Variant report

Variant	nsv1059766
Chromosome Location	chr17:45130765-45203468
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1580)
CpG islands
(count:794)
Chromatin interactive
region (count:36)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1580 , 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	chr17:45144527-45145208	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:45191135-45191603	K562	blood:	n/a	n/a
3	ARID3A	chr17:45178080-45178088	HepG2	liver:	n/a	n/a
4	ARID3A	chr17:45165062-45165080	K562	blood:	n/a	n/a
5	ARID3A	chr17:45140347-45140388	K562	blood:	n/a	n/a
6	ARID3A	chr17:45144743-45145166	K562	blood:	n/a	n/a
7	ATF1	chr17:45148562-45148592	K562	blood:	n/a	n/a
8	ATF1	chr17:45176347-45176414	K562	blood:	n/a	n/a
9	ATF2	chr17:45144587-45145135	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr17:45144604-45145036	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr17:45144575-45145188	GM12878	blood:	n/a	n/a
12	ATF2	chr17:45144651-45145146	GM12878	blood:	n/a	n/a
13	ATF3	chr17:45144719-45145135	K562	blood:	n/a	n/a
14	ATF3	chr17:45144278-45145192	A549	lung:	n/a	n/a
15	ATF3	chr17:45144521-45145080	A549	lung:	n/a	n/a
16	BACH1	chr17:45177408-45177655	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr17:45142639-45142681	K562	blood:	n/a	n/a
18	BACH1	chr17:45191283-45191331	K562	blood:	n/a	n/a
19	BACH1	chr17:45144464-45144994	K562	blood:	n/a	n/a
20	BATF	chr17:45144747-45145054	GM12878	blood:	n/a	n/a
21	BCL11A	chr17:45144770-45145045	GM12878	blood:	n/a	n/a
22	BCL11A	chr17:45144678-45144962	GM12878	blood:	n/a	n/a
23	BCL3	chr17:45177585-45178094	A549	lung:	n/a	n/a
24	BCL3	chr17:45144478-45145168	A549	lung:	n/a	n/a
25	BCL3	chr17:45143945-45145197	A549	lung:	n/a	n/a
26	BCL3	chr17:45144494-45145057	GM12878	blood:	n/a	n/a
27	BCLAF1	chr17:45144096-45145119	GM12878	blood:	n/a	n/a
28	BCLAF1	chr17:45144518-45145177	K562	blood:	n/a	n/a
29	BCLAF1	chr17:45177412-45177731	GM12878	blood:	n/a	n/a
30	BCLAF1	chr17:45144491-45145085	GM12878	blood:	n/a	n/a
31	BCLAF1	chr17:45144545-45145178	K562	blood:	n/a	n/a
32	BHLHE40	chr17:45177425-45177752	K562	blood:	n/a	n/a
33	BHLHE40	chr17:45177528-45177799	GM12878	blood:	n/a	n/a
34	BHLHE40	chr17:45176199-45176524	GM12878	blood:	n/a	n/a
35	BHLHE40	chr17:45147784-45147837	A549	lung:	n/a	n/a
36	BHLHE40	chr17:45176257-45176572	K562	blood:	n/a	n/a
37	BHLHE40	chr17:45144608-45145047	K562	blood:	n/a	n/a
38	BHLHE40	chr17:45144674-45145149	GM12878	blood:	n/a	n/a
39	BRCA1	chr17:45144688-45145138	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr17:45177718-45177810	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr17:45144647-45144987	HepG2	liver:	n/a	n/a
42	BRCA1	chr17:45147769-45147988	Hela-S3	cervix:	n/a	n/a
43	CBX3	chr17:45142102-45142392	K562	blood:	n/a	n/a
44	CBX3	chr17:45144579-45145091	K562	blood:	n/a	n/a
45	CBX3	chr17:45141967-45142458	K562	blood:	n/a	n/a
46	CBX3	chr17:45183455-45183828	K562	blood:	n/a	n/a
47	CBX3	chr17:45148405-45148864	K562	blood:	n/a	n/a
48	CBX3	chr17:45144515-45145100	K562	blood:	n/a	n/a
49	CBX3	chr17:45176116-45176464	K562	blood:	n/a	n/a
50	CCNT2	chr17:45144623-45145013	K562	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45177859-45177909	NT2-D1	testis:	n/a
2	chr17:45177859-45177909	NT2-D1	testis:	n/a
3	chr17:45183984-45184034	H1-hESC	embryonic stem cell:	embryo
4	chr17:45177429-45177479	U87	brain:	n/a
5	chr17:45177859-45177909	HRPEpiC	eye:	n/a
6	chr17:45177598-45177648	HEK293	kidney:	embryo
7	chr17:45177429-45177479	HIPEpiC	eye:	n/a
8	chr17:45198207-45198257	HEEpiC	esophagus:	n/a
9	chr17:45177429-45177479	AG10803	skin:	n/a
10	chr17:45177598-45177648	HUVEC	blood vessel:	n/a
11	chr17:45177431-45177481	GM12891	blood:	n/a
12	chr17:45177429-45177479	AG04449	skin:	fetal
13	chr17:45177859-45177909	H1-hESC	embryonic stem cell:	embryo
14	chr17:45177859-45177909	HUVEC	blood vessel:	n/a
15	chr17:45183984-45184034	PFSK-1	brain:	n/a
16	chr17:45134721-45134771	HCT-116	colon:	n/a
17	chr17:45143871-45143921	ovcar-3	ovarian:	n/a
18	chr17:45177859-45177909	U87	brain:	n/a
19	chr17:45177859-45177909	BE2_C	brain:	n/a
20	chr17:45174155-45174205	HAEpiC	amniotic membrane:	n/a
21	chr17:45134721-45134771	MCF-7	breast:	n/a
22	chr17:45134721-45134771	SK-N-SH	brain:	n/a
23	chr17:45177628-45177678	HPAEpiC	pulmonary alveolar:	n/a
24	chr17:45177598-45177648	GM06990	blood:	n/a
25	chr17:45177429-45177479	NHDF-neo	bronchial:	n/a
26	chr17:45198207-45198257	AG04449	skin:	fetal
27	chr17:45177859-45177909	SK-N-MC	brain:	n/a
28	chr17:45174155-45174205	IMR90	lung:	fetal
29	chr17:45198207-45198257	AG09309	skin:	n/a
