Variant report

Variant	nsv468094
Chromosome Location	chr1:214654965-214687725
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:291)
CpG islands
(count:184)
Chromatin interactive
region (count:21)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:291 , 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	ARID3A	chr1:214680221-214680889	HepG2	liver:	n/a	n/a
2	BACH1	chr1:214668142-214668148	K562	blood:	n/a	n/a
3	BCL11A	chr1:214687393-214687543	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr1:214680127-214680866	A549	lung:	n/a	chr1:214680412-214680421 chr1:214680411-214680420
5	BHLHE40	chr1:214680341-214680553	GM12878	blood:	n/a	n/a
6	BHLHE40	chr1:214683670-214683747	K562	blood:	n/a	n/a
7	CBX3	chr1:214667636-214668598	HCT-116	colon:	n/a	n/a
8	CBX3	chr1:214680279-214680973	HCT-116	colon:	n/a	n/a
9	CEBPB	chr1:214662073-214662393	A549	lung:	n/a	chr1:214662132-214662143 chr1:214662232-214662243 chr1:214662230-214662247
10	CEBPB	chr1:214679623-214679673	K562	blood:	n/a	n/a
11	CEBPB	chr1:214666764-214667109	IMR90	lung:	n/a	chr1:214666905-214666918 chr1:214666905-214666916 chr1:214666905-214666916
12	CEBPB	chr1:214662050-214662401	IMR90	lung:	n/a	chr1:214662132-214662143 chr1:214662232-214662243 chr1:214662230-214662247
13	CEBPB	chr1:214662084-214662392	HepG2	liver:	n/a	chr1:214662132-214662143 chr1:214662232-214662243 chr1:214662230-214662247
14	CHD2	chr1:214680585-214680815	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr1:214680477-214680809	GM12878	blood:	n/a	n/a
16	CHD2	chr1:214680519-214680722	HepG2	liver:	n/a	n/a
17	CTCF	chr1:214665040-214665052	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr1:214678560-214678710	RPTEC	kidney:	n/a	n/a
19	CTCF	chr1:214678540-214678690	RPTEC	kidney:	n/a	n/a
20	CTCF	chr1:214678520-214678670	HFF-Myc	foreskin:	n/a	n/a
21	CTCF	chr1:214678532-214678665	HepG2	liver:	n/a	n/a
22	CTCF	chr1:214678520-214678670	MCF-7	breast:	n/a	n/a
23	CTCF	chr1:214678500-214678650	HMF	breast:	n/a	n/a
24	CTCF	chr1:214664920-214665070	HEK293	kidney:	n/a	n/a
25	CTCF	chr1:214664920-214665170	GM06990	blood:	n/a	n/a
26	CTCF	chr1:214678540-214678690	K562	blood:	n/a	n/a
27	CTCF	chr1:214678500-214678650	HRE	kidney:	n/a	n/a
28	CTCF	chr1:214664880-214665030	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr1:214664960-214665110	GM12873	blood:	n/a	n/a
30	CTCF	chr1:214678496-214678713	MCF-7	breast:	n/a	n/a
31	CTCF	chr1:214655421-214655535	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr1:214655405-214655507	LNCaP	prostate:	n/a	n/a
33	CTCF	chr1:214664969-214665100	HepG2	liver:	n/a	n/a
34	CTCF	chr1:214678560-214678710	HCT-116	colon:	n/a	n/a
35	CTCF	chr1:214685940-214686090	A549	lung:	n/a	n/a
36	CTCF	chr1:214678540-214678690	HCT-116	colon:	n/a	n/a
37	CTCF	chr1:214678540-214678690	HRE	kidney:	n/a	n/a
38	CTCF	chr1:214678574-214678611	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr1:214664980-214665130	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr1:214673780-214673930	AG09319	gingival:	n/a	n/a
41	CTCF	chr1:214673860-214674010	AG10803	skin:	n/a	n/a
42	CTCF	chr1:214678572-214678608	K562	blood:	n/a	n/a
43	CTCF	chr1:214678480-214678630	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr1:214678520-214678670	HepG2	liver:	n/a	n/a
45	CTCF	chr1:214678520-214678670	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr1:214664920-214665070	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr1:214678540-214678687	MCF-7	breast:	n/a	n/a
48	CTCF	chr1:214665020-214665170	HepG2	liver:	n/a	n/a
49	CTCF	chr1:214678440-214678590	HAc	cerebellar:	n/a	n/a
50	CTCF	chr1:214671516-214671550	Pancreas_OC	pancreas:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:214657859-214657909	PANC-1	pancreas:	n/a
2	chr1:214657859-214657909	PANC-1	pancreas:	n/a
3	chr1:214657859-214657909	HCF	heart:	n/a
4	chr1:214657859-214657909	Caco-2	colon:	n/a
5	chr1:214668616-214668666	HMEC	breast:	n/a
