Variant report

Variant	nsv888047
Chromosome Location	chr7:53813283-54031396
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:53878746-53879008	K562	blood:	n/a	chr7:53878805-53878821
2	ARID3A	chr7:53877206-53877492	K562	blood:	n/a	n/a
3	ARID3A	chr7:53880056-53880500	K562	blood:	n/a	n/a
4	BHLHE40	chr7:53879156-53880313	K562	blood:	n/a	n/a
5	BRCA1	chr7:53919533-53919557	GM12878	blood:	n/a	n/a
6	CCNT2	chr7:53879220-53879790	K562	blood:	n/a	n/a
7	CEBPB	chr7:53929924-53930105	K562	blood:	n/a	n/a
8	CEBPB	chr7:53950666-53950975	H1-hESC	embryonic stem cell:	n/a	chr7:53950802-53950815 chr7:53950804-53950813 chr7:53950804-53950813 chr7:53950863-53950874 chr7:53950804-53950813
9	CEBPB	chr7:53991460-53991780	IMR90	lung:	n/a	chr7:53991604-53991615
10	CEBPB	chr7:53950673-53950917	A549	lung:	n/a	chr7:53950802-53950815 chr7:53950804-53950813 chr7:53950804-53950813 chr7:53950863-53950874 chr7:53950804-53950813
11	CEBPB	chr7:53923660-53923836	HepG2	liver:	n/a	chr7:53923796-53923807
12	CEBPB	chr7:53995168-53995489	A549	lung:	n/a	chr7:53995333-53995344 chr7:53995333-53995346
13	CEBPB	chr7:53937222-53937545	IMR90	lung:	n/a	chr7:53937391-53937402
14	CEBPB	chr7:53995164-53995500	IMR90	lung:	n/a	chr7:53995333-53995344 chr7:53995333-53995346
15	CEBPB	chr7:53950649-53950861	HepG2	liver:	n/a	chr7:53950802-53950815 chr7:53950804-53950813 chr7:53950804-53950813 chr7:53950804-53950813
16	CEBPB	chr7:53863849-53863877	K562	blood:	n/a	n/a
17	CEBPB	chr7:53991434-53991756	A549	lung:	n/a	chr7:53991604-53991615
18	CEBPB	chr7:54013426-54013673	IMR90	lung:	n/a	chr7:54013519-54013532 chr7:54013520-54013531 chr7:54013519-54013530 chr7:54013519-54013532 chr7:54013519-54013532
19	CEBPB	chr7:53960408-53960716	HepG2	liver:	n/a	chr7:53960576-53960587 chr7:53960436-53960449
20	CEBPB	chr7:54013455-54013662	A549	lung:	n/a	chr7:54013519-54013532 chr7:54013520-54013531 chr7:54013519-54013530 chr7:54013519-54013532 chr7:54013519-54013532
21	CEBPB	chr7:53873750-53874089	K562	blood:	n/a	n/a
22	CEBPB	chr7:53875149-53875349	K562	blood:	n/a	n/a
23	CEBPB	chr7:53950630-53950964	IMR90	lung:	n/a	chr7:53950802-53950815 chr7:53950804-53950813 chr7:53950804-53950813 chr7:53950863-53950874 chr7:53950804-53950813
24	CEBPB	chr7:53980037-53980386	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:53995177-53995525	HepG2	liver:	n/a	chr7:53995333-53995344 chr7:53995333-53995346
26	CEBPB	chr7:53877399-53877749	K562	blood:	n/a	n/a
27	CEBPB	chr7:53879534-53880394	K562	blood:	n/a	n/a
28	CEBPB	chr7:53937236-53937500	HepG2	liver:	n/a	chr7:53937391-53937402
29	CEBPB	chr7:54013432-54013580	H1-hESC	embryonic stem cell:	n/a	chr7:54013519-54013532 chr7:54013520-54013531 chr7:54013519-54013530 chr7:54013519-54013532 chr7:54013519-54013532
30	CEBPB	chr7:54013434-54013638	HepG2	liver:	n/a	chr7:54013519-54013532 chr7:54013520-54013531 chr7:54013519-54013530 chr7:54013519-54013532 chr7:54013519-54013532
31	CEBPB	chr7:53960534-53960671	A549	lung:	n/a	chr7:53960576-53960587
32	CEBPB	chr7:53991425-53991786	HepG2	liver:	n/a	chr7:53991604-53991615
33	CEBPB	chr7:53995228-53995491	K562	blood:	n/a	chr7:53995333-53995344 chr7:53995333-53995346
34	CEBPB	chr7:53950795-53950824	K562	blood:	n/a	chr7:53950802-53950815 chr7:53950804-53950813 chr7:53950804-53950813 chr7:53950804-53950813
35	CEBPB	chr7:53879553-53879905	K562	blood:	n/a	n/a
36	CEBPB	chr7:53960493-53960651	K562	blood:	n/a	chr7:53960576-53960587
37	CEBPB	chr7:53980061-53980369	A549	lung:	n/a	n/a
38	CEBPB	chr7:53916135-53916381	HepG2	liver:	n/a	chr7:53916256-53916265 chr7:53916254-53916267 chr7:53916255-53916266
39	CHD2	chr7:53827893-53827955	HepG2	liver:	n/a	n/a
40	CHD2	chr7:53879367-53879877	K562	blood:	n/a	n/a
41	CTCF	chr7:53965772-53966093	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:54005623-54005663	Fibrobl	skin:	n/a	n/a
43	CTCF	chr7:53968649-53968816	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:53968704-53968796	K562	blood:	n/a	n/a
45	CTCF	chr7:53965833-53966001	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:53968680-53968830	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr7:53968760-53968910	NB4	blood:	n/a	n/a
48	CTCF	chr7:53975620-53975770	BE2_C	brain:	n/a	n/a
49	CTCF	chr7:53975600-53975750	MCF-7	breast:	n/a	n/a
50	CTCF	chr7:53965840-53965990	SK-N-SH_RA	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:53879728-53879778	SK-N-SH	brain:	n/a
2	chr7:53879728-53879778	SK-N-SH	brain:	n/a
3	chr7:53879728-53879778	RPTEC	kidney:	n/a
4	chr7:53879377-53879427	MCF10A-Er-Src	breast:	n/a
5	chr7:53879377-53879427	RPTEC	kidney:	n/a
