Variant report

Variant	nsv1034730
Chromosome Location	chr5:17437494-17515789
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:328)
CpG islands
(count:550)
Chromatin interactive
region (count:17)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:17492224-17492379	K562	blood:	n/a	n/a
2	ATF3	chr5:17443879-17444164	K562	blood:	n/a	n/a
3	BATF	chr5:17499625-17499833	GM12878	blood:	n/a	n/a
4	BCL11A	chr5:17499603-17499787	GM12878	blood:	n/a	n/a
5	BCL11A	chr5:17499619-17499851	GM12878	blood:	n/a	n/a
6	BHLHE40	chr5:17456049-17456242	GM12878	blood:	n/a	n/a
7	CEBPB	chr5:17449006-17449365	IMR90	lung:	n/a	chr5:17449175-17449186
8	CEBPB	chr5:17443973-17444164	K562	blood:	n/a	n/a
9	CEBPB	chr5:17448970-17449405	A549	lung:	n/a	chr5:17449175-17449186
10	CEBPB	chr5:17449024-17449337	HepG2	liver:	n/a	chr5:17449175-17449186
11	CEBPB	chr5:17483315-17483373	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr5:17449019-17449300	K562	blood:	n/a	chr5:17449175-17449186
13	CEBPB	chr5:17504178-17504267	HepG2	liver:	n/a	n/a
14	CEBPB	chr5:17486902-17487265	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr5:17479590-17479792	HepG2	liver:	n/a	chr5:17479700-17479711
16	CEBPB	chr5:17445308-17445697	MCF-7	breast:	n/a	n/a
17	CEBPB	chr5:17443930-17444116	HepG2	liver:	n/a	n/a
18	CEBPB	chr5:17444051-17444276	K562	blood:	n/a	n/a
19	CEBPB	chr5:17449051-17449354	A549	lung:	n/a	chr5:17449175-17449186
20	CEBPB	chr5:17444001-17444214	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr5:17443942-17444214	A549	lung:	n/a	n/a
22	CEBPB	chr5:17449048-17449320	Hela-S3	cervix:	n/a	chr5:17449175-17449186
23	CEBPB	chr5:17479634-17479713	H1-hESC	embryonic stem cell:	n/a	chr5:17479700-17479711
24	CTCF	chr5:17438296-17438408	MCF-7	breast:	n/a	chr5:17438327-17438348
25	CTCF	chr5:17451566-17451641	GM10248	blood:	n/a	n/a
26	CTCF	chr5:17468460-17468610	MCF-7	breast:	n/a	n/a
27	CTCF	chr5:17443960-17444110	HL-60	blood:	n/a	n/a
28	CTCF	chr5:17481912-17482004	MCF-7	breast:	n/a	n/a
29	CTCF	chr5:17438160-17438425	H1-hESC	embryonic stem cell:	n/a	chr5:17438327-17438348
30	CTCF	chr5:17481780-17481930	MCF-7	breast:	n/a	n/a
31	CTCF	chr5:17443602-17443683	K562	blood:	n/a	n/a
32	CTCF	chr5:17468440-17468590	GM12873	blood:	n/a	n/a
33	CTCF	chr5:17443930-17444182	K562	blood:	n/a	n/a
34	CTCF	chr5:17468443-17468530	GM19238	blood:	n/a	n/a
35	CTCF	chr5:17468447-17468543	GM12878	blood:	n/a	n/a
36	CTCF	chr5:17438299-17438367	MCF-7	breast:	n/a	chr5:17438327-17438348
37	CTCF	chr5:17481912-17481950	Medullo	brain:	n/a	n/a
38	CTCF	chr5:17443500-17443650	GM12865	blood:	n/a	n/a
39	CTCF	chr5:17468454-17468538	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr5:17438309-17438355	Pancreas_OC	pancreas:	n/a	chr5:17438327-17438348
41	CTCF	chr5:17481946-17481996	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr5:17468453-17468523	GM10266	blood:	n/a	n/a
43	CTCF	chr5:17456692-17456725	Fibrobl	skin:	n/a	n/a
44	CTCF	chr5:17468421-17468553	K562	blood:	n/a	n/a
45	CTCF	chr5:17468405-17468580	GM19239	blood:	n/a	n/a
46	CTCF	chr5:17438300-17438372	H1-hESC	embryonic stem cell:	n/a	chr5:17438327-17438348
47	CTCF	chr5:17464299-17464386	Fibrobl	skin:	n/a	n/a
48	CTCF	chr5:17473433-17473489	GM13976	blood:	n/a	n/a
49	CTCF	chr5:17443850-17444181	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr5:17468420-17468570	A549	lung:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17491941-17491991	CMK	blood:	n/a
2	chr5:17491941-17491991	CMK	blood:	n/a
3	chr5:17488879-17488929	K562	blood:	n/a
4	chr5:17495781-17495831	HAEpiC	amniotic membrane:	n/a
5	chr5:17491469-17491519	NT2-D1	testis:	n/a
6	chr5:17491604-17491654	Hepatocyte	liver:	n/a
7	chr5:17491586-17491636	SK-N-SH	brain:	n/a
8	chr5:17491469-17491519	SK-N-SH	brain:	n/a
9	chr5:17485435-17485485	HL-60	blood:	n/a
10	chr5:17491941-17491991	IMR90	lung:	fetal
11	chr5:17491469-17491519	GM06990	blood:	n/a
12	chr5:17491586-17491636	ECC-1	luminal epithelium:	n/a
13	chr5:17488879-17488929	HCM	heart:	n/a
14	chr5:17491941-17491991	HCT-116	colon:	n/a
15	chr5:17490778-17490828	RPTEC	kidney:	n/a
16	chr5:17491469-17491519	CMK	blood:	n/a
17	chr5:17495781-17495831	HMEC	breast:	n/a
18	chr5:17444401-17444451	Caco-2	colon:	n/a
19	chr5:17490778-17490828	AG09319	gingival:	n/a
20	chr5:17444401-17444451	HAEpiC	amniotic membrane:	n/a
21	chr5:17491604-17491654	GM19239	blood:	n/a
22	chr5:17490778-17490828	BJ	skin:	n/a
