Variant report

Variant	nsv945765
Chromosome Location	chr1:9633634-9639115
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:300)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr1:9634686-9634968	HepG2	liver:	n/a	n/a
2	CEBPB	chr1:9637526-9637560	K562	blood:	n/a	n/a
3	CTCF	chr1:9633860-9634010	BE2_C	brain:	n/a	n/a
4	CTCF	chr1:9633880-9634030	HPAF	blood vessel:	n/a	n/a
5	CTCF	chr1:9636608-9636735	K562	blood:	n/a	n/a
6	CTCF	chr1:9633888-9634067	GM13977	blood:	n/a	n/a
7	CTCF	chr1:9633867-9634089	Pancreas_OC	pancreas:	n/a	n/a
8	CTCF	chr1:9633911-9634050	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr1:9633920-9634070	GM12868	blood:	n/a	n/a
10	CTCF	chr1:9637047-9637231	K562	blood:	n/a	chr1:9637151-9637169 chr1:9637154-9637167
11	CTCF	chr1:9633880-9634030	SAEC	small airway:	n/a	n/a
12	CTCF	chr1:9633881-9634062	K562	blood:	n/a	n/a
13	CTCF	chr1:9633940-9634090	WI-38	lung:	n/a	n/a
14	CTCF	chr1:9633880-9634030	GM12875	blood:	n/a	n/a
15	CTCF	chr1:9633920-9634070	HBMEC	blood vessel:	n/a	n/a
16	CTCF	chr1:9636520-9636670	HAc	cerebellar:	n/a	n/a
17	CTCF	chr1:9633780-9633930	HA-sp	spinal cord:	n/a	n/a
18	CTCF	chr1:9633860-9634010	NHDF-neo	bronchial:	n/a	n/a
19	CTCF	chr1:9637080-9637230	HCPEpiC	choroid plexus:	n/a	chr1:9637151-9637169 chr1:9637154-9637167
20	CTCF	chr1:9637093-9637216	Hela-S3	cervix:	n/a	chr1:9637151-9637169 chr1:9637154-9637167
21	CTCF	chr1:9633870-9634077	HepG2	liver:	n/a	n/a
22	CTCF	chr1:9636631-9636675	Gliobla	brain:	n/a	n/a
23	CTCF	chr1:9636580-9636730	RPTEC	kidney:	n/a	n/a
24	CTCF	chr1:9633783-9634186	MCF-7	breast:	n/a	n/a
25	CTCF	chr1:9633882-9634066	A549	lung:	n/a	n/a
26	CTCF	chr1:9637080-9637230	HRPEpiC	eye:	n/a	chr1:9637151-9637169 chr1:9637154-9637167
27	CTCF	chr1:9633927-9634026	GM20000	blood:	n/a	n/a
28	CTCF	chr1:9633940-9634090	GM12870	blood:	n/a	n/a
29	CTCF	chr1:9633920-9634070	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr1:9633940-9634090	GM12864	blood:	n/a	n/a
31	CTCF	chr1:9633560-9633710	GM12872	blood:	n/a	n/a
32	CTCF	chr1:9633960-9634110	NHEK	skin:	n/a	n/a
33	CTCF	chr1:9633860-9634010	GM12874	blood:	n/a	n/a
34	CTCF	chr1:9633915-9633978	GM12891	blood:	n/a	n/a
35	CTCF	chr1:9633880-9634030	HEK293	kidney:	n/a	n/a
36	CTCF	chr1:9637060-9637210	HCPEpiC	choroid plexus:	n/a	chr1:9637151-9637169 chr1:9637154-9637167
37	CTCF	chr1:9632836-9634174	A549	lung:	n/a	chr1:9633140-9633158 chr1:9633215-9633236 chr1:9633135-9633156
38	CTCF	chr1:9633893-9634062	Lung_OC	lung:	n/a	n/a
39	CTCF	chr1:9633880-9634030	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr1:9634257-9634307	GM19238	blood:	n/a	n/a
41	CTCF	chr1:9633821-9634175	IMR90	lung:	n/a	n/a
42	CTCF	chr1:9637120-9637270	HUVEC	blood vessel:	n/a	chr1:9637151-9637169 chr1:9637154-9637167
43	CTCF	chr1:9633877-9634101	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr1:9633640-9633790	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr1:9637100-9637250	HAc	cerebellar:	n/a	chr1:9637151-9637169 chr1:9637154-9637167
46	CTCF	chr1:9637120-9637270	RPTEC	kidney:	n/a	chr1:9637151-9637169 chr1:9637154-9637167
47	CTCF	chr1:9633900-9634050	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr1:9633920-9634070	GM06990	blood:	n/a	n/a
49	CTCF	chr1:9633900-9634050	HPF	lung:	n/a	n/a
50	CTCF	chr1:9637120-9637270	HBMEC	blood vessel:	n/a	chr1:9637151-9637169 chr1:9637154-9637167

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:9635799-9635849	K562	blood:	n/a
2	chr1:9635799-9635849	HMEC	breast:	n/a
3	chr1:9635799-9635849	NH-A	brain:	n/a
4	chr1:9635799-9635849	NHBE	bronchial:	n/a
5	chr1:9635799-9635849	BE2_C	brain:	n/a
6	chr1:9635799-9635849	NB4	blood:	n/a
7	chr1:9635799-9635849	HRPEpiC	eye:	n/a
8	chr1:9635799-9635849	GM06990	blood:	n/a
9	chr1:9635799-9635849	GM12891	blood:	n/a
10	chr1:9635799-9635849	AG10803	skin:	n/a
11	chr1:9635799-9635849	PANC-1	pancreas:	n/a
12	chr1:9635799-9635849	LNCaP	prostate:	n/a
13	chr1:9635799-9635849	AG09309	skin:	n/a
14	chr1:9635799-9635849	SK-N-MC	brain:	n/a
15	chr1:9635799-9635849	Jurkat	blood:	n/a
16	chr1:9635799-9635849	MCF10A-Er-Src	breast:	n/a
17	chr1:9635799-9635849	ECC-1	luminal epithelium:	n/a
18	chr1:9635799-9635849	HNPCEpiC	eye:	n/a
19	chr1:9635799-9635849	H1-hESC	embryonic stem cell:	embryo
20	chr1:9635799-9635849	PFSK-1	brain:	n/a
21	chr1:9635799-9635849	IMR90	lung:	fetal
22	chr1:9635799-9635849	HEK293	kidney:	embryo
23	chr1:9635799-9635849	HCT-116	colon:	n/a
24	chr1:9635799-9635849	GM19239	blood:	n/a
25	chr1:9635799-9635849	HPAEpiC	pulmonary alveolar:	n/a
26	chr1:9635799-9635849	HCPEpiC	choroid plexus:	n/a
27	chr1:9635799-9635849	HEEpiC	esophagus:	n/a
28	chr1:9635799-9635849	BJ	skin:	n/a
29	chr1:9635799-9635849	HCF	heart:	n/a
30	chr1:9635799-9635849	SK-N-SH	brain:	n/a
31	chr1:9635799-9635849	HAEpiC	amniotic membrane:	n/a
32	chr1:9635799-9635849	ovcar-3	ovarian:	n/a