6	chr7:53879422-53879472	HCM	heart:	n/a
7	chr7:53879377-53879427	PANC-1	pancreas:	n/a
8	chr7:53879377-53879427	AG10803	skin:	n/a
9	chr7:53879377-53879427	HCF	heart:	n/a
10	chr7:53879377-53879427	BE2_C	brain:	n/a
11	chr7:53879728-53879778	NHDF-neo	bronchial:	n/a
12	chr7:53879377-53879427	HCPEpiC	choroid plexus:	n/a
13	chr7:53879253-53879303	HL-60	blood:	n/a
14	chr7:53879377-53879427	HNPCEpiC	eye:	n/a
15	chr7:53879253-53879303	AG09319	gingival:	n/a
16	chr7:53879377-53879427	HAEpiC	amniotic membrane:	n/a
17	chr7:53879377-53879427	HEK293	kidney:	embryo
18	chr7:53879377-53879427	Jurkat	blood:	n/a
19	chr7:53879422-53879472	RPTEC	kidney:	n/a
20	chr7:53879377-53879427	HCM	heart:	n/a
21	chr7:53879422-53879472	HCF	heart:	n/a
22	chr7:53879728-53879778	AG09319	gingival:	n/a
23	chr7:53879728-53879778	PrEC	prostate:	n/a
24	chr7:53879377-53879427	LNCaP	prostate:	n/a
25	chr7:53879377-53879427	AoSMC	blood vessel:	n/a
26	chr7:53879728-53879778	HL-60	blood:	n/a
27	chr7:53879253-53879303	MCF10A-Er-Src	breast:	n/a
28	chr7:53879377-53879427	H1-hESC	embryonic stem cell:	embryo
29	chr7:53879728-53879778	HIPEpiC	eye:	n/a
30	chr7:53879728-53879778	LNCaP	prostate:	n/a
31	chr7:53879377-53879427	PFSK-1	brain:	n/a
32	chr7:53879253-53879303	NT2-D1	testis:	n/a
33	chr7:53879253-53879303	Hepatocyte	liver:	n/a
34	chr7:53879253-53879303	HPAEpiC	pulmonary alveolar:	n/a
35	chr7:53879422-53879472	Jurkat	blood:	n/a
36	chr7:53879422-53879472	NT2-D1	testis:	n/a
37	chr7:53879377-53879427	GM12892	blood:	n/a
38	chr7:53879377-53879427	T-47D	breast:	n/a
39	chr7:53879422-53879472	NH-A	brain:	n/a
40	chr7:53879253-53879303	A549	lung:	n/a
41	chr7:53879253-53879303	GM06990	blood:	n/a
42	chr7:53879253-53879303	SKMC	muscle:	n/a
43	chr7:53879253-53879303	NH-A	brain:	n/a
44	chr7:53879377-53879427	SK-N-SH_RA	brain:	n/a
45	chr7:53879728-53879778	GM12878	blood:	n/a
46	chr7:53879377-53879427	AG09309	skin:	n/a
47	chr7:53879728-53879778	HepG2	liver:	n/a
48	chr7:53879253-53879303	Hela-S3	cervix:	n/a
49	chr7:53879728-53879778	AG09309	skin:	n/a
50	chr7:53879422-53879472	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:53841058..53842718-chr7:53850373..53853368,2	K562	blood:
2	chr7:53857172..53859056-chr7:53860252..53862922,2	K562	blood:
3	chr5:135485656..135486185-chr7:53838517..53839265,2	MCF-7	breast:
4	chr7:53961627..53964439-chr7:53965222..53967400,2	K562	blood:
5	chr7:54009097..54010852-chr7:54010877..54012495,2	MCF-7	breast:
6	chr7:53818690..53823967-chr7:53825430..53828073,4	K562	blood:
7	chr7:53975341..53977191-chr7:53977217..53978871,2	MCF-7	breast:
8	chr3:73159725..73160594-chr7:53843395..53843920,2	HCT-116	colon:
9	chr7:53871548..53874105-chr7:53878796..53880658,2	K562	blood:
10	chr7:53848619..53849339-chr7:53918094..53918709,2	MCF-7	breast:
11	chr7:53841458..53843486-chr7:53862183..53865020,2	K562	blood:
12	chr7:53820582..53822348-chr7:53824215..53825903,2	K562	blood:
13	chr7:53841458..53843486-chr7:53862183..53865020,2	K562	blood:
14	chr7:53849409..53852274-chr7:53856069..53858017,2	K562	blood:
15	chr7:53870278..53873063-chr7:53876211..53878158,2	K562	blood:
16	chr7:53870278..53873063-chr7:53876211..53878158,2	K562	blood:
17	chr7:53817997..53820497-chr7:53821045..53822573,2	K562	blood:
18	chr7:53820582..53822348-chr7:53824215..53825903,2	K562	blood:
19	chr7:53865812..53868107-chr7:53870179..53872741,2	K562	blood:
20	chr7:54009097..54010852-chr7:54010877..54012495,2	MCF-7	breast:
21	chr7:53975341..53977191-chr7:53977217..53978871,2	MCF-7	breast:
22	chr7:53817997..53820497-chr7:53821045..53822573,2	K562	blood:
23	chr7:53961627..53964439-chr7:53965222..53967400,2	K562	blood:
24	chr7:53818690..53823967-chr7:53825430..53828073,4	K562	blood:
25	chr7:53857172..53859056-chr7:53860252..53862922,2	K562	blood:
26	chr7:53827998..53830937-chr7:53834103..53836205,2	K562	blood:
27	chr7:53848619..53849339-chr7:53918094..53918709,2	MCF-7	breast:
28	chr7:53841058..53842718-chr7:53850373..53853368,2	K562	blood:
29	chr7:53849409..53852274-chr7:53856069..53858017,2	K562	blood:
30	chr7:53827998..53830937-chr7:53834103..53836205,2	K562	blood:
31	chr7:53865812..53868107-chr7:53870179..53872741,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POM121L12-10	chr7:53847476-53847617	NONHSAT120643
2	lnc-SEC61G-3	chr7:53994369-53994678	XLOC_006448
3	lnc-SEC61G-3	chr7:53997721-53997941	XLOC_006448
4	lnc-SEC61G-3	chr7:54015344-54015437	XLOC_006448
5	lnc-POM121L12-9	chr7:53832374-53832647	NONHSAT120640
6	lnc-POM121L12-10	chr7:53847707-53847956	NONHSAT120643
7	lnc-POM121L12-9	chr7:53832905-53833852	NONHSAT120640

