Variant report

Variant	nsv517049
Chromosome Location	chr5:90003131-90262475
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2617)
CpG islands
(count:549)
Chromatin interactive
region (count:243)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2617 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:90009369-90009462	K562	blood:	n/a	n/a
2	ARID3A	chr5:90206923-90207944	HepG2	liver:	n/a	chr5:90207495-90207511
3	ARID3A	chr5:90261062-90261124	K562	blood:	n/a	n/a
4	ARID3A	chr5:90197091-90197433	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:90003713-90003798	K562	blood:	n/a	n/a
6	ARID3A	chr5:90230187-90230369	K562	blood:	n/a	n/a
7	ARID3A	chr5:90162128-90163576	HepG2	liver:	n/a	chr5:90162475-90162491 chr5:90162476-90162492
8	ARID3A	chr5:90212860-90212970	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:90194700-90195645	HepG2	liver:	n/a	n/a
10	ARID3A	chr5:90184275-90184537	K562	blood:	n/a	n/a
11	ARID3A	chr5:90210840-90211953	HepG2	liver:	n/a	n/a
12	ARID3A	chr5:90227845-90228288	HepG2	liver:	n/a	n/a
13	ARID3A	chr5:90005141-90005474	K562	blood:	n/a	n/a
14	ARID3A	chr5:90162160-90162498	K562	blood:	n/a	chr5:90162475-90162491 chr5:90162476-90162492
15	ARID3A	chr5:90079524-90079811	K562	blood:	n/a	n/a
16	ARID3A	chr5:90245526-90246112	HepG2	liver:	n/a	n/a
17	ARID3A	chr5:90184320-90184992	HepG2	liver:	n/a	n/a
18	ATF1	chr5:90162183-90162383	K562	blood:	n/a	n/a
19	ATF1	chr5:90057649-90057656	K562	blood:	n/a	n/a
20	ATF2	chr5:90245438-90245964	GM12878	blood:	n/a	n/a
21	ATF3	chr5:90227822-90228413	A549	lung:	n/a	n/a
22	BACH1	chr5:90043108-90043170	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr5:90036137-90036320	K562	blood:	n/a	n/a
24	BATF	chr5:90139293-90139576	GM12878	blood:	n/a	chr5:90139462-90139473
25	BATF	chr5:90005602-90005915	GM12878	blood:	n/a	n/a
26	BATF	chr5:90245542-90245849	GM12878	blood:	n/a	chr5:90245689-90245699 chr5:90245685-90245695
27	BATF	chr5:90005582-90005917	GM12878	blood:	n/a	n/a
28	BATF	chr5:90139290-90139599	GM12878	blood:	n/a	chr5:90139462-90139473
29	BATF	chr5:90245562-90245948	GM12878	blood:	n/a	chr5:90245689-90245699 chr5:90245685-90245695
30	BCL11A	chr5:90245586-90245830	GM12878	blood:	n/a	n/a
31	BCL3	chr5:90162692-90163515	A549	lung:	n/a	chr5:90162899-90162906
32	BCL3	chr5:90194750-90195316	A549	lung:	n/a	n/a
33	BCL3	chr5:90245397-90245975	A549	lung:	n/a	n/a
34	BCL3	chr5:90184120-90185126	A549	lung:	n/a	chr5:90184818-90184827 chr5:90184817-90184826
35	BCLAF1	chr5:90139329-90139633	GM12878	blood:	n/a	n/a
36	BHLHE40	chr5:90005339-90005398	K562	blood:	n/a	n/a
37	BHLHE40	chr5:90148737-90148775	K562	blood:	n/a	n/a
38	BHLHE40	chr5:90174055-90174180	K562	blood:	n/a	n/a
39	BHLHE40	chr5:90184515-90184606	HepG2	liver:	n/a	n/a
40	BHLHE40	chr5:90245630-90245847	HepG2	liver:	n/a	n/a
41	BHLHE40	chr5:90036161-90036469	K562	blood:	n/a	n/a
42	BHLHE40	chr5:90236516-90236728	GM12878	blood:	n/a	n/a