33	chr1:9635799-9635849	HRCEpiC	kidney:	n/a
34	chr1:9635799-9635849	MCF-7	breast:	n/a
35	chr1:9635799-9635849	HepG2	liver:	n/a
36	chr1:9635799-9635849	A549	lung:	n/a
37	chr1:9635799-9635849	SK-N-SH_RA	brain:	n/a
38	chr1:9635799-9635849	HRE	kidney:	n/a
39	chr1:9635799-9635849	CMK	blood:	n/a
40	chr1:9635799-9635849	HCM	heart:	n/a
41	chr1:9635799-9635849	AG04450	lung:	fetal
42	chr1:9635799-9635849	Hela-S3	cervix:	n/a
43	chr1:9635799-9635849	RPTEC	kidney:	n/a
44	chr1:9635799-9635849	PrEC	prostate:	n/a
45	chr1:9635799-9635849	GM12892	blood:	n/a
46	chr1:9635799-9635849	ProgFib	skin:	n/a
47	chr1:9635799-9635849	AG09319	gingival:	n/a
48	chr1:9635799-9635849	T-47D	breast:	n/a
49	chr1:9635799-9635849	U87	brain:	n/a
50	chr1:9635799-9635849	Hepatocyte	liver:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:9598681..9600930-chr1:9633895..9636058,2	K562	blood:
2	chr1:9349206..9350728-chr1:9637393..9640357,2	MCF-7	breast:
3	chr1:9554983..9555919-chr1:9632720..9634161,5	MCF-7	breast:
4	chr1:9555024..9555849-chr1:9633147..9634000,2	K562	blood:
5	chr1:9637454..9639176-chr1:9647301..9649460,2	MCF-7	breast:
6	chr1:9629513..9631020-chr1:9637855..9640503,2	K562	blood:
7	chr1:9628204..9631020-chr1:9637855..9640358,2	K562	blood:
8	chr1:9554978..9555932-chr1:9632759..9633994,4	MCF-7	breast:
9	chr1:9633719..9635859-chr1:9647624..9649218,2	K562	blood:
10	chr1:9636153..9639901-chr1:9648602..9651962,4	K562	blood:
11	chr1:9553945..9555814-chr1:9634241..9636152,2	K562	blood:
12	chr1:9602754..9605108-chr1:9639045..9641242,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000231181	TF binding region
ENSG00000231181	CpG island
ENSG00000171612	chromatin interactions
ENSG00000188807	chromatin interactions

Extended variants
information (count: 190 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:190 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544592071	chr1:9633659-9633660	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs559853537	chr1:9633671-9633672	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs564662991	chr1:9633675-9633676	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs114732044	chr1:9633714-9633715	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs144271026	chr1:9633716-9633717	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs547227082	chr1:9633722-9633723	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs6540953	chr1:9633723-9633724	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs372998218	chr1:9633761-9633762	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs540257432	chr1:9633775-9633776	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs549829808	chr1:9633783-9633784	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs140830967	chr1:9633784-9633785	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs533400480	chr1:9633800-9633801	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs551796172	chr1:9633812-9633813	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs566824335	chr1:9633905-9633906	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs534042572	chr1:9633928-9633929	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs549421525	chr1:9633963-9633964	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs567783617	chr1:9633981-9633982	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs144578659	chr1:9633988-9633989	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs556470817	chr1:9633993-9633994	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs558569928	chr1:9634010-9634011	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs577910339	chr1:9634032-9634033	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs372493170	chr1:9634033-9634034	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs538296246	chr1:9634035-9634036	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs188699251	chr1:9634161-9634162	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs57215050	chr1:9634192-9634193	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs71643064	chr1:9634194-9634195	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs544251119	chr1:9634218-9634219	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs192316263	chr1:9634231-9634232	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs571968384	chr1:9634260-9634261	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs147457612	chr1:9634291-9634292	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs561010720	chr1:9634292-9634293	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs139919097	chr1:9634304-9634305	Weak transcription ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs543587990	chr1:9634420-9634421	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs115876988	chr1:9634429-9634430	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs116244440	