Variant report

Variant	nsv537989
Chromosome Location	chr5:180112337-180218662
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:950)
CpG islands
(count:856)
Chromatin interactive
region (count:50)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:950 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:180212679-180213244	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr5:180144959-180145359	GM12878	blood:	n/a	n/a
3	ATF2	chr5:180212570-180213141	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr5:180145040-180145312	GM12878	blood:	n/a	chr5:180145207-180145218
5	BATF	chr5:180169789-180169977	GM12878	blood:	n/a	n/a
6	BATF	chr5:180145061-180145379	GM12878	blood:	n/a	chr5:180145207-180145218
7	BCL11A	chr5:180145100-180145299	GM12878	blood:	n/a	chr5:180145235-180145244
8	BCL11A	chr5:180145000-180145348	GM12878	blood:	n/a	chr5:180145235-180145244
9	CBX3	chr5:180208858-180209504	K562	blood:	n/a	n/a
10	CBX3	chr5:180215613-180215981	K562	blood:	n/a	n/a
11	CBX3	chr5:180198844-180199194	K562	blood:	n/a	n/a
12	CBX3	chr5:180198766-180199290	K562	blood:	n/a	n/a
13	CBX3	chr5:180127492-180127736	K562	blood:	n/a	n/a
14	CBX3	chr5:180208965-180209392	K562	blood:	n/a	n/a
15	CEBPB	chr5:180209005-180209250	K562	blood:	n/a	n/a
16	CEBPB	chr5:180131341-180131657	K562	blood:	n/a	n/a
17	CEBPB	chr5:180208882-180209430	K562	blood:	n/a	n/a
18	CEBPD	chr5:180208780-180209396	K562	blood:	n/a	n/a
19	CEBPD	chr5:180208777-180209303	K562	blood:	n/a	n/a
20	CEBPD	chr5:180131384-180131803	K562	blood:	n/a	n/a
21	CREB1	chr5:180144917-180145413	GM12878	blood:	n/a	n/a
22	CREB1	chr5:180144836-180145451	GM12878	blood:	n/a	n/a
23	CTCF	chr5:180214815-180214885	Medullo	brain:	n/a	n/a
24	CTCF	chr5:180145632-180146378	SK-N-SH	brain:	n/a	n/a
25	CTCF	chr5:180146259-180146315	MCF-7	breast:	n/a	n/a
26	CTCF	chr5:180217085-180217299	Fibrobl	skin:	n/a	chr5:180217158-180217179 chr5:180217156-180217174 chr5:180217245-180217258 chr5:180217159-180217172 chr5:180217242-180217260 chr5:180217157-180217173
27	CTCF	chr5:180145840-180145990	AG09309	skin:	n/a	n/a
28	CTCF	chr5:180146200-180146350	HepG2	liver:	n/a	n/a
29	CTCF	chr5:180145840-180145990	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr5:180146180-180146330	GM12878	blood:	n/a	n/a
31	CTCF	chr5:180145860-180146010	GM06990	blood:	n/a	n/a
32	CTCF	chr5:180146160-180146310	SAEC	small airway:	n/a	n/a
33	CTCF	chr5:180146220-180146370	GM12865	blood:	n/a	n/a
34	CTCF	chr5:180217080-180217230	HCT-116	colon:	n/a	chr5:180217158-180217179 chr5:180217156-180217174 chr5:180217159-180217172 chr5:180217157-180217173
35	CTCF	chr5:180211565-180211811	GM19239	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
36	CTCF	chr5:180146140-180146290	GM12878	blood:	n/a	n/a
37	CTCF	chr5:180147520-180147670	MCF-7	breast:	n/a	n/a
38	CTCF	chr5:180146100-180146250	AG09309	skin:	n/a	n/a
39	CTCF	chr5:180145840-180145990	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr5:180211640-180211790	BJ	skin:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
41	CTCF	chr5:180145820-180145970	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr5:180216920-180217070	BE2_C	brain:	n/a	n/a
43	CTCF	chr5:180211571-180211813	Hela-S3	cervix:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
44	CTCF	chr5:180211455-180211919	A549	lung:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
45	CTCF	chr5:180211640-180211790	GM12872	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
46	CTCF	chr5:180145840-180145990	HCFaa	heart:	n/a	n/a
47	CTCF	chr5:180211640-180211790	GM12871	blood:	n/a	chr5:180211685-180211706 chr5:180211683-180211701
48	CTCF	chr5:180216060-180216210	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr5:180212320-180212470	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr5:180146167-180146335	Gliobla	brain:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:180217700-180217750	PrEC	prostate:	n/a
2	chr5:180167724-180167774	AoSMC	blood vessel:	n/a
3	chr5:180217700-180217750	PrEC	prostate:	n/a
4	chr5:180167724-180167774	AoSMC	blood vessel:	n/a
5	chr5:180166694-180166744	T-47D	breast:	n/a
6	chr5:180167566-180167616	MCF10A-Er-Src	breast:	n/a
7	chr5:180217700-180217750	ProgFib	skin:	n/a
8	chr5:180167724-180167774	K562	blood:	n/a
9	chr5:180166492-180166542	HPAEpiC	pulmonary alveolar:	n/a
10	chr5:180113357-180113407	HRE	kidney:	n/a
11	chr5:180116385-180116435	AG09319	gingival:	n/a
12	chr5:180166492-180166542	LNCaP	prostate:	n/a
13	chr5:180167965-180168015	MCF10A-Er-Src	breast:	n/a
14	chr5:180166694-180166744	Hela-S3	cervix:	n/a
15	chr5:180112929-180112979	BE2_C	brain:	n/a
16	chr5:180166694-180166744	HUVEC	blood vessel:	n/a
17	chr5:180116385-180116435	Hela-S3	cervix:	n/a
18	chr5:180167566-180167616	H1-hESC	embryonic stem cell:	embryo
19	chr5:180166694-180166744	NB4	blood:	n/a
20	chr5:180217700-180217750	Hela-S3	cervix:	n/a