43	BHLHE40	chr5:90121660-90121705	GM12878	blood:	n/a	n/a
44	BHLHE40	chr5:90245564-90245856	GM12878	blood:	n/a	n/a
45	BHLHE40	chr5:90226805-90226844	K562	blood:	n/a	n/a
46	BHLHE40	chr5:90139361-90139665	GM12878	blood:	n/a	n/a
47	BRCA1	chr5:90079672-90079809	HepG2	liver:	n/a	n/a
48	BRCA1	chr5:90260989-90261559	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr5:90098539-90098758	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr5:90005179-90005502	H1-hESC	embryonic stem cell:	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	chr5:90076860-90076910	HAEpiC	amniotic membrane:	n/a
2	chr5:90172358-90172408	HCPEpiC	choroid plexus:	n/a
3	chr5:90225181-90225231	SK-N-SH	brain:	n/a
4	chr5:90075932-90075982	GM12892	blood:	n/a
5	chr5:90172358-90172408	LNCaP	prostate:	n/a
6	chr5:90185030-90185080	HCM	heart:	n/a
7	chr5:90236557-90236607	H1-hESC	embryonic stem cell:	embryo
8	chr5:90236557-90236607	PrEC	prostate:	n/a
9	chr5:90236557-90236607	AoSMC	blood vessel:	n/a
10	chr5:90185030-90185080	HNPCEpiC	eye:	n/a
11	chr5:90042723-90042773	NH-A	brain:	n/a
12	chr5:90236557-90236607	MCF10A-Er-Src	breast:	n/a
13	chr5:90036436-90036486	IMR90	lung:	fetal
14	chr5:90075932-90075982	GM06990	blood:	n/a
15	chr5:90076292-90076342	HEEpiC	esophagus:	n/a
16	chr5:90042723-90042773	NB4	blood:	n/a
17	chr5:90225181-90225231	HAEpiC	amniotic membrane:	n/a
18	chr5:90042723-90042773	GM12892	blood:	n/a
19	chr5:90185030-90185080	PANC-1	pancreas:	n/a
20	chr5:90075932-90075982	CMK	blood:	n/a
21	chr5:90042723-90042773	BJ	skin:	n/a
22	chr5:90076860-90076910	NH-A	brain:	n/a
23	chr5:90185030-90185080	T-47D	breast:	n/a
24	chr5:90076860-90076910	AoSMC	blood vessel:	n/a
25	chr5:90185030-90185080	RPTEC	kidney:	n/a
26	chr5:90185030-90185080	HUVEC	blood vessel:	n/a
27	chr5:90036436-90036486	AG09319	gingival:	n/a
28	chr5:90225181-90225231	ovcar-3	ovarian:	n/a
29	chr5:90036436-90036486	HUVEC	blood vessel:	n/a
30	chr5:90036436-90036486	RPTEC	kidney:	n/a
31	chr5:90225181-90225231	HEK293	kidney:	embryo
32	chr5:90036436-90036486	AG04449	skin:	fetal
33	chr5:90076292-90076342	HCPEpiC	choroid plexus:	n/a
34	chr5:90236557-90236607	HEK293	kidney:	embryo
35	chr5:90172358-90172408	IMR90	lung:	fetal
36	chr5:90076860-90076910	PANC-1	pancreas:	n/a
37	chr5:90036436-90036486	MCF10A-Er-Src	breast:	n/a
38	chr5:90036436-90036486	MCF-7	breast:	n/a
39	chr5:90036436-90036486	HAEpiC	amniotic membrane:	n/a
40	chr5:90036436-90036486	K562	blood:	n/a
41	chr5:90042723-90042773	HNPCEpiC	eye:	n/a
42	chr5:90172358-90172408	PFSK-1	brain:	n/a
43	chr5:90042723-90042773	PANC-1	pancreas:	n/a
44	chr5:90185030-90185080	HRE	kidney:	n/a
45	chr5:90076292-90076342	AG09319	gingival:	n/a
46	chr5:90076292-90076342	HL-60	blood:	n/a
47	chr5:90225181-90225231	HepG2	liver:	n/a
48	chr5:90075932-90075982	AG10803	skin:	n/a
49	chr5:90075932-90075982	HNPCEpiC	eye:	n/a
50	chr5:90172358-90172408	HCM	heart:	n/a

