Variant report

Variant	nsv830413
Chromosome Location	chr5:96450582-96509294
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:939)
CpG islands
(count:549)
Chromatin interactive
region (count:44)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:939 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:96465539-96465890	K562	blood:	n/a	n/a
2	ATF1	chr5:96466940-96467134	K562	blood:	n/a	n/a
3	ATF1	chr5:96463534-96463724	K562	blood:	n/a	n/a
4	ATF2	chr5:96503022-96503427	GM12878	blood:	n/a	n/a
5	ATF2	chr5:96503064-96503603	GM12878	blood:	n/a	n/a
6	ATF2	chr5:96470286-96470816	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr5:96485448-96485735	K562	blood:	n/a	n/a
8	BATF	chr5:96503162-96503595	GM12878	blood:	n/a	chr5:96503383-96503394
9	BATF	chr5:96503177-96503536	GM12878	blood:	n/a	chr5:96503383-96503394
10	BCL11A	chr5:96470502-96470707	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr5:96470396-96470707	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCLAF1	chr5:96503107-96503654	GM12878	blood:	n/a	n/a
13	CBX3	chr5:96493412-96493733	K562	blood:	n/a	n/a
14	CBX3	chr5:96493401-96493849	HCT-116	colon:	n/a	n/a
15	CBX3	chr5:96493372-96493804	K562	blood:	n/a	n/a
16	CCNT2	chr5:96499379-96499468	K562	blood:	n/a	n/a
17	CCNT2	chr5:96497890-96498055	K562	blood:	n/a	n/a
18	CCNT2	chr5:96498838-96498954	K562	blood:	n/a	n/a
19	CEBPB	chr5:96485406-96485752	HepG2	liver:	n/a	chr5:96485581-96485592
20	CEBPB	chr5:96485406-96485773	IMR90	lung:	n/a	chr5:96485581-96485592
21	CEBPB	chr5:96500583-96500873	IMR90	lung:	n/a	n/a
22	CEBPB	chr5:96485434-96485660	K562	blood:	n/a	chr5:96485581-96485592
23	CEBPB	chr5:96500665-96500821	A549	lung:	n/a	n/a
24	CEBPB	chr5:96485462-96485733	K562	blood:	n/a	chr5:96485581-96485592
25	CEBPB	chr5:96485429-96485757	A549	lung:	n/a	chr5:96485581-96485592
26	CEBPB	chr5:96485430-96485730	Hela-S3	cervix:	n/a	chr5:96485581-96485592
27	CEBPB	chr5:96485403-96485775	K562	blood:	n/a	chr5:96485581-96485592
28	CEBPB	chr5:96485518-96485718	H1-hESC	embryonic stem cell:	n/a	chr5:96485581-96485592
29	CEBPB	chr5:96498422-96498631	A549	lung:	n/a	n/a
30	CEBPB	chr5:96500572-96500849	Hela-S3	cervix:	n/a	n/a
31	CHD1	chr5:96478357-96478799	IMR90	lung:	n/a	n/a
32	CHD1	chr5:96503652-96503697	GM12878	blood:	n/a	n/a
33	CHD1	chr5:96503008-96503369	GM12878	blood:	n/a	n/a
34	CHD2	chr5:96470366-96470872	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr5:96503118-96503458	GM12878	blood:	n/a	n/a
36	CREB1	chr5:96503023-96503523	GM12878	blood:	n/a	n/a
37	CREB1	chr5:96502889-96503626	GM12878	blood:	n/a	n/a
38	CTCF	chr5:96478444-96478637	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr5:96497720-96497870	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr5:96470480-96470630	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr5:96470560-96470710	HepG2	liver:	n/a	n/a
42	CTCF	chr5:96478338-96478746	IMR90	lung:	n/a	n/a
43	CTCF	chr5:96478442-96478672	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr5:96497780-96497930	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr5:96498809-96499546	SK-N-SH	brain:	n/a	chr5:96499153-96499169 chr5:96499147-96499168 chr5:96499152-96499170 chr5:96499159-96499166
46	CTCF	chr5:96497800-96497950	GM12801	blood:	n/a	n/a
47	CTCF	chr5:96499016-96499368	Spleen_OC	spleen:	n/a	chr5:96499153-96499169 chr5:96499147-96499168 chr5:96499152-96499170 chr5:96499159-96499166
48	CTCF	chr5:96499036-96499286	Kidney_OC	kidney:	n/a	chr5:96499153-96499169 chr5:96499147-96499168 chr5:96499152-96499170 chr5:96499159-96499166
49	CTCF	chr5:96478400-96478550	HCT-116	colon:	n/a	n/a
50	CTCF	chr5:96497780-96497930	MCF-7	breast:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:96478573-96478623	PANC-1	pancreas:	n/a
2	chr5:96478514-96478564	NB4	blood:	n/a
3	chr5:96478495-96478545	NH-A	brain:	n/a
4	chr5:96477502-96477552	HCF	heart:	n/a
5	chr5:96477502-96477552	HepG2	liver:	n/a
6	chr5:96471792-96471842	HEK293	kidney:	embryo
7	chr5:96478573-96478623	HCF	heart:	n/a
8	chr5:96478573-96478623	HEK293	kidney:	embryo
9	chr5:96477502-96477552	RPTEC	kidney:	n/a
10	chr5:96471792-96471842	H1-hESC	embryonic stem cell:	embryo
11	chr5:96478495-96478545	AG04450	lung:	fetal
12	chr5:96479253-96479303	HEEpiC	esophagus:	n/a
13	chr5:96479253-96479303	K562	blood:	n/a
14	chr5:96479353-96479403	AG09319	gingival:	n/a
15	chr5:96479253-96479303	HIPEpiC	eye:	n/a
16	chr5:96478495-96478545	RPTEC	kidney:	n/a
