Variant report

Variant	nsv870734
Chromosome Location	chr1:71469583-71485036
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:67)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:67 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:71472265-71472284	K562	blood:	n/a	n/a
2	ARID3A	chr1:71481128-71481217	K562	blood:	n/a	n/a
3	BHLHE40	chr1:71480894-71480941	K562	blood:	n/a	n/a
4	CCNT2	chr1:71474825-71475012	K562	blood:	n/a	n/a
5	CEBPB	chr1:71477204-71477504	K562	blood:	n/a	chr1:71477360-71477371
6	CEBPB	chr1:71470760-71470839	HepG2	liver:	n/a	chr1:71470810-71470821
7	CEBPB	chr1:71483442-71483555	IMR90	lung:	n/a	n/a
8	CEBPB	chr1:71477312-71477504	HepG2	liver:	n/a	chr1:71477360-71477371
9	CEBPB	chr1:71474287-71474494	K562	blood:	n/a	n/a
10	CEBPB	chr1:71469996-71470196	K562	blood:	n/a	chr1:71470127-71470140 chr1:71470129-71470140
11	CTCF	chr1:71478740-71478890	GM12866	blood:	n/a	n/a
12	CUX1	chr1:71481194-71481342	K562	blood:	n/a	n/a
13	EP300	chr1:71484234-71487033	SK-N-SH	brain:	n/a	chr1:71486260-71486269 chr1:71484313-71484327 chr1:71484888-71484895 chr1:71485709-71485723
14	EP300	chr1:71470322-71470837	ECC-1	luminal epithelium:	n/a	chr1:71470375-71470384
15	EP300	chr1:71484967-71485666	SK-N-SH_RA	brain:	n/a	n/a
16	EP300	chr1:71484933-71485359	SK-N-SH_RA	brain:	n/a	n/a
17	FOS	chr1:71483560-71483868	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr1:71481218-71481788	MCF10A-Er-Src	breast:	n/a	chr1:71481328-71481339
19	FOS	chr1:71481183-71481603	HUVEC	blood vessel:	n/a	chr1:71481328-71481339
20	FOS	chr1:71483558-71483802	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr1:71483562-71483805	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr1:71481207-71481680	MCF10A-Er-Src	breast:	n/a	chr1:71481328-71481339
23	FOS	chr1:71481167-71481790	MCF10A-Er-Src	breast:	n/a	chr1:71481328-71481339
24	FOS	chr1:71483560-71483887	MCF10A-Er-Src	breast:	n/a	n/a
25	FOXP2	chr1:71479770-71480138	SK-N-MC	brain:	n/a	n/a
26	GATA2	chr1:71484602-71485670	SH-SY5Y	brain:	n/a	chr1:71485136-71485145 chr1:71485611-71485620 chr1:71485610-71485620 chr1:71485503-71485513
27	GATA3	chr1:71473605-71473835	SH-SY5Y	brain:	n/a	n/a
28	GATA3	chr1:71479609-71480122	SK-N-SH	brain:	n/a	n/a
29	GATA3	chr1:71484920-71485481	SK-N-SH	brain:	n/a	chr1:71485136-71485145
30	GATA3	chr1:71484963-71486094	SH-SY5Y	brain:	n/a	chr1:71485136-71485145 chr1:71485611-71485620 chr1:71485610-71485620 chr1:71485503-71485513
31	GATA3	chr1:71479599-71480290	SK-N-SH	brain:	n/a	n/a
32	GATA3	chr1:71484932-71485641	SK-N-SH	brain:	n/a	chr1:71485136-71485145 chr1:71485611-71485620 chr1:71485610-71485620 chr1:71485503-71485513
33	JUN	chr1:71478258-71478560	K562	blood:	n/a	n/a
34	JUN	chr1:71481286-71481449	K562	blood:	n/a	n/a
35	JUND	chr1:71481186-71481455	K562	blood:	n/a	n/a
36	MAFF	chr1:71481238-71481422	K562	blood:	n/a	n/a
37	MAFK	chr1:71481311-71481361	HepG2	liver:	n/a	n/a
38	MAFK	chr1:71481242-71481456	K562	blood:	n/a	n/a
39	MXI1	chr1:71473675-71473677	GM12878	blood:	n/a	n/a
40	MXI1	chr1:71483643-71486068	SK-N-SH	brain:	n/a	chr1:71485096-71485105
41	MXI1	chr1:71474235-71474348	K562	blood:	n/a	n/a
42	MYC	chr1:71484933-71485162	K562	blood:	n/a	n/a
43	MYC	chr1:71483557-71483773	MCF10A-Er-Src	breast:	n/a	n/a
44	NR3C1	chr1:71470459-71470716	ECC-1	luminal epithelium:	n/a	n/a