30	chr17:45177429-45177479	PANC-1	pancreas:	n/a
31	chr17:45177859-45177909	GM19239	blood:	n/a
32	chr17:45177859-45177909	SAEC	small airway:	n/a
33	chr17:45177378-45177428	AG04450	lung:	fetal
34	chr17:45198207-45198257	Caco-2	colon:	n/a
35	chr17:45177431-45177481	HEK293	kidney:	embryo
36	chr17:45177598-45177648	CMK	blood:	n/a
37	chr17:45183984-45184034	BJ	skin:	n/a
38	chr17:45198207-45198257	HL-60	blood:	n/a
39	chr17:45134721-45134771	HEEpiC	esophagus:	n/a
40	chr17:45177429-45177479	PFSK-1	brain:	n/a
41	chr17:45177598-45177648	HCF	heart:	n/a
42	chr17:45177598-45177648	Jurkat	blood:	n/a
43	chr17:45177431-45177481	AG04450	lung:	fetal
44	chr17:45177378-45177428	HRPEpiC	eye:	n/a
45	chr17:45177859-45177909	HRE	kidney:	n/a
46	chr17:45174155-45174205	Hepatocyte	liver:	n/a
47	chr17:45177628-45177678	Caco-2	colon:	n/a
48	chr17:45143871-45143921	HEEpiC	esophagus:	n/a
49	chr17:45177429-45177479	GM12892	blood:	n/a
50	chr17:45198207-45198257	NHBE	bronchial:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:45141024..45142587-chr17:45143013..45146312,3	K562	blood:
2	chr17:45156502..45159050-chr17:45162212..45165184,2	K562	blood:
3	chr17:45137333..45141674-chr17:45143017..45146181,5	MCF-7	breast:
4	chr17:45142727..45145152-chr17:45150394..45151973,2	K562	blood:
5	chr17:45143352..45144907-chr17:45399301..45401186,2	K562	blood:
6	chr17:45136707..45138287-chr17:45138390..45140418,2	K562	blood:
7	chr17:45148479..45151206-chr17:45175479..45177922,2	K562	blood:
8	chr1:28655193..28655793-chr17:45144387..45145240,2	Hela-S3	cervix:
9	chr17:45162074..45163604-chr17:45171046..45173992,2	MCF-7	breast:
10	chr17:45145658..45148463-chr17:45161187..45163786,2	MCF-7	breast:
11	chr17:45170129..45171669-chr17:45173350..45174934,2	K562	blood:
12	chr17:45155821..45158287-chr17:45163734..45167832,3	K562	blood:
13	chr17:45143436..45146346-chr17:45178059..45181405,3	K562	blood:
14	chr17:45138815..45142587-chr17:45143506..45146312,3	K562	blood:
15	chr17:45179866..45182150-chr17:45185203..45188192,2	K562	blood:
16	chr17:45179866..45182150-chr17:45185203..45188192,2	K562	blood:
17	chr17:45136707..45138287-chr17:45138390..45140418,2	K562	blood:
18	chr17:44302347..44303352-chr17:45177408..45178065,4	HCT-116	colon:
19	chr17:45155821..45158287-chr17:45163734..45167832,3	K562	blood:
20	chr17:45163760..45166072-chr17:45166357..45168655,2	K562	blood:
21	chr17:45143258..45146165-chr17:45178013..45180632,2	K562	blood:
22	chr17:45156502..45159050-chr17:45162212..45165184,2	K562	blood:
23	chr17:45170129..45171669-chr17:45173350..45174934,2	K562	blood:
24	chr17:45159211..45163683-chr17:45163741..45168313,5	K562	blood:
25	chr17:45145658..45148463-chr17:45161187..45163786,2	MCF-7	breast:
26	chr17:45195494..45197087-chr17:45199093..45201965,2	K562	blood:
27	chr17:45169541..45171629-chr17:45172586..45174850,2	K562	blood:
28	chr17:45177573..45179138-chr17:45179846..45181452,2	MCF-7	breast:
29	chr17:45195494..45197087-chr17:45199093..45201965,2	K562	blood:
30	chr17:45143352..45146051-chr17:45399301..45401762,3	K562	blood:
31	chr17:45159211..45163683-chr17:45163741..45168313,5	K562	blood:
32	chr17:45169541..45171629-chr17:45172586..45174850,2	K562	blood:
33	chr17:45144506..45145240-chr9:130213283..130213833,2	Hela-S3	cervix:
34	chr17:45163760..45166072-chr17:45166357..45168655,2	K562	blood:
35	chr17:45162074..45163604-chr17:45171046..45173992,2	MCF-7	breast:
36	chr17:45190584..45193064-chr17:45401116..45402656,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPRML-3	chr17:45149838-45149925	NONHSAT054277
2	lnc-RPRML-3	chr17:45133975-45134119	ENSG00000262879.1
3	lnc-RPRML-3	chr17:45177201-45177560	NONHSAT054278
4	lnc-GOSR2-2	chr17:45126422-45131777	NONHSAT054246
5	lnc-RPRML-3	chr17:45177201-45177605	ENSG00000262879.1
6	lnc-RPRML-3	chr17:45176744-45177617	NONHSAT054281
7	lnc-RPRML-3	chr17:45149838-45149925	ENSG00000262879.1
8	lnc-GOSR2-2	chr17:45131884-45134124	NONHSAT054246
9	lnc-RPRML-3	chr17:45159286-45159716	ENSG00000262879.1
10	lnc-RPRML-3	chr17:45148881-45148978	NONHSAT054277
11	lnc-RPRML-3	chr17:45158273-45158298	NONHSAT054279
12	lnc-RPRML-3	chr17:45177201-45177631	NONHSAT054279
13	lnc-CDC27-3	chr17:45135517-45136457	NONHSAT054275
14	lnc-RPRML-3	chr17:45149723-45149925	NONHSAT054278
15	lnc-GOSR2-2	chr17:45131638-45133274	NONHSAT054261
16	lnc-GOSR2-2	chr17:45131093-45131559	NONHSAT054261
17	lnc-RPRML-3	chr17:45129892-45131988	NONHSAT054259
18	lnc-RPRML-3	chr17:45177201-45177614	ENSG00000262879.1
19	lnc-RPRML-3	chr17:45177201-45177614	NONHSAT054277

