Variant report

Variant	nsv543245
Chromosome Location	chr17:18098110-18136330
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:936)
CpG islands
(count:917)
Chromatin interactive
region (count:46)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:936 , 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	ARID3A	chr17:18127583-18128021	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:18124217-18124321	K562	blood:	n/a	n/a
3	ATF1	chr17:18128364-18129077	K562	blood:	n/a	n/a
4	ATF2	chr17:18127515-18127982	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr17:18127659-18128609	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr17:18128866-18129108	K562	blood:	n/a	n/a
7	ATF3	chr17:18128570-18128864	K562	blood:	n/a	chr17:18128797-18128806 chr17:18128707-18128716
8	ATF3	chr17:18124160-18124439	K562	blood:	n/a	n/a
9	BACH1	chr17:18129337-18129543	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr17:18127800-18129072	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr17:18124087-18124429	GM12878	blood:	n/a	chr17:18124255-18124266
12	BATF	chr17:18124151-18124384	GM12878	blood:	n/a	chr17:18124255-18124266
13	BCL3	chr17:18120697-18121186	A549	lung:	n/a	n/a
14	BCLAF1	chr17:18128522-18128812	GM12878	blood:	n/a	chr17:18128709-18128722 chr17:18128707-18128720
15	BHLHE40	chr17:18124560-18124680	K562	blood:	n/a	n/a
16	BHLHE40	chr17:18128456-18129081	GM12878	blood:	n/a	n/a
17	BHLHE40	chr17:18131594-18131940	K562	blood:	n/a	n/a
18	BHLHE40	chr17:18128203-18128848	K562	blood:	n/a	n/a
19	BHLHE40	chr17:18106619-18107024	HepG2	liver:	n/a	n/a
20	BRCA1	chr17:18127940-18128566	H1-hESC	embryonic stem cell:	n/a	n/a
21	CCNT2	chr17:18128578-18129357	K562	blood:	n/a	chr17:18128792-18128801
22	CEBPB	chr17:18127531-18128523	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr17:18116828-18117051	K562	blood:	n/a	chr17:18116939-18116950 chr17:18116936-18116953
24	CEBPB	chr17:18119525-18119783	K562	blood:	n/a	n/a
25	CEBPB	chr17:18116828-18117139	Hela-S3	cervix:	n/a	chr17:18116939-18116950 chr17:18116936-18116953
26	CEBPB	chr17:18116828-18117093	HepG2	liver:	n/a	chr17:18116939-18116950 chr17:18116936-18116953
27	CEBPB	chr17:18119567-18119795	K562	blood:	n/a	n/a
28	CEBPD	chr17:18104796-18105321	K562	blood:	n/a	n/a
29	CEBPD	chr17:18128788-18129094	HepG2	liver:	n/a	n/a
30	CHD1	chr17:18128198-18128639	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr17:18128356-18128887	K562	blood:	n/a	chr17:18128793-18128803
32	CHD2	chr17:18122270-18122279	GM12878	blood:	n/a	n/a
33	CHD2	chr17:18128510-18129025	Hela-S3	cervix:	n/a	chr17:18128793-18128803
34	CHD2	chr17:18128468-18128849	HepG2	liver:	n/a	chr17:18128793-18128803
35	CHD2	chr17:18128502-18128960	GM12878	blood:	n/a	chr17:18128793-18128803
36	CHD2	chr17:18127654-18128898	H1-hESC	embryonic stem cell:	n/a	chr17:18128793-18128803
37	CREB1	chr17:18128506-18128885	ECC-1	luminal epithelium:	n/a	n/a
38	CREB1	chr17:18128499-18129113	HepG2	liver:	n/a	n/a
39	CREB1	chr17:18127687-18129222	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr17:18128542-18129088	A549	lung:	n/a	n/a
41	CREB1	chr17:18128502-18129093	GM12878	blood:	n/a	n/a
42	CREB1	chr17:18127418-18129485	HepG2	liver:	n/a	n/a
43	CREB1	chr17:18127504-18129217	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr17:18128472-18129261	K562	blood:	n/a	n/a
45	CREB1	chr17:18128625-18128852	A549	lung:	n/a	n/a
46	CTBP2	chr17:18127453-18128791	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr17:18120755-18121038	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr17:18135260-18135410	GM12878	blood:	n/a	n/a
49	CTCF	chr17:18120860-18121010	MCF-7	breast:	n/a	n/a
50	CTCF	chr17:18120820-18120970	HepG2	liver:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:18128578-18128628	CMK	blood:	n/a
2	chr17:18128806-18128856	ECC-1	luminal epithelium:	n/a
3	chr17:18128578-18128628	CMK	blood:	n/a
4	chr17:18128806-18128856	ECC-1	luminal epithelium:	n/a
5	chr17:18106813-18106863	GM12878	blood:	n/a
6	chr17:18101567-18101617	SKMC	muscle:	n/a
7	chr17:18128022-18128072	PrEC	prostate:	n/a
8	chr17:18128581-18128631	BJ	skin:	n/a
9	chr17:18128581-18128631	AG09319	gingival:	n/a
10	chr17:18125250-18125300	HPAEpiC	pulmonary alveolar:	n/a
11	chr17:18101567-18101617	Hela-S3	cervix:	n/a
12	chr17:18128022-18128072	PANC-1	pancreas:	n/a
13	chr17:18112356-18112406	SK-N-SH_RA	brain:	n/a
14	chr17:18131641-18131691	HRCEpiC	kidney:	n/a
15	chr17:18128735-18128785	HNPCEpiC	eye:	n/a
16	chr17:18125250-18125300	HepG2	liver:	n/a
17	chr17:18125250-18125300	NB4	blood:	n/a
18	chr17:18128745-18128795	PANC-1	pancreas:	n/a
