Variant report

Variant	nsv945838
Chromosome Location	chr1:26213812-26218468
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:250)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:250 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr1:26217000-26217392	Hela-S3	cervix:	n/a	n/a
2	CBX3	chr1:26216968-26217591	HCT-116	colon:	n/a	n/a
3	CBX3	chr1:26217003-26217577	HCT-116	colon:	n/a	n/a
4	CEBPB	chr1:26214203-26214307	A549	lung:	n/a	n/a
5	CEBPB	chr1:26217021-26217409	Hela-S3	cervix:	n/a	n/a
6	CHD2	chr1:26217051-26217384	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr1:26216060-26216210	WI-38	lung:	n/a	n/a
8	CTCF	chr1:26216056-26216264	MCF-7	breast:	n/a	n/a
9	CTCF	chr1:26216140-26216290	AG09319	gingival:	n/a	n/a
10	CTCF	chr1:26217120-26217270	HEEpiC	esophagus:	n/a	n/a
11	CTCF	chr1:26216140-26216290	HRPEpiC	eye:	n/a	n/a
12	CTCF	chr1:26216040-26216190	HA-sp	spinal cord:	n/a	n/a
13	CTCF	chr1:26216079-26216228	MCF-7	breast:	n/a	n/a
14	CTCF	chr1:26216080-26216230	AG04449	skin:	n/a	n/a
15	CTCF	chr1:26217060-26217210	HMEC	breast:	n/a	n/a
16	CTCF	chr1:26217100-26217250	NHEK	skin:	n/a	n/a
17	CTCF	chr1:26216080-26216230	HCT-116	colon:	n/a	n/a
18	CTCF	chr1:26216080-26216230	RPTEC	kidney:	n/a	n/a
19	CTCF	chr1:26216040-26216190	SAEC	small airway:	n/a	n/a
20	CTCF	chr1:26216040-26216190	HMEC	breast:	n/a	n/a
21	CTCF	chr1:26216080-26216230	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr1:26216380-26216530	HFF-Myc	foreskin:	n/a	n/a
23	CTCF	chr1:26216100-26216250	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr1:26216122-26216204	HepG2	liver:	n/a	n/a
25	CTCF	chr1:26216120-26216270	SAEC	small airway:	n/a	n/a
26	CTCF	chr1:26216360-26216510	K562	blood:	n/a	n/a
27	CTCF	chr1:26216020-26216170	HCM	heart:	n/a	n/a
28	CTCF	chr1:26216080-26216230	HPF	lung:	n/a	n/a
29	CTCF	chr1:26216100-26216250	MCF-7	breast:	n/a	n/a
30	CTCF	chr1:26216100-26216250	HRE	kidney:	n/a	n/a
31	CTCF	chr1:26216160-26216165	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr1:26216100-26216250	NHEK	skin:	n/a	n/a
33	CTCF	chr1:26216100-26216250	HCT-116	colon:	n/a	n/a
34	CTCF	chr1:26216120-26216270	AG04450	lung:	n/a	n/a
35	CTCF	chr1:26216065-26216259	K562	blood:	n/a	n/a
36	CTCF	chr1:26216060-26216210	HMF	breast:	n/a	n/a
37	CTCF	chr1:26216040-26216190	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr1:26216040-26216190	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr1:26216070-26216191	MCF-7	breast:	n/a	n/a
40	CTCF	chr1:26216100-26216250	K562	blood:	n/a	n/a
41	CTCF	chr1:26216220-26216370	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr1:26216074-26216241	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr1:26216120-26216270	HRE	kidney:	n/a	n/a
44	CTCF	chr1:26216060-26216210	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr1:26215916-26216373	K562	blood:	n/a	n/a
46	CTCF	chr1:26216100-26216250	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr1:26216080-26216230	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr1:26216020-26216170	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr1:26216060-26216210	HVMF	connective:	n/a	n/a
50	CTCF	chr1:26216066-26216255	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:26217268-26217318	LNCaP	prostate:	n/a
2	chr1:26217268-26217318	HL-60	blood:	n/a
3	chr1:26217268-26217318	NHDF-neo	bronchial:	n/a