21	chr5:180116385-180116435	Caco-2	colon:	n/a
22	chr5:180218509-180218559	RPTEC	kidney:	n/a
23	chr5:180112929-180112979	PANC-1	pancreas:	n/a
24	chr5:180113357-180113407	CMK	blood:	n/a
25	chr5:180217700-180217750	HCPEpiC	choroid plexus:	n/a
26	chr5:180112929-180112979	MCF10A-Er-Src	breast:	n/a
27	chr5:180167724-180167774	CMK	blood:	n/a
28	chr5:180112929-180112979	SAEC	small airway:	n/a
29	chr5:180217700-180217750	HRE	kidney:	n/a
30	chr5:180216985-180217035	SK-N-MC	brain:	n/a
31	chr5:180112929-180112979	U87	brain:	n/a
32	chr5:180116385-180116435	HNPCEpiC	eye:	n/a
33	chr5:180213189-180213239	AoSMC	blood vessel:	n/a
34	chr5:180166492-180166542	NT2-D1	testis:	n/a
35	chr5:180218509-180218559	AG09319	gingival:	n/a
36	chr5:180218509-180218559	SK-N-SH_RA	brain:	n/a
37	chr5:180116385-180116435	AG04450	lung:	fetal
38	chr5:180213189-180213239	PANC-1	pancreas:	n/a
39	chr5:180166492-180166542	HEK293	kidney:	embryo
40	chr5:180217700-180217750	RPTEC	kidney:	n/a
41	chr5:180167566-180167616	HRCEpiC	kidney:	n/a
42	chr5:180116385-180116435	AG10803	skin:	n/a
43	chr5:180167566-180167616	AG10803	skin:	n/a
44	chr5:180216985-180217035	GM12891	blood:	n/a
45	chr5:180167132-180167182	CMK	blood:	n/a
46	chr5:180167132-180167182	HNPCEpiC	eye:	n/a
47	chr5:180166492-180166542	Jurkat	blood:	n/a
48	chr5:180167724-180167774	HEEpiC	esophagus:	n/a
49	chr5:180166492-180166542	GM19239	blood:	n/a
50	chr5:180167724-180167774	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:180130605..180132994-chr5:180134010..180136773,2	MCF-7	breast:
2	chr5:180212092..180214294-chr5:180453988..180456472,2	K562	blood:
3	chr5:180202113..180204208-chr5:180208493..180210882,2	K562	blood:
4	chr5:180037911..180038640-chr5:180145288..180145999,2	MCF-7	breast:
5	chr5:180217067..180219759-chr5:180269419..180271439,2	K562	blood:
6	chr5:180207548..180210211-chr5:180589188..180591545,3	K562	blood:
7	chr5:180170663..180173512-chr5:180175093..180176860,2	K562	blood:
8	chr5:180143140..180144948-chr5:180229622..180231793,2	K562	blood:
9	chr5:180210073..180212750-chr5:180649135..180651698,2	MCF-7	breast:
10	chr5:180154735..180156600-chr5:180159240..180161653,2	MCF-7	breast:
11	chr5:180209019..180210957-chr5:180453882..180456380,2	K562	blood:
12	chr5:180170663..180173512-chr5:180175093..180176860,2	K562	blood:
13	chr5:180208714..180211702-chr5:180212096..180213803,2	K562	blood:
14	chr5:180097643..180098351-chr5:180145367..180146387,3	MCF-7	breast:
15	chr5:180114639..180117305-chr5:180118582..180121501,2	MCF-7	breast:
16	chr5:180208714..180211260-chr5:180212096..180214924,3	K562	blood:
17	chr5:180168390..180170515-chr5:180204872..180207367,2	K562	blood:
18	chr5:180208714..180211702-chr5:180212096..180213803,2	K562	blood:
19	chr5:180217057..180217623-chr5:180228458..180229188,2	MCF-7	breast:
20	chr5:179919075..179921338-chr5:180210769..180213087,2	MCF-7	breast:
21	chr5:180211640..180213961-chr5:180214094..180219248,5	K562	blood:
22	chr5:180113673..180116367-chr5:180119581..180121156,3	K562	blood:
23	chr5:180171538..180174150-chr5:180179388..180180987,2	K562	blood:
24	chr5:180207628..180210924-chr5:180228309..180230947,5	MCF-7	breast:
25	chr5:180217957..180220948-chr5:180429295..180431970,2	K562	blood:
26	chr5:180171538..180174150-chr5:180179388..180180987,2	K562	blood:
27	chr5:180168390..180170515-chr5:180204872..180207367,2	K562	blood:
28	chr5:180147687..180149481-chr5:180151717..180153867,2	K562	blood:
29	chr5:180216327..180219256-chr5:180485099..180486798,2	K562	blood:
30	chr5:180147687..180149481-chr5:180151717..180153867,2	K562	blood:
31	chr5:180211185..180212156-chr5:180225940..180226892,9	MCF-7	breast:
32	chr5:180211281..180211887-chr5:180586366..180586939,2	MCF-7	breast:
33	chr5:180153993..180156519-chr5:180159947..180161759,2	K562	blood:
34	chr5:180153993..180156519-chr5:180159947..180161759,2	K562	blood:
35	chr5:180211375..180212214-chr5:180226180..180226854,2	MCF-7	breast:
36	chr5:180158275..180159905-chr5:180163258..180165205,2	K562	blood:
37	chr5:180202113..180204208-chr5:180208493..180210882,2	K562	blood:
38	chr5:180136617..180138276-chr5:180153652..180155749,2	K562	blood:
39	chr5:180158275..180159905-chr5:180163258..180165205,2	K562	blood:
40	chr5:180216578..180217657-chr5:180225674..180226614,3	MCF-7	breast:
41	chr5:180048663..180050730-chr5:180113911..180116171,2	K562	blood:
42	chr5:180146148..180147851-chr5:180235768..180238086,2	K562	blood:
43	chr5:180208930..180211085-chr5:180226767..180229407,2	K562	blood:
44	chr5:180130605..180132994-chr5:180134010..180136773,2	MCF-7	breast:
45	chr5:180210430..180214631-chr5:180286463..180290673,6	MCF-7	breast:
46	chr5:180168086..180169925-chr5:180190599..180192805,2	K562	blood:
47	chr5:180136617..180138276-chr5:180153652..180155749,2	K562	blood:
48	chr5:180168086..180169925-chr5:180190599..180192805,2	K562	blood:
49	chr5:180172009..180174376-chr5:180240608..180243076,2	MCF-7	breast:
50	chr5:180202321..180205166-chr5:180643152..180645917,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTNL8-8	chr5:180190563-180190835	ucscGeneNc_uc003mmk_2
2	lnc-OR2Y1-1	chr5:180155280-180155484	expReg_chr5_11028_-
3	lnc-BTNL8-8	chr5:180192279-180192466	ucscGeneNc_uc003mmk_2
4	lnc-BTNL8-8	chr5:180193918-180195284	ucscGeneNc_uc003mmk_2
5	lnc-OR2Y1-2	chr5:180189565-180191201	ucscGeneNc_uc003mmj_1
6	lnc-CNOT6-3	chr5:180112648-180113546	NONHSAT105706
7	lnc-CNOT6-3	chr5:180112649-180113546	XLOC_004682

No data

Variant related genes	Relation type
RNU1-17P	TF binding region
ENSG00000260841	TF binding region
OR2Y1	TF binding region
OR2AI1P	TF binding region
RNU1-17P	CpG island
ENSG00000260841	CpG island
OR2Y1	CpG island
OR2AI1P	CpG island
ENSG00000260841	chromatin interactions
ENSG00000131446	chromatin interactions
ENSG00000236791	chromatin interactions
ENSG00000196670	chromatin interactions
ENSG00000199892	chromatin interactions
ENSG00000264732	chromatin interactions
ENSG00000146063	chromatin interactions

Extended variants
information (count: 2733 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:2733 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183632097	chr5:180112349-180112350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs187992203	chr5:180112363-180112364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs368816602	chr5:180112402-180112403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116625790	chr5:180112403-180112404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7704656	chr5:180112519-180112520	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs554374737	chr5:180112559-180112560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11386975	chr5:180112600-180112601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200719258	chr5:180112618-180112619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6601133	chr5:180112627-180112628	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs540912937	chr5:180112640-180112641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562999960	chr5:180112642-180112643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574897070	chr5:180112661-180112662	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs543771209	chr5:180112663-180112664	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs560802563	chr5:180112664-180112665	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs367920478	chr5:180112713-180112714	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs546372860	chr5:180112720-180112721	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs144744164	chr5:180112735-180112736	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs532164125	chr5:180112766-180112767	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs182304442	chr5:180112781-180112782	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs35298401	chr5:180112929-180112930	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs6601134	chr5:180112934-180112935	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs187381630	chr5:180112936-180112937	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs190108584	chr5:180112991-180112992	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs568445954	chr5:180113053-180113054	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs11748961	chr5:180113065-180113066	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs553966178	chr5:180113070-180113071	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs577379039	chr5:180113098-180113099	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs529035667	chr5:180113103-180113104	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs556454305	chr5:180113105-180113106	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs367691152	chr5:180113129-180113130	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs576361850	chr5:180113159-180113160	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs542096203	chr5:180113208-180113209	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs73812670	chr5:180113216-180113217	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs371436955	chr5:180113238-180113239	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs115052724	chr5:180113244-180113245	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs540330109	chr5:180113268-180113269	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs566121380	chr5:180113284-180113285	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs559943946	chr5:180113357-180113358	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs532356565	chr5:180113375-180113376	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs552054588	chr5:180113462-180113463	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs113997439	