Variant report

Variant	esv1831777
Chromosome Location	chr1:62086216-62119201
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	BHLHE40	chr1:62098847-62098861	K562	blood:	n/a	n/a
8	CBX3	chr1:62107266-62107746	K562	blood:	n/a	n/a
9	CCNT2	chr1:62107450-62107689	K562	blood:	n/a	chr1:62107646-62107655
10	CEBPB	chr1:62094958-62095094	K562	blood:	n/a	n/a
11	CEBPB	chr1:62093161-62093304	K562	blood:	n/a	n/a
12	CEBPB	chr1:62101288-62101356	A549	lung:	n/a	n/a
13	CEBPB	chr1:62103904-62104253	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:62103918-62104248	K562	blood:	n/a	n/a
15	CEBPB	chr1:62113754-62113947	K562	blood:	n/a	n/a
16	CEBPB	chr1:62090802-62090847	A549	lung:	n/a	n/a
17	CEBPB	chr1:62103933-62104217	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:62107061-62107294	K562	blood:	n/a	n/a
19	CEBPB	chr1:62103922-62104265	A549	lung:	n/a	n/a
20	CEBPB	chr1:62113772-62113972	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr1:62108063-62109003	MCF-7	breast:	n/a	n/a
22	CEBPB	chr1:62103903-62104255	IMR90	lung:	n/a	n/a
23	CEBPB	chr1:62108004-62108991	MCF-7	breast:	n/a	n/a
24	CHD1	chr1:62107168-62107238	GM12878	blood:	n/a	n/a
25	CHD1	chr1:62107411-62107699	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr1:62107400-62107674	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr1:62107427-62107745	A549	lung:	n/a	n/a
28	CTCF	chr1:62107520-62107670	HPAF	blood vessel:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
29	CTCF	chr1:62107466-62107712	MCF-7	breast:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
30	CTCF	chr1:62107540-62107690	GM12869	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
31	CTCF	chr1:62107500-62107650	HRE	kidney:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
32	CTCF	chr1:62107427-62107680	T-47D	breast:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
33	CTCF	chr1:62107520-62107670	HBMEC	blood vessel:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
34	CTCF	chr1:62091617-62091640	GM13976	blood:	n/a	n/a
35	CTCF	chr1:62107459-62107721	MCF-7	breast:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
36	CTCF	chr1:62107333-62107788	K562	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
37	CTCF	chr1:62107620-62107770	A549	lung:	n/a	n/a
38	CTCF	chr1:62107520-62107670	GM12878	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
39	CTCF	chr1:62107540-62107690	BJ	skin:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
40	CTCF	chr1:62107105-62107909	A549	lung:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
41	CTCF	chr1:62092580-62092730	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr1:62107540-62107690	K562	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
43	CTCF	chr1:62107468-62107751	A549	lung:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
44	CTCF	chr1:62107560-62107710	GM12872	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
45	CTCF	chr1:62107479-62107696	Pancreas_OC	pancreas:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
46	CTCF	chr1:62107520-62107670	GM12874	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
47	CTCF	chr1:62107500-62107650	GM12864	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
48	CTCF	chr1:62107453-62107728	MCF-7	breast:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
49	CTCF	chr1:62107520-62107670	HEEpiC	esophagus:	n/a	chr1:62107580-62107598 chr1:62107575-62107596
50	CTCF	chr1:62107308-62107741	K562	blood:	n/a	chr1:62107580-62107598 chr1:62107575-62107596

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62107477-62107527	GM12891	blood:	n/a
2	chr1:62107477-62107527	GM12891	blood:	n/a
3	chr1:62107624-62107674	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:62107624-62107674	H1-hESC	embryonic stem cell:	embryo
5	chr1:62107430-62107480	Jurkat	blood:	n/a
6	chr1:62107542-62107592	GM12891	blood:	n/a
7	chr1:62107542-62107592	SK-N-MC	brain:	n/a
8	chr1:62107430-62107480	BE2_C	brain:	n/a
9	chr1:62107624-62107674	NHBE	bronchial:	n/a
10	chr1:62107430-62107480	HRPEpiC	eye:	n/a
11	chr1:62107477-62107527	MCF10A-Er-Src	breast:	n/a
12	chr1:62107624-62107674	HCF	heart:	n/a
13	chr1:62107477-62107527	AG10803	skin:	n/a
14	chr1:62107624-62107674	HAEpiC	amniotic membrane:	n/a
15	chr1:62102363-62102413	GM12891	blood:	n/a
16	chr1:62102363-62102413	RPTEC	kidney:	n/a
17	chr1:62107542-62107592	HIPEpiC	eye:	n/a
18	chr1:62102363-62102413	AG09319	gingival:	n/a
19	chr1:62102363-62102413	MCF10A-Er-Src	breast:	n/a
20	chr1:62107624-62107674	HNPCEpiC	eye:	n/a
21	chr1:62102363-62102413	AG04449	skin:	fetal
22	chr1:62107542-62107592	U87	brain:	n/a
23	chr1:62107477-62107527	Caco-2	colon:	n/a
24	chr1:62107477-62107527	SK-N-SH_RA	brain:	n/a
25	chr1:62107477-62107527	HCPEpiC	choroid plexus:	n/a
26	chr1:62107624-62107674	NHDF-neo	bronchial:	n/a
27	chr1:62107624-62107674	AG09309	skin:	n/a
28	chr1:62107624-62107674	AG04450	lung:	fetal
29	chr1:62107477-62107527	K562	blood:	n/a
30	chr1:62107430-62107480	MCF10A-Er-Src	breast:	n/a
31	chr1:62107477-62107527	HCF	heart:	n/a
32	chr1:62102363-62102413	NHDF-neo	bronchial:	n/a
