Variant report

Variant	esv1829975
Chromosome Location	chr9:43045290-43831337
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2523)
CpG islands
(count:368)
Chromatin interactive
region (count:0)
LncRNA
region (count:50)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2523 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:43155080-43155340	K562	blood:	n/a	n/a
2	ARID3A	chr9:43498011-43498345	K562	blood:	n/a	n/a
3	BACH1	chr9:43686226-43686817	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr9:43456004-43456520	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr9:43078198-43078425	GM12878	blood:	n/a	n/a
6	BATF	chr9:43121853-43122095	GM12878	blood:	n/a	n/a
7	BATF	chr9:43380741-43381310	GM12878	blood:	n/a	n/a
8	BATF	chr9:43380711-43381300	GM12878	blood:	n/a	n/a
9	BATF	chr9:43122109-43123723	GM12878	blood:	n/a	n/a
10	BATF	chr9:43103941-43104337	GM12878	blood:	n/a	chr9:43104053-43104061
11	BATF	chr9:43391498-43391789	GM12878	blood:	n/a	n/a
12	BATF	chr9:43160512-43160671	GM12878	blood:	n/a	n/a
13	BATF	chr9:43374503-43374725	GM12878	blood:	n/a	n/a
14	BATF	chr9:43080437-43080600	GM12878	blood:	n/a	n/a
15	BATF	chr9:43393256-43393475	GM12878	blood:	n/a	n/a
16	BATF	chr9:43110560-43110802	GM12878	blood:	n/a	n/a
17	BATF	chr9:43120659-43120859	GM12878	blood:	n/a	n/a
18	BATF	chr9:43714519-43714714	GM12878	blood:	n/a	n/a
19	BATF	chr9:43123059-43123716	GM12878	blood:	n/a	n/a
20	BATF	chr9:43117281-43117481	GM12878	blood:	n/a	n/a
21	BATF	chr9:43087580-43087916	GM12878	blood:	n/a	chr9:43087721-43087732
22	BATF	chr9:43097243-43097501	GM12878	blood:	n/a	n/a
23	BATF	chr9:43087590-43087949	GM12878	blood:	n/a	chr9:43087721-43087732
24	BATF	chr9:43140357-43140594	GM12878	blood:	n/a	n/a
25	BATF	chr9:43393230-43393466	GM12878	blood:	n/a	n/a
26	BATF	chr9:43080508-43080818	GM12878	blood:	n/a	n/a
27	BATF	chr9:43091491-43091786	GM12878	blood:	n/a	n/a
28	BATF	chr9:43148308-43148516	GM12878	blood:	n/a	chr9:43148436-43148444
29	BATF	chr9:43392171-43392418	GM12878	blood:	n/a	n/a
30	BATF	chr9:43653838-43653993	GM12878	blood:	n/a	n/a
31	BATF	chr9:43139074-43139379	GM12878	blood:	n/a	n/a
32	BATF	chr9:43418541-43419033	GM12878	blood:	n/a	chr9:43418699-43418707
33	BATF	chr9:43445858-43446598	GM12878	blood:	n/a	n/a
34	BATF	chr9:43446919-43447105	GM12878	blood:	n/a	n/a
35	BATF	chr9:43133516-43133712	GM12878	blood:	n/a	n/a
36	BATF	chr9:43391601-43391805	GM12878	blood:	n/a	n/a
37	BATF	chr9:43397934-43398253	GM12878	blood:	n/a	n/a
38	BATF	chr9:43133225-43133467	GM12878	blood:	n/a	n/a
39	BATF	chr9:43091426-43091832	GM12878	blood:	n/a	n/a
40	BATF	chr9:43529040-43529422	GM12878	blood:	n/a	n/a
41	BATF	chr9:43133474-43133863	GM12878	blood:	n/a	n/a
42	BATF	chr9:43123789-43123988	GM12878	blood:	n/a	n/a
43	BATF	chr9:43445830-43446625	GM12878	blood:	n/a	n/a
44	BATF	chr9:43127672-43127998	GM12878	blood:	n/a	n/a
45	BATF	chr9:43127650-43128051	GM12878	blood:	n/a	n/a
46	BATF	chr9:43115481-43115981	GM12878	blood:	n/a	chr9:43115613-43115623
47	BATF	chr9:43418592-43418991	GM12878	blood:	n/a	chr9:43418699-43418707
48	BATF	chr9:43101328-43101584	GM12878	blood:	n/a	n/a
49	BATF	chr9:43488473-43488768	GM12878	blood:	n/a	chr9:43488642-43488653
50	BATF	chr9:43397875-43398296	GM12878	blood:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:43135418-43135468	PrEC	prostate:	n/a
2	chr9:43631161-43631211	ProgFib	skin:	n/a
3	chr9:43135418-43135468	PrEC	prostate:	n/a
4	chr9:43631161-43631211	ProgFib	skin:	n/a
5	chr9:43135418-43135468	AoSMC	blood vessel:	n/a
6	chr9:43134033-43134083	HCF	heart:	n/a
7	chr9:43135418-43135468	AG10803	skin:	n/a