chr1:9634453-9634454	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs547673440	chr1:9634485-9634486	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs560493994	chr1:9634544-9634545	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs527655081	chr1:9634546-9634547	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs113533006	chr1:9634575-9634576	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs78833413	chr1:9634606-9634607	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs184533980	chr1:9634690-9634691	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs374712981	chr1:9634712-9634713	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs549545672	chr1:9634724-9634725	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs142968769	chr1:9634725-9634726	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs151125013	chr1:9634822-9634823	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs12123479	chr1:9634838-9634839	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs188797048	chr1:9634880-9634881	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs72646725	chr1:9634881-9634882	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs554012229	chr1:9634909-9634910	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs529942883	chr1:9634934-9634935	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	20406844	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:9616200-9648200	Weak transcription	Esophagus	oesophagus
2	chr1:9616400-9638400	Weak transcription	Pancreas	Pancrea
3	chr1:9616800-9636600	Weak transcription	Gastric	stomach
4	chr1:9617000-9640200	Weak transcription	Placenta	Placenta
5	chr1:9618600-9648200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:9619200-9635800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:9619200-9635800	Weak transcription	Brain Cingulate Gyrus	brain
8	chr1:9619200-9635800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr1:9619200-9636000	Weak transcription	Brain Angular Gyrus	brain
10	chr1:9619200-9636000	Weak transcription	Spleen	Spleen
11	chr1:9619200-9648400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr1:9619200-9648400	Weak transcription	Aorta	Aorta
13	chr1:9619200-9648400	Weak transcription	Right Atrium	heart
14	chr1:9619400-9636000	Weak transcription	Brain Substantia Nigra	brain
15	chr1:9619600-9636000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr1:9619800-9639400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr1:9620000-9635000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr1:9620200-9648200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr1:9620200-9648400	Weak transcription	Psoas Muscle	Psoas
20	chr1:9621400-9636200	Weak transcription	Lung	lung
21	chr1:9621600-9648400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr1:9621800-9636200	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr1:9621800-9637400	Weak transcription	Colonic Mucosa	Colon
24	chr1:9622000-9635800	Weak transcription	Brain Hippocampus Middle	brain
25	chr1:9622000-9636000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr1:9622000-9636000	Weak transcription	HMEC	breast
27	chr1:9622000-9636200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr1:9622000-9638800	Weak transcription	Right Ventricle	heart
29	chr1:9622000-9639400	Weak transcription	A549	lung
30	chr1:9622000-9641000	Weak transcription	NHDF-Ad	bronchial
31	chr1:9622000-9648200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr1:9622000-9648200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr1:9622000-9648200	Weak transcription	Fetal Brain Female	brain
34	chr1:9622000-9648200	Weak transcription	Fetal Kidney	kidney
35	chr1:9622000-9648200	Weak transcription	NHLF	lung
36	chr1:9622000-9648400	Weak transcription	Fetal Lung	lung
37	chr1:9622200-9634400	Weak transcription	Stomach Mucosa	stomach
38	chr1:9622200-9636000	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr1:9622200-9636000	Weak transcription	Osteobl	bone
40	chr1:9622200-9637800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr1:9622200-9648200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr1:9622200-9648200	Weak transcription	HUVEC	blood vessel
43	chr1:9622200-9648200	Weak transcription	NH-A	brain
44	chr1:9622200-9648800	Weak transcription	Small Intestine	intestine
45	chr1:9622400-9636000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr1:9622400-9636000	Weak transcription	Left Ventricle	heart
47	chr1:9622400-9636000	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr1:9622400-9638800	Weak transcription	Colon Smooth Muscle	Colon
49	chr1:9622400-9638800	Weak transcription	Rectal Smooth Muscle	rectum
50	chr1:9623000-9645800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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