Variant report

Variant	nsv871193
Chromosome Location	chr1:80970978-81056946
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:170)
CpG islands
(count:62)
Chromatin interactive
region (count:1)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:170 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:81022589-81022754	K562	blood:	n/a	n/a
2	BACH1	chr1:80998868-80999129	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr1:80975728-80975960	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr1:80996803-80997369	HCT-116	colon:	n/a	n/a
5	CBX3	chr1:81000531-81001133	HCT-116	colon:	n/a	n/a
6	CEBPB	chr1:81000182-81001093	HCT-116	colon:	n/a	n/a
7	CEBPB	chr1:81006302-81006643	HepG2	liver:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
8	CEBPB	chr1:80989668-80989956	A549	lung:	n/a	n/a
9	CEBPB	chr1:81006300-81006629	A549	lung:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
10	CEBPB	chr1:81006278-81006649	IMR90	lung:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
11	CEBPB	chr1:81004063-81004214	A549	lung:	n/a	chr1:81004073-81004086 chr1:81004075-81004086 chr1:81004073-81004086 chr1:81004073-81004086
12	CEBPB	chr1:80991202-80991443	HepG2	liver:	n/a	chr1:80991301-80991314 chr1:80991302-80991313
13	CEBPB	chr1:80991969-80992035	HepG2	liver:	n/a	chr1:80992011-80992022 chr1:80992011-80992024
14	CEBPB	chr1:80989649-80990016	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr1:81006283-81006695	Hela-S3	cervix:	n/a	chr1:81006455-81006466 chr1:81006455-81006468
16	CEBPB	chr1:81009753-81009933	HepG2	liver:	n/a	chr1:81009799-81009812 chr1:81009799-81009810
17	CEBPB	chr1:80991142-80991478	IMR90	lung:	n/a	chr1:80991301-80991314 chr1:80991302-80991313
18	CEBPB	chr1:81000600-81001165	HCT-116	colon:	n/a	n/a
19	CHD1	chr1:80998537-80998660	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr1:80975773-80976006	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr1:80998820-80998970	HRE	kidney:	n/a	chr1:80998881-80998888
22	CTCF	chr1:81000698-81000888	GM12878	blood:	n/a	n/a
23	CTCF	chr1:81049281-81049353	Fibrobl	skin:	n/a	n/a
24	CTCF	chr1:81020220-81020370	AG09319	gingival:	n/a	n/a
25	CTCF	chr1:81000760-81000910	HEK293	kidney:	n/a	n/a
26	CTCF	chr1:81000680-81000830	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr1:81000724-81000893	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr1:81000746-81000849	Gliobla	brain:	n/a	n/a
29	CTCF	chr1:81001636-81001652	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr1:80998880-80999030	RPTEC	kidney:	n/a	chr1:80998881-80998888
31	CTCF	chr1:81000765-81000851	MCF-7	breast:	n/a	n/a
32	CTCF	chr1:81000720-81000870	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr1:81000789-81000814	MCF-7	breast:	n/a	n/a
34	E2F4	chr1:81021556-81021890	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr1:81051688-81051984	MCF10A-Er-Src	breast:	n/a	n/a
36	EBF1	chr1:81025827-81026001	GM12878	blood:	n/a	chr1:81025887-81025898 chr1:81025867-81025878
37	EP300	chr1:80975532-80975535	K562	blood:	n/a	n/a
38	EP300	chr1:80996904-80997290	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr1:80975614-80976036	H1-hESC	embryonic stem cell:	n/a	n/a
40	EP300	chr1:80996848-80997428	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr1:81004195-81004219	GM12878	blood:	n/a	n/a
42	FAM48A	chr1:81015128-81015211	GM12878	blood:	n/a	n/a
43	FAM48A	chr1:81024665-81024835	GM12878	blood:	n/a	n/a