6	chr1:214657859-214657909	HEEpiC	esophagus:	n/a
7	chr1:214668616-214668666	AoSMC	blood vessel:	n/a
8	chr1:214679247-214679297	U87	brain:	n/a
9	chr1:214679247-214679297	HMEC	breast:	n/a
10	chr1:214679247-214679297	HEK293	kidney:	embryo
11	chr1:214668616-214668666	ovcar-3	ovarian:	n/a
12	chr1:214668616-214668666	HUVEC	blood vessel:	n/a
13	chr1:214668616-214668666	GM12878	blood:	n/a
14	chr1:214668616-214668666	Jurkat	blood:	n/a
15	chr1:214668616-214668666	Hela-S3	cervix:	n/a
16	chr1:214657859-214657909	HPAEpiC	pulmonary alveolar:	n/a
17	chr1:214679247-214679297	LNCaP	prostate:	n/a
18	chr1:214657859-214657909	ovcar-3	ovarian:	n/a
19	chr1:214668616-214668666	GM06990	blood:	n/a
20	chr1:214668616-214668666	T-47D	breast:	n/a
21	chr1:214657859-214657909	BE2_C	brain:	n/a
22	chr1:214679247-214679297	AoSMC	blood vessel:	n/a
23	chr1:214668616-214668666	AG04450	lung:	fetal
24	chr1:214668616-214668666	AG09319	gingival:	n/a
25	chr1:214657859-214657909	HNPCEpiC	eye:	n/a
26	chr1:214679247-214679297	SK-N-SH_RA	brain:	n/a
27	chr1:214657859-214657909	GM19239	blood:	n/a
28	chr1:214679247-214679297	HIPEpiC	eye:	n/a
29	chr1:214679247-214679297	RPTEC	kidney:	n/a
30	chr1:214657859-214657909	AG04449	skin:	fetal
31	chr1:214679247-214679297	HPAEpiC	pulmonary alveolar:	n/a
32	chr1:214679247-214679297	HRE	kidney:	n/a
33	chr1:214657859-214657909	NHBE	bronchial:	n/a
34	chr1:214679247-214679297	GM12878	blood:	n/a
35	chr1:214657859-214657909	IMR90	lung:	fetal
36	chr1:214668616-214668666	H1-hESC	embryonic stem cell:	embryo
37	chr1:214679247-214679297	GM19239	blood:	n/a
38	chr1:214679247-214679297	Caco-2	colon:	n/a
39	chr1:214679247-214679297	MCF10A-Er-Src	breast:	n/a
40	chr1:214657859-214657909	SK-N-MC	brain:	n/a
41	chr1:214657859-214657909	U87	brain:	n/a
42	chr1:214679247-214679297	SK-N-MC	brain:	n/a
43	chr1:214657859-214657909	AG09319	gingival:	n/a
44	chr1:214657859-214657909	HCPEpiC	choroid plexus:	n/a
45	chr1:214679247-214679297	BJ	skin:	n/a
46	chr1:214668616-214668666	PANC-1	pancreas:	n/a
47	chr1:214679247-214679297	HUVEC	blood vessel:	n/a
48	chr1:214679247-214679297	A549	lung:	n/a
49	chr1:214657859-214657909	AG10803	skin:	n/a
50	chr1:214679247-214679297	HCPEpiC	choroid plexus:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:214679463..214680976-chr1:214683287..214685488,2	K562	blood:
2	chr1:214659692..214662430-chr1:214669544..214671221,2	K562	blood:
3	chr1:214673174..214674823-chr1:214674925..214678786,3	K562	blood:
4	chr1:214679463..214680976-chr1:214683287..214685488,2	K562	blood:
5	chr1:214648053..214650360-chr1:214683258..214686104,2	MCF-7	breast:
6	chr1:214656600..214658506-chr1:214723643..214725822,2	MCF-7	breast:
7	chr1:214659692..214662430-chr1:214669544..214671221,2	K562	blood:
8	chr1:214677154..214678655-chr1:214700789..214703552,2	MCF-7	breast:
9	chr1:214660865..214663396-chr1:214666846..214669507,2	MCF-7	breast:
10	chr1:214665493..214668241-chr1:214672288..214674423,2	K562	blood:
11	chr1:214660024..214663647-chr1:214669721..214672544,3	K562	blood:
12	chr1:214665493..214668241-chr1:214672288..214674423,2	K562	blood:
13	chr1:214677645..214681280-chr1:214723322..214726744,5	MCF-7	breast:
14	chr1:214648961..214651838-chr1:214664599..214667382,2	K562	blood:
15	chr1:214660865..214663396-chr1:214666846..214669507,2	MCF-7	breast:
16	chr1:214683964..214686596-chr1:214687813..214690608,3	MCF-7	breast:
17	chr1:214647353..214649494-chr1:214677849..214679754,2	MCF-7	breast:
18	chr1:214678638..214681169-chr1:214682598..214685287,2	MCF-7	breast:
19	chr1:214673174..214674823-chr1:214674925..214678786,3	K562	blood:
20	chr1:214660024..214663647-chr1:214669721..214672544,3	K562	blood:
21	chr1:214678638..214681169-chr1:214682598..214685287,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USH2A-4	chr1:214656156-214656730	NONHSAT009464
2	lnc-USH2A-4	chr1:214655882-214656819	NONHSAT009463

