Variant report

Variant	nsv597681
Chromosome Location	chr5:27426728-27526060
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:782)
CpG islands
(count:367)
Chromatin interactive
region (count:17)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:782 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:27471950-27472762	HepG2	liver:	n/a	n/a
2	ATF1	chr5:27428887-27428920	K562	blood:	n/a	n/a
3	ATF2	chr5:27472335-27472849	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr5:27480439-27480694	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:27472100-27472589	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:27472602-27472610	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr5:27473140-27473798	GM12878	blood:	n/a	n/a
8	BHLHE40	chr5:27473085-27473935	K562	blood:	n/a	n/a
9	BHLHE40	chr5:27473428-27473653	HepG2	liver:	n/a	n/a
10	BHLHE40	chr5:27523477-27524035	K562	blood:	n/a	n/a
11	BHLHE40	chr5:27473142-27473831	HepG2	liver:	n/a	n/a
12	BHLHE40	chr5:27472077-27472614	GM12878	blood:	n/a	n/a
13	BHLHE40	chr5:27523586-27524110	HepG2	liver:	n/a	n/a
14	BHLHE40	chr5:27473412-27473860	A549	lung:	n/a	n/a
15	BRCA1	chr5:27472043-27473952	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr5:27448587-27448827	HepG2	liver:	n/a	chr5:27448671-27448682
17	CEBPB	chr5:27431090-27431379	A549	lung:	n/a	n/a
18	CEBPB	chr5:27510117-27510388	Hela-S3	cervix:	n/a	chr5:27510236-27510247
19	CEBPB	chr5:27465277-27465509	HepG2	liver:	n/a	chr5:27465370-27465381
20	CEBPB	chr5:27496435-27496760	HepG2	liver:	n/a	chr5:27496587-27496600 chr5:27496589-27496598 chr5:27496589-27496600 chr5:27496587-27496600 chr5:27496587-27496598
21	CEBPB	chr5:27521019-27521350	HepG2	liver:	n/a	chr5:27521082-27521099 chr5:27521085-27521098
22	CEBPB	chr5:27510109-27510409	A549	lung:	n/a	chr5:27510236-27510247
23	CEBPB	chr5:27488786-27488986	HepG2	liver:	n/a	chr5:27488807-27488820 chr5:27488848-27488857 chr5:27488846-27488857 chr5:27488809-27488820 chr5:27488809-27488820 chr5:27488807-27488818 chr5:27488807-27488820
24	CEBPB	chr5:27434380-27434748	ECC-1	luminal epithelium:	n/a	chr5:27434536-27434547 chr5:27434534-27434547 chr5:27434534-27434545 chr5:27434726-27434743
25	CEBPB	chr5:27444220-27444223	A549	lung:	n/a	n/a
26	CEBPB	chr5:27448645-27448696	Hela-S3	cervix:	n/a	chr5:27448671-27448682
27	CEBPB	chr5:27472147-27472690	HepG2	liver:	n/a	n/a
28	CEBPB	chr5:27520976-27521265	A549	lung:	n/a	chr5:27521082-27521099 chr5:27521085-27521098
29	CEBPB	chr5:27459726-27459987	HepG2	liver:	n/a	chr5:27459841-27459854 chr5:27459841-27459852 chr5:27459842-27459853
30	CEBPB	chr5:27496445-27496749	K562	blood:	n/a	chr5:27496587-27496600 chr5:27496589-27496598 chr5:27496589-27496600 chr5:27496587-27496600 chr5:27496587-27496598
31	CEBPB	chr5:27496448-27496745	Hela-S3	cervix:	n/a	chr5:27496587-27496600 chr5:27496589-27496598 chr5:27496589-27496600 chr5:27496587-27496600 chr5:27496587-27496598
32	CEBPB	chr5:27510195-27510392	K562	blood:	n/a	chr5:27510236-27510247
33	CEBPB	chr5:27434401-27434672	HepG2	liver:	n/a	chr5:27434536-27434547 chr5:27434534-27434547 chr5:27434534-27434545
34	CEBPB	chr5:27521041-27521386	IMR90	lung:	n/a	chr5:27521082-27521099 chr5:27521085-27521098
35	CEBPB	chr5:27434396-27434708	A549	lung:	n/a	chr5:27434536-27434547 chr5:27434534-27434547 chr5:27434534-27434545
36	CEBPB	chr5:27472163-27473883	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr5:27496438-27496767	A549	lung:	n/a	chr5:27496587-27496600 chr5:27496589-27496598 chr5:27496589-27496600 chr5:27496587-27496600 chr5:27496587-27496598
38	CEBPB	chr5:27496418-27496770	IMR90	lung:	n/a	chr5:27496587-27496600 chr5:27496589-27496598 chr5:27496589-27496600 chr5:27496587-27496600 chr5:27496587-27496598
39	CEBPB	chr5:27497947-27498299	HepG2	liver:	n/a	chr5:27498130-27498139 chr5:27498130-27498139
40	CEBPB	chr5:27510098-27510421	HepG2	liver:	n/a	chr5:27510236-27510247
41	CEBPB	chr5:27459716-27459960	A549	lung:	n/a	chr5:27459841-27459854 chr5:27459841-27459852 chr5:27459842-27459853
42	CEBPD	chr5:27472396-27472646	HepG2	liver:	n/a	n/a
43	CEBPD	chr5:27472200-27472594	HepG2	liver:	n/a	n/a
44	CHD1	chr5:27473616-27473621	GM12878	blood:	n/a	n/a
45	CHD1	chr5:27476041-27476172	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr5:27472064-27474597	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr5:27472063-27472656	GM12878	blood:	n/a	n/a
48	CHD2	chr5:27472182-27472643	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr5:27523744-27523834	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr5:27478298-27478421	H1-hESC	embryonic stem cell:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:27438836-27438886	BJ	skin:	n/a
2	chr5:27438836-27438886	BJ	skin:	n/a