chr5:180113472-180113473	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs141556003	chr5:180113492-180113493	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs548502308	chr5:180113502-180113503	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs181780926	chr5:180113509-180113510	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs115956295	chr5:180113536-180113537	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs548766329	chr5:180113561-180113562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147034282	chr5:180113594-180113595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376685622	chr5:180113595-180113596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186618058	chr5:180113710-180113711	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs556365166	chr5:180113735-180113736	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	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
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	17440070	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:770 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:180109200-180113600	Enhancers	Primary T helper cells fromperipheralblood	blood
2	chr5:180109200-180115800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr5:180109600-180112800	Enhancers	Primary T cells fromperipheralblood	blood
4	chr5:180109600-180115400	Enhancers	Fetal Thymus	thymus
5	chr5:180109600-180115400	Enhancers	Thymus	Thymus
6	chr5:180109600-180115600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr5:180109600-180116200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:180109800-180113000	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr5:180109800-180116000	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr5:180110000-180113600	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr5:180110800-180113800	Weak transcription	Dnd41	blood
12	chr5:180110800-180116000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr5:180111000-180115400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr5:180111600-180112400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr5:180111600-180115600	Enhancers	Primary T cells from cord blood	blood
16	chr5:180111800-180114600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr5:180112200-180119400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr5:180112400-180114000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr5:180112400-180114800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr5:180112800-180114000	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr5:180113000-180114000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr5:180113600-180114600	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr5:180113600-180114600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr5:180113800-180115000	Enhancers	Dnd41	blood
25	chr5:180114000-180114400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
26	chr5:180114000-180115400	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr5:180114000-180116200	Enhancers	Primary T cells fromperipheralblood	blood
28	chr5:180114400-180115400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr5:180114400-180116200	Weak transcription	Pancreas	Pancrea
30	chr5:180114600-180114800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr5:180114600-180115600	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr5:180114600-180115800	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr5:180114600-180118400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr5:180114800-180115200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr5:180114800-180115600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr5:180115000-180117000	Flanking Active TSS	Dnd41	blood
37	chr5:180115200-180115800	Enhancers	Fetal Lung	lung
38	chr5:180115200-180116000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr5:180115400-180115600	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
40	chr5:180115400-180115600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
41	chr5:180115400-180115600	Flanking Active TSS	Fetal Thymus	thymus
42	chr5:180115400-180115600	Active TSS	Thymus	Thymus
43	chr5:180115400-180117000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr5:180115400-180117000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:180115400-180117000	Enhancers	Primary hematopoietic stem cells	blood
46	chr5:180115400-180117200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr5:180115400-180117200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
48	chr5:180115600-180115800	Flanking Active TSS	Thymus	Thymus
49	chr5:180115600-180116000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr5:180115600-180116200	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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