19	chr17:18128578-18128628	T-47D	breast:	n/a
20	chr17:18128581-18128631	HRE	kidney:	n/a
21	chr17:18101567-18101617	ProgFib	skin:	n/a
22	chr17:18121946-18121996	T-47D	breast:	n/a
23	chr17:18112356-18112406	AG04449	skin:	fetal
24	chr17:18128581-18128631	HepG2	liver:	n/a
25	chr17:18129026-18129076	GM06990	blood:	n/a
26	chr17:18128745-18128795	SK-N-SH_RA	brain:	n/a
27	chr17:18112356-18112406	SKMC	muscle:	n/a
28	chr17:18134744-18134794	PFSK-1	brain:	n/a
29	chr17:18128578-18128628	HEEpiC	esophagus:	n/a
30	chr17:18128578-18128628	Caco-2	colon:	n/a
31	chr17:18128022-18128072	K562	blood:	n/a
32	chr17:18128806-18128856	GM12892	blood:	n/a
33	chr17:18129026-18129076	SKMC	muscle:	n/a
34	chr17:18106813-18106863	HUVEC	blood vessel:	n/a
35	chr17:18134744-18134794	PANC-1	pancreas:	n/a
36	chr17:18112356-18112406	HEK293	kidney:	embryo
37	chr17:18101567-18101617	NB4	blood:	n/a
38	chr17:18131641-18131691	H1-hESC	embryonic stem cell:	embryo
39	chr17:18128735-18128785	HepG2	liver:	n/a
40	chr17:18128735-18128785	Caco-2	colon:	n/a
41	chr17:18106813-18106863	LNCaP	prostate:	n/a
42	chr17:18101567-18101617	T-47D	breast:	n/a
43	chr17:18129087-18129137	PrEC	prostate:	n/a
44	chr17:18121946-18121996	ovcar-3	ovarian:	n/a
45	chr17:18106813-18106863	AG09319	gingival:	n/a
46	chr17:18106813-18106863	ProgFib	skin:	n/a
47	chr17:18134744-18134794	NH-A	brain:	n/a
48	chr17:18121946-18121996	SKMC	muscle:	n/a
49	chr17:18128745-18128795	SK-N-SH	brain:	n/a
50	chr17:18125250-18125300	RPTEC	kidney:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:18101503..18103754-chr17:18111699..18113934,2	K562	blood:
2	chr17:18088851..18092330-chr17:18106978..18109728,3	K562	blood:
3	chr17:18092817..18094681-chr17:18097736..18100155,2	MCF-7	breast:
4	chr17:18100028..18102220-chr17:18112479..18114725,2	K562	blood:
5	chr17:18122942..18125259-chr17:18127493..18129477,3	MCF-7	breast:
6	chr17:18121617..18124692-chr17:18126477..18129347,3	MCF-7	breast:
7	chr17:18132797..18135774-chr17:18137041..18139017,2	K562	blood:
8	chr17:18086176..18087752-chr17:18106920..18108922,2	MCF-7	breast:
9	chr17:18044115..18044841-chr17:18120469..18121362,2	K562	blood:
10	chr17:18136077..18142771-chr17:18143654..18157956,22	MCF-7	breast:
11	chr17:18086116..18088007-chr17:18126945..18129861,2	K562	blood:
12	chr17:18127671..18130325-chr17:18161981..18165246,3	K562	blood:
13	chr17:18093548..18096318-chr17:18098737..18101675,3	MCF-7	breast:
14	chr17:18128446..18130837-chr17:18148104..18152552,6	MCF-7	breast:
15	chr17:18124389..18126686-chr17:18128291..18130726,2	K562	blood:
16	chr17:18135343..18136871-chr17:18137313..18139125,2	MCF-7	breast:
17	chr17:18111005..18113844-chr17:18114465..18116043,2	K562	blood:
18	chr17:18130971..18132517-chr17:18148096..18150971,2	MCF-7	breast:
19	chr17:18128609..18130304-chr17:18157638..18159883,2	K562	blood:
20	chr17:18134113..18135746-chr17:18160892..18162821,2	MCF-7	breast:
21	chr17:18130743..18132299-chr17:18139265..18141956,2	K562	blood:
22	chr17:18127264..18129965-chr17:18170745..18172525,2	K562	blood:
23	chr17:18127269..18131326-chr17:18216439..18220320,6	MCF-7	breast:
24	chr17:18080216..18082835-chr17:18097056..18098956,2	MCF-7	breast:
25	chr17:18128887..18137475-chr17:18144772..18151698,11	K562	blood:
26	chr17:18124758..18126506-chr17:18160763..18163317,2	MCF-7	breast:
27	chr17:18128637..18131335-chr17:18133166..18135080,2	MCF-7	breast:
28	chr17:18101503..18103754-chr17:18111699..18113934,2	K562	blood:
29	chr17:18127100..18135567-chr17:18158023..18168767,25	MCF-7	breast:
30	chr17:18111005..18113844-chr17:18114465..18116043,2	K562	blood:
31	chr17:18135795..18137603-chr17:18160135..18163013,2	MCF-7	breast:
32	chr17:18126073..18132705-chr17:18158327..18165323,14	MCF-7	breast:
33	chr17:18118058..18120854-chr17:18219963..18222284,2	K562	blood:
34	chr17:18055964..18057548-chr17:18123395..18125960,2	K562	blood:
35	chr17:18125152..18133137-chr17:18145532..18152012,9	K562	blood:
36	chr17:18085712..18088140-chr17:18106871..18109334,2	MCF-7	breast:
37	chr17:18087388..18090875-chr17:18103511..18106213,4	K562	blood:
38	chr17:18127536..18130433-chr17:18148836..18151541,2	MCF-7	breast:
39	chr17:18132550..18134440-chr17:18155290..18157461,2	MCF-7	breast:
40	chr17:18135872..18138183-chr17:18147458..18150169,3	K562	blood:
41	chr17:18086669..18088482-chr17:18100484..18103236,2	K562	blood:
42	chr17:18129178..18131592-chr17:18137709..18139287,2	MCF-7	breast:
43	chr17:18127210..18129786-chr17:18153749..18156676,2	MCF-7	breast:
44	chr17:18100028..18102220-chr17:18112479..18114725,2	K562	blood:
45	chr17:18128940..18129457-chr19:55896848..55897657,2	Hela-S3	cervix:
46	chr17:18107127..18109986-chr17:18112573..18114376,2	MCF-7	breast:

No data

Variant related genes	Relation type
ALKBH5	TF binding region
LLGL1	TF binding region
ALKBH5	CpG island
LLGL1	CpG island
ENSG00000131899	chromatin interactions
ENSG00000177302	chromatin interactions
ENSG00000260647	chromatin interactions
ENSG00000091536	chromatin interactions
ENSG00000091542	chromatin interactions
ENSG00000108107	chromatin interactions
ENSG00000176994	chromatin interactions
ENSG00000266677	chromatin interactions
ENSG00000177427	chromatin interactions
ENSG00000177731	chromatin interactions

Extended variants
information (count: 1473 )
Associated
traits (count: 160 )

Variant overlapped rSNPs/rCNVs (count:1473 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181852449	chr17:18098124-18098125	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs17436616	chr17:18098180-18098181	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs572802937	chr17:18098182-18098183	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114322620	chr17:18098185-18098186	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186450598	chr17:18098210-18098211	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575638750	chr17:18098236-18098237	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs374762911	chr17:18098240-18098241	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs28694704	chr17:18098253-18098254	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs371842345	chr17:18098272-18098273	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534288301	chr17:18098371-18098372	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533164130	chr17:18098495-18098496	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540008502	chr17:18098500-18098501	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557352953	chr17:18098537-18098538	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559817740	chr17:18098560-18098561	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528541968	chr17:18098579-18098580	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190914882	chr17:18098580-18098581	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577272990	chr17:18098593-18098594	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs568089810	chr17:18098602-18098603	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538014187	chr17:18098619-18098620	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531156122	chr17:18098662-18098663	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556819703	chr17:18098677-18098678	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550853281	chr17:18098736-18098737	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571015291	chr17:18098743-18098744	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540025816	chr17:18098776-18098777	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs148285040	chr17:18098846-18098847	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs139944498	chr17:18098872-18098873	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566596859	chr17:18098950-18098951	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs535521200	chr17:18098975-18098976	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs376660628	chr17:18098986-18098987	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575305090	chr17:18099005-18099006	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537803513	chr17:18099018-18099019	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs558037099	chr17:18099049-18099050	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73288251	chr17:18099087-18099088	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs545435595	chr17:18099107-18099108	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563439357	chr17:18099131-18099132	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114633125	chr17:18099150-18099151	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370989315	chr17:18099187-18099188	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560073101	chr17:18099239-18099240	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181509703	chr17:18099243-18099244	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs187032194	chr17:18099306-18099307	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs375993534	chr17:18099315-18099316	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530823167	chr17:18099325-18099326	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149434460	chr17:18099376-18099377	