3	chr5:27523974-27524024	RPTEC	kidney:	n/a
4	chr5:27472542-27472592	AG09319	gingival:	n/a
5	chr5:27523909-27523959	HCF	heart:	n/a
6	chr5:27523974-27524024	HCPEpiC	choroid plexus:	n/a
7	chr5:27523909-27523959	Hela-S3	cervix:	n/a
8	chr5:27472029-27472079	HMEC	breast:	n/a
9	chr5:27472029-27472079	HCM	heart:	n/a
10	chr5:27472520-27472570	GM19239	blood:	n/a
11	chr5:27472542-27472592	SAEC	small airway:	n/a
12	chr5:27523974-27524024	ProgFib	skin:	n/a
13	chr5:27472542-27472592	ECC-1	luminal epithelium:	n/a
14	chr5:27523974-27524024	K562	blood:	n/a
15	chr5:27472520-27472570	AG04449	skin:	fetal
16	chr5:27523909-27523959	GM19239	blood:	n/a
17	chr5:27438836-27438886	NT2-D1	testis:	n/a
18	chr5:27472029-27472079	Hepatocyte	liver:	n/a
19	chr5:27472520-27472570	BJ	skin:	n/a
20	chr5:27438836-27438886	ovcar-3	ovarian:	n/a
21	chr5:27438836-27438886	BE2_C	brain:	n/a
22	chr5:27438836-27438886	AG09309	skin:	n/a
23	chr5:27523974-27524024	BJ	skin:	n/a
24	chr5:27523909-27523959	NHBE	bronchial:	n/a
25	chr5:27472029-27472079	GM19239	blood:	n/a
26	chr5:27523909-27523959	MCF-7	breast:	n/a
27	chr5:27472029-27472079	HRPEpiC	eye:	n/a
28	chr5:27438836-27438886	AG04450	lung:	fetal
29	chr5:27472029-27472079	PFSK-1	brain:	n/a
30	chr5:27438836-27438886	H1-hESC	embryonic stem cell:	embryo
31	chr5:27472520-27472570	RPTEC	kidney:	n/a
32	chr5:27523909-27523959	NHDF-neo	bronchial:	n/a
33	chr5:27523909-27523959	HEK293	kidney:	embryo
34	chr5:27472029-27472079	HL-60	blood:	n/a
35	chr5:27472029-27472079	AG04450	lung:	fetal
36	chr5:27523974-27524024	Caco-2	colon:	n/a
37	chr5:27438836-27438886	HCT-116	colon:	n/a
38	chr5:27472542-27472592	SK-N-SH_RA	brain:	n/a
39	chr5:27523909-27523959	HRCEpiC	kidney:	n/a
40	chr5:27523974-27524024	HEK293	kidney:	embryo
41	chr5:27472029-27472079	GM12892	blood:	n/a
42	chr5:27472520-27472570	HUVEC	blood vessel:	n/a
43	chr5:27472520-27472570	AG10803	skin:	n/a
44	chr5:27472029-27472079	SAEC	small airway:	n/a
45	chr5:27472542-27472592	GM12892	blood:	n/a
46	chr5:27472542-27472592	NB4	blood:	n/a
47	chr5:27523974-27524024	HUVEC	blood vessel:	n/a
48	chr5:27438836-27438886	NB4	blood:	n/a
49	chr5:27472542-27472592	HRCEpiC	kidney:	n/a
50	chr5:27472029-27472079	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:27441556..27444509-chr5:27447634..27449803,2	K562	blood:
2	chr5:27465898..27467546-chr5:27470324..27472509,2	K562	blood:
3	chr5:27467308..27469302-chr5:27473283..27475423,2	K562	blood:
4	chr5:27415884..27418944-chr5:27423264..27427119,3	K562	blood:
5	chr5:27467308..27469302-chr5:27473283..27475423,2	K562	blood:
6	chr5:27483953..27485836-chr5:27487380..27490659,3	K562	blood:
7	chr10:69644380..69644911-chr5:27472591..27473140,2	Hela-S3	cervix:
8	chr5:27483622..27485658-chr5:27500054..27501684,2	K562	blood:
9	chr5:27483953..27485836-chr5:27487380..27490659,3	K562	blood:
10	chr5:27466020..27468393-chr5:27470324..27473144,3	K562	blood:
11	chr5:27470415..27473388-chr5:27486185..27488435,2	K562	blood:
12	chr19:45907739..45908484-chr5:27472364..27473126,2	Hela-S3	cervix:
13	chr5:27483622..27485658-chr5:27500054..27501684,2	K562	blood:
14	chr5:27483953..27486391-chr5:27488039..27490659,3	K562	blood:
15	chr5:27483953..27486391-chr5:27488039..27490659,3	K562	blood:
16	chr5:27422999..27425291-chr5:27429898..27432218,2	K562	blood:
17	chr5:27441556..27444509-chr5:27447634..27449803,2	K562	blood:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf17-8	chr5:27485033-27485136	ENSG00000250337
2	lnc-C5orf17-8	chr5:27475642-27475802	XLOC_004323
3	lnc-C5orf17-8	chr5:27475642-27475802	ENSG00000250337
4	lnc-C5orf17-8	chr5:27489389-27489493	ENSG00000250337
5	lnc-C5orf17-14	chr5:27520790-27521692	ucscGeneNc_uc003jgv_1
6	lnc-C5orf17-8	chr5:27472414-27472626	ENSG00000250337
7	lnc-C5orf17-8	chr5:27485033-27485136	ENSG00000250337
8	lnc-CDH9-2	chr5:27428267-27428320	XLOC_004761
9	lnc-C5orf17-8	chr5:27494342-27494425	ENSG00000250337
10	lnc-C5orf17-13	chr5:27497127-27497768	NONHSAT100808
11	lnc-CDH9-9	chr5:27442394-27442634	l_2893_chr5:27442393-27446144_testes
12	lnc-C5orf17-8	chr5:27475642-27475802	ENSG00000250337
13	lnc-C5orf17-8	chr5:27489389-27489493	ENSG00000250337
14	lnc-CDH9-2	chr5:27436260-27436518	XLOC_004761
15	lnc-C5orf17-8	chr5:27496056-27496274	XLOC_004323
16	lnc-C5orf17-8	chr5:27485033-27487999	XLOC_004323
17	lnc-C5orf17-8	chr5:27472414-27472626	ENSG00000250337
18	lnc-C5orf17-8	chr5:27475642-27475802	ENSG00000250337
19	lnc-C5orf17-8	chr5:27494342-27494425	ENSG00000250337
20	lnc-C5orf17-14	chr5:27508148-27508383	ucscGeneNc_uc003jgv_1
21	lnc-CDH9-9	chr5:27446084-27446144	l_2893_chr5:27442393-27446144_testes
22	lnc-C5orf17-14	chr5:27511399-27511559	ucscGeneNc_uc003jgv_1
23	lnc-C5orf17-8	chr5:27494420-27494442	XLOC_004323
