Variant report

Variant	nsv881187
Chromosome Location	chr5:16514269-16654960
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1565)
CpG islands
(count:976)
Chromatin interactive
region (count:129)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1565 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:16550399-16550821	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:16577678-16577890	K562	blood:	n/a	n/a
3	ARID3A	chr5:16539344-16539662	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:16588602-16589051	HepG2	liver:	n/a	n/a
5	ATF1	chr5:16577726-16578073	K562	blood:	n/a	n/a
6	ATF1	chr5:16593833-16594059	K562	blood:	n/a	n/a
7	ATF1	chr5:16629496-16629795	K562	blood:	n/a	n/a
8	ATF1	chr5:16522308-16522571	K562	blood:	n/a	n/a
9	ATF1	chr5:16532087-16532196	K562	blood:	n/a	n/a
10	ATF1	chr5:16521684-16521987	K562	blood:	n/a	n/a
11	BACH1	chr5:16517741-16517782	K562	blood:	n/a	n/a
12	BACH1	chr5:16575267-16575690	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr5:16561794-16562126	GM12878	blood:	n/a	n/a
14	BCLAF1	chr5:16528331-16528963	K562	blood:	n/a	n/a
15	BCLAF1	chr5:16528395-16528951	K562	blood:	n/a	n/a
16	BHLHE40	chr5:16522161-16522412	K562	blood:	n/a	n/a
17	BHLHE40	chr5:16618270-16618591	HepG2	liver:	n/a	n/a
18	BHLHE40	chr5:16585289-16585498	K562	blood:	n/a	n/a
19	BHLHE40	chr5:16539371-16539641	HepG2	liver:	n/a	n/a
20	BHLHE40	chr5:16577242-16577759	K562	blood:	n/a	n/a
21	BHLHE40	chr5:16581299-16581421	K562	blood:	n/a	n/a
22	BHLHE40	chr5:16552970-16553079	K562	blood:	n/a	n/a
23	BHLHE40	chr5:16556181-16556402	GM12878	blood:	n/a	n/a
24	BHLHE40	chr5:16552998-16553046	HepG2	liver:	n/a	n/a
25	BRCA1	chr5:16577794-16578035	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr5:16521255-16521283	HepG2	liver:	n/a	n/a
27	CCNT2	chr5:16522236-16522538	K562	blood:	n/a	n/a
28	CCNT2	chr5:16543316-16543516	K562	blood:	n/a	n/a
29	CEBPB	chr5:16539360-16539740	A549	lung:	n/a	chr5:16539565-16539576
30	CEBPB	chr5:16650246-16650516	HepG2	liver:	n/a	chr5:16650360-16650371
31	CEBPB	chr5:16539304-16539715	IMR90	lung:	n/a	chr5:16539565-16539576
32	CEBPB	chr5:16650213-16650472	IMR90	lung:	n/a	chr5:16650360-16650371
33	CEBPB	chr5:16589841-16590180	HepG2	liver:	n/a	n/a
34	CEBPB	chr5:16628711-16628905	Hela-S3	cervix:	n/a	chr5:16628824-16628835
35	CEBPB	chr5:16629482-16629754	Hela-S3	cervix:	n/a	chr5:16629609-16629620
36	CEBPB	chr5:16639393-16639682	A549	lung:	n/a	chr5:16639515-16639526
37	CEBPB	chr5:16593718-16594096	K562	blood:	n/a	chr5:16593877-16593888
38	CEBPB	chr5:16528718-16529061	K562	blood:	n/a	n/a
39	CEBPB	chr5:16629458-16629730	K562	blood:	n/a	chr5:16629609-16629620
40	CEBPB	chr5:16557563-16557826	H1-hESC	embryonic stem cell:	n/a	chr5:16557713-16557722 chr5:16557713-16557722 chr5:16557712-16557723 chr5:16557713-16557722 chr5:16557711-16557724 chr5:16557713-16557722 chr5:16557711-16557724 chr5:16557568-16557580
41	CEBPB	chr5:16575611-16575725	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr5:16546771-16547116	IMR90	lung:	n/a	chr5:16546948-16546959
43	CEBPB	chr5:16629469-16629718	IMR90	lung:	n/a	chr5:16629609-16629620
44	CEBPB	chr5:16557528-16557897	K562	blood:	n/a	chr5:16557713-16557722 chr5:16557713-16557722 chr5:16557712-16557723 chr5:16557713-16557722 chr5:16557711-16557724 chr5:16557713-16557722 chr5:16557711-16557724 chr5:16557568-16557580
45	CEBPB	chr5:16612355-16612364	HepG2	liver:	n/a	n/a
46	CEBPB	chr5:16556578-16556882	K562	blood:	n/a	chr5:16556734-16556745
47	CEBPB	chr5:16618752-16618920	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr5:16639368-16639660	K562	blood:	n/a	chr5:16639515-16639526
49	CEBPB	chr5:16593801-16593949	A549	lung:	n/a	chr5:16593877-16593888
50	CEBPB	chr5:16546771-16547051	K562	blood:	n/a	chr5:16546948-16546959

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:16617388-16617438	LNCaP	prostate:	n/a