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	CDC27	hsa-miR-16-5p	chr17:45195640-45195634
2	CDC27	hsa-miR-32-5p	chr17:45198131-45198124
3	CDC27	hsa-miR-16-5p	chr17:45195634-45195658
4	CDC27	hsa-miR-32-5p	chr17:45198125-45198146

Variant related genes	Relation type
ENSG00000221016	TF binding region
CDC27	TF binding region
ENSG00000262879	TF binding region
ENSG00000221016	CpG island
CDC27	CpG island
ENSG00000262879	CpG island
ENSG00000197958	chromatin interactions
ENSG00000263293	chromatin interactions
ENSG00000130772	chromatin interactions
ENSG00000262879	chromatin interactions
ENSG00000178852	chromatin interactions
ENSG00000221016	chromatin interactions
ENSG00000148356	chromatin interactions
ENSG00000120071	chromatin interactions
ENSG00000004897	chromatin interactions

Extended variants
information (count: 2612 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:2612 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377399299	chr17:45130769-45130770	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs138238695	chr17:45130810-45130811	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs4257261	chr17:45130836-45130837	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs550186350	chr17:45130876-45130877	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs570382129	chr17:45130911-45130912	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs146318501	chr17:45130991-45130992	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs553261799	chr17:45130992-45130993	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs572950514	chr17:45131014-45131015	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs373670903	chr17:45131019-45131020	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs535681723	chr17:45131108-45131109	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs139039678	chr17:45131149-45131150	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs543065860	chr17:45131205-45131206	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs188575165	chr17:45131256-45131257	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs544581577	chr17:45131288-45131289	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs564457043	chr17:45131307-45131308	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs578089492	chr17:45131362-45131363	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs142849329	chr17:45131426-45131427	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs560879492	chr17:45131434-45131435	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs529423550	chr17:45131438-45131439	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs192871243	chr17:45131491-45131492	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs184917728	chr17:45131519-45131520	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs377253091	chr17:45131526-45131527	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs188330693	chr17:45131531-45131532	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs529385932	chr17:45131532-45131533	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs191236229	chr17:45131566-45131567	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs148033190	chr17:45131598-45131599	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs141749331	chr17:45131605-45131606	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs183826806	chr17:45131638-45131639	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs150531623	chr17:45131664-45131665	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs535266033	chr17:45131671-45131672	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs555552658	chr17:45131680-45131681	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs569104993	chr17:45131704-45131705	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs61181097	chr17:45131712-45131713	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs558327966	chr17:45131718-45131719	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs578061766	chr17:45131727-45131728	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs540627873	chr17:45131739-45131740	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs554120401	chr17:45131743-45131744	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs574300420	chr17:45131754-45131755	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs7220777	chr17:45131755-45131756	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs562729282	chr17:45131787-45131788	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs531817504	chr17:45131836-45131837	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs543901537	