Variant report

Variant	nsv462199
Chromosome Location	chr5:60129361-60329624
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2270)
CpG islands
(count:2137)
Chromatin interactive
region (count:95)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2270 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:60224933-60225228	K562	blood:	n/a	n/a
2	ARID3A	chr5:60140010-60140140	K562	blood:	n/a	n/a
3	ARID3A	chr5:60179163-60179195	K562	blood:	n/a	n/a
4	ARID3A	chr5:60274848-60275124	K562	blood:	n/a	n/a
5	ARID3A	chr5:60181991-60182269	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:60314308-60314387	K562	blood:	n/a	chr5:60314370-60314386
7	ARID3A	chr5:60227642-60227690	K562	blood:	n/a	n/a
8	ARID3A	chr5:60240718-60241241	HepG2	liver:	n/a	n/a
9	ATF1	chr5:60148865-60149065	K562	blood:	n/a	n/a
10	ATF1	chr5:60140322-60140612	K562	blood:	n/a	n/a
11	ATF1	chr5:60137790-60137795	K562	blood:	n/a	n/a
12	ATF1	chr5:60257644-60257861	K562	blood:	n/a	n/a
13	ATF1	chr5:60274513-60275143	K562	blood:	n/a	n/a
14	ATF1	chr5:60148344-60148514	K562	blood:	n/a	n/a
15	ATF2	chr5:60240675-60241129	GM12878	blood:	n/a	n/a
16	ATF3	chr5:60257617-60257921	K562	blood:	n/a	n/a
17	ATF3	chr5:60139979-60140240	K562	blood:	n/a	chr5:60140013-60140022
18	BACH1	chr5:60241238-60241531	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr5:60274899-60275146	K562	blood:	n/a	n/a
20	BACH1	chr5:60139641-60140505	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr5:60140730-60140830	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCLAF1	chr5:60241147-60241621	GM12878	blood:	n/a	n/a
23	BHLHE40	chr5:60274319-60275283	K562	blood:	n/a	n/a
24	BHLHE40	chr5:60148834-60149083	K562	blood:	n/a	n/a
25	BHLHE40	chr5:60240684-60241301	GM12878	blood:	n/a	chr5:60241008-60241024
26	BHLHE40	chr5:60273867-60274075	K562	blood:	n/a	n/a
27	BHLHE40	chr5:60139857-60140324	GM12878	blood:	n/a	n/a
28	BHLHE40	chr5:60139760-60140304	HepG2	liver:	n/a	chr5:60139813-60139829
29	BHLHE40	chr5:60168934-60168938	GM12878	blood:	n/a	n/a
30	BHLHE40	chr5:60139908-60140548	K562	blood:	n/a	n/a
31	BHLHE40	chr5:60240872-60241581	K562	blood:	n/a	chr5:60241008-60241024
32	BHLHE40	chr5:60241820-60242140	K562	blood:	n/a	n/a
33	BRCA1	chr5:60139999-60140699	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr5:60306630-60306773	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr5:60242705-60242764	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr5:60231541-60231761	K562	blood:	n/a	n/a
37	CBX3	chr5:60289190-60289610	K562	blood:	n/a	n/a
38	CBX3	chr5:60166733-60166960	K562	blood:	n/a	n/a
39	CBX3	chr5:60289241-60289660	HCT-116	colon:	n/a	n/a
40	CBX3	chr5:60277815-60278245	K562	blood:	n/a	n/a
41	CBX3	chr5:60240930-60241613	K562	blood:	n/a	n/a
42	CBX3	chr5:60274796-60275180	K562	blood:	n/a	n/a
43	CBX3	chr5:60251024-60251519	HCT-116	colon:	n/a	n/a
44	CBX3	chr5:60274711-60275276	K562	blood:	n/a	n/a
45	CBX3	chr5:60289206-60289789	K562	blood:	n/a	n/a
46	CCNT2	chr5:60240705-60241024	K562	blood:	n/a	n/a
47	CCNT2	chr5:60241747-60241947	K562	blood:	n/a	n/a
48	CCNT2	chr5:60274822-60275307	K562	blood:	n/a	n/a
49	CCNT2	chr5:60139486-60140436	K562	blood:	n/a	n/a
50	CCNT2	chr5:60257762-60257798	K562	blood:	n/a	n/a

(count:2137 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:60240926-60240976	AG09319	gingival:	n/a
2	chr5:60241324-60241374	AG09319	gingival:	n/a
3	chr5:60240926-60240976	AG09319	gingival:	n/a
4	chr5:60241324-60241374	AG09319	gingival:	n/a
5	chr5:60138883-60138933	PFSK-1	brain:	n/a
6	chr5:60141082-60141132	PrEC	prostate:	n/a
7	chr5:60139938-60139988	NHDF-neo	bronchial:	n/a
8	chr5:60139293-60139343	AG10803	skin:	n/a
9	chr5:60138761-60138811	SK-N-SH_RA	brain:	n/a
10	chr5:60241019-60241069	ProgFib	skin:	n/a
11	chr5:60141082-60141132	HNPCEpiC	eye:	n/a
12	chr5:60239580-60239630	AG10803	skin:	n/a
13	chr5:60139708-60139758	ovcar-3	ovarian:	n/a
14	chr5:60138761-60138811	LNCaP	prostate:	n/a
15	chr5:60139516-60139566	AG09309	skin:	n/a
16	chr5:60240891-60240941	SAEC	small airway:	n/a
17	chr5:60139420-60139470	RPTEC	kidney:	n/a
18	chr5:60139941-60139991	A549	lung:	n/a
19	chr5:60241428-60241478	NH-A	brain:	n/a
20	chr5:60138761-60138811	SKMC	muscle:	n/a
21	chr5:60148273-60148323	GM19239	blood:	n/a
22	chr5:60187211-60187261	A549	lung:	n/a
23	chr5:60140824-60140874	ECC-1	luminal epithelium:	n/a
24	chr5:60239580-60239630	HL-60	blood:	n/a
25	chr5:60239580-60239630	BE2_C	brain:	n/a
26	chr5:60240838-60240888	Hela-S3	cervix:	n/a
27	chr5:60138838-60138888	HepG2	liver:	n/a
28	chr5:60132712-60132762	ECC-1	luminal epithelium:	n/a
29	chr5:60240568-60240618	ovcar-3	ovarian:	n/a