23	chr5:17444401-17444451	LNCaP	prostate:	n/a
24	chr5:17491604-17491654	IMR90	lung:	fetal
25	chr5:17491469-17491519	HRPEpiC	eye:	n/a
26	chr5:17491469-17491519	HCM	heart:	n/a
27	chr5:17488879-17488929	LNCaP	prostate:	n/a
28	chr5:17485435-17485485	H1-hESC	embryonic stem cell:	embryo
29	chr5:17491941-17491991	HCPEpiC	choroid plexus:	n/a
30	chr5:17495781-17495831	HRPEpiC	eye:	n/a
31	chr5:17491586-17491636	GM12891	blood:	n/a
32	chr5:17488879-17488929	HRE	kidney:	n/a
33	chr5:17495781-17495831	ProgFib	skin:	n/a
34	chr5:17490778-17490828	GM12891	blood:	n/a
35	chr5:17485435-17485485	GM06990	blood:	n/a
36	chr5:17485435-17485485	HRE	kidney:	n/a
37	chr5:17444401-17444451	NH-A	brain:	n/a
38	chr5:17490778-17490828	BE2_C	brain:	n/a
39	chr5:17491941-17491991	A549	lung:	n/a
40	chr5:17491586-17491636	Hepatocyte	liver:	n/a
41	chr5:17495781-17495831	Caco-2	colon:	n/a
42	chr5:17488879-17488929	AoSMC	blood vessel:	n/a
43	chr5:17491604-17491654	ECC-1	luminal epithelium:	n/a
44	chr5:17444401-17444451	SK-N-SH	brain:	n/a
45	chr5:17491604-17491654	HMEC	breast:	n/a
46	chr5:17485435-17485485	GM12891	blood:	n/a
47	chr5:17491941-17491991	SK-N-SH_RA	brain:	n/a
48	chr5:17495781-17495831	ovcar-3	ovarian:	n/a
49	chr5:17488879-17488929	AG04449	skin:	fetal
50	chr5:17491469-17491519	GM19239	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:17448288..17450803-chr5:17469886..17472287,2	K562	blood:
2	chr5:17463203..17464706-chr5:17470171..17472480,2	MCF-7	breast:
3	chr5:17491440..17494172-chr5:17495062..17497549,2	MCF-7	breast:
4	chr5:17444658..17447223-chr5:17452681..17454773,2	MCF-7	breast:
5	chr5:17216689..17219268-chr5:17450632..17453590,2	MCF-7	breast:
6	chr5:17448288..17450803-chr5:17469886..17472287,2	K562	blood:
7	chr5:17482145..17483996-chr5:17485919..17488626,2	MCF-7	breast:
8	chr5:17445953..17448807-chr5:17455324..17457089,2	K562	blood:
9	chr5:17463203..17464706-chr5:17470171..17472480,2	MCF-7	breast:
10	chr5:17223492..17225946-chr5:17474747..17476783,2	MCF-7	breast:
11	chr5:17491440..17494172-chr5:17495062..17497549,2	MCF-7	breast:
12	chr5:17445953..17448807-chr5:17455324..17457089,2	K562	blood:
13	chr5:17445129..17446748-chr5:17447906..17450127,2	MCF-7	breast:
14	chr5:17446833..17449235-chr5:17452939..17454886,2	MCF-7	breast:
15	chr5:17445129..17446748-chr5:17447906..17450127,2	MCF-7	breast:
16	chr5:17444658..17447223-chr5:17452681..17454773,2	MCF-7	breast:
17	chr5:17446833..17449235-chr5:17452939..17454886,2	MCF-7	breast:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYO10-8	chr5:17437952-17438549	ucscGeneNc_uc003jga_2
2	lnc-BASP1-4	chr5:17483841-17484055	XLOC_004309
3	lnc-BASP1-3	chr5:17441578-17442654	XLOC_004308
4	lnc-BASP1-3	chr5:17441578-17441787	XLOC_004308
5	lnc-BASP1-4	chr5:17483931-17484068	XLOC_004309
6	lnc-BASP1-3	chr5:17441578-17441803	XLOC_004308
7	lnc-BASP1-4	chr5:17444119-17444343	XLOC_004309
8	lnc-MYO10-8	chr5:17440311-17440416	ucscGeneNc_uc003jga_2
9	lnc-BASP1-11	chr5:17465001-17465207	l_2885_chr5:17456969-17494846_brain
10	lnc-BASP1-11	chr5:17456970-17457429	l_2885_chr5:17456969-17494846_brain
11	lnc-BASP1-3	chr5:17441578-17441846	XLOC_004308
12	lnc-BASP1-3	chr5:17440223-17440293	XLOC_004308
13	lnc-BASP1-3	chr5:17441578-17441787	XLOC_004308
14	lnc-BASP1-3	chr5:17441577-17441809	NONHSAT100641
15	lnc-BASP1-4	chr5:17445736-17446039	XLOC_004309
16	lnc-BASP1-3	chr5:17441578-17442297	XLOC_004308
17	lnc-BASP1-3	chr5:17441578-17441826	NONHSAT100634
18	lnc-BASP1-3	chr5:17441578-17441787	XLOC_004308
19	lnc-BASP1-11	chr5:17457474-17457838	l_2885_chr5:17456969-17494846_brain
20	lnc-BASP1-11	chr5:17494578-17494846	l_2885_chr5:17456969-17494846_brain
21	lnc-BASP1-3	chr5:17441578-17441809	XLOC_004308
22	lnc-BASP1-3	chr5:17440222-17440293	NONHSAT100641
23	lnc-BASP1-4	chr5:17477724-17477865	XLOC_004309
24	lnc-BASP1-4	chr5:17485639-17485937	XLOC_004309
25	lnc-BASP1-4	chr5:17444119-17444343	XLOC_004309

No data

Variant related genes	Relation type
ENSG00000251304	TF binding region
ENSG00000248861	TF binding region
ENSG00000248205	TF binding region
ENSG00000250667	TF binding region
ENSG00000249662	TF binding region
ENSG00000268799	TF binding region
ENSG00000185041	TF binding region
ENSG00000249620	TF binding region
ENSG00000251304	CpG island
ENSG00000248861	CpG island
ENSG00000248205	CpG island
ENSG00000250667	CpG island
ENSG00000249662	CpG island