8	chr9:43631161-43631211	GM19239	blood:	n/a
9	chr9:43525320-43525370	HEEpiC	esophagus:	n/a
10	chr9:43631161-43631211	HEEpiC	esophagus:	n/a
11	chr9:43525948-43525998	HMEC	breast:	n/a
12	chr9:43525948-43525998	BE2_C	brain:	n/a
13	chr9:43134756-43134806	SK-N-MC	brain:	n/a
14	chr9:43631161-43631211	NHBE	bronchial:	n/a
15	chr9:43135418-43135468	A549	lung:	n/a
16	chr9:43135418-43135468	HIPEpiC	eye:	n/a
17	chr9:43631161-43631211	A549	lung:	n/a
18	chr9:43134756-43134806	HCF	heart:	n/a
19	chr9:43135418-43135468	HepG2	liver:	n/a
20	chr9:43135418-43135468	K562	blood:	n/a
21	chr9:43134033-43134083	NB4	blood:	n/a
22	chr9:43134033-43134083	PFSK-1	brain:	n/a
23	chr9:43525948-43525998	HEK293	kidney:	embryo
24	chr9:43525948-43525998	HNPCEpiC	eye:	n/a
25	chr9:43525320-43525370	HMEC	breast:	n/a
26	chr9:43135418-43135468	AG09319	gingival:	n/a
27	chr9:43631161-43631211	HepG2	liver:	n/a
28	chr9:43134756-43134806	MCF-7	breast:	n/a
29	chr9:43135418-43135468	HNPCEpiC	eye:	n/a
30	chr9:43525320-43525370	GM12878	blood:	n/a
31	chr9:43525320-43525370	HPAEpiC	pulmonary alveolar:	n/a
32	chr9:43135418-43135468	HAEpiC	amniotic membrane:	n/a
33	chr9:43134033-43134083	HEEpiC	esophagus:	n/a
34	chr9:43525948-43525998	SK-N-MC	brain:	n/a
35	chr9:43525320-43525370	HRPEpiC	eye:	n/a
36	chr9:43135418-43135468	GM06990	blood:	n/a
37	chr9:43631161-43631211	AG10803	skin:	n/a
38	chr9:43525320-43525370	NT2-D1	testis:	n/a
39	chr9:43631161-43631211	K562	blood:	n/a
40	chr9:43631161-43631211	HCT-116	colon:	n/a
41	chr9:43525320-43525370	HEK293	kidney:	embryo
42	chr9:43134033-43134083	HAEpiC	amniotic membrane:	n/a
43	chr9:43135418-43135468	CMK	blood:	n/a
44	chr9:43135418-43135468	HCM	heart:	n/a
45	chr9:43134756-43134806	GM19239	blood:	n/a
46	chr9:43134756-43134806	ovcar-3	ovarian:	n/a
47	chr9:43525948-43525998	AG09309	skin:	n/a
48	chr9:43134033-43134083	SK-N-SH	brain:	n/a
49	chr9:43134756-43134806	PFSK-1	brain:	n/a
50	chr9:43631161-43631211	HMEC	breast:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXD4L2-1	chr9:43102670-43102758	ENSG00000237587.2
2	lnc-FOXD4L2-7	chr9:43065382-43065609	NONHSAT131343
3	lnc-RP11-160N1.10.1-8	chr9:43828157-43828221	NONHSAT131364
4	lnc-ANKRD20A3-2	chr9:43075209-43075490	ENSG00000176057.5
5	lnc-ANKRD20A3-2	chr9:43074401-43074612	ENSG00000176057.5
6	lnc-CNTNAP3B-6	chr9:43399987-43401315	NONHSAT131358
7	lnc-FAM75A6-10	chr9:43130533-43130803	NONHSAT131349
8	lnc-ANKRD20A3-2	chr9:43089717-43089866	ENSG00000176057.5
9	lnc-FOXD4L2-1	chr9:43113254-43113526	ENSG00000237587.2
10	lnc-ANKRD20A3-11	chr9:43318619-43318952	NONHSAT131357
11	lnc-ANKRD20A3-7	chr9:43177955-43178014	NONHSAT131355
12	lnc-ANKRD20A3-2	chr9:43082756-43082885	ENSG00000176057.5
13	lnc-ANKRD20A3-2	chr9:43064966-43065135	ENSG00000176057.5
14	lnc-FOXD4L2-1	chr9:43113254-43113467	ENSG00000237587.1
15	lnc-RP11-160N1.10.1-8	chr9:43822613-43822699	NONHSAT131364
16	lnc-ANKRD20A3-13	chr9:43628634-43628694	NONHSAT131362
17	lnc-FAM75A6-10	chr9:43132625-43132735	NONHSAT131349
18	lnc-ANKRD20A3-2	chr9:43066677-43066795	ENSG00000176057.5
19	lnc-ANKRD20A3-2	chr9:43067596-43067649	ENSG00000176057.5
20	lnc-FOXD4L2-1	chr9:43102670-43102758	ENSG00000237587.1
21	lnc-ANKRD20A3-11	chr9:43319264-43319576	NONHSAT131357
22	lnc-FAM75A6-11	chr9:43099327-43099506	NONHSAT131344
23	lnc-ANKRD20A3-1	chr9:43144980-43145567	XLOC_007693
24	lnc-ANKRD20A3-7	chr9:43179365-43179407	NONHSAT131355
25	lnc-ANKRD20A3-1	chr9:43159864-43160103	XLOC_007693
26	lnc-RP11-160N1.10.1-8	chr9:43822729-43822779	NONHSAT131364
27	lnc-ANKRD20A3-7	chr9:43178104-43178145	NONHSAT131355
28	lnc-ANKRD20A3-2	chr9:43075209-43075490	ENSG00000176057.5
