Variant report

Variant	nsv1014937
Chromosome Location	chr1:180360900-180399555
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	ATF1	chr1:180361304-180361367	K562	blood:	n/a	n/a
2	ATF1	chr1:180398354-180398477	K562	blood:	n/a	n/a
3	ATF1	chr1:180379529-180379568	K562	blood:	n/a	n/a
4	BACH1	chr1:180386975-180387028	K562	blood:	n/a	n/a
5	BATF	chr1:180372837-180373078	GM12878	blood:	n/a	n/a
6	CBX3	chr1:180385127-180385514	K562	blood:	n/a	n/a
7	CCNT2	chr1:180385308-180385408	K562	blood:	n/a	n/a
8	CEBPB	chr1:180371284-180371457	H1-hESC	embryonic stem cell:	n/a	chr1:180371352-180371361
9	CEBPB	chr1:180398171-180398565	Hela-S3	cervix:	n/a	chr1:180398307-180398318
10	CEBPB	chr1:180366360-180366690	IMR90	lung:	n/a	chr1:180366529-180366540 chr1:180366518-180366529
11	CEBPB	chr1:180366366-180366686	HepG2	liver:	n/a	chr1:180366529-180366540 chr1:180366518-180366529
12	CEBPB	chr1:180381765-180382042	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr1:180381719-180382060	MCF-7	breast:	n/a	n/a
14	CEBPB	chr1:180366394-180366645	Hela-S3	cervix:	n/a	chr1:180366529-180366540 chr1:180366518-180366529
15	CEBPB	chr1:180366365-180366698	K562	blood:	n/a	chr1:180366529-180366540 chr1:180366518-180366529
16	CEBPB	chr1:180376043-180376273	A549	lung:	n/a	chr1:180376122-180376134 chr1:180376161-180376172
17	CEBPB	chr1:180381696-180382185	MCF-7	breast:	n/a	n/a
18	CEBPB	chr1:180398139-180398627	A549	lung:	n/a	chr1:180398307-180398318
19	CEBPB	chr1:180381745-180382056	A549	lung:	n/a	n/a
20	CEBPB	chr1:180381716-180382102	K562	blood:	n/a	n/a
21	CEBPB	chr1:180381754-180382062	IMR90	lung:	n/a	n/a
22	CEBPB	chr1:180398123-180398505	IMR90	lung:	n/a	chr1:180398307-180398318
23	CEBPB	chr1:180398178-180398452	HepG2	liver:	n/a	chr1:180398307-180398318
24	CEBPB	chr1:180376010-180376276	HepG2	liver:	n/a	chr1:180376122-180376134 chr1:180376161-180376172
25	CEBPB	chr1:180381735-180382093	K562	blood:	n/a	n/a
26	CEBPB	chr1:180376077-180376264	K562	blood:	n/a	chr1:180376122-180376134 chr1:180376161-180376172
27	CEBPB	chr1:180366355-180366681	A549	lung:	n/a	chr1:180366529-180366540 chr1:180366518-180366529
28	CEBPB	chr1:180366370-180366611	MCF-7	breast:	n/a	chr1:180366529-180366540 chr1:180366518-180366529
29	CEBPB	chr1:180398165-180398467	H1-hESC	embryonic stem cell:	n/a	chr1:180398307-180398318
30	CEBPB	chr1:180381698-180382027	A549	lung:	n/a	n/a
31	CEBPB	chr1:180381737-180382098	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr1:180381782-180382051	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr1:180398143-180398676	K562	blood:	n/a	chr1:180398307-180398318
34	CEBPB	chr1:180381711-180382074	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr1:180381744-180382095	HepG2	liver:	n/a	n/a
36	CTCF	chr1:180385280-180385430	HEEpiC	esophagus:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
37	CTCF	chr1:180385089-180385446	HCT-116	colon:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
38	CTCF	chr1:180385253-180385393	MCF-7	breast:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
39	CTCF	chr1:180385180-180385450	HVMF	connective:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
40	CTCF	chr1:180385240-180385390	GM12872	blood:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
41	CTCF	chr1:180385224-180385482	Lung_OC	lung:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
42	CTCF	chr1:180385300-180385450	AG09319	gingival:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
43	CTCF	chr1:180385260-180385410	GM12864	blood:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
44	CTCF	chr1:180385280-180385430	HAc	cerebellar:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
45	CTCF	chr1:180385260-180385410	GM06990	blood:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
46	CTCF	chr1:180385254-180385404	HepG2	liver:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
47	CTCF	chr1:180385200-180385350	NHDF-neo	bronchial:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344
48	CTCF	chr1:180371303-180371364	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:180371244-180371455	GM12878	blood:	n/a	n/a
50	CTCF	chr1:180385229-180385465	GM12878	blood:	n/a	chr1:180385328-180385346 chr1:180385329-180385345 chr1:180385333-180385341 chr1:180385323-180385344

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:180374455-180374505	HepG2	liver:	n/a
2	chr1:180374455-180374505	ovcar-3	ovarian:	n/a
3	chr1:180374455-180374505	HCM	heart:	n/a