chr17:45131838-45131839	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs563880714	chr17:45131863-45131864	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs532726619	chr17:45131901-45131902	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs546579670	chr17:45131906-45131907	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs189426932	chr17:45131914-45131915	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs182082003	chr17:45131925-45131926	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs549035142	chr17:45131960-45131961	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs569067979	chr17:45131973-45131974	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs538077680	chr17:45132023-45132024	Weak transcription Strong transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	17142309	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2054 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45090000-45131600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr17:45090200-45131000	Weak transcription	Dnd41	blood
3	chr17:45096200-45131000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr17:45121400-45142200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr17:45123800-45143600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr17:45124000-45131400	Weak transcription	GM12878-XiMat	blood
7	chr17:45124800-45130800	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr17:45125000-45133400	Weak transcription	Fetal Brain Female	brain
9	chr17:45125200-45130800	Weak transcription	Fetal Kidney	kidney
10	chr17:45125200-45132400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr17:45125200-45143600	Weak transcription	HepG2	liver
12	chr17:45125400-45132400	Weak transcription	Right Ventricle	heart
13	chr17:45125400-45133200	Weak transcription	Gastric	stomach
14	chr17:45125400-45133400	Weak transcription	Pancreas	Pancrea
15	chr17:45125400-45143800	Weak transcription	NHLF	lung
16	chr17:45127000-45133400	Weak transcription	Ovary	ovary
17	chr17:45127200-45131400	Weak transcription	HSMM	muscle
18	chr17:45128200-45133200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr17:45128200-45133400	Weak transcription	Brain Angular Gyrus	brain
20	chr17:45128200-45140000	Weak transcription	K562	blood
21	chr17:45128200-45143600	Weak transcription	HSMMtube	muscle
22	chr17:45128200-45143800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr17:45128400-45131000	Weak transcription	Primary neutrophils fromperipheralblood	blood
24	chr17:45128400-45131200	Weak transcription	Brain Cingulate Gyrus	brain
25	chr17:45128400-45131400	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr17:45128400-45133200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr17:45128600-45130800	Weak transcription	Left Ventricle	heart
28	chr17:45128600-45134200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr17:45128800-45133400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr17:45128800-45143600	Weak transcription	HUVEC	blood vessel
31	chr17:45128800-45144600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr17:45129000-45131400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr17:45129000-45131600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr17:45129000-45131600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr17:45129000-45133600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr17:45129200-45131600	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr17:45129200-45132400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr17:45129200-45133000	Weak transcription	Esophagus	oesophagus
39	chr17:45129200-45137200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr17:45129400-45131000	Weak transcription	Colonic Mucosa	Colon
41	chr17:45129400-45131000	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr17:45129400-45144200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr17:45129600-45131000	Strong transcription	Brain Hippocampus Middle	brain
44	chr17:45129600-45131800	Strong transcription	Osteobl	bone
45	chr17:45129600-45132000	Strong transcription	Duodenum Smooth Muscle	Duodenum
46	chr17:45129600-45132000	Strong transcription	Spleen	Spleen
47	chr17:45129600-45133800	Strong transcription	Primary T helper cells PMA-I stimulated	--
48	chr17:45129600-45134000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr17:45129600-45134000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr17:45129600-45134000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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