29	lnc-ANKRD20A3-1	chr9:43151785-43152008	XLOC_007693
30	lnc-FOXD4L2-1	chr9:43102670-43102758	ENSG00000237587.1
31	lnc-FOXD4L2-1	chr9:43108319-43108363	ENSG00000237587.1
32	lnc-ANKRD20A3-2	chr9:43068816-43068861	ENSG00000176057.5
33	lnc-ANKRD20A3-2	chr9:43072271-43072493	ENSG00000176057.5
34	lnc-ANKRD20A3-13	chr9:43629020-43629117	NONHSAT131362
35	lnc-ANKRD20A3-13	chr9:43627769-43628378	NONHSAT131362
36	lnc-CNTNAP3B-2	chr9:43617727-43618056	NONHSAT131361
37	lnc-ANKRD20A3-2	chr9:43091403-43091472	ENSG00000176057.5
38	lnc-ANKRD20A3-1	chr9:43159864-43160008	XLOC_007693
39	lnc-FAM75A6-11	chr9:43095105-43095268	NONHSAT131344
40	lnc-ANKRD20A3-2	chr9:43091403-43091857	ENSG00000176057.5
41	lnc-FOXD4L2-1	chr9:43113254-43113375	ENSG00000237587.1
42	lnc-ANKRD20A3-2	chr9:43074435-43074612	ENSG00000176057.5
43	lnc-CNTNAP3B-5	chr9:43403148-43403646	NONHSAT131359
44	lnc-ANKRD20A3-7	chr9:43174019-43175549	NONHSAT131355
45	lnc-FAM75A6-6	chr9:43830636-43831108	NONHSAT131365
46	lnc-FAM75A6-11	chr9:43093621-43093677	NONHSAT131344
47	lnc-ANKRD20A3-1	chr9:43151637-43152008	XLOC_007693
48	lnc-ANKRD20A3-7	chr9:43177211-43177295	NONHSAT131355
49	lnc-ANKRD20A3-2	chr9:43089717-43089866	ENSG00000176057.5
50	lnc-FAM75A6-5	chr9:43802781-43803039	NONHSAT131363

No data

Variant related genes	Relation type
MEP1AP3	TF binding region
ENSG00000236322	TF binding region
ENSG00000237587	TF binding region
ENSG00000233074	TF binding region
ENSG00000239986	TF binding region
ENSG00000232866	TF binding region
ENSG00000223512	TF binding region
SNX18P4	TF binding region
ENSG00000269474	TF binding region
ENSG00000232863	TF binding region
RNU6-538P	TF binding region
ATP5A1P5	TF binding region
SPATA31A6	TF binding region
ANKRD20A3	TF binding region
ENSG00000197805	TF binding region
RN7SL343P	TF binding region
ENSG00000224828	TF binding region
CNTNAP3B	TF binding region
ENSG00000224303	TF binding region
MEP1AP3	CpG island
ENSG00000236322	CpG island
ENSG00000237587	CpG island
ENSG00000233074	CpG island
ENSG00000239986	CpG island
ENSG00000232866	CpG island
ENSG00000223512	CpG island
SNX18P4	CpG island
ENSG00000269474	CpG island
ENSG00000232863	CpG island
RNU6-538P	CpG island
ATP5A1P5	CpG island
SPATA31A6	CpG island
ANKRD20A3	CpG island
ENSG00000197805	CpG island
RN7SL343P	CpG island
ENSG00000224828	CpG island
CNTNAP3B	CpG island
ENSG00000224303	CpG island

Extended variants
information (count: 4039 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4039 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112953427	chr9:43048011-43048012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs80203406	chr9:43048025-43048026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs3132250	chr9:43048050-43048051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555654566	chr9:43048058-43048059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs369793363	chr9:43048076-43048077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200940129	chr9:43048096-43048097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573817885	chr9:43048098-43048099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs71243292	chr9:43048109-43048110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs62535947	chr9:43048161-43048162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12340313	chr9:43048190-43048191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs199616309	chr9:43060449-43060450	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs549059603	chr9:43060585-43060586	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs567190884	chr9:43060597-43060598	