4	chr1:180374455-180374505	PrEC	prostate:	n/a
5	chr1:180374455-180374505	HL-60	blood:	n/a
6	chr1:180374455-180374505	SAEC	small airway:	n/a
7	chr1:180374455-180374505	IMR90	lung:	fetal
8	chr1:180374455-180374505	HEEpiC	esophagus:	n/a
9	chr1:180374455-180374505	GM06990	blood:	n/a
10	chr1:180374455-180374505	MCF10A-Er-Src	breast:	n/a
11	chr1:180374455-180374505	NHDF-neo	bronchial:	n/a
12	chr1:180374455-180374505	BJ	skin:	n/a
13	chr1:180374455-180374505	HAEpiC	amniotic membrane:	n/a
14	chr1:180374455-180374505	Caco-2	colon:	n/a
15	chr1:180374455-180374505	AoSMC	blood vessel:	n/a
16	chr1:180374455-180374505	PANC-1	pancreas:	n/a
17	chr1:180374455-180374505	HRCEpiC	kidney:	n/a
18	chr1:180374455-180374505	BE2_C	brain:	n/a
19	chr1:180374455-180374505	HRPEpiC	eye:	n/a
20	chr1:180374455-180374505	K562	blood:	n/a
21	chr1:180374455-180374505	LNCaP	prostate:	n/a
22	chr1:180374455-180374505	MCF-7	breast:	n/a
23	chr1:180374455-180374505	HIPEpiC	eye:	n/a
24	chr1:180374455-180374505	HCPEpiC	choroid plexus:	n/a
25	chr1:180374455-180374505	Hela-S3	cervix:	n/a
26	chr1:180374455-180374505	SKMC	muscle:	n/a
27	chr1:180374455-180374505	AG04449	skin:	fetal
28	chr1:180374455-180374505	GM12891	blood:	n/a
29	chr1:180374455-180374505	H1-hESC	embryonic stem cell:	embryo
30	chr1:180374455-180374505	SK-N-SH	brain:	n/a
31	chr1:180374455-180374505	HCT-116	colon:	n/a
32	chr1:180374455-180374505	HRE	kidney:	n/a
33	chr1:180374455-180374505	HPAEpiC	pulmonary alveolar:	n/a
34	chr1:180374455-180374505	GM19239	blood:	n/a
35	chr1:180374455-180374505	RPTEC	kidney:	n/a
36	chr1:180374455-180374505	AG09319	gingival:	n/a
37	chr1:180374455-180374505	NT2-D1	testis:	n/a
38	chr1:180374455-180374505	AG09309	skin:	n/a
39	chr1:180374455-180374505	PFSK-1	brain:	n/a
40	chr1:180374455-180374505	GM12878	blood:	n/a
41	chr1:180374455-180374505	HUVEC	blood vessel:	n/a
42	chr1:180374455-180374505	NH-A	brain:	n/a
43	chr1:180374455-180374505	NHBE	bronchial:	n/a
44	chr1:180374455-180374505	HCF	heart:	n/a
45	chr1:180374455-180374505	HEK293	kidney:	embryo
46	chr1:180374455-180374505	ECC-1	luminal epithelium:	n/a
47	chr1:180374455-180374505	A549	lung:	n/a
48	chr1:180374455-180374505	CMK	blood:	n/a
49	chr1:180374455-180374505	SK-N-MC	brain:	n/a
50	chr1:180374455-180374505	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:180385266..180387346-chr1:180425240..180427346,2	K562	blood:
2	chr1:180380729..180383084-chr1:180391274..180393848,2	K562	blood:
3	chr1:180396509..180398136-chr1:180400657..180403081,2	MCF-7	breast:
4	chr1:180384412..180386137-chr1:180393141..180396163,3	K562	blood:
5	chr1:180383756..180385501-chr1:180395011..180397819,2	K562	blood:
6	chr1:180383756..180385501-chr1:180395011..180397819,2	K562	blood:
7	chr1:180373412..180375725-chr1:180377296..180379670,2	MCF-7	breast:
8	chr1:180374275..180377221-chr1:180383343..180386300,2	K562	blood:
9	chr1:180374275..180378586-chr1:180383335..180386300,4	K562	blood:
10	chr1:180382343..180384575-chr1:180387330..180389916,2	MCF-7	breast:
11	chr1:180221511..180222402-chr1:180384611..180385850,8	K562	blood:
12	chr1:180383396..180385405-chr1:180470493..180472141,2	MCF-7	breast:
13	chr1:180374275..180377221-chr1:180383343..180386300,2	K562	blood:
14	chr1:180338174..180341966-chr1:180380791..180382462,3	MCF-7	breast:
15	chr1:180374275..180378586-chr1:180383335..180386300,4	K562	blood:
16	chr1:180384412..180386137-chr1:180393141..180396163,3	K562	blood:
17	chr1:180333422..180334593-chr1:180384864..180385775,6	MCF-7	breast:
18	chr1:180354979..180356991-chr1:180360915..180363474,2	MCF-7	breast:
19	chr1:180353732..180356120-chr1:180367249..180368760,2	MCF-7	breast:
20	chr1:180221010..180222431-chr1:180384882..180385873,4	MCF-7	breast:
21	chr1:180373412..180375725-chr1:180377296..180379670,2	MCF-7	breast:
22	chr1:180333279..180333792-chr1:180384823..180385385,2	MCF-7	breast:
23	chr1:180391869..180395184-chr1:180397658..180400952,4	K562	blood:
24	chr1:180156865..180157706-chr1:180384959..180385623,2	K562	blood:
25	chr1:180338679..180340699-chr1:180366769..180368773,2	K562	blood:
26	chr1:180381265..180383323-chr1:180383973..180385553,2	K562	blood:
27	chr1:180222556..180224240-chr1:180362387..180364458,2	MCF-7	breast:
28	chr1:180157564..180158553-chr1:180385566..180386276,2	MCF-7	breast:
29	chr1:180345449..180347535-chr1:180362052..180364147,2	MCF-7	breast:
30	chr1:180156740..180157798-chr1:180384923..180385820,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TOR1AIP2-7	chr1:180363055-180363304	NONHSAT008259
2	lnc-TOR1AIP2-7	chr1:180363569-180363685	NONHSAT008259
3	lnc-TOR1AIP2-7	chr1:180364163-180364423	NONHSAT008259

Variant related genes	Relation type
ACBD6	TF binding region
VDAC1P4	TF binding region
ACBD6	CpG island
VDAC1P4	CpG island
ENSG00000135847	chromatin interactions

Extended variants
information (count: 1463 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1463 , 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	rs10913980	chr1:180360900-180360901	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377161823	chr1:180360995-180360996	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs66994364	chr1:180361029-180361030	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs200147933	chr1:180361035-180361036	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs370091432	chr1:180361037-180361038	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs371514962	chr1:180361054-180361055	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs148809344	chr1:180361075-180361076	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs560897238	chr1:180361116-180361117	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs543237433	chr1:180361120-180361121	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs529849150	chr1:180361169-180361170	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs142390486	chr1:180361252-180361253	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs150886499	chr1:180361294-180361295	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs576674060	chr1:180361350-180361351	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs201188190	chr1:180361399-180361400	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs199693077	chr1:180361414-180361415	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs201820900	chr1:180361416-180361417	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs59508850	chr1:180361417-180361418	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs201600545	chr1:180361418-180361419	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs532099614	chr1:180361520-180361521	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs183783078	chr1:180361567-180361568	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs6661208	chr1:180361630-180361631	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs527901480	chr1:180361748-180361749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558704552	chr1:180361783-180361784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188465841	chr1:180361790-180361791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs180849861	chr1:180361854-180361855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs184909442	chr1:180361872-180361873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569722181	chr1:180361887-180361888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538987408	chr1:180361892-180361893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558597234	chr1:180361923-180361924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144311810	chr1:180361958-180361959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs147761254	chr1:180361977-180361978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554843750	chr1:180361989-180361990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs58677059	chr1:180362003-180362004	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs67025020	chr1:180362037-180362038	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs77380313	chr1:180362041-180362042	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs115286768	chr1:180362107-180362108	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs74544942	chr1:180362133-180362134	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576930543	chr1:180362153-180362154	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs367872270	chr1:180362158-180362159	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs35966816	chr1:180362183-180362184	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs559066759	chr1:180362225-180362226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189750712	chr1:180362234-180362235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs181800862	chr1:180362238-180362239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547765846	chr1:180362257-180362258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185718637	chr1:180362295-180362296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530190827	chr1:180362344-180362345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs116723425	chr1:180362350-180362351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569783573	chr1:180362439-180362440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538732672	chr1:180362445-180362446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552575789	chr1:180362510-180362511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	16397240	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	23248035	CNVD