17	chr5:96497888-96497938	BJ	skin:	n/a
18	chr5:96497888-96497938	HCT-116	colon:	n/a
19	chr5:96478514-96478564	HCM	heart:	n/a
20	chr5:96471792-96471842	PANC-1	pancreas:	n/a
21	chr5:96478495-96478545	HRE	kidney:	n/a
22	chr5:96471792-96471842	U87	brain:	n/a
23	chr5:96479253-96479303	Caco-2	colon:	n/a
24	chr5:96478514-96478564	NHBE	bronchial:	n/a
25	chr5:96497888-96497938	MCF10A-Er-Src	breast:	n/a
26	chr5:96479353-96479403	AG04450	lung:	fetal
27	chr5:96479353-96479403	PrEC	prostate:	n/a
28	chr5:96471792-96471842	HPAEpiC	pulmonary alveolar:	n/a
29	chr5:96452274-96452324	AG09319	gingival:	n/a
30	chr5:96478514-96478564	HRE	kidney:	n/a
31	chr5:96479353-96479403	HepG2	liver:	n/a
32	chr5:96452274-96452324	HIPEpiC	eye:	n/a
33	chr5:96471792-96471842	SK-N-SH_RA	brain:	n/a
34	chr5:96452274-96452324	SAEC	small airway:	n/a
35	chr5:96452274-96452324	NH-A	brain:	n/a
36	chr5:96479353-96479403	SK-N-MC	brain:	n/a
37	chr5:96479253-96479303	Hepatocyte	liver:	n/a
38	chr5:96452274-96452324	HepG2	liver:	n/a
39	chr5:96478495-96478545	Jurkat	blood:	n/a
40	chr5:96497888-96497938	H1-hESC	embryonic stem cell:	embryo
41	chr5:96479353-96479403	AG10803	skin:	n/a
42	chr5:96471792-96471842	GM12878	blood:	n/a
43	chr5:96452274-96452324	AG04449	skin:	fetal
44	chr5:96479353-96479403	A549	lung:	n/a
45	chr5:96497888-96497938	PFSK-1	brain:	n/a
46	chr5:96497888-96497938	HEK293	kidney:	embryo
47	chr5:96471792-96471842	LNCaP	prostate:	n/a
48	chr5:96479253-96479303	U87	brain:	n/a
49	chr5:96477502-96477552	HUVEC	blood vessel:	n/a
50	chr5:96478514-96478564	AG04450	lung:	fetal

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:96087839..96088456-chr5:96497483..96498165,2	MCF-7	breast:
2	chr5:96360377..96362346-chr5:96465459..96468207,2	MCF-7	breast:
3	chr5:96447147..96449161-chr5:96455236..96457694,2	K562	blood:
4	chr5:96505549..96507976-chr5:96519747..96521338,2	MCF-7	breast:
5	chr5:96381504..96384488-chr5:96474189..96476207,2	K562	blood:
6	chr5:96087099..96087726-chr5:96498883..96499456,2	MCF-7	breast:
7	chr5:96078120..96080024-chr5:96498248..96500707,2	K562	blood:
8	chr5:96422481..96423221-chr5:96497763..96498668,2	K562	blood:
9	chr5:96461333..96463342-chr5:96466148..96468249,2	K562	blood:
10	chr5:96507787..96509709-chr5:96511038..96513163,2	K562	blood:
11	chr5:96089762..96090275-chr5:96497777..96498553,2	K562	blood:
12	chr5:96087427..96088455-chr5:96497429..96498297,3	MCF-7	breast:
13	chr5:96484050..96486367-chr5:96488023..96491599,3	K562	blood:
14	chr5:95680165..95680955-chr5:96498665..96499236,2	K562	blood:
15	chr5:96484050..96486367-chr5:96488023..96491599,3	K562	blood:
16	chr5:96423649..96425360-chr5:96459657..96461691,2	K562	blood:
17	chr5:96087837..96088851-chr5:96497370..96499403,9	K562	blood:
18	chr5:96452324..96455301-chr5:96461206..96463835,3	K562	blood:
19	chr5:96381723..96383480-chr5:96500362..96502420,2	K562	blood:
20	chr5:96496779..96498459-chr5:96502787..96504322,2	K562	blood:
21	chr5:96496426..96497975-chr5:96509660..96511880,2	K562	blood:
22	chr5:96087835..96088823-chr5:96498655..96499598,4	MCF-7	breast:
23	chr5:96469286..96471593-chr5:96474372..96477073,2	K562	blood:
24	chr5:96351534..96353188-chr5:96493803..96496020,2	K562	blood:
25	chr5:96447006..96449161-chr5:96454353..96456736,3	K562	blood:
26	chr5:96454080..96455959-chr5:96463185..96466174,2	MCF-7	breast:
27	chr5:96270867..96272370-chr5:96475978..96478536,2	MCF-7	breast:
28	chr5:96379467..96380324-chr5:96497473..96498285,2	MCF-7	breast:
29	chr5:96203527..96205559-chr5:96508441..96510333,2	K562	blood:
30	chr5:96503041..96507630-chr5:96507953..96511468,4	K562	blood:
31	chr5:96332674..96333555-chr5:96497655..96498457,3	K562	blood:
32	chr5:96414990..96416706-chr5:96466146..96468878,2	MCF-7	breast:
33	chr5:96461333..96463342-chr5:96466148..96468249,2	K562	blood:
34	chr5:95949882..95950863-chr5:96497777..96498341,2	K562	blood:
35	chr5:96508014..96513294-chr5:96513654..96520413,9	K562	blood:
36	chr5:96469286..96471593-chr5:96474372..96477073,2	K562	blood:
37	chr5:96504565..96506934-chr5:96511490..96513264,2	K562	blood:
38	chr5:96449374..96451547-chr5:96453007..96458409,4	K562	blood:
39	chr5:96332659..96333410-chr5:96497323..96498128,4	MCF-7	breast:
40	chr5:96452324..96455301-chr5:96461206..96463835,3	K562	blood:
41	chr5:96271154..96273754-chr5:96462535..96464231,2	K562	blood:
42	chr5:96454080..96455959-chr5:96463185..96466174,2	MCF-7	breast:
43	chr5:96425765..96427339-chr5:96454933..96458511,3	K562	blood:
44	chr5:96449374..96451547-chr5:96453007..96458409,4	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RIOK2	hsa-miR-101-3p	chr5:96498716-96498737
2	RIOK2	hsa-miR-155-5p	chr5:96498413-96498438

Variant related genes	Relation type
LIX1	TF binding region
RIOK2	TF binding region
LIX1	CpG island
RIOK2	CpG island
ENSG00000251606	chromatin interactions
ENSG00000249180	chromatin interactions
ENSG00000251513	chromatin interactions
ENSG00000113441	chromatin interactions
ENSG00000153113	chromatin interactions
ENSG00000206698	chromatin interactions
ENSG00000247121	chromatin interactions
ENSG00000058729	chromatin interactions

Extended variants
information (count: 2114 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2114 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76638491	chr5:96450605-96450606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115387123	chr5:96450606-96450607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs556848023	chr5:96450633-96450634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575050412	chr5:96450700-96450701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147179258	chr5:96450709-96450710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554510404	chr5:96450711-96450712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573272858	chr5:96450715-96450716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575513050	chr5:96450771-96450772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148636379	chr5:96450781-96450782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs565244334	chr5:96450829-96450830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544050747	chr5:96450873-96450874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs532558226	chr5:96451026-96451027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183925775	chr5:96451065-96451066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563170787	chr5:96451174-96451175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188925806	chr5:96451222-96451223	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs141156875	chr5:96451225-96451226	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs75681564	chr5:96451229-96451230	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs79444362	chr5:96451294-96451295	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs546308374	chr5:96451313-96451314	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs570871658	chr5:96451369-96451370	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs538252949	chr5:96451385-96451386	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs549292836	chr5:96451394-96451395	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs140144197	chr5:96451407-96451408	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs61659537	chr5:96451412-96451413	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs139211994	chr5:96451416-96451417	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs60482981	chr5:96451417-96451418	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs554659065	chr5:96451460-96451461	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs35264000	chr5:96451461-96451462	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs554728254	chr5:96451475-96451476	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs367720649	chr5:96451497-96451498	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs561664053	chr5:96451564-96451565	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs540690143	chr5:96451603-96451604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs527555474	chr5:96451661-96451662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144131880	chr5:96451697-96451698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs544605955	chr5:96451765-96451766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562902408	chr5:96451777-96451778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34918010	chr5:96451811-96451812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540371545	chr5:96451822-96451823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575051934	chr5:96451854-96451855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560187421	chr5:96451887-96451888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs560704522	chr5:96451888-96451889	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs527892958	chr5:96451925-96451926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546244943	