Variant report

Variant	nsv546377
Chromosome Location	chr1:62103021-62116913
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:62112891-62113154	HepG2	liver:	n/a	n/a
2	ATF1	chr1:62106776-62107045	K562	blood:	n/a	n/a
3	ATF2	chr1:62107397-62107804	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:62106882-62107105	K562	blood:	n/a	n/a
5	BHLHE40	chr1:62107382-62107766	K562	blood:	n/a	chr1:62107530-62107546
6	BHLHE40	chr1:62106799-62107118	K562	blood:	n/a	n/a
7	CBX3	chr1:62107266-62107746	K562	blood:	n/a	n/a
8	CCNT2	chr1:62107450-62107689	K562	blood:	n/a	chr1:62107646-62107655
9	CEBPB	chr1:62103933-62104217	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:62103922-62104265	A549	lung:	n/a	n/a
11	CEBPB	chr1:62103904-62104253	HepG2	liver:	n/a	n/a
12	CEBPB	chr1:62113754-62113947	K562	blood:	n/a	n/a
13	CEBPB	chr1:62103918-62104248	K562	blood:	n/a	n/a
14	CEBPB	chr1:62108004-62108991	MCF-7	breast:	n/a	n/a
15	CEBPB	chr1:62113772-62113972	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr1:62103903-62104255	IMR90	lung:	n/a	n/a
17	CEBPB	chr1:62107061-62107294	K562	blood:	n/a	n/a
18	CEBPB	chr1:62108063-62109003	MCF-7	breast:	n/a	n/a
19	CHD1	chr1:62107168-62107238	GM12878	blood:	n/a	n/a
20	CHD1	chr1:62107411-62107699	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr1:62107400-62107674	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr1:62107427-62107745	A549	lung:	n/a	n/a
23	CTCF	chr1:62107427-62107680	T-47D	breast:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
24	CTCF	chr1:62107476-62107685	GM20000	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
25	CTCF	chr1:62107520-62107670	WERI-Rb-1	eye:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
26	CTCF	chr1:62107480-62107630	HMEC	breast:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
27	CTCF	chr1:62107500-62107650	GM12875	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
28	CTCF	chr1:62106858-62106932	GM13976	blood:	n/a	n/a
29	CTCF	chr1:62107321-62107831	MCF-7	breast:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
30	CTCF	chr1:62107466-62107712	MCF-7	breast:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
31	CTCF	chr1:62107502-62107637	SK-N-SH_RA	brain:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
32	CTCF	chr1:62107501-62107695	LNCaP	prostate:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
33	CTCF	chr1:62107560-62107710	GM12801	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
34	CTCF	chr1:62108120-62108270	HPF	lung:	n/a	n/a
35	CTCF	chr1:62108280-62108430	GM12864	blood:	n/a	n/a
36	CTCF	chr1:62107520-62107670	HFF-Myc	foreskin:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
37	CTCF	chr1:62107105-62107909	A549	lung:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
38	CTCF	chr1:62107374-62107811	GM12878	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
39	CTCF	chr1:62107540-62107690	HVMF	connective:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
40	CTCF	chr1:62107520-62107670	GM06990	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
41	CTCF	chr1:62107520-62107670	SK-N-SH_RA	brain:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
42	CTCF	chr1:62111272-62111424	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:62107520-62107670	K562	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
44	CTCF	chr1:62107466-62107703	MCF-7	breast:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
45	CTCF	chr1:62107500-62107650	GM12871	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
46	CTCF	chr1:62107540-62107690	WI-38	lung:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
47	CTCF	chr1:62107540-62107690	BE2_C	brain:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
48	CTCF	chr1:62107348-62107753	T-47D	breast:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
49	CTCF	chr1:62107463-62107728	Lung_OC	lung:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
50	CTCF	chr1:62107480-62107704	H1-hESC	embryonic stem cell:	n/a	chr1:62107580-62107598 chr1:62107575-62107596