33	chr1:62107542-62107592	AG10803	skin:	n/a
34	chr1:62107477-62107527	HMEC	breast:	n/a
35	chr1:62107430-62107480	HIPEpiC	eye:	n/a
36	chr1:62107624-62107674	IMR90	lung:	fetal
37	chr1:62107430-62107480	HRCEpiC	kidney:	n/a
38	chr1:62107624-62107674	A549	lung:	n/a
39	chr1:62107624-62107674	SK-N-SH_RA	brain:	n/a
40	chr1:62107477-62107527	PANC-1	pancreas:	n/a
41	chr1:62107542-62107592	GM12878	blood:	n/a
42	chr1:62102363-62102413	HCT-116	colon:	n/a
43	chr1:62107430-62107480	IMR90	lung:	fetal
44	chr1:62107624-62107674	GM06990	blood:	n/a
45	chr1:62102363-62102413	HEEpiC	esophagus:	n/a
46	chr1:62107542-62107592	IMR90	lung:	fetal
47	chr1:62107430-62107480	MCF-7	breast:	n/a
48	chr1:62107542-62107592	HMEC	breast:	n/a
49	chr1:62107430-62107480	HNPCEpiC	eye:	n/a
50	chr1:62107542-62107592	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:62110139..62113045-chr1:62113882..62116057,2	K562	blood:
2	chr1:62106350..62108369-chr1:62114638..62116326,2	K562	blood:
3	chr1:61519880..61523708-chr1:62105298..62109732,4	MCF-7	breast:
4	chr1:61961790..61962305-chr1:62107717..62108447,2	MCF-7	breast:
5	chr1:62104103..62106324-chr1:62108881..62110470,2	K562	blood:
6	chr1:62078266..62080827-chr1:62086486..62088051,2	K562	blood:
7	chr1:62107133..62108121-chr1:62124846..62125524,3	MCF-7	breast:
8	chr1:62110139..62113045-chr1:62113882..62116057,2	K562	blood:
9	chr1:62106350..62108369-chr1:62114638..62116326,2	K562	blood:
10	chr1:62107692..62111975-chr1:62207507..62210400,5	MCF-7	breast:
11	chr1:61681397..61683015-chr1:62107574..62109680,2	MCF-7	breast:
12	chr1:62109498..62111908-chr1:62214585..62216451,2	MCF-7	breast:
13	chr1:62104103..62106324-chr1:62108881..62110470,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-INADL-1	chr1:62102824-62102980	XLOC_000227
2	lnc-INADL-1	chr1:62113728-62113990	XLOC_000227

Variant related genes	Relation type
ENSG00000223920	TF binding region
ENSG00000264551	TF binding region
ENSG00000223920	CpG island
ENSG00000264551	CpG island
ENSG00000132849	chromatin interactions
ENSG00000271200	chromatin interactions

Extended variants
information (count: 1201 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1201 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs61583138	chr1:62086220-62086221	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527718293	chr1:62086251-62086252	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs542571335	chr1:62086271-62086272	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs561434885	chr1:62086274-62086275	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs531683467	chr1:62086275-62086276	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs183595919	chr1:62086337-62086338	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs188196144	chr1:62086408-62086409	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs192760499	chr1:62086493-62086494	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs72672304	chr1:62086515-62086516	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs183523664	chr1:62086531-62086532	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs533700622	chr1:62086615-62086616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548676273	chr1:62086616-62086617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186711343	chr1:62086618-62086619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs192337494	chr1:62086635-62086636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556199853	chr1:62086644-62086645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs577860772	chr1:62086652-62086653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs7519731	chr1:62086670-62086671	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs554051293	chr1:62086678-62086679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7554347	chr1:62086690-62086691	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs7519830	chr1:62086728-62086729	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs530415869	chr1:62086771-62086772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561091636	chr1:62086814-62086815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576369539	chr1:62086825-62086826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs7542856	chr1:62086889-62086890	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs147273192	chr1:62086926-62086927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs7542870	chr1:62086934-62086935	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs551555076	chr1:62086945-62086946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs560471444	chr1:62086969-62086970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184726473	chr1:62086970-62086971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140684931	chr1:62086980-62086981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546710732	chr1:62087035-62087036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs549247637	chr1:62087042-62087043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567181032	chr1:62087056-62087057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7522515	