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs537827301	chr9:43060631-43060632	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs556206949	chr9:43060633-43060634	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs62552303	chr9:43060646-43060647	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs2474200	chr9:43062308-43062309	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs9412466	chr9:43062387-43062388	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs199760472	chr9:43063236-43063237	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs368424083	chr9:43063384-43063385	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs111561185	chr9:43063553-43063554	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs372005239	chr9:43063764-43063765	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs375374597	chr9:43064640-43064641	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs577974360	chr9:43064826-43064827	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs147507978	chr9:43064853-43064854	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs548618095	chr9:43064858-43064859	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs369960650	chr9:43064938-43064939	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs371315858	chr9:43065152-43065153	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs369881600	chr9:43066548-43066549	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs374176816	chr9:43066620-43066621	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs553964734	chr9:43066637-43066638	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs572268481	chr9:43066643-43066644	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs542797838	chr9:43066679-43066680	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs142964543	chr9:43066687-43066688	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs111356121	chr9:43066693-43066694	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs576384368	chr9:43066756-43066757	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs2507527	chr9:43067962-43067963	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs2444135	chr9:43067979-43067980	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs547586260	chr9:43072303-43072304	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs28566160	chr9:43072420-43072421	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs28595406	chr9:43072421-43072422	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs57165819	chr9:43072454-43072455	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs373667248	chr9:43075445-43075446	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs62552310	chr9:43091509-43091510	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs536427463	chr9:43092088-43092089	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs559602789	chr9:43099272-43099273	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs4247563	chr9:43099893-43099894	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs9645048	chr9:43100609-43100610	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs62552311	chr9:43101400-43101401	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs183183755	chr9:43101414-43101415	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	20409316	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Lung adenocarcinoma	17086460	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	22522925	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Lung cancer	17086460	CNVD
Rhabdomyosarcoma	16790082	CNVD