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62107430-62107480	A549	lung:	n/a
2	chr1:62107542-62107592	HUVEC	blood vessel:	n/a
3	chr1:62107477-62107527	NHDF-neo	bronchial:	n/a
4	chr1:62107624-62107674	HRPEpiC	eye:	n/a
5	chr1:62107542-62107592	ECC-1	luminal epithelium:	n/a
6	chr1:62107477-62107527	HRCEpiC	kidney:	n/a
7	chr1:62107477-62107527	SKMC	muscle:	n/a
8	chr1:62107477-62107527	T-47D	breast:	n/a
9	chr1:62107430-62107480	RPTEC	kidney:	n/a
10	chr1:62107542-62107592	NB4	blood:	n/a
11	chr1:62107477-62107527	PFSK-1	brain:	n/a
12	chr1:62107542-62107592	HRCEpiC	kidney:	n/a
13	chr1:62107430-62107480	AG09309	skin:	n/a
14	chr1:62107542-62107592	MCF-7	breast:	n/a
15	chr1:62107542-62107592	ProgFib	skin:	n/a
16	chr1:62107624-62107674	GM12878	blood:	n/a
17	chr1:62107624-62107674	HEEpiC	esophagus:	n/a
18	chr1:62107542-62107592	RPTEC	kidney:	n/a
19	chr1:62107477-62107527	AG09319	gingival:	n/a
20	chr1:62107542-62107592	MCF10A-Er-Src	breast:	n/a
21	chr1:62107542-62107592	NT2-D1	testis:	n/a
22	chr1:62107430-62107480	HUVEC	blood vessel:	n/a
23	chr1:62107430-62107480	AG04450	lung:	fetal
24	chr1:62107542-62107592	A549	lung:	n/a
25	chr1:62107542-62107592	GM06990	blood:	n/a
26	chr1:62107542-62107592	T-47D	breast:	n/a
27	chr1:62107624-62107674	HNPCEpiC	eye:	n/a
28	chr1:62107477-62107527	AG10803	skin:	n/a
29	chr1:62107624-62107674	MCF-7	breast:	n/a
30	chr1:62107624-62107674	RPTEC	kidney:	n/a
31	chr1:62107430-62107480	Caco-2	colon:	n/a
32	chr1:62107542-62107592	SK-N-SH_RA	brain:	n/a
33	chr1:62107477-62107527	HRPEpiC	eye:	n/a
34	chr1:62107477-62107527	HCPEpiC	choroid plexus:	n/a
35	chr1:62107542-62107592	IMR90	lung:	fetal
36	chr1:62107430-62107480	GM06990	blood:	n/a
37	chr1:62107430-62107480	HCF	heart:	n/a
38	chr1:62107430-62107480	PANC-1	pancreas:	n/a
39	chr1:62107624-62107674	ECC-1	luminal epithelium:	n/a
40	chr1:62107624-62107674	HCT-116	colon:	n/a
41	chr1:62107477-62107527	AoSMC	blood vessel:	n/a
42	chr1:62107430-62107480	Hepatocyte	liver:	n/a
43	chr1:62107542-62107592	BJ	skin:	n/a
44	chr1:62107624-62107674	HEK293	kidney:	embryo
45	chr1:62107542-62107592	PANC-1	pancreas:	n/a
46	chr1:62107542-62107592	GM12892	blood:	n/a
47	chr1:62107430-62107480	GM12891	blood:	n/a
48	chr1:62107542-62107592	Hela-S3	cervix:	n/a
49	chr1:62107542-62107592	NHBE	bronchial:	n/a
50	chr1:62107542-62107592	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:62110139..62113045-chr1:62113882..62116057,2	K562	blood:
2	chr1:61519880..61523708-chr1:62105298..62109732,4	MCF-7	breast:
3	chr1:62104103..62106324-chr1:62108881..62110470,2	K562	blood:
4	chr1:62107692..62111975-chr1:62207507..62210400,5	MCF-7	breast:
5	chr1:62106350..62108369-chr1:62114638..62116326,2	K562	blood:
6	chr1:62104103..62106324-chr1:62108881..62110470,2	K562	blood:
7	chr1:62106350..62108369-chr1:62114638..62116326,2	K562	blood:
8	chr1:61681397..61683015-chr1:62107574..62109680,2	MCF-7	breast:
9	chr1:62110139..62113045-chr1:62113882..62116057,2	K562	blood:
10	chr1:62109498..62111908-chr1:62214585..62216451,2	MCF-7	breast:
11	chr1:62107133..62108121-chr1:62124846..62125524,3	MCF-7	breast:
12	chr1:61961790..61962305-chr1:62107717..62108447,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-INADL-1	chr1:62113728-62113990	XLOC_000227

Variant related genes	Relation type
ENSG00000223920	TF binding region
ENSG00000223920	CpG island
ENSG00000271200	chromatin interactions
ENSG00000132849	chromatin interactions