ENSG00000268799	CpG island
ENSG00000185041	CpG island
ENSG00000249620	CpG island
ENSG00000176788	chromatin interactions
ENSG00000268799	chromatin interactions
ENSG00000250667	chromatin interactions
ENSG00000251304	chromatin interactions
ENSG00000215196	chromatin interactions
RAE1	miRNA target sites
RNF41	miRNA target sites
PRKCE	miRNA target sites

Extended variants
information (count: 2360 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2360 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs871722	chr5:17437494-17437495	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs535275262	chr5:17437500-17437501	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs555192474	chr5:17437511-17437512	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs572053490	chr5:17437521-17437522	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs531204364	chr5:17437552-17437553	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs541017982	chr5:17437577-17437578	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs148955532	chr5:17437587-17437588	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs578032071	chr5:17437592-17437593	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs143687767	chr5:17437640-17437641	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs114343678	chr5:17437651-17437652	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs574246310	chr5:17437703-17437704	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs543247076	chr5:17437722-17437723	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs75728684	chr5:17437724-17437725	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs537454491	chr5:17437736-17437737	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs6893246	chr5:17437742-17437743	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs575912316	chr5:17437753-17437754	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs528837142	chr5:17437762-17437763	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs189447608	chr5:17437763-17437764	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs35873426	chr5:17437786-17437787	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs71611037	chr5:17437791-17437792	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs563956326	chr5:17437793-17437794	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs532967647	chr5:17437817-17437818	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs549569645	chr5:17437820-17437821	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs569733015	chr5:17437878-17437879	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs535264501	chr5:17437879-17437880	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs140961893	chr5:17437938-17437939	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs546165157	chr5:17437947-17437948	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs565623258	chr5:17437951-17437952	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs146325165	chr5:17438013-17438014	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
30	rs181802673	chr5:17438026-17438027	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
31	rs186267395	chr5:17438086-17438087	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
32	rs138227579	chr5:17438115-17438116	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
33	rs143698384	chr5:17438116-17438117	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
34	rs574232331	chr5:17438154-17438155	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
35	rs80252216	chr5:17438156-17438157	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
36	rs560026226	chr5:17438168-17438169	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
37	rs573355125	chr5:17438177-17438178	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
38	rs2459828	chr5:17438198-17438199	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs12108943	chr5:17438223-17438224	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
40	rs565579893	chr5:17438276-17438277	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
41	rs367762898	chr5:17438307-17438308	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
42	rs190739829	chr5:17438324-17438325	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
43	rs76228081	chr5:17438327-17438328	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