4	chr1:26217268-26217318	AG09309	skin:	n/a
5	chr1:26217268-26217318	T-47D	breast:	n/a
6	chr1:26217268-26217318	HRCEpiC	kidney:	n/a
7	chr1:26217268-26217318	PrEC	prostate:	n/a
8	chr1:26217268-26217318	AoSMC	blood vessel:	n/a
9	chr1:26217268-26217318	SKMC	muscle:	n/a
10	chr1:26217268-26217318	AG09319	gingival:	n/a
11	chr1:26217268-26217318	A549	lung:	n/a
12	chr1:26217268-26217318	H1-hESC	embryonic stem cell:	embryo
13	chr1:26217268-26217318	Hela-S3	cervix:	n/a
14	chr1:26217268-26217318	Hepatocyte	liver:	n/a
15	chr1:26217268-26217318	HCM	heart:	n/a
16	chr1:26217268-26217318	SK-N-MC	brain:	n/a
17	chr1:26217268-26217318	K562	blood:	n/a
18	chr1:26217268-26217318	HAEpiC	amniotic membrane:	n/a
19	chr1:26217268-26217318	GM12892	blood:	n/a
20	chr1:26217268-26217318	BE2_C	brain:	n/a
21	chr1:26217268-26217318	PFSK-1	brain:	n/a
22	chr1:26217268-26217318	ovcar-3	ovarian:	n/a
23	chr1:26217268-26217318	MCF10A-Er-Src	breast:	n/a
24	chr1:26217268-26217318	AG04449	skin:	fetal
25	chr1:26217268-26217318	HCT-116	colon:	n/a
26	chr1:26217268-26217318	IMR90	lung:	fetal
27	chr1:26217268-26217318	NHBE	bronchial:	n/a
28	chr1:26217268-26217318	PANC-1	pancreas:	n/a
29	chr1:26217268-26217318	HCF	heart:	n/a
30	chr1:26217268-26217318	GM12878	blood:	n/a
31	chr1:26217268-26217318	ECC-1	luminal epithelium:	n/a
32	chr1:26217268-26217318	HUVEC	blood vessel:	n/a
33	chr1:26217268-26217318	HRE	kidney:	n/a
34	chr1:26217268-26217318	U87	brain:	n/a
35	chr1:26217268-26217318	NH-A	brain:	n/a
36	chr1:26217268-26217318	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:26217268-26217318	HEK293	kidney:	embryo
38	chr1:26217268-26217318	SAEC	small airway:	n/a
39	chr1:26217268-26217318	HepG2	liver:	n/a
40	chr1:26217268-26217318	GM12891	blood:	n/a
41	chr1:26217268-26217318	HCPEpiC	choroid plexus:	n/a
42	chr1:26217268-26217318	CMK	blood:	n/a
43	chr1:26217268-26217318	HNPCEpiC	eye:	n/a
44	chr1:26217268-26217318	BJ	skin:	n/a
45	chr1:26217268-26217318	GM19239	blood:	n/a
46	chr1:26217268-26217318	MCF-7	breast:	n/a
47	chr1:26217268-26217318	AG10803	skin:	n/a
48	chr1:26217268-26217318	RPTEC	kidney:	n/a
49	chr1:26217268-26217318	HRPEpiC	eye:	n/a
50	chr1:26217268-26217318	GM06990	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:26217587..26219092-chr1:26220601..26223352,2	MCF-7	breast:
2	chr1:26163508..26164526-chr1:26215722..26216468,3	MCF-7	breast:
3	chr1:26144584..26148504-chr1:26213993..26219242,5	MCF-7	breast:
4	chr1:26202371..26204003-chr1:26213732..26216671,3	K562	blood:
5	chr1:26218143..26237631-chr1:26312847..26343326,142	K562	blood:
6	chr1:26201074..26204512-chr1:26213787..26217646,3	MCF-7	breast:
7	chr1:26215724..26217394-chr1:26322376..26325233,3	K562	blood:
8	chr1:26153734..26156719-chr1:26216356..26218396,2	K562	blood:
9	chr1:26184421..26187513-chr1:26216151..26218029,3	MCF-7	breast:
10	chr1:26186031..26187953-chr1:26217090..26219316,2	MCF-7	breast:
11	chr1:26212750..26219919-chr1:26322810..26327399,10	K562	blood:
12	chr1:26203993..26207196-chr1:26215838..26218866,3	MCF-7	breast:
13	chr1:26138071..26140044-chr1:26215489..26217914,2	K562	blood:
14	chr1:26215670..26217483-chr1:26231406..26232966,2	MCF-7	breast:
15	chr1:26184665..26187275-chr1:26210707..26214954,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM54B-2	chr1:26213851-26214101	NONHSAT001760

