Variant report

Variant	nsv871140
Chromosome Location	chr1:79095581-79155134
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	chr1:79142134-79142380	HepG2	liver:	n/a	n/a
2	BATF	chr1:79130482-79130746	GM12878	blood:	n/a	chr1:79130659-79130669
3	BATF	chr1:79106163-79106472	GM12878	blood:	n/a	n/a
4	BCL11A	chr1:79106121-79106496	GM12878	blood:	n/a	n/a
5	BCL11A	chr1:79106219-79106467	GM12878	blood:	n/a	n/a
6	BCLAF1	chr1:79098766-79099277	GM12878	blood:	n/a	n/a
7	BCLAF1	chr1:79115359-79115671	GM12878	blood:	n/a	chr1:79115456-79115465
8	BCLAF1	chr1:79099901-79100397	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:79099259-79099288	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:79142056-79142383	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:79105213-79105250	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:79097726-79097845	GM12878	blood:	n/a	n/a
13	BRCA1	chr1:79099377-79099420	GM12878	blood:	n/a	n/a
14	CEBPB	chr1:79153084-79153397	MCF-7	breast:	n/a	n/a
15	CEBPB	chr1:79154345-79154687	Hela-S3	cervix:	n/a	chr1:79154499-79154512
16	CEBPB	chr1:79115863-79116154	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr1:79146975-79147333	IMR90	lung:	n/a	chr1:79147144-79147155
18	CEBPB	chr1:79143505-79143845	IMR90	lung:	n/a	chr1:79143655-79143666 chr1:79143655-79143668
19	CEBPB	chr1:79147025-79147182	H1-hESC	embryonic stem cell:	n/a	chr1:79147144-79147155
20	CEBPB	chr1:79146981-79147334	HepG2	liver:	n/a	chr1:79147144-79147155
21	CEBPB	chr1:79143504-79143812	A549	lung:	n/a	chr1:79143655-79143666 chr1:79143655-79143668
22	CEBPB	chr1:79147022-79147222	K562	blood:	n/a	chr1:79147144-79147155
23	CEBPB	chr1:79143503-79143822	HepG2	liver:	n/a	chr1:79143655-79143666 chr1:79143655-79143668
24	CEBPB	chr1:79116826-79116982	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:79146995-79147309	A549	lung:	n/a	chr1:79147144-79147155
26	CEBPB	chr1:79098035-79098245	HepG2	liver:	n/a	n/a
27	CEBPB	chr1:79146973-79147328	Hela-S3	cervix:	n/a	chr1:79147144-79147155
28	CHD1	chr1:79096937-79096978	GM12878	blood:	n/a	n/a
29	CHD1	chr1:79116720-79117589	GM12878	blood:	n/a	n/a
30	CHD1	chr1:79097821-79098005	GM12878	blood:	n/a	n/a
31	CHD1	chr1:79121360-79121497	GM12878	blood:	n/a	n/a
32	CHD1	chr1:79115356-79116503	GM12878	blood:	n/a	n/a
33	CTCF	chr1:79154480-79154630	MCF-7	breast:	n/a	chr1:79154555-79154576 chr1:79154553-79154571 chr1:79154554-79154570
34	CTCF	chr1:79154436-79154686	HUVEC	blood vessel:	n/a	chr1:79154555-79154576 chr1:79154553-79154571 chr1:79154554-79154570
35	CTCF	chr1:79142094-79142408	Spleen_OC	spleen:	n/a	chr1:79142229-79142242 chr1:79142227-79142245 chr1:79142233-79142242 chr1:79142228-79142244 chr1:79142222-79142243
36	CTCF	chr1:79154310-79154725	MCF-7	breast:	n/a	chr1:79154555-79154576 chr1:79154553-79154571 chr1:79154554-79154570
37	CTCF	chr1:79142180-79142330	HCFaa	heart:	n/a	chr1:79142229-79142242 chr1:79142227-79142245 chr1:79142233-79142242 chr1:79142228-79142244 chr1:79142222-79142243
38	CTCF	chr1:79154540-79154690	HRE	kidney:	n/a	chr1:79154555-79154576 chr1:79154553-79154571 chr1:79154554-79154570
39	CTCF	chr1:79138924-79139051	GM19238	blood:	n/a	n/a
40	CTCF	chr1:79154400-79154550	RPTEC	kidney:	n/a	n/a
41	CTCF	chr1:79142180-79142330	K562	blood:	n/a	chr1:79142229-79142242 chr1:79142227-79142245 chr1:79142233-79142242 chr1:79142228-79142244 chr1:79142222-79142243
42	CTCF	chr1:79142160-79142310	BE2_C	brain:	n/a	chr1:79142229-79142242 chr1:79142227-79142245 chr1:79142233-79142242 chr1:79142228-79142244 chr1:79142222-79142243
43	CTCF	chr1:79142145-79142358	GM10248	blood:	n/a	chr1:79142229-79142242 chr1:79142227-79142245 chr1:79142233-79142242 chr1:79142228-79142244 chr1:79142222-79142243
44	CTCF	chr1:79142160-79142310	GM12870	blood:	n/a	chr1:79142229-79142242 chr1:79142227-79142245 chr1:79142233-79142242 chr1:79142228-79142244 chr1:79142222-79142243
45	CTCF	chr1:79138900-79139050	GM12871	blood:	n/a	n/a
46	CTCF	chr1:79138880-79139030	GM12872	blood:	n/a	n/a
47	CTCF	chr1:79113000-79113150	GM12869	blood:	n/a	n/a
48	CTCF	chr1:79142120-79142270	GM12878	blood:	n/a	chr1:79142229-79142242 chr1