chr5:96451928-96451929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191349841	chr5:96451947-96451948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs316217	chr5:96451980-96451981	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs550147453	chr5:96451997-96451998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547353727	chr5:96451999-96452000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs7707850	chr5:96452007-96452008	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs548197544	chr5:96452008-96452009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372333201	chr5:96452020-96452021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1006 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96438600-96454800	Weak transcription	Brain Hippocampus Middle	brain
2	chr5:96442400-96460200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr5:96444200-96454000	Weak transcription	Primary B cells from peripheral blood	blood
4	chr5:96446000-96453800	Weak transcription	Primary B cells from cord blood	blood
5	chr5:96447600-96454000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr5:96447800-96451000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr5:96447800-96451600	Weak transcription	Brain Germinal Matrix	brain
8	chr5:96447800-96453200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr5:96448000-96459600	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr5:96448000-96460000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr5:96448000-96465800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:96448800-96452400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr5:96448800-96453400	Weak transcription	Fetal Muscle Leg	muscle
14	chr5:96449000-96451600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr5:96449000-96454800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:96449000-96463400	Weak transcription	Brain Anterior Caudate	brain
17	chr5:96450200-96451400	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr5:96450200-96452800	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr5:96451000-96451200	Enhancers	Fetal Heart	heart
20	chr5:96451000-96452200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr5:96451200-96451600	Flanking Active TSS	Fetal Heart	heart
22	chr5:96451400-96452200	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr5:96451600-96452000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr5:96451600-96452200	Enhancers	Brain Germinal Matrix	brain
25	chr5:96451600-96453200	Enhancers	Fetal Heart	heart
26	chr5:96451600-96454400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr5:96452200-96452400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr5:96452200-96453000	Weak transcription	Brain Germinal Matrix	brain
29	chr5:96452400-96453200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr5:96452800-96454600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr5:96453000-96453200	Enhancers	Brain Germinal Matrix	brain
32	chr5:96453200-96453400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr5:96453200-96453600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr5:96453200-96453600	Weak transcription	Brain Germinal Matrix	brain
35	chr5:96453200-96454600	Weak transcription	Fetal Heart	heart
36	chr5:96453400-96455400	Enhancers	Fetal Muscle Leg	muscle
37	chr5:96453600-96453800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr5:96453600-96454200	Enhancers	Brain Germinal Matrix	brain
39	chr5:96453600-96455000	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr5:96453800-96454600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr5:96453800-96454600	Enhancers	GM12878-XiMat	blood
42	chr5:96453800-96455000	Enhancers	Primary B cells from cord blood	blood
43	chr5:96454000-96454200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr5:96454000-96455000	Enhancers	Brain Substantia Nigra	brain
45	chr5:96454000-96455200	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr5:96454000-96455400	Enhancers	Primary B cells from peripheral blood	blood
47	chr5:96454200-96454800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr5:96454400-96454800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr5:96454400-96455400	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr5:96454600-96454800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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