44	rs138561287	chr5:17438341-17438342	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
45	rs563031214	chr5:17438408-17438409	Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
46	rs528988332	chr5:17438432-17438433	Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
47	rs180710219	chr5:17438468-17438469	Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
48	rs565508552	chr5:17438492-17438493	Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
49	rs375524363	chr5:17438537-17438538	Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
50	rs551347484	chr5:17438548-17438549	Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	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
Melanoma	22183965	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	19287141	CNVD

Chromatin state (count:130 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17430800-17463800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:17435400-17439000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
3	chr5:17436000-17437600	Flanking Active TSS	Primary B cells from cord blood	blood
4	chr5:17436000-17437800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr5:17436200-17437600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr5:17436600-17437600	Flanking Active TSS	GM12878-XiMat	blood
7	chr5:17436800-17437600	Active TSS	Primary hematopoietic stem cells	blood
8	chr5:17437000-17437600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
9	chr5:17437200-17437600	Enhancers	Colon Smooth Muscle	Colon
10	chr5:17437200-17437600	Enhancers	Fetal Kidney	kidney
11	chr5:17437200-17437600	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr5:17437200-17437800	Enhancers	Primary B cells from peripheral blood	blood
13	chr5:17437200-17438400	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr5:17437400-17437600	Enhancers	HUVEC	blood vessel
15	chr5:17437400-17437800	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr5:17437400-17438000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr5:17437400-17438000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr5:17437400-17440800	Weak transcription	Osteobl	bone
19	chr5:17437600-17437800	Flanking Active TSS	Primary hematopoietic stem cells	blood
20	chr5:17437600-17437800	Enhancers	GM12878-XiMat	blood
21	chr5:17437600-17438000	Enhancers	Primary B cells from cord blood	blood
22	chr5:17437600-17438200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr5:17437800-17438000	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr5:17439000-17442400	Enhancers	Primary neutrophils fromperipheralblood	blood
25	chr5:17440200-17441400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr5:17440600-17442200	Enhancers	NH-A	brain
27	chr5:17440800-17442600	Enhancers	Osteobl	bone
28	chr5:17441000-17442200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr5:17441400-17441600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr5:17441600-17442400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr5:17442200-17444200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr5:17442200-17444200	Weak transcription	NH-A	brain
33	chr5:17442400-17442600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr5:17442400-17444200	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr5:17442400-17444400	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr5:17442400-17446200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
37	chr5:17442600-17443200	Enhancers	Primary B cells from cord blood	blood
38	chr5:17442600-17448400	Weak transcription	Osteobl	bone
39	chr5:17443200-17444000	Weak transcription	Primary B cells from cord blood	blood
40	chr5:17443400-17443800	Enhancers	Gastric	stomach
41	chr5:17443600-17444400	Enhancers	Fetal Brain Male	brain
42	chr5:17443800-17445000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr5:17443800-17445000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr5:17443800-17445400	Weak transcription	Gastric	stomach
45	chr5:17444000-17445600	Active TSS	Primary B cells from cord blood	blood
46	chr5:17444000-17446200	Enhancers	Stomach Mucosa	stomach
47	chr5:17444200-17444400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
48	chr5:17444200-17445200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr5:17444200-17445600	Enhancers	NH-A	brain
50	chr5:17444200-17446200	Enhancers	A549	lung

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