24	lnc-C5orf17-8	chr5:27494226-27494425	ENSG00000250337
25	lnc-C5orf17-8	chr5:27477746-27477908	ENSG00000250337
26	lnc-CDH9-9	chr5:27448470-27448525	l_2893_chr5:27442393-27446144_testes
27	lnc-C5orf17-8	chr5:27472414-27472626	ENSG00000250337
28	lnc-C5orf17-8	chr5:27472418-27472626	XLOC_004323
29	lnc-C5orf17-8	chr5:27476194-27477201	XLOC_004323
30	lnc-C5orf17-8	chr5:27476833-27477908	XLOC_004323

No data

Variant related genes	Relation type
LINC01021	TF binding region
ENSG00000248490	TF binding region
LINC01021	CpG island
ENSG00000248490	CpG island
ENSG00000104881	chromatin interactions
ENSG00000250337	chromatin interactions
ENSG00000096717	chromatin interactions
KRAS	miRNA target sites
NUDT12	miRNA target sites
BTAF1	miRNA target sites
SIRT1	miRNA target sites
SYNJ1	miRNA target sites
CKAP5	miRNA target sites
TERF2	miRNA target sites
RANBP10	miRNA target sites
SCCPDH	miRNA target sites
PTPN22	miRNA target sites
BCL2	miRNA target sites

Extended variants
information (count: 2204 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2204 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548703559	chr5:27428268-27428269	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs563729780	chr5:27428294-27428295	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs190380145	chr5:27428308-27428309	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs77609755	chr5:27428312-27428313	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs140856724	chr5:27434005-27434006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535155072	chr5:27434031-27434032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs149743688	chr5:27434033-27434034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78249773	chr5:27434105-27434106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147833744	chr5:27434157-27434158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557985494	chr5:27434177-27434178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542867836	chr5:27434186-27434187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181303316	chr5:27434202-27434203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541481520	chr5:27434205-27434206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559782923	chr5:27434238-27434239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184983476	chr5:27434253-27434254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542307358	chr5:27434260-27434261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143772538	chr5:27434263-27434264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371760789	chr5:27434264-27434265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563749555	chr5:27434289-27434290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188328244	chr5:27434312-27434313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs143561751	chr5:27434317-27434318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10942246	chr5:27434339-27434340	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs114112817	chr5:27434360-27434361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528756284	chr5:27434378-27434379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73069843	chr5:27434386-27434387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs145799396	chr5:27434402-27434403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs76535507	chr5:27434405-27434406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs34509367	chr5:27434406-27434407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs397777060	chr5:27434410-27434411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs80133265	chr5:27434411-27434412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs375640386	chr5:27434413-27434414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs370468763	chr5:27434417-27434418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567701069	chr5:27434443-27434444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535191370	chr5:27434449-27434450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs77460626	chr5:27434453-27434454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs77434721	chr5:27434567-27434568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs66701456	chr5:27434608-27434609	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs181760315	chr5:27434624-27434625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs187200386	chr5:27434643-27434644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs116420874	chr5:27434660-27434661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374247872	chr5:27434734-27434735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs76136649	chr5:27434746-27434747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548035620	chr5:27434760-27434761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs376113178	chr5:27434798-27434799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs191728105	chr5:27434839-27434840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs368955353	chr5:27434841-27434842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372300361	chr5:27434861-27434862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183515276	chr5:27434866-27434867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs575637359	chr5:27434884-27434885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs546424337	chr5:27434886-27434887	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