(count:243 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr5:90153756..90156660-chr5:90161187..90163810,2	K562	blood:
2	chr5:90048477..90050312-chr5:90052878..90054667,2	K562	blood:
3	chr5:90066656..90069234-chr5:90677139..90680259,3	K562	blood:
4	chr5:90012587..90015508-chr5:90022676..90025221,2	K562	blood:
5	chr5:90146306..90149323-chr5:90149920..90152363,3	K562	blood:
6	chr5:90076080..90077925-chr5:90078435..90080138,2	K562	blood:
7	chr5:90004946..90006140-chr5:90079283..90080191,6	MCF-7	breast:
8	chr5:90161853..90166366-chr5:90170217..90173249,4	K562	blood:
9	chr5:90145396..90148045-chr5:90150505..90152535,3	K562	blood:
10	chr5:90261974..90263559-chr5:90264503..90266718,2	MCF-7	breast:
11	chr5:90163456..90166184-chr5:90179464..90181248,2	K562	blood:
12	chr5:90118775..90121270-chr5:90123736..90126038,2	K562	blood:
13	chr5:90079294..90080237-chr5:90089325..90090028,2	MCF-7	breast:
14	chr5:90161853..90164383-chr5:90169834..90171717,3	K562	blood:
15	chr5:90055288..90058176-chr5:90059292..90060804,2	MCF-7	breast:
16	chr5:90190412..90192818-chr5:90363374..90365459,2	K562	blood:
17	chr5:90162422..90165076-chr5:90191582..90194100,2	MCF-7	breast:
18	chr5:90033178..90036416-chr5:90039651..90042855,4	K562	blood:
19	chr5:90205974..90208499-chr5:90214592..90217001,3	K562	blood:
20	chr5:90239303..90242044-chr5:90248874..90251643,2	K562	blood:
21	chr5:90184114..90185772-chr5:90277640..90279396,2	K562	blood:
22	chr5:90159385..90163869-chr5:90675528..90680815,7	MCF-7	breast:
23	chr5:90066747..90069663-chr5:90070261..90074130,4	K562	blood:
24	chr5:90001172..90003183-chr5:90006013..90008402,2	K562	blood:
25	chr5:90258002..90260372-chr5:90677122..90679413,2	MCF-7	breast:
26	chr5:90055144..90057508-chr5:90058506..90061459,3	K562	blood:
27	chr5:90175343..90178087-chr5:90180223..90182478,2	MCF-7	breast:
28	chr5:90227664..90228224-chr5:90680158..90680912,2	K562	blood:
29	chr5:90228093..90228615-chr5:90680787..90681318,2	MCF-7	breast:
30	chr5:90226670..90228954-chr5:90237004..90239086,2	K562	blood:
31	chr5:90183752..90186174-chr5:90676365..90680151,3	MCF-7	breast:
32	chr5:90100827..90103086-chr5:90108487..90111195,2	K562	blood:
33	chr5:90026342..90028789-chr5:90031725..90034231,3	K562	blood:
34	chr5:90124795..90126326-chr5:90127337..90129683,2	K562	blood:
35	chr5:90205974..90208499-chr5:90214592..90217001,3	K562	blood:
36	chr5:90184781..90186579-chr5:90679255..90681231,2	MCF-7	breast:
37	chr5:90226329..90230726-chr5:90675433..90680039,8	MCF-7	breast:
38	chr5:90046899..90048953-chr5:90056620..90058436,2	K562	blood:
39	chr5:90229694..90231320-chr5:90235004..90237466,2	K562	blood:
40	chr5:90180905..90184179-chr5:90184592..90187757,3	K562	blood:
41	chr5:90215673..90217953-chr5:90675761..90678552,2	K562	blood:
42	chr5:90021626..90023836-chr5:90049567..90052309,2	K562	blood:
43	chr5:90227817..90228486-chr5:90521512..90522261,2	MCF-7	breast:
44	chr5:90099252..90099895-chr5:90145585..90146206,2	MCF-7	breast:
45	chr5:90026342..90028789-chr5:90031725..90034231,3	K562	blood:
46	chr5:90185745..90188136-chr5:90190208..90193028,2	K562	blood:
47	chr5:90050605..90053422-chr5:90072276..90073803,2	K562	blood:
48	chr5:89703602..89706051-chr5:90235055..90237032,2	K562	blood:
49	chr5:90021626..90023836-chr5:90049567..90052309,2	K562	blood:
50	chr5:90105553..90108677-chr5:90109621..90112137,3	MCF-7	breast:

No data

Variant related genes	Relation type
GPR98	TF binding region
GPR98	CpG island
ENSG00000133302	chromatin interactions
ENSG00000113369	chromatin interactions
ENSG00000189167	chromatin interactions
ENSG00000164199	chromatin interactions
ENSG00000255647	chromatin interactions
ENSG00000176055	chromatin interactions
ENSG00000153140	chromatin interactions
ENSG00000113356	chromatin interactions
ENSG00000139618	chromatin interactions

Extended variants
information (count: 9379 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:9379 , 50 per page) page: 1 2 3 4 5 6 7 ... 188

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6869935	chr5:90003131-90003132	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs200890971	chr5:90003192-90003193	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541126225	chr5:90003211-90003212	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531844871	chr5:90003250-90003251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551661399	chr5:90003259-90003260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2176624	chr5:90003274-90003275	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs189168480	chr5:90003279-90003280	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548915491	chr5:90003354-90003355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567725767	chr5:90003394-90003395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536393362	chr5:90003404-90003405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139865095	chr5:90003436-90003437	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568964642	chr5:90003488-90003489	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538089871	chr5:90003504-90003505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565953343	chr5:90003540-90003541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558104810	chr5:90003586-90003587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4916686	chr5:90003594-90003595	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs540213884	chr5:90003617-90003618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs193121546	chr5:90003633-90003634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557884657	chr5:90003662-90003663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573674040	chr5:90003667-90003668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185148571	chr5:90003674-90003675	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563052082	chr5:90003675-90003676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs78666623	chr5:90003681-90003682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs151057914	chr5:90003726-90003727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs79290391	chr5:90003728-90003729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528005855	chr5:90003733-90003734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547765591	chr5:90003734-90003735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113284328	chr5:90003802-90003803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149813785	chr5:90003819-90003820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550007621	chr5:90003826-90003827	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569042944	chr5:90003842-90003843	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538051519	chr5:90003924-90003925	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539905941	chr5:90003927-90003928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182097470	chr5:90003939-90003940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571565305	chr5:90003959-90003960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112866927	chr5:90003967-90003968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79659716	chr5:90003987-90003988	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553688402	chr5:90003996-90003997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75422449	chr5:90004005-90004006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185697761	chr5:90004025-90004026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536318443	chr5:90004062-90004063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556002550	chr5:90004156-90004157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188844963	chr5:90004161-90004162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs73193258	chr5:90004180-90004181	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs542235919	chr5:90004218-90004219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555796650	chr5:90004233-90004234	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34939014	chr5:90004255-90004256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs398084285	chr5:90004264-90004265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200561374	chr5:90004265-90004266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs541366824	chr5:90004268-90004269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	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
Esophageal adenocarcinoma	18519675	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
Ovarian cancer	21720365	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
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	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
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Obesity	20950786	CNVD

Chromatin state (count:1625 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89950400-90033400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr5:89982000-90004600	Weak transcription	Fetal Brain Female	brain
3	chr5:89987800-90007200	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr5:89991800-90014000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
5	chr5:89995000-90025800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr5:89997800-90017600	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr5:89998800-90018000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:89999600-90010000	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr5:89999800-90004200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr5:90001800-90006000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:90002000-90005600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr5:90002200-90012200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:90002200-90022000	Weak transcription	Brain Germinal Matrix	brain
14	chr5:90002200-90023200	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr5:90002400-90005600	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr5:90003000-90003600	Weak transcription	K562	blood
17	chr5:90003600-90004600	Strong transcription	K562	blood
18	chr5:90004200-90005600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:90004600-90005200	Genic enhancers	K562	blood
20	chr5:90005200-90009400	Strong transcription	K562	blood
21	chr5:90005400-90005800	Enhancers	GM12878-XiMat	blood
22	chr5:90005600-90007800	Strong transcription	H1 Cell Line	embryonic stem cell
23	chr5:90005600-90009000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
24	chr5:90005600-90009600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:90005800-90006000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr5:90006000-90008200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr5:90006000-90011000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr5:90007200-90007800	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr5:90007800-90008000	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr5:90007800-90012200	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr5:90008000-90008200	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr5:90008200-90021600	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr5:90008200-90022000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr5:90008400-90011600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr5:90009000-90012200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr5:90009400-90011000	Weak transcription	K562	blood
37	chr5:90009600-90011800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr5:90010000-90011800	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr5:90010600-90035200	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr5:90011000-90011200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:90011000-90013000	Strong transcription	K562	blood
42	chr5:90011200-90027200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr5:90011800-90013200	Strong transcription	HUES64 Cell Line	embryonic stem cell
44	chr5:90011800-90017800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr5:90012200-90012800	Strong transcription	H1 Cell Line	embryonic stem cell
46	chr5:90012200-90013000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
47	chr5:90012200-90013200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:90012800-90016800	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr5:90013000-90015200	Weak transcription	K562	blood
50	chr5:90013000-90021200	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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