45	PBX3	chr1:71484978-71485376	SK-N-SH	brain:	n/a	n/a
46	POLR2A	chr1:71470403-71471404	SK-N-MC	brain:	n/a	n/a
47	POLR2A	chr1:71485013-71485751	SK-N-MC	brain:	n/a	n/a
48	POLR2A	chr1:71479717-71481198	SK-N-MC	brain:	n/a	n/a
49	POLR2A	chr1:71479579-71480341	SK-N-MC	brain:	n/a	n/a
50	POLR2A	chr1:71471360-71471361	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:71472738-71472788	BJ	skin:	n/a
2	chr1:71472738-71472788	Jurkat	blood:	n/a
3	chr1:71472738-71472788	MCF10A-Er-Src	breast:	n/a
4	chr1:71472738-71472788	HL-60	blood:	n/a
5	chr1:71472738-71472788	AG09309	skin:	n/a
6	chr1:71472738-71472788	GM12892	blood:	n/a
7	chr1:71472738-71472788	AG04449	skin:	fetal
8	chr1:71472738-71472788	HEEpiC	esophagus:	n/a
9	chr1:71472738-71472788	PANC-1	pancreas:	n/a
10	chr1:71472738-71472788	HRPEpiC	eye:	n/a
11	chr1:71472738-71472788	SK-N-MC	brain:	n/a
12	chr1:71472738-71472788	ovcar-3	ovarian:	n/a
13	chr1:71472738-71472788	HRCEpiC	kidney:	n/a
14	chr1:71472738-71472788	T-47D	breast:	n/a
15	chr1:71472738-71472788	GM19239	blood:	n/a
16	chr1:71472738-71472788	U87	brain:	n/a
17	chr1:71472738-71472788	IMR90	lung:	fetal
18	chr1:71472738-71472788	PrEC	prostate:	n/a
19	chr1:71472738-71472788	SKMC	muscle:	n/a
20	chr1:71472738-71472788	GM12891	blood:	n/a
21	chr1:71472738-71472788	NHDF-neo	bronchial:	n/a
22	chr1:71472738-71472788	GM12878	blood:	n/a
23	chr1:71472738-71472788	AG09319	gingival:	n/a
24	chr1:71472738-71472788	Hepatocyte	liver:	n/a
25	chr1:71472738-71472788	K562	blood:	n/a
26	chr1:71472738-71472788	SAEC	small airway:	n/a
27	chr1:71472738-71472788	RPTEC	kidney:	n/a
28	chr1:71472738-71472788	Hela-S3	cervix:	n/a
29	chr1:71472738-71472788	SK-N-SH	brain:	n/a
30	chr1:71472738-71472788	HPAEpiC	pulmonary alveolar:	n/a
31	chr1:71472738-71472788	AG04450	lung:	fetal
32	chr1:71472738-71472788	HepG2	liver:	n/a
33	chr1:71472738-71472788	HRE	kidney:	n/a
34	chr1:71472738-71472788	NHBE	bronchial:	n/a
35	chr1:71472738-71472788	H1-hESC	embryonic stem cell:	embryo
36	chr1:71472738-71472788	PFSK-1	brain:	n/a
37	chr1:71472738-71472788	HMEC	breast:	n/a
38	chr1:71472738-71472788	HIPEpiC	eye:	n/a
39	chr1:71472738-71472788	HCF	heart:	n/a
40	chr1:71472738-71472788	ECC-1	luminal epithelium:	n/a
41	chr1:71472738-71472788	NB4	blood:	n/a
42	chr1:71472738-71472788	LNCaP	prostate:	n/a
43	chr1:71472738-71472788	A549	lung:	n/a
44	chr1:71472738-71472788	ProgFib	skin:	n/a
45	chr1:71472738-71472788	HNPCEpiC	eye:	n/a
46	chr1:71472738-71472788	NT2-D1	testis:	n/a
47	chr1:71472738-71472788	HCPEpiC	choroid plexus:	n/a
48	chr1:71472738-71472788	HCT-116	colon:	n/a
49	chr1:71472738-71472788	NH-A	brain:	n/a
50	chr1:71472738-71472788	AG10803	skin:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:71475910..71477737-chr1:71480653..71482581,2	MCF-7	breast:
2	chr1:71473756..71476164-chr1:71480981..71482752,2	K562	blood:
3	chr1:71475910..71477737-chr1:71480653..71482581,2	MCF-7	breast:
4	chr1:71484257..71486555-chr1:71489083..71490597,2	MCF-7	breast:
5	chr1:71473756..71476164-chr1:71480981..71482752,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZRANB2-3	chr1:71471537-71472185	ENSG00000269933.1
2	lnc-CTH-14	chr1:71475926-71475982	l_71_chr1:71319635-71475982_testes
3	lnc-ZRANB2-2	chr1:71472542-71473814	NONHSAT003875
4	lnc-CTH-14	chr1:71475401-71475924	l_71_chr1:71319635-71475982_testes