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
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	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
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Compulsive disorder	18923513	CNVD
Epilepsy	18923513	CNVD
Prader-willi syndrome	18923513	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:206 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:27434000-27435200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr5:27434200-27435200	Enhancers	NHEK	skin
3	chr5:27435000-27435200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:27435000-27435400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr5:27435000-27435400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr5:27435000-27435600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr5:27435200-27436200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr5:27436200-27436600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:27436400-27436600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr5:27436800-27449400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr5:27442800-27443200	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr5:27446600-27449200	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr5:27447600-27448400	ZNF genes & repeats	Spleen	Spleen
14	chr5:27450600-27451200	Enhancers	Fetal Heart	heart
15	chr5:27450800-27451000	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr5:27450800-27451200	Enhancers	Rectal Smooth Muscle	rectum
17	chr5:27450800-27451400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr5:27451000-27451400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
19	chr5:27451400-27452000	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr5:27467800-27468400	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr5:27467800-27468600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr5:27468000-27468400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:27468000-27468600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr5:27468400-27472000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr5:27468400-27472200	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr5:27468600-27470000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr5:27468600-27472000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr5:27470000-27470400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr5:27470000-27470600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr5:27470400-27471800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr5:27470600-27471800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr5:27471000-27471800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr5:27471200-27471600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr5:27471400-27472000	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr5:27471600-27471800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr5:27471600-27471800	Enhancers	A549	lung
37	chr5:27471600-27472000	Enhancers	Hela-S3	cervix
38	chr5:27471600-27472400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr5:27471800-27472000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr5:27471800-27472000	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr5:27471800-27472000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr5:27471800-27472200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
43	chr5:27471800-27472200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr5:27471800-27472200	Flanking Active TSS	A549	lung
45	chr5:27471800-27472200	Enhancers	HepG2	liver
46	chr5:27471800-27474600	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr5:27472000-27472200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:27472000-27472200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr5:27472000-27472200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
50	chr5:27472000-27472200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell

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