44	FOS	chr1:81006323-81006657	MCF10A-Er-Src	breast:	n/a	chr1:81006491-81006501 chr1:81006492-81006500
45	FOS	chr1:81007986-81008262	MCF10A-Er-Src	breast:	n/a	chr1:81008039-81008048 chr1:81008131-81008140
46	FOS	chr1:81006306-81006702	MCF10A-Er-Src	breast:	n/a	chr1:81006491-81006501 chr1:81006492-81006500
47	FOS	chr1:81000650-81001004	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr1:80998934-80999189	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr1:80998908-80999081	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr1:81000687-81001000	MCF10A-Er-Src	breast:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:81001617-81001667	AG09309	skin:	n/a
2	chr1:81001617-81001667	AG09309	skin:	n/a
3	chr1:81001617-81001667	HIPEpiC	eye:	n/a
4	chr1:81001617-81001667	ovcar-3	ovarian:	n/a
5	chr1:81001617-81001667	A549	lung:	n/a
6	chr1:81001617-81001667	HCT-116	colon:	n/a
7	chr1:81001617-81001667	RPTEC	kidney:	n/a
8	chr1:81001617-81001667	HAEpiC	amniotic membrane:	n/a
9	chr1:81001617-81001667	HRPEpiC	eye:	n/a
10	chr1:81001617-81001667	NHBE	bronchial:	n/a
11	chr1:81001617-81001667	HRCEpiC	kidney:	n/a
12	chr1:81001617-81001667	AG04450	lung:	fetal
13	chr1:81001617-81001667	SK-N-SH_RA	brain:	n/a
14	chr1:81001617-81001667	H1-hESC	embryonic stem cell:	embryo
15	chr1:81001617-81001667	AoSMC	blood vessel:	n/a
16	chr1:81001617-81001667	PFSK-1	brain:	n/a
17	chr1:81001617-81001667	ProgFib	skin:	n/a
18	chr1:81001617-81001667	AG09319	gingival:	n/a
19	chr1:81001617-81001667	HL-60	blood:	n/a
20	chr1:81001617-81001667	HEK293	kidney:	embryo
21	chr1:81001617-81001667	SAEC	small airway:	n/a
22	chr1:81001617-81001667	LNCaP	prostate:	n/a
23	chr1:81001617-81001667	Hepatocyte	liver:	n/a
24	chr1:81001617-81001667	SK-N-SH	brain:	n/a
25	chr1:81001617-81001667	PANC-1	pancreas:	n/a
26	chr1:81001617-81001667	GM19239	blood:	n/a
27	chr1:81001617-81001667	CMK	blood:	n/a
28	chr1:81001617-81001667	HCM	heart:	n/a
29	chr1:81001617-81001667	MCF-7	breast:	n/a
30	chr1:81001617-81001667	HMEC	breast:	n/a
31	chr1:81001617-81001667	HCF	heart:	n/a
32	chr1:81001617-81001667	U87	brain:	n/a
33	chr1:81001617-81001667	HEEpiC	esophagus:	n/a
34	chr1:81001617-81001667	Jurkat	blood:	n/a
35	chr1:81001617-81001667	BJ	skin:	n/a
36	chr1:81001617-81001667	BE2_C	brain:	n/a
37	chr1:81001617-81001667	GM12892	blood:	n/a
38	chr1:81001617-81001667	NH-A	brain:	n/a
39	chr1:81001617-81001667	AG04449	skin:	fetal
40	chr1:81001617-81001667	GM06990	blood:	n/a
41	chr1:81001617-81001667	HepG2	liver:	n/a
42	chr1:81001617-81001667	IMR90	lung:	fetal
43	chr1:81001617-81001667	SKMC	muscle:	n/a
44	chr1:81001617-81001667	NHDF-neo	bronchial:	n/a
45	chr1:81001617-81001667	AG10803	skin:	n/a
46	chr1:81001617-81001667	SK-N-MC	brain:	n/a
47	chr1:81001617-81001667	MCF10A-Er-Src	breast:	n/a
48	chr1:81001617-81001667	GM12891	blood:	n/a
49	chr1:81001617-81001667	Hela-S3	cervix:	n/a
50	chr1:81001617-81001667	PrEC	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:81001450..81003092-chr6:32940222..32942950,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LPHN2-1	chr1:81001440-81001627	XLOC_000268
2	lnc-LPHN2-1	chr1:81001445-81001627	XLOC_000268
3	lnc-LPHN2-1	chr1:81001440-81001627	XLOC_000268
4	lnc-LPHN2-1	chr1:81001424-81001627	NONHSAT004117
5	lnc-ELTD1-8	chr1:81000663-81000937	XLOC_000883
6	lnc-ELTD1-8	chr1:81049975-81050048	XLOC_000883
7	lnc-LPHN2-1	chr1:81006273-81006321	NONHSAT004118
8	lnc-LPHN2-1	chr1:81006274-81006321	XLOC_000268
9	lnc-LPHN2-1	chr1:81001439-81001627	NONHSAT004118