Metanephric adenoma	20802469	CNVD
Renal cell carcinoma	18765545	CNVD
Nephroblastoma	17189400	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:180341200-180401400	Weak transcription	Osteobl	bone
2	chr1:180348200-180382600	Weak transcription	Pancreas	Pancrea
3	chr1:180349400-180364200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr1:180349400-180407000	Weak transcription	Esophagus	oesophagus
5	chr1:180351600-180378400	Weak transcription	HSMM	muscle
6	chr1:180352400-180381400	Weak transcription	Hela-S3	cervix
7	chr1:180352800-180399400	Weak transcription	Fetal Thymus	thymus
8	chr1:180354200-180364200	Weak transcription	NH-A	brain
9	chr1:180354600-180374000	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr1:180354800-180386600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr1:180355200-180364800	Weak transcription	K562	blood
12	chr1:180355200-180402600	Weak transcription	HMEC	breast
13	chr1:180355400-180361200	Weak transcription	Small Intestine	intestine
14	chr1:180355400-180378800	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr1:180355600-180378400	Weak transcription	Placenta	Placenta
16	chr1:180355600-180390800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr1:180356400-180363800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr1:180356600-180364200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr1:180356600-180364200	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr1:180356600-180381400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr1:180356600-180394000	Weak transcription	NHDF-Ad	bronchial
22	chr1:180356800-180363600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr1:180356800-180364200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:180356800-180364800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr1:180356800-180373000	Weak transcription	Fetal Intestine Small	intestine
26	chr1:180356800-180378600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr1:180356800-180378800	Weak transcription	Left Ventricle	heart
28	chr1:180356800-180380800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr1:180356800-180406200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr1:180356800-180407000	Weak transcription	Aorta	Aorta
31	chr1:180357000-180361200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr1:180357000-180364000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr1:180357000-180364200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:180357000-180364200	Weak transcription	Fetal Intestine Large	intestine
35	chr1:180357000-180364200	Weak transcription	Ovary	ovary
36	chr1:180357000-180364400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr1:180357000-180378400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr1:180357800-180366600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr1:180358200-180374000	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr1:180358600-180364200	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr1:180359800-180361000	ZNF genes & repeats	A549	lung
42	chr1:180359800-180361200	ZNF genes & repeats	Primary B cells from cord blood	blood
43	chr1:180360000-180361000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr1:180360000-180363800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:180360200-180378000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr1:180360400-180364200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr1:180360400-180364200	Weak transcription	Fetal Lung	lung
48	chr1:180360400-180394200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:180360600-180361000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
50	chr1:180360600-180361000	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood

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