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191067866	chr17:18099406-18099407	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144662019	chr17:18099418-18099419	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs543232022	chr17:18099436-18099437	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368562559	chr17:18099447-18099448	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575337257	chr17:18099528-18099529	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79832126	chr17:18099543-18099544	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs8066590	chr17:18099584-18099585	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:160)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	22543975	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Sezary syndrome	18413736	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1873 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:18090200-18103400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr17:18090800-18098200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr17:18090800-18098400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr17:18090800-18104000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr17:18091200-18104600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr17:18091400-18098800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr17:18091400-18114000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr17:18091800-18098200	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr17:18091800-18114400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr17:18092000-18104000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr17:18092200-18098200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr17:18093000-18098800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr17:18094200-18098200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr17:18094200-18114600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr17:18094400-18098200	Weak transcription	Fetal Heart	heart
16	chr17:18094400-18114600	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr17:18094600-18114600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr17:18094800-18098200	Weak transcription	Fetal Lung	lung
19	chr17:18094800-18098200	Weak transcription	HSMM	muscle
20	chr17:18094800-18098600	Weak transcription	HSMMtube	muscle
21	chr17:18094800-18098600	Weak transcription	NH-A	brain
22	chr17:18094800-18101800	Strong transcription	Rectal Mucosa Donor 29	rectum
23	chr17:18094800-18103400	Strong transcription	Fetal Intestine Large	intestine
24	chr17:18095000-18098200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr17:18095000-18098200	Weak transcription	Ovary	ovary
26	chr17:18095000-18108600	Strong transcription	Cortex derived primary cultured neurospheres	brain
27	chr17:18095000-18114600	Strong transcription	Sigmoid Colon	Sigmoid Colon
28	chr17:18095000-18114800	Strong transcription	Fetal Thymus	thymus
29	chr17:18095200-18098200	Weak transcription	Colonic Mucosa	Colon
30	chr17:18095200-18098200	Weak transcription	Esophagus	oesophagus
31	chr17:18095200-18101000	Strong transcription	Thymus	Thymus
32	chr17:18095400-18098200	Weak transcription	Rectal Smooth Muscle	rectum
33	chr17:18095400-18101800	Weak transcription	Small Intestine	intestine
34	chr17:18095400-18116000	Strong transcription	Fetal Stomach	stomach
35	chr17:18095600-18098200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr17:18095600-18098200	Weak transcription	Fetal Brain Male	brain
37	chr17:18095600-18098200	Weak transcription	Pancreas	Pancrea
38	chr17:18095600-18098200	Weak transcription	HUVEC	blood vessel
39	chr17:18095600-18098800	Weak transcription	Psoas Muscle	Psoas
40	chr17:18095600-18099600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr17:18095600-18100600	Strong transcription	GM12878-XiMat	blood
42	chr17:18095600-18103600	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chr17:18095600-18114600	Strong transcription	Dnd41	blood
44	chr17:18095800-18098400	Weak transcription	Stomach Mucosa	stomach
45	chr17:18095800-18100400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr17:18095800-18102200	Strong transcription	Duodenum Mucosa	Duodenum
47	chr17:18095800-18103200	Strong transcription	Fetal Intestine Small	intestine
48	chr17:18095800-18108600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr17:18096000-18098200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr17:18096000-18098200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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