chr1:62087091-62087092	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs549649228	chr1:62087095-62087096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568142004	chr1:62087101-62087102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10789096	chr1:62087116-62087117	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs373664573	chr1:62087127-62087128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553918412	chr1:62087147-62087148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs550594262	chr1:62087152-62087153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs60613275	chr1:62087153-62087154	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs537393549	chr1:62087167-62087168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs536576735	chr1:62087195-62087196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555221927	chr1:62087225-62087226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144634444	chr1:62087235-62087236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559011043	chr1:62087271-62087272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs117701085	chr1:62087277-62087278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs151256373	chr1:62087312-62087313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs112915580	chr1:62087370-62087371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550425238	chr1:62087389-62087390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62073200-62086400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:62073200-62098800	Weak transcription	Right Atrium	heart
3	chr1:62085200-62093000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:62086000-62086600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr1:62086000-62086600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr1:62086000-62087400	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr1:62086400-62086600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:62086600-62088000	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr1:62090600-62091200	Enhancers	Fetal Lung	lung
10	chr1:62091000-62091200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr1:62091400-62092200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:62092200-62093400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr1:62092400-62093000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:62092400-62093200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:62092600-62093400	Enhancers	Aorta	Aorta
16	chr1:62093400-62096400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:62096400-62096600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr1:62098800-62099400	Enhancers	Right Atrium	heart
19	chr1:62099200-62100000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr1:62099400-62099800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr1:62099400-62104800	Weak transcription	Right Atrium	heart
22	chr1:62099800-62101400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr1:62100000-62101400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr1:62101400-62102000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:62101400-62103000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr1:62101800-62102200	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr1:62101800-62103000	Enhancers	HUVEC	blood vessel
28	chr1:62102000-62102800	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr1:62102000-62102800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr1:62102200-62102600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr1:62102200-62102600	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr1:62102200-62102600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
33	chr1:62102200-62102800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr1:62102200-62102800	Active TSS	Adipose Nuclei	Adipose
35	chr1:62102200-62103000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr1:62102200-62103000	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr1:62102200-62103000	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr1:62102200-62103200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr1:62102400-62103000	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr1:62102400-62103200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr1:62102600-62102800	Enhancers	H1 Cell Line	embryonic stem cell
42	chr1:62102600-62102800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr1:62102600-62102800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr1:62102600-62102800	Enhancers	Stomach Mucosa	stomach
45	chr1:62102600-62102800	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr1:62102600-62103000	Enhancers	Fetal Lung	lung
47	chr1:62102600-62106600	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr1:62102600-62107000	Enhancers	Ovary	ovary
49	chr1:62102800-62103000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr1:62102800-62103200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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