Extended variants
information (count: 471 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:471 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13375459	chr1:62103021-62103022	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10889245	chr1:62103029-62103030	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs12407058	chr1:62103072-62103073	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs147963181	chr1:62103083-62103084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558191917	chr1:62103179-62103180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140534194	chr1:62103194-62103195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150452489	chr1:62103197-62103198	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs77065069	chr1:62103266-62103267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573687695	chr1:62103268-62103269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs13375467	chr1:62103284-62103285	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs188938970	chr1:62103290-62103291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs13375468	chr1:62103309-62103310	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs545948064	chr1:62103385-62103386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs114293559	chr1:62103404-62103405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs6686620	chr1:62103414-62103415	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs182166153	chr1:62103427-62103428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568105084	chr1:62103468-62103469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs138289783	chr1:62103473-62103474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs13375477	chr1:62103500-62103501	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs17122568	chr1:62103502-62103503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs117084476	chr1:62103532-62103533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12407106	chr1:62103548-62103549	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs11585057	chr1:62103566-62103567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149164090	chr1:62103627-62103628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145077910	chr1:62103674-62103675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs555598441	chr1:62103684-62103685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573698126	chr1:62103702-62103703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544564415	chr1:62103726-62103727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs75687238	chr1:62103734-62103735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563965201	chr1:62103750-62103751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559062329	chr1:62103781-62103782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186310737	chr1:62103804-62103805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs12118986	chr1:62103814-62103815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370085591	chr1:62103838-62103839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs138791226	chr1:62103868-62103869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191550656	chr1:62103889-62103890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs12407152	chr1:62103890-62103891	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs561918305	chr1:62103955-62103956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528918805	chr1:62103983-62103984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs78784354	chr1:62104069-62104070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs546244775	chr1:62104100-62104101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs180781080	chr1:62104115-62104116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533078145	chr1:62104145-62104146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529466435	chr1:62104258-62104259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs75002563	chr1:62104268-62104269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534078632	chr1:62104293-62104294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547875153	chr1:62104304-62104305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs549285486	chr1:62104307-62104308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs12402429	chr1:62104383-62104384	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs369837203	chr1:62104401-62104402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62099400-62104800	Weak transcription	Right Atrium	heart
2	chr1:62102200-62103200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr1:62102400-62103200	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr1:62102600-62106600	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr1:62102600-62107000	Enhancers	Ovary	ovary
6	chr1:62102800-62103200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:62102800-62103200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:62102800-62103800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr1:62102800-62104600	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr1:62102800-62106000	Enhancers	Adipose Nuclei	Adipose
11	chr1:62102800-62106400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr1:62102800-62107200	Weak transcription	Stomach Mucosa	stomach
13	chr1:62103000-62105000	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr1:62103000-62105000	Weak transcription	Fetal Lung	lung
15	chr1:62103000-62106400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr1:62103000-62107200	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr1:62103000-62107200	Weak transcription	HUVEC	blood vessel
18	chr1:62103200-62103400	Enhancers	Gastric	stomach
19	chr1:62103200-62103600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr1:62103200-62104800	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr1:62103200-62106200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr1:62103200-62106600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr1:62103400-62108000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr1:62103400-62146400	Weak transcription	Gastric	stomach
25	chr1:62103600-62104600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr1:62103600-62104800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr1:62103600-62105400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr1:62103800-62104600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr1:62103800-62104800	Enhancers	NHDF-Ad	bronchial
30	chr1:62103800-62105400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr1:62103800-62107400	Enhancers	Aorta	Aorta
32	chr1:62103800-62108000	Enhancers	Fetal Stomach	stomach
33	chr1:62103800-62108000	Enhancers	Rectal Smooth Muscle	rectum
34	chr1:62104200-62105000	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr1:62104200-62105200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr1:62104400-62107000	Enhancers	Stomach Smooth Muscle	stomach
37	chr1:62104400-62108400	Enhancers	Fetal Muscle Leg	muscle
38	chr1:62104600-62105200	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr1:62104600-62105800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr1:62104600-62106400	Enhancers	Colon Smooth Muscle	Colon
41	chr1:62104600-62106600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr1:62104600-62106800	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr1:62104600-62107000	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr1:62104800-62105000	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr1:62104800-62105200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr1:62104800-62105200	Enhancers	Fetal Heart	heart
47	chr1:62104800-62105200	Enhancers	Left Ventricle	heart
48	chr1:62104800-62105200	Enhancers	Lung	lung
49	chr1:62104800-62105200	Enhancers	Right Atrium	heart
50	chr1:62104800-62107200	Weak transcription	NHDF-Ad	bronchial

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