No data

Variant related genes	Relation type
ENSG00000269933	TF binding region
ENSG00000269933	CpG island

Extended variants
information (count: 517 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:517 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2744914	chr1:71469583-71469584	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142341219	chr1:71469595-71469596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556265638	chr1:71469628-71469629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144751985	chr1:71469644-71469645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191782921	chr1:71469704-71469705	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558605979	chr1:71469706-71469707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371091520	chr1:71469735-71469736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs74087147	chr1:71469759-71469760	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs373246307	chr1:71469776-71469777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541348429	chr1:71469804-71469805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183858140	chr1:71469807-71469808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2250312	chr1:71469819-71469820	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs200735757	chr1:71469845-71469846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187404218	chr1:71469850-71469851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370458175	chr1:71469916-71469917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546758211	chr1:71469934-71469935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74087148	chr1:71469946-71469947	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs185747011	chr1:71470008-71470009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544969702	chr1:71470081-71470082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564974811	chr1:71470140-71470141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527958040	chr1:71470141-71470142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548117391	chr1:71470192-71470193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs373612759	chr1:71470239-71470240	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs151270666	chr1:71470241-71470242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568143258	chr1:71470272-71470273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190567589	chr1:71470410-71470411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528933694	chr1:71470428-71470429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550399720	chr1:71470438-71470439	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569739958	chr1:71470565-71470566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538753237	chr1:71470596-71470597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs114975528	chr1:71470622-71470623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565695488	chr1:71470637-71470638	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534607826	chr1:71470654-71470655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555348965	chr1:71470671-71470672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574651132	chr1:71470696-71470697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs150462662	chr1:71470716-71470717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556756038	chr1:71470733-71470734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576114604	chr1:71470744-71470745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115771519	chr1:71470758-71470759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138248080	chr1:71470794-71470795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572445139	chr1:71470799-71470800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs114196477	chr1:71470804-71470805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141465575	chr1:71470910-71470911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74760954	chr1:71470944-71470945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550362906	chr1:71470945-71470946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs76792052	chr1:71470950-71470951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543707181	chr1:71471001-71471002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115787560	chr1:71471002-71471003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529567962	chr1:71471021-71471022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145159819	chr1:71471058-71471059	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
small cell lung cancer	20016488	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
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	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
Cancer	20164920	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71465800-71485000	Weak transcription	Pancreas	Pancrea
2	chr1:71466000-71475200	Weak transcription	K562	blood
3	chr1:71467400-71469600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:71467800-71475400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:71468400-71472800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr1:71469600-71469800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:71469800-71470200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:71470200-71470800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr1:71470400-71470600	Enhancers	Adipose Nuclei	Adipose
10	chr1:71470400-71470800	Enhancers	Placenta	Placenta
11	chr1:71470600-71477600	Weak transcription	Adipose Nuclei	Adipose
12	chr1:71472800-71474000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:71473600-71478000	Weak transcription	Aorta	Aorta
14	chr1:71474000-71474600	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr1:71474600-71478200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr1:71475200-71476200	Strong transcription	K562	blood
17	chr1:71475400-71478200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr1:71476200-71477200	Weak transcription	K562	blood
19	chr1:71477200-71478600	Strong transcription	K562	blood
20	chr1:71477600-71478200	Strong transcription	Adipose Nuclei	Adipose
21	chr1:71477800-71478200	Enhancers	Fetal Stomach	stomach
22	chr1:71478000-71478200	Enhancers	Aorta	Aorta
23	chr1:71478200-71479600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:71478200-71479600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:71478200-71482600	Weak transcription	Aorta	Aorta
26	chr1:71478200-71483200	Weak transcription	Adipose Nuclei	Adipose
27	chr1:71478600-71480400	Weak transcription	K562	blood
28	chr1:71479600-71481600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:71479600-71482000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr1:71479800-71480600	Enhancers	Fetal Heart	heart
31	chr1:71480400-71481800	Enhancers	K562	blood
32	chr1:71480600-71484400	Weak transcription	Fetal Heart	heart
33	chr1:71481600-71482800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:71481800-71501000	Weak transcription	K562	blood
35	chr1:71482000-71483400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr1:71482600-71483800	Enhancers	Aorta	Aorta
37	chr1:71482800-71484000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr1:71483000-71483800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:71483000-71483800	Enhancers	Placenta	Placenta
40	chr1:71483200-71483600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr1:71483200-71483600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr1:71483200-71484000	Enhancers	Adipose Nuclei	Adipose
43	chr1:71483400-71483800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr1:71483800-71486800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr1:71483800-71491400	Weak transcription	Aorta	Aorta
46	chr1:71484000-71484400	Weak transcription	Adipose Nuclei	Adipose
47	chr1:71484000-71485000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:71484400-71485000	Enhancers	Fetal Brain Male	brain
49	chr1:71484400-71485800	Enhancers	Adipose Nuclei	Adipose
50	chr1:71484400-71486000	Enhancers	Fetal Heart	heart

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