2	chr5:16617587-16617637	GM12891	blood:	n/a
3	chr5:16617388-16617438	SAEC	small airway:	n/a
4	chr5:16617290-16617340	Jurkat	blood:	n/a
5	chr5:16614241-16614291	BJ	skin:	n/a
6	chr5:16617388-16617438	HCM	heart:	n/a
7	chr5:16615081-16615131	CMK	blood:	n/a
8	chr5:16617290-16617340	IMR90	lung:	fetal
9	chr5:16616834-16616884	HEK293	kidney:	embryo
10	chr5:16616510-16616560	HRE	kidney:	n/a
11	chr5:16616834-16616884	H1-hESC	embryonic stem cell:	embryo
12	chr5:16615081-16615131	HMEC	breast:	n/a
13	chr5:16621256-16621306	GM12878	blood:	n/a
14	chr5:16614632-16614682	NH-A	brain:	n/a
15	chr5:16616459-16616509	GM12892	blood:	n/a
16	chr5:16617587-16617637	HCM	heart:	n/a
17	chr5:16617290-16617340	HUVEC	blood vessel:	n/a
18	chr5:16616510-16616560	H1-hESC	embryonic stem cell:	embryo
19	chr5:16618052-16618102	Caco-2	colon:	n/a
20	chr5:16616510-16616560	ovcar-3	ovarian:	n/a
21	chr5:16617388-16617438	K562	blood:	n/a
22	chr5:16616459-16616509	GM19239	blood:	n/a
23	chr5:16615081-16615131	NT2-D1	testis:	n/a
24	chr5:16616510-16616560	T-47D	breast:	n/a
25	chr5:16559541-16559591	HL-60	blood:	n/a
26	chr5:16559541-16559591	AG04449	skin:	fetal
27	chr5:16615750-16615800	NB4	blood:	n/a
28	chr5:16616459-16616509	U87	brain:	n/a
29	chr5:16616834-16616884	ProgFib	skin:	n/a
30	chr5:16614241-16614291	LNCaP	prostate:	n/a
31	chr5:16559541-16559591	GM06990	blood:	n/a
32	chr5:16621256-16621306	IMR90	lung:	fetal
33	chr5:16615750-16615800	AG10803	skin:	n/a
34	chr5:16559541-16559591	HAEpiC	amniotic membrane:	n/a
35	chr5:16617427-16617477	HepG2	liver:	n/a
36	chr5:16614241-16614291	Jurkat	blood:	n/a
37	chr5:16617388-16617438	Caco-2	colon:	n/a
38	chr5:16616510-16616560	HCM	heart:	n/a
39	chr5:16621256-16621306	HMEC	breast:	n/a
40	chr5:16617587-16617637	HEK293	kidney:	embryo
41	chr5:16615750-16615800	ECC-1	luminal epithelium:	n/a
42	chr5:16617427-16617477	NT2-D1	testis:	n/a
43	chr5:16614241-16614291	HL-60	blood:	n/a
44	chr5:16616834-16616884	Jurkat	blood:	n/a
45	chr5:16615750-16615800	AG04450	lung:	fetal
46	chr5:16617587-16617637	Caco-2	colon:	n/a
47	chr5:16617290-16617340	A549	lung:	n/a
48	chr5:16615081-16615131	ProgFib	skin:	n/a
49	chr5:16614632-16614682	ECC-1	luminal epithelium:	n/a
50	chr5:16617290-16617340	HRCEpiC	kidney:	n/a

(count:129 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:16562738..16565686-chr5:16598984..16600839,2	MCF-7	breast:
2	chr5:14870477..14872982-chr5:16567170..16569965,2	K562	blood:
3	chr5:16577162..16580474-chr5:16583638..16586521,3	MCF-7	breast:
4	chr5:16508708..16509534-chr5:16549932..16550748,2	MCF-7	breast:
5	chr5:16552702..16553520-chr5:16666199..16667543,5	MCF-7	breast:
6	chr5:16464646..16468132-chr5:16626735..16630201,3	MCF-7	breast:
7	chr5:16498229..16500270-chr5:16516001..16517832,2	K562	blood:
8	chr5:16535725..16538550-chr5:16541937..16543644,2	K562	blood:
9	chr5:16588416..16589500-chr5:16674631..16675555,5	MCF-7	breast:
10	chr5:16511492..16513352-chr5:16516670..16518535,2	MCF-7	breast:
11	chr5:16529119..16532127-chr5:16532204..16536269,4	MCF-7	breast:
12	chr5:16490936..16491477-chr5:16550200..16551088,2	MCF-7	breast:
13	chr5:16588327..16590123-chr5:16591920..16594377,2	MCF-7	breast:
14	chr5:16552594..16553429-chr5:16666387..16667201,2	MCF-7	breast:
15	chr5:16515644..16517588-chr5:16520879..16522535,2	K562	blood:
16	chr5:16464191..16467356-chr5:16550758..16555048,4	MCF-7	breast:
17	chr5:16552565..16553606-chr5:16568821..16570258,3	MCF-7	breast:
18	chr5:16513910..16515735-chr5:16529020..16530796,2	K562	blood:
19	chr5:16581461..16583771-chr5:16590436..16593206,2	MCF-7	breast:
20	chr5:16588331..16589560-chr5:16626475..16627361,9	MCF-7	breast:
21	chr5:16562738..16565686-chr5:16598984..16600839,2	MCF-7	breast:
22	chr5:16588331..16589560-chr5:16626475..16627361,9	MCF-7	breast:
23	chr5:16560688..16562479-chr5:16569806..16571624,2	K562	blood:
24	chr5:16600836..16605070-chr5:16611486..16614397,4	MCF-7	breast:
25	chr5:16544591..16547039-chr5:16547595..16549857,2	K562	blood:
26	chr5:16590135..16590892-chr5:16626779..16627328,2	MCF-7	breast:
27	chr5:16577676..16580941-chr5:16584093..16586155,5	K562	blood:
28	chr5:16515851..16518543-chr5:16577137..16579059,2	K562	blood:
29	chr5:16417923..16420482-chr5:16527282..16529023,2	K562	blood:
30	chr5:16615493..16618797-chr5:16619529..16623976,5	MCF-7	breast:
31	chr5:16625039..16627888-chr5:16628424..16629990,2	MCF-7	breast:
32	chr5:16489246..16489886-chr5:16550234..16551055,2	MCF-7	breast:
33	chr21:47647239..47649885-chr5:16575581..16577546,2	MCF-7	breast:
34	chr5:16588651..16589517-chr5:16626683..16627384,4	MCF-7	breast:
35	chr5:16529383..16532195-chr5:16534622..16538676,4	MCF-7	breast:
36	chr5:16521375..16523909-chr5:16526389..16530359,4	K562	blood:
37	chr5:16489110..16490011-chr5:16552358..16553386,3	MCF-7	breast:
38	chr5:16577676..16580941-chr5:16584093..16586155,5	K562	blood:
39	chr5:16593743..16596156-chr5:16613042..16615565,2	MCF-7	breast:
40	chr5:16551810..16554386-chr5:16638970..16640642,2	MCF-7	breast:
41	chr5:16598185..16599797-chr5:16601466..16603741,2	MCF-7	breast:
42	chr5:16482049..16483952-chr5:16545895..16548159,2	MCF-7	breast:
43	chr5:16489161..16490030-chr5:16550533..16551034,2	K562	blood:
44	chr5:16577676..16580941-chr5:16582189..16586155,5	K562	blood:
45	chr5:16491767..16494434-chr5:16547644..16549811,2	K562	blood:
46	chr5:16588526..16589249-chr5:16628201..16629134,3	MCF-7	breast:
47	chr5:16588331..16589560-chr5:16626475..16627361,14	MCF-7	breast:
48	chr5:16514469..16516231-chr5:16522718..16524786,2	MCF-7	breast:
49	chr5:16581461..16583771-chr5:16590436..16593206,2	MCF-7	breast:
50	chr5:16464577..16466598-chr5:16578860..16580566,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BASP1-6	chr5:16616035-16616595	ENSG00000246214
2	lnc-BASP1-6	chr5:16629563-16630078	ENSG00000246214
3	lnc-BASP1-6	chr5:16615996-16616595	NONHSAT100608
4	lnc-BASP1-5	chr5:16617334-16617664	ENSG00000250415.1
5	lnc-BASP1-5	chr5:16621154-16621238	ENSG00000250415.1
6	lnc-BASP1-5	chr5:16621317-16621385	ENSG00000250415.1
7	lnc-BASP1-5	chr5:16617928-16618146	ENSG00000250415.1
8	lnc-BASP1-6	chr5:16617388-16617435	NONHSAT100608
9	lnc-BASP1-6	chr5:16621887-16622141	ENSG00000246214
10	lnc-BASP1-6	chr5:16625524-16625865	ENSG00000246214

No data

Variant related genes	Relation type
FAM134B	TF binding region
ENSG00000246214	TF binding region
ENSG00000250415	TF binding region
ENSG00000201370	TF binding region
FAM134B	CpG island
ENSG00000246214	CpG island
ENSG00000250415	CpG island
ENSG00000201370	CpG island
ENSG00000246214	chromatin interactions
ENSG00000250415	chromatin interactions
ENSG00000154153	chromatin interactions
ENSG00000173545	chromatin interactions
ENSG00000154122	chromatin interactions
ENSG00000201370	chromatin interactions
ENSG00000272057	chromatin interactions
ENSG00000160285	chromatin interactions
ENSG00000215424	chromatin interactions

Extended variants
information (count: 5223 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:5223 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4702150	chr5:16514269-16514270	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543398063	chr5:16514334-16514335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560426114	chr5:16514362-16514363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs527663430	chr5:16514397-16514398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545911097	chr5:16514405-16514406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs188939218	chr5:16514478-16514479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561976076	chr5:16514497-16514498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531530245	