No data

Variant related genes	Relation type
ENSG00000223624	TF binding region
SNRPFP2	TF binding region
ENSG00000223624	CpG island
SNRPFP2	CpG island
ENSG00000158006	chromatin interactions
ENSG00000223474	chromatin interactions
ENSG00000162430	chromatin interactions
ENSG00000127423	chromatin interactions
ENSG00000252190	chromatin interactions
ENSG00000228172	chromatin interactions
ENSG00000207302	chromatin interactions
ENSG00000264021	chromatin interactions
ENSG00000117640	chromatin interactions
ENSG00000117632	chromatin interactions
ENSG00000252691	chromatin interactions
ENSG00000236528	chromatin interactions

Extended variants
information (count: 159 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:159 , 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	rs529609770	chr1:26213817-26213818	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs528687530	chr1:26213871-26213872	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
3	rs561757148	chr1:26213878-26213879	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
4	rs72881367	chr1:26213880-26213881	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs186480747	chr1:26213903-26213904	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
6	rs570567081	chr1:26213926-26213927	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
7	rs533019497	chr1:26213930-26213931	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
8	rs115789164	chr1:26213940-26213941	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
9	rs159525	chr1:26213991-26213992	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs146165820	chr1:26214010-26214011	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
11	rs139034814	chr1:26214015-26214016	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
12	rs34918616	chr1:26214095-26214096	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
13	rs565778779	chr1:26214121-26214122	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs77765189	chr1:26214139-26214140	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	mRNA abundance
15	rs190439345	chr1:26214167-26214168	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs577729216	chr1:26214171-26214172	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs201696246	chr1:26214174-26214175	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs367886306	chr1:26214194-26214195	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs537119563	chr1:26214218-26214219	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs557560121	chr1:26214230-26214231	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs181680018	chr1:26214287-26214288	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs186250741	chr1:26214305-26214306	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs559791587	chr1:26214323-26214324	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs375973094	chr1:26214397-26214398	Weak transcription Strong transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs190715804	chr1:26214455-26214456	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs564037580	chr1:26214472-26214473	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs533081424	chr1:26214481-26214482	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs532033656	chr1:26214545-26214546	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs532948641	chr1:26214558-26214559	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs549592199	chr1:26214601-26214602	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs159524	chr1:26214603-26214604	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs549475590	chr1:26214713-26214714	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs78728552	chr1:26214831-26214832	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs371983123	chr1:26214843-26214844	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs61179488	chr1:26214868-26214869	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs565645281	chr1:26214877-26214878	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs369589870	chr1:26214893-26214894	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs534569086	chr1:26214927-26214928	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs551381153	chr1:26214948-26214949	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs571282307	chr1:26214968-26214969	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs372021377	chr1:26214988-26214989	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs569633640	chr1:26215035-26215036	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs529175291	chr1:26215085-26215086	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs114378653	chr1:26215092-26215093	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs548859713	chr1:26215096-26215097	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs76974781	chr1:26215112-26215113	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs76717683	chr1:26215113-26215114	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs536448802	chr1:26215150-26215151	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs183930800	chr1:26215164-26215165	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs187747639	chr1:26215226-26215227	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:119)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Ovarian neoplasms	16753589	CNVD
Melanoma	17363583	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Biliary cancer	19435499	CNVD
Breast cancer	16397240	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
Schizophrenia	22118685	CNVD
Myelofibrosis	22110671	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung cancer	18438408	CNVD
Obesity	17160897	CNVD
Endometrial cancer	19261849	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21364760	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:249 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:26201800-26219000	Weak transcription	Fetal Heart	heart
2	chr1:26202400-26216200	Weak transcription	Lung	lung
3	chr1:26202800-26214600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr1:26202800-26214600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr1:26202800-26214600	Weak transcription	HSMM	muscle
6	chr1:26202800-26215000	Weak transcription	HSMMtube	muscle
7	chr1:26202800-26216200	Weak transcription	NH-A	brain
8	chr1:26202800-26216400	Weak transcription	Osteobl	bone
9	chr1:26202800-26220400	Weak transcription	Primary hematopoietic stem cells	blood
10	chr1:26203000-26216200	Weak transcription	NHLF	lung
11	chr1:26203000-26219200	Weak transcription	Right Atrium	heart
12	chr1:26203000-26222200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:26203200-26215000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr1:26203400-26214400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr1:26203400-26217200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr1:26203600-26216000	Weak transcription	Fetal Kidney	kidney
17	chr1:26203600-26216200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr1:26203600-26216400	Weak transcription	Fetal Lung	lung
19	chr1:26204200-26219000	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr1:26206600-26216200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr1:26206600-26216200	Weak transcription	Brain Substantia Nigra	brain
22	chr1:26206800-26219000	Strong transcription	Fetal Brain Female	brain
23	chr1:26207000-26215800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr1:26207200-26215000	Weak transcription	Brain Angular Gyrus	brain
25	chr1:26207200-26219000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr1:26207400-26215000	Weak transcription	K562	blood
27	chr1:26207800-26215800	Weak transcription	Pancreas	Pancrea
28	chr1:26208000-26214000	Strong transcription	Fetal Stomach	stomach
29	chr1:26208200-26214800	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr1:26208200-26224600	Weak transcription	Spleen	Spleen
31	chr1:26208400-26214600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr1:26208800-26215400	Weak transcription	Ovary	ovary
33	chr1:26209400-26216000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr1:26210000-26222000	Strong transcription	Brain Germinal Matrix	brain
35	chr1:26211000-26214200	Enhancers	Fetal Intestine Large	intestine
36	chr1:26211200-26214400	Weak transcription	Fetal Thymus	thymus
37	chr1:26211200-26221800	Strong transcription	Thymus	Thymus
38	chr1:26211400-26216200	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr1:26211400-26216200	Strong transcription	Fetal Muscle Trunk	muscle
40	chr1:26211400-26218600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr1:26212000-26219200	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr1:26212000-26222200	Weak transcription	Brain Anterior Caudate	brain
43	chr1:26212200-26215400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr1:26212200-26215400	Weak transcription	Brain Hippocampus Middle	brain
45	chr1:26212200-26215800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr1:26212200-26215800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr1:26212200-26216800	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr1:26212400-26214600	Weak transcription	Dnd41	blood
49	chr1:26212400-26214800	Weak transcription	Fetal Muscle Leg	muscle
50	chr1:26212400-26215800	Enhancers	Fetal Intestine Small	intestine

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