Variant related genes	Relation type
RNU2-29P	TF binding region
ENSG00000271306	TF binding region
ENSG00000232418	TF binding region
ENSG00000205628	TF binding region
ENSG00000235454	TF binding region
ENSG00000238131	TF binding region
RNU2-29P	CpG island
ENSG00000271306	CpG island
ENSG00000232418	CpG island
ENSG00000205628	CpG island
ENSG00000235454	CpG island
ENSG00000238131	CpG island
ENSG00000205628	chromatin interactions
ENSG00000223247	chromatin interactions

Extended variants
information (count: 1370 )
Associated
traits (count: 143 )

Variant overlapped rSNPs/rCNVs (count:1370 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549570061	chr7:53827814-53827815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs114442738	chr7:53827847-53827848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536691302	chr7:53827850-53827851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs79054450	chr7:53827909-53827910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565713942	chr7:53827924-53827925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539035845	chr7:53827964-53827965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551098393	chr7:53827965-53827966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201556154	chr7:53827969-53827970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147798530	chr7:53827993-53827994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536871847	chr7:53827998-53827999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs555505755	chr7:53827999-53828000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs79438059	chr7:53828001-53828002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536510120	chr7:53828028-53828029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs141330044	chr7:53828066-53828067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183575699	chr7:53828072-53828073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569814414	chr7:53828121-53828122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564728763	chr7:53828136-53828137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149940209	chr7:53828142-53828143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537292750	chr7:53828152-53828153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76807440	chr7:53828160-53828161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543253022	chr7:53828176-53828177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561482824	chr7:53828187-53828188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570505896	chr7:53832037-53832038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537825428	chr7:53832056-53832057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs369492777	chr7:53832078-53832079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574446449	chr7:53832093-53832094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148436710	chr7:53832115-53832116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs180989106	chr7:53832185-53832186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371946802	chr7:53832192-53832193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs142574950	chr7:53832258-53832259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150975192	chr7:53832327-53832328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs62445425	chr7:53832366-53832367	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs143437092	chr7:53832372-53832373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543768525	chr7:53832390-53832391	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs377167857	chr7:53832403-53832404	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs559639650	chr7:53832410-53832411	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs562054190	chr7:53832455-53832456	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs529345953	chr7:53832484-53832485	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs115849376	chr7:53832486-53832487	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs114345931	chr7:53832495-53832496	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs373540583	chr7:53832511-53832512	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs186062200	chr7:53832521-53832522	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs62445426	chr7:53832526-53832527	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs76414888	chr7:53832528-53832529	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs191357048	chr7:53832560-53832561	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs549717662	chr7:53832563-53832564	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs75758283	chr7:53832584-53832585	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs146771410	chr7:53832634-53832635	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs183219492	chr7:53832636-53832637	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs140504564	chr7:53832670-53832671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:143)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioblastoma multiforme	21525872	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Intracranial ependymoma	16609018	CNVD