chr5:16514498-16514499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs144913508	chr5:16514506-16514507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371879075	chr5:16514507-16514508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs62369679	chr5:16514511-16514512	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs338330	chr5:16514551-16514552	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs547495878	chr5:16514556-16514557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs16868708	chr5:16514564-16514565	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs539387834	chr5:16514565-16514566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557492887	chr5:16514566-16514567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs138669474	chr5:16514581-16514582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs374903360	chr5:16514594-16514595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs62369680	chr5:16514619-16514620	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs62369681	chr5:16514635-16514636	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs193251029	chr5:16514706-16514707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574686970	chr5:16514732-16514733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552630111	chr5:16514750-16514751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535678848	chr5:16514767-16514768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113815326	chr5:16514769-16514770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537852335	chr5:16514779-16514780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572462998	chr5:16514792-16514793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs184366457	chr5:16514807-16514808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs62369682	chr5:16514887-16514888	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs576547776	chr5:16514925-16514926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369948126	chr5:16514993-16514994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551880015	chr5:16515004-16515005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs143463663	chr5:16515009-16515010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs142825924	chr5:16515010-16515011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144991707	chr5:16515019-16515020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs61346860	chr5:16515022-16515023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs13170136	chr5:16515023-16515024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs13190361	chr5:16515024-16515025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189300275	chr5:16515030-16515031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs13190362	chr5:16515031-16515032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561992591	chr5:16515043-16515044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs13190376	chr5:16515056-16515057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13170150	chr5:16515057-16515058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs13170653	chr5:16515063-16515064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs13170264	chr5:16515067-16515068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs13190491	chr5:16515075-16515076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs13170268	chr5:16515076-16515077	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs547626421	chr5:16515079-16515080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs199787021	chr5:16515088-16515089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115666259	chr5:16515089-16515090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
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
Cervical squamous cell carcinoma	21590768	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