No data

Variant related genes	Relation type
ENSG00000213036	TF binding region
ENSG00000213036	CpG island
ENSG00000152104	chromatin interactions

Extended variants
information (count: 1426 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1426 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7537274	chr1:214654965-214654966	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181173856	chr1:214654980-214654981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576884700	chr1:214655049-214655050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115265386	chr1:214655056-214655057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs61819640	chr1:214655057-214655058	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs148762463	chr1:214655066-214655067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs61819641	chr1:214655071-214655072	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs531513307	chr1:214655095-214655096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572449581	chr1:214655146-214655147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541453061	chr1:214655199-214655200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs61819642	chr1:214655238-214655239	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs533472022	chr1:214655244-214655245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543600706	chr1:214655286-214655287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7539848	chr1:214655298-214655299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564786051	chr1:214655315-214655316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs117740158	chr1:214655369-214655370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527386237	chr1:214655411-214655412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188713274	chr1:214655422-214655423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs116701914	chr1:214655430-214655431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139651810	chr1:214655447-214655448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs180829824	chr1:214655548-214655549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs61017156	chr1:214655562-214655563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144199090	chr1:214655587-214655588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539514342	chr1:214655632-214655633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556025121	chr1:214655676-214655677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs56089935	chr1:214655681-214655682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144688026	chr1:214655689-214655690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111411721	chr1:214655701-214655702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs55760423	chr1:214655743-214655744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs79295541	chr1:214655758-214655759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185185513	chr1:214655800-214655801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139694394	chr1:214655814-214655815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529665899	chr1:214655815-214655816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs111690740	chr1:214655823-214655824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111806866	chr1:214655833-214655834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs17790652	chr1:214655840-214655841	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs572381167	chr1:214655884-214655885	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs12096551	chr1:214655890-214655891	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs111335858	chr1:214655895-214655896	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs191922109	chr1:214655908-214655909	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs201517619	chr1:214655922-214655923	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs554641505	chr1:214655923-214655924	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs59662579	chr1:214655933-214655934	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs201085884	chr1:214655934-214655935	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs186643566	chr1:214655940-214655941	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs563661143	chr1:214655941-214655942	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs112095945	chr1:214655943-214655944	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs112370571	chr1:214655979-214655980	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs112854551	chr1:214655986-214655987	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs542831561	chr1:214655990-214655991	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Liposarcoma	21253554	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	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
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Breast cancer	22522925	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD

Chromatin state (count:975 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:214641400-214667800	Weak transcription	Hela-S3	cervix
2	chr1:214645200-214656600	Weak transcription	Fetal Intestine Large	intestine
3	chr1:214645800-214666000	Weak transcription	Fetal Muscle Trunk	muscle
4	chr1:214646000-214672200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr1:214647200-214661600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr1:214648000-214669400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr1:214649200-214660800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr1:214650200-214657400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr1:214650200-214658000	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr1:214650200-214666000	Weak transcription	Fetal Muscle Leg	muscle
11	chr1:214650600-214657400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr1:214650800-214656400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr1:214650800-214657400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr1:214650800-214660000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:214650800-214662600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:214651000-214655000	Weak transcription	Stomach Mucosa	stomach
17	chr1:214651000-214656200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr1:214651000-214656200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr1:214651000-214656400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr1:214651000-214656800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr1:214651000-214666400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr1:214651200-214656200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr1:214651200-214657400	Weak transcription	Psoas Muscle	Psoas
24	chr1:214651200-214659400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr1:214651200-214664600	Weak transcription	Left Ventricle	heart
26	chr1:214651200-214665600	Weak transcription	NHLF	lung
27	chr1:214651200-214666000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr1:214651200-214666400	Weak transcription	Adipose Nuclei	Adipose
29	chr1:214651400-214655600	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr1:214651600-214656200	Weak transcription	Colon Smooth Muscle	Colon
31	chr1:214651600-214661400	Weak transcription	Fetal Heart	heart
32	chr1:214651800-214655600	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr1:214651800-214655800	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr1:214651800-214655800	Weak transcription	A549	lung
35	chr1:214651800-214656600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr1:214651800-214658000	Weak transcription	NH-A	brain
37	chr1:214651800-214663000	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr1:214651800-214665400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:214651800-214668000	Weak transcription	HSMMtube	muscle
40	chr1:214652000-214665800	Weak transcription	NHDF-Ad	bronchial
41	chr1:214652000-214666000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr1:214652200-214658000	Weak transcription	HSMM	muscle
43	chr1:214652200-214664800	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr1:214652400-214655400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr1:214652600-214656000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr1:214652600-214656200	Weak transcription	HMEC	breast
47	chr1:214652600-214657400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:214652600-214662000	Weak transcription	HUVEC	blood vessel
49	chr1:214654200-214656200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:214654200-214656400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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