Lung cancer	21911935	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	21990379	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17925434	CNVD
Glioma	24330732	CNVD
Lung adenocarcinoma	23938291	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	17634744	CNVD
Oral squamous cell carcinoma	19276369	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Lung cancer	20031968	CNVD
Glioblastoma	17090523	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Glioma	17123091	CNVD
Glioblastoma multiforme	19115005	CNVD

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:53827800-53828200	Enhancers	Brain Hippocampus Middle	brain
2	chr7:53832000-53837800	Weak transcription	K562	blood
3	chr7:53836200-53836600	Enhancers	Fetal Stomach	stomach
4	chr7:53837800-53839200	Strong transcription	K562	blood
5	chr7:53838200-53838800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:53839000-53839400	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr7:53839200-53847000	Weak transcription	K562	blood
8	chr7:53839400-53844200	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr7:53840400-53840800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:53840800-53843200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:53841200-53842000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:53843200-53843400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:53843400-53843600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:53844000-53844200	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr7:53844200-53844600	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr7:53844600-53844800	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr7:53844800-53845200	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr7:53847000-53847200	Strong transcription	K562	blood
19	chr7:53847200-53848400	Weak transcription	K562	blood
20	chr7:53861800-53862000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:53864000-53864400	Enhancers	K562	blood
22	chr7:53868200-53868800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr7:53877200-53880200	Active TSS	K562	blood
24	chr7:53879000-53879400	Active TSS	NHEK	skin
25	chr7:53879000-53879600	ZNF genes & repeats	Fetal Intestine Large	intestine
26	chr7:53879000-53879600	Active TSS	Fetal Intestine Small	intestine
27	chr7:53879000-53879600	Active TSS	Right Ventricle	heart
28	chr7:53879000-53880000	Active TSS	Placenta	Placenta
29	chr7:53879200-53879600	Active TSS	HUVEC	blood vessel
30	chr7:53893800-53894200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:53899000-53899400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr7:53903000-53903200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr7:53916800-53917200	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr7:53936000-53936200	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr7:53959400-53959600	Active TSS	HSMM	muscle
36	chr7:53959600-53959800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr7:53959600-53959800	Flanking Active TSS	HSMM	muscle
38	chr7:53971800-53972200	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr7:53971800-53972600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr7:53972000-53972200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr7:53972000-53972400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:53972000-53972600	Enhancers	H1 Cell Line	embryonic stem cell
43	chr7:53972000-53972600	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr7:53972200-53973000	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr7:53972600-53975200	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr7:53973000-53973400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
47	chr7:54014000-54016200	Enhancers	Fetal Lung	lung
48	chr7:54014400-54015000	Enhancers	Fetal Stomach	stomach
49	chr7:54014800-54016000	Enhancers	Fetal Brain Male	brain
50	chr7:54015400-54015600	Enhancers	Fetal Brain Female	brain

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