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21364760	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	22183965	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2810 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:16509200-16524200	Weak transcription	Brain Cingulate Gyrus	brain
2	chr5:16509400-16515600	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr5:16509600-16515600	Weak transcription	Brain Substantia Nigra	brain
4	chr5:16509600-16528800	Weak transcription	Brain Hippocampus Middle	brain
5	chr5:16509800-16521000	Weak transcription	Fetal Heart	heart
6	chr5:16511200-16519200	Weak transcription	Fetal Intestine Large	intestine
7	chr5:16511600-16522000	Weak transcription	Primary T cells from cord blood	blood
8	chr5:16511800-16519000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr5:16512000-16519000	Weak transcription	Fetal Intestine Small	intestine
10	chr5:16513200-16519200	Weak transcription	Left Ventricle	heart
11	chr5:16513200-16519800	Weak transcription	Right Ventricle	heart
12	chr5:16513400-16517000	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr5:16514200-16514800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr5:16514800-16516000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr5:16515200-16516400	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr5:16515600-16515800	Enhancers	Brain Angular Gyrus	brain
17	chr5:16515600-16516000	Enhancers	Brain Substantia Nigra	brain
18	chr5:16515600-16517000	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr5:16515600-16519200	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr5:16515800-16516000	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr5:16515800-16518800	Weak transcription	Brain Angular Gyrus	brain
22	chr5:16516000-16518000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr5:16516000-16519000	Weak transcription	Brain Substantia Nigra	brain
24	chr5:16516000-16519600	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr5:16516000-16540800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr5:16517000-16517400	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr5:16517000-16518400	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr5:16517400-16518600	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr5:16518000-16519000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr5:16518400-16519200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr5:16518400-16520000	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr5:16518600-16519600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr5:16518800-16519400	Enhancers	HSMMtube	muscle
34	chr5:16518800-16519400	Enhancers	NHDF-Ad	bronchial
35	chr5:16518800-16520200	Enhancers	Brain Angular Gyrus	brain
36	chr5:16519000-16519200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr5:16519000-16519400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr5:16519000-16519800	Enhancers	Fetal Intestine Small	intestine
39	chr5:16519000-16520200	Enhancers	Brain Substantia Nigra	brain
40	chr5:16519200-16519600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr5:16519200-16520200	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr5:16519200-16520400	Enhancers	Left Ventricle	heart
43	chr5:16519200-16521200	Enhancers	Fetal Intestine Large	intestine
44	chr5:16519400-16519800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr5:16519400-16521400	Enhancers	Pancreas	Pancrea
46	chr5:16519400-16523200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr5:16519600-16520400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr5:16519600-16520800	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr5:16519800-16520400	Enhancers	Colonic Mucosa	Colon
50	chr5:16519800-16520400	Genic enhancers	Fetal Intestine Small	intestine

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