No data

Variant related genes	Relation type
ENSG00000234184	TF binding region
ENSG00000224326	TF binding region
ENSG00000234184	CpG island
ENSG00000224326	CpG island
ENSG00000204256	chromatin interactions
ENSG00000263756	chromatin interactions
NUFIP2	miRNA target sites

Extended variants
information (count: 1385 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1385 , 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	rs184812	chr1:80970978-80970979	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149198100	chr1:80970988-80970989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544905154	chr1:80971234-80971235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565175449	chr1:80971244-80971245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575495681	chr1:80971247-80971248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544497185	chr1:80971321-80971322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560906580	chr1:80971358-80971359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113903771	chr1:80971366-80971367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs207460259	chr1:80971416-80971417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11800144	chr1:80971443-80971444	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs79932016	chr1:80971447-80971448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570871588	chr1:80971491-80971492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113031063	chr1:80971499-80971500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552538553	chr1:80971525-80971526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569533334	chr1:80971527-80971528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76230680	chr1:80971549-80971550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs11803485	chr1:80971580-80971581	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs61774396	chr1:80971638-80971639	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs536276436	chr1:80971731-80971732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs553083420	chr1:80971736-80971737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566607089	chr1:80971749-80971750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs200951181	chr1:80971755-80971756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538822812	chr1:80971784-80971785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191146822	chr1:80971786-80971787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575405692	chr1:80971810-80971811	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544144831	chr1:80971821-80971822	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554464223	chr1:80971836-80971837	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574470113	chr1:80971894-80971895	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376741611	chr1:80971903-80971904	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115961056	chr1:80971921-80971922	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183579489	chr1:80971933-80971934	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536425143	chr1:80971935-80971936	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546283235	chr1:80971952-80971953	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111605431	chr1:80971998-80971999	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531951853	chr1:80972048-80972049	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs556740732	chr1:80972061-80972062	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs548874712	chr1:80972087-80972088	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs568801080	chr1:80972095-80972096	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs138322318	chr1:80972186-80972187	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs142334110	chr1:80972198-80972199	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs189709824	chr1:80972212-80972213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146579536	chr1:80972229-80972230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181344551	chr1:80972239-80972240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186949656	chr1:80972244-80972245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576374237	chr1:80972257-80972258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568930536	chr1:80972272-80972273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs117954228	chr1:80972273-80972274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377616793	chr1:80972290-80972291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554427216	chr1:80972304-80972305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76101638	chr1:80972305-80972306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	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
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	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
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	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
Breast cancer	17603634	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
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	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
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:158 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:80970800-80971000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:80971200-80972000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:80971600-80971800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr1:80971600-80972600	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr1:80971800-80972200	Enhancers	H1 Cell Line	embryonic stem cell
6	chr1:80971800-80972200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr1:80971800-80972200	Active TSS	iPS-20b Cell Line	embryonic stem cell
8	chr1:80971800-80972400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr1:80971800-80972400	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr1:80971800-80972600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr1:80972000-80972200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:80972000-80972200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr1:80972000-80972400	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr1:80972200-80972600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr1:80972200-80975600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr1:80972400-80975400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr1:80972400-80975600	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr1:80975400-80975800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr1:80975400-80975800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:80975400-80975800	Enhancers	HSMMtube	muscle
21	chr1:80975400-80976000	Enhancers	H9 Cell Line	embryonic stem cell
22	chr1:80975600-80975800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr1:80975600-80975800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr1:80975600-80975800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr1:80975600-80976200	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr1:80975600-80976200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr1:80987400-80988000	Enhancers	Adipose Nuclei	Adipose
28	chr1:80989800-80990000	Enhancers	Adipose Nuclei	Adipose
29	chr1:80989800-80990400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr1:80996400-80997600	Enhancers	Primary T cells from cord blood	blood
31	chr1:80996800-80997200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr1:80996800-80997200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:80997000-80997200	Enhancers	H9 Cell Line	embryonic stem cell
34	chr1:80997000-80997200	Enhancers	Fetal Kidney	kidney
35	chr1:80997000-80997400	Enhancers	Dnd41	blood
36	chr1:80997000-80999400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr1:80997200-80997400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr1:80997200-80997400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:80997200-80998000	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr1:80997200-80998600	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr1:80997200-80998600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr1:80997200-80998600	Weak transcription	Fetal Kidney	kidney
43	chr1:80997400-81000600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:80997600-80997800	Enhancers	Ovary	ovary
45	chr1:80997600-80998000	Bivalent Enhancer	Primary T cells from cord blood	blood
46	chr1:80998000-80998200	Enhancers	Colon Smooth Muscle	Colon
47	chr1:80998000-80998400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr1:80998000-81001800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr1:80998200-80998800	Weak transcription	Colon Smooth Muscle	Colon
50	chr1:80998400-80999200	Enhancers	HUES64 Cell Line	embryonic stem cell

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