30	chr5:60139293-60139343	BE2_C	brain:	n/a
31	chr5:60138761-60138811	MCF-7	breast:	n/a
32	chr5:60141082-60141132	T-47D	breast:	n/a
33	chr5:60138761-60138811	T-47D	breast:	n/a
34	chr5:60139293-60139343	LNCaP	prostate:	n/a
35	chr5:60148273-60148323	CMK	blood:	n/a
36	chr5:60132712-60132762	HPAEpiC	pulmonary alveolar:	n/a
37	chr5:60142446-60142496	HNPCEpiC	eye:	n/a
38	chr5:60142446-60142496	HPAEpiC	pulmonary alveolar:	n/a
39	chr5:60138761-60138811	HCPEpiC	choroid plexus:	n/a
40	chr5:60240926-60240976	H1-hESC	embryonic stem cell:	embryo
41	chr5:60170058-60170108	HMEC	breast:	n/a
42	chr5:60241003-60241053	HCF	heart:	n/a
43	chr5:60241324-60241374	SAEC	small airway:	n/a
44	chr5:60241636-60241686	SK-N-SH	brain:	n/a
45	chr5:60142446-60142496	HRE	kidney:	n/a
46	chr5:60138883-60138933	T-47D	breast:	n/a
47	chr5:60139516-60139566	NH-A	brain:	n/a
48	chr5:60240952-60241002	IMR90	lung:	fetal
49	chr5:60142446-60142496	HCPEpiC	choroid plexus:	n/a
50	chr5:60241424-60241474	AG04450	lung:	fetal

(count:95 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:60199648..60201758-chr5:60214066..60215878,2	K562	blood:
2	chr5:60198217..60200090-chr5:60210725..60213432,2	K562	blood:
3	chr5:60244987..60247970-chr5:60252320..60254157,2	K562	blood:
4	chr5:59995891..59998683-chr5:60261062..60263658,2	K562	blood:
5	chr5:60248322..60251287-chr5:60256158..60258205,2	K562	blood:
6	chr5:60307463..60309346-chr5:60317381..60319314,2	K562	blood:
7	chr5:60138677..60141411-chr5:60155273..60157219,2	MCF-7	breast:
8	chr5:60134031..60135823-chr5:60138767..60140768,2	MCF-7	breast:
9	chr5:60182235..60184103-chr5:60240425..60242925,2	MCF-7	breast:
10	chr5:60307333..60308996-chr5:60311645..60313281,2	K562	blood:
11	chr5:60238903..60241711-chr5:60255745..60258195,2	K562	blood:
12	chr5:60143868..60145505-chr5:60146013..60148610,2	K562	blood:
13	chr5:60244730..60246591-chr5:60250985..60252968,2	MCF-7	breast:
14	chr5:60307333..60308996-chr5:60311645..60313281,2	K562	blood:
15	chr5:60306690..60309499-chr5:60316229..60318083,2	MCF-7	breast:
16	chr5:60305681..60307942-chr5:60309957..60312620,2	MCF-7	breast:
17	chr5:60311498..60313138-chr5:60318136..60319841,2	K562	blood:
18	chr5:60248420..60251083-chr5:60253409..60255301,2	K562	blood:
19	chr5:60239573..60241896-chr5:60245590..60248548,2	K562	blood:
20	chr5:60142106..60144527-chr5:60240837..60243388,2	K562	blood:
21	chr5:60308495..60310817-chr5:60337811..60340272,2	K562	blood:
22	chr5:60234928..60236588-chr5:60398367..60400919,2	K562	blood:
23	chr5:60244987..60247970-chr5:60252320..60254157,2	K562	blood:
24	chr5:60168971..60171964-chr5:60184118..60186790,2	K562	blood:
25	chr5:60147000..60148847-chr5:60149735..60152461,2	MCF-7	breast:
26	chr5:60241626..60243235-chr5:60252135..60253778,2	K562	blood:
27	chr5:60232184..60235811-chr5:60236501..60239833,3	K562	blood:
28	chr5:60261942..60265146-chr5:60457137..60459002,3	MCF-7	breast:
29	chr5:60234642..60236205-chr5:60241471..60243288,2	MCF-7	breast:
30	chr5:60248420..60251083-chr5:60253409..60255301,2	K562	blood:
31	chr1:156698013..156698560-chr5:60240745..60241454,2	Hela-S3	cervix:
32	chr5:60132825..60135249-chr5:60136200..60138330,2	K562	blood:
33	chr19:10314099..10314599-chr5:60155075..60155644,2	Hela-S3	cervix:
34	chr5:60180292..60182864-chr5:60197652..60199480,2	MCF-7	breast:
35	chr5:60180292..60182864-chr5:60197652..60199480,2	MCF-7	breast:
36	chr5:60248322..60251287-chr5:60256158..60258205,2	K562	blood:
37	chr5:60244730..60246591-chr5:60250985..60252968,2	MCF-7	breast:
38	chr5:60305681..60307942-chr5:60309957..60312620,2	MCF-7	breast:
39	chr5:60268329..60270384-chr5:60275561..60277405,2	K562	blood:
40	chr5:60100541..60102761-chr5:60130219..60132557,2	K562	blood:
41	chr5:60238903..60240533-chr5:60255101..60257245,2	K562	blood:
42	chr5:60246470..60249444-chr5:60252320..60255288,2	K562	blood:
43	chr5:60309345..60311074-chr5:60313385..60316097,2	K562	blood:
44	chr2:25194755..25195595-chr5:60240745..60241487,2	Hela-S3	cervix:
45	chr5:59995106..59997535-chr5:60240120..60242292,3	K562	blood:
46	chr5:60307463..60309346-chr5:60317381..60319314,2	K562	blood:
47	chr5:60242359..60244736-chr5:60254537..60257581,3	K562	blood:
48	chr5:60254798..60255532-chr5:60954065..60954863,2	K562	blood:
49	chr5:60306690..60309499-chr5:60316229..60318083,2	MCF-7	breast:
50	chr5:60268329..60270384-chr5:60275561..60277405,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDUFAF2-1	chr5:60214122-60214254	ENSG00000233847.1
2	lnc-ERCC8-1	chr5:60162284-60162762	ENSG00000272308.1
3	lnc-NDUFAF2-1	chr5:60213317-60213394	ENSG00000233847.1
4	lnc-ZSWIM6-4	chr5:60241056-60241209	NONHSAT101655