Chromatin state (count:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:43048000-43048200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:43133000-43133200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr9:43133000-43133800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr9:43133000-43133800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr9:43133000-43134200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr9:43133000-43134200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr9:43133000-43134200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr9:43133000-43134800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr9:43133000-43135000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr9:43133000-43135000	Active TSS	Brain Germinal Matrix	brain
11	chr9:43133200-43134000	Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr9:43133200-43134000	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr9:43133200-43134200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr9:43133200-43134200	Active TSS	Brain Angular Gyrus	brain
15	chr9:43133200-43134200	Active TSS	Esophagus	oesophagus
16	chr9:43133200-43134200	Active TSS	Right Ventricle	heart
17	chr9:43133600-43133800	Active TSS	Adipose Nuclei	Adipose
18	chr9:43133800-43134000	Active TSS	H1 Cell Line	embryonic stem cell
19	chr9:43133800-43134000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr9:43133800-43134000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr9:43133800-43134000	Enhancers	Muscle Satellite Cultured Cells	--
22	chr9:43133800-43134000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr9:43133800-43134000	Active TSS	Fetal Intestine Large	intestine
24	chr9:43133800-43134000	Active TSS	Fetal Muscle Leg	muscle
25	chr9:43133800-43134000	Active TSS	Rectal Mucosa Donor 31	rectum
26	chr9:43133800-43134000	Active TSS	HMEC	breast
27	chr9:43133800-43134000	Active TSS	NHEK	skin
28	chr9:43133800-43134200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr9:43133800-43134200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr9:43133800-43134200	Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr9:43133800-43134200	Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr9:43133800-43134200	Enhancers	Primary hematopoietic stem cells	blood
33	chr9:43133800-43134200	Active TSS	Primary hematopoietic stem cells short term culture	blood
34	chr9:43133800-43134200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
35	chr9:43133800-43134200	Active TSS	Primary T helper cells PMA-I stimulated	--
36	chr9:43133800-43134200	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr9:43133800-43134200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
38	chr9:43133800-43134200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr9:43133800-43134200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr9:43133800-43134200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr9:43133800-43134200	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr9:43133800-43134200	Active TSS	Brain Hippocampus Middle	brain
43	chr9:43133800-43134200	Active TSS	Brain Inferior Temporal Lobe	brain
44	chr9:43133800-43134200	Active TSS	Duodenum Mucosa	Duodenum
45	chr9:43133800-43134200	Active TSS	Duodenum Smooth Muscle	Duodenum
46	chr9:43133800-43134200	Active TSS	Rectal Smooth Muscle	rectum
47	chr9:43133800-43134200	Active TSS	Sigmoid Colon	Sigmoid Colon
48	chr9:43133800-43134200	Active TSS	Skeletal Muscle Male	skeletal muscle
49	chr9:43133800-43134200	Active TSS	Skeletal Muscle Female	skeletal muscle
50	chr9:43133800-43134200	Active TSS	Stomach Smooth Muscle	stomach

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