2	chr5:14744600-14775800	Weak transcription	NH-A	brain
3	chr5:14744800-14776000	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr5:14746000-14790200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr5:14746200-14775800	Weak transcription	Spleen	Spleen
6	chr5:14746600-14776000	Weak transcription	Placenta	Placenta
7	chr5:14749000-14776000	Weak transcription	Esophagus	oesophagus
8	chr5:14751400-14775800	Weak transcription	Pancreas	Pancrea
9	chr5:14752200-14776600	Weak transcription	Stomach Smooth Muscle	stomach
10	chr5:14753400-14775600	Weak transcription	Lung	lung
11	chr5:14753400-14777000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr5:14753600-14790000	Weak transcription	Ovary	ovary
13	chr5:14753600-14801600	Weak transcription	Rectal Smooth Muscle	rectum
14	chr5:14753800-14775800	Weak transcription	Gastric	stomach
15	chr5:14756800-14779000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr5:14756800-14780200	Weak transcription	Fetal Stomach	stomach
17	chr5:14756800-14781200	Weak transcription	Thymus	Thymus
18	chr5:14757400-14775800	Weak transcription	HMEC	breast
19	chr5:14758800-14783800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr5:14759200-14790200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr5:14761000-14776000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr5:14761000-14777800	Weak transcription	HSMMtube	muscle
23	chr5:14761400-14772200	Weak transcription	Aorta	Aorta
24	chr5:14761400-14772200	Weak transcription	Right Ventricle	heart
25	chr5:14761400-14775800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr5:14761600-14772400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr5:14761600-14773800	Weak transcription	Fetal Heart	heart
28	chr5:14761600-14776000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr5:14761800-14772800	Weak transcription	Brain Anterior Caudate	brain
30	chr5:14763200-14771400	Weak transcription	Psoas Muscle	Psoas
31	chr5:14765200-14775800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr5:14766000-14773000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr5:14766600-14780000	Weak transcription	Fetal Intestine Large	intestine
34	chr5:14767400-14809800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr5:14768400-14776000	Weak transcription	Hela-S3	cervix
36	chr5:14768400-14789800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr5:14768600-14771600	Weak transcription	Brain Angular Gyrus	brain
38	chr5:14768600-14771600	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr5:14768600-14772200	Weak transcription	Brain Cingulate Gyrus	brain
40	chr5:14768600-14772600	Weak transcription	HepG2	liver
41	chr5:14768600-14773200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr5:14768600-14773600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr5:14768600-14773800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr5:14768600-14775600	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr5:14768600-14779400	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr5:14768600-14790000	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr5:14768600-14790200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr5:14768600-14790200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
49	chr5:14768600-14790200	Weak transcription	Dnd41	blood
50	chr5:14768800-14772400	Weak transcription	Brain Hippocampus Middle	brain

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