5	lnc-NDUFAF2-1	chr5:60215204-60215400	ENSG00000233847.1

No data

Variant related genes	Relation type
NDUFAF2	TF binding region
ELOVL7	TF binding region
ENSG00000272308	TF binding region
ERCC8	TF binding region
GNL3LP1	TF binding region
ENSG00000233847	TF binding region
NDUFAF2	CpG island
ELOVL7	CpG island
ENSG00000272308	CpG island
ERCC8	CpG island
GNL3LP1	CpG island
ENSG00000233847	CpG island
ENSG00000112977	chromatin interactions
ENSG00000049167	chromatin interactions
ENSG00000115137	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000233847	chromatin interactions
ENSG00000188725	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000224165	chromatin interactions
ENSG00000035499	chromatin interactions
ENSG00000164181	chromatin interactions
ENSG00000164182	chromatin interactions
ENSG00000251279	chromatin interactions

Extended variants
information (count: 6945 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:6945 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6869332	chr5:60129361-60129362	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188263234	chr5:60129369-60129370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs200543771	chr5:60129403-60129404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs150126104	chr5:60129421-60129422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192254080	chr5:60129430-60129431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553160074	chr5:60129537-60129538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574068624	chr5:60129672-60129673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542701729	chr5:60129689-60129690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145518663	chr5:60129695-60129696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35257212	chr5:60129741-60129742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs185776811	chr5:60129748-60129749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577273095	chr5:60129777-60129778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550759141	chr5:60129787-60129788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113521314	chr5:60129794-60129795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556680390	chr5:60129876-60129877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190201287	chr5:60129903-60129904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565550398	chr5:60129934-60129935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148815341	chr5:60129991-60129992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547971763	chr5:60129992-60129993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182014950	chr5:60129998-60129999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184695856	chr5:60130054-60130055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548734060	chr5:60130064-60130065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568822285	chr5:60130146-60130147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561210852	chr5:60130174-60130175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548962044	chr5:60130181-60130182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573061307	chr5:60130184-60130185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs551262796	chr5:60130209-60130210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369059400	chr5:60130214-60130215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372511698	chr5:60130215-60130216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189069426	chr5:60130218-60130219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181372632	chr5:60130219-60130220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574078187	chr5:60130256-60130257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536735227	chr5:60130264-60130265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556348218	chr5:60130326-60130327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576528329	chr5:60130367-60130368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185654137	chr5:60130381-60130382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs143458330	chr5:60130511-60130512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191101380	chr5:60130533-60130534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs541672074	chr5:60130554-60130555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370772924	chr5:60130557-60130558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529017273	chr5:60130558-60130559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138528745	chr5:60130587-60130588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144133227	chr5:60130602-60130603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527974247	chr5:60130609-60130610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531223996	chr5:60130614-60130615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550949198	chr5:60130617-60130618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541329953	chr5:60130693-60130694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571236794	chr5:60130737-60130738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs180753448	chr5:60130739-60130740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547316796	chr5:60130746-60130747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
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
Thoracic aortic aneurysm	21092924	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
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	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
Hepatocellular carcinoma	16750200	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
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Contiguous gene syndrome	19525295	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2639 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60102200-60137800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr5:60120800-60132200	Weak transcription	K562	blood
3	chr5:60122800-60131200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr5:60124000-60133600	Weak transcription	Pancreas	Pancrea
5	chr5:60126000-60131600	Weak transcription	HMEC	breast
6	chr5:60127000-60131200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr5:60127000-60133600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr5:60129000-60129400	Enhancers	Fetal Intestine Large	intestine
9	chr5:60129000-60129400	Enhancers	Fetal Intestine Small	intestine
10	chr5:60129400-60133400	Weak transcription	Fetal Intestine Large	intestine
11	chr5:60129400-60137200	Weak transcription	Fetal Intestine Small	intestine
12	chr5:60131000-60132600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr5:60131200-60132000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr5:60131200-60132400	Enhancers	A549	lung
15	chr5:60131200-60132600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr5:60131200-60134600	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr5:60131400-60131800	Enhancers	HUVEC	blood vessel
18	chr5:60131400-60132000	Enhancers	HSMM	muscle
19	chr5:60131400-60132400	Enhancers	NHEK	skin
20	chr5:60131600-60132000	Enhancers	HMEC	breast
21	chr5:60131600-60133600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:60131600-60133600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr5:60131600-60134000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr5:60131600-60134400	Enhancers	H1 Cell Line	embryonic stem cell
25	chr5:60131600-60134400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr5:60131800-60132000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr5:60131800-60133000	Enhancers	H9 Cell Line	embryonic stem cell
28	chr5:60131800-60133000	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr5:60131800-60133600	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr5:60131800-60134200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr5:60131800-60134400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr5:60132000-60132800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr5:60132000-60133000	Weak transcription	HSMM	muscle
34	chr5:60132000-60133800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr5:60132000-60138600	Weak transcription	HMEC	breast
36	chr5:60132200-60132400	Enhancers	K562	blood
37	chr5:60132200-60133000	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr5:60132400-60133000	Weak transcription	K562	blood
39	chr5:60132400-60133800	Weak transcription	NHEK	skin
40	chr5:60132400-60138600	Weak transcription	A549	lung
41	chr5:60132600-60133600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr5:60132600-60133600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr5:60132800-60133200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr5:60133000-60133200	Flanking Active TSS	HSMM	muscle
45	chr5:60133000-60134000	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr5:60133000-60134000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr5:60133000-60134200	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr5:60133000-60134600	Enhancers	K562	blood
49	chr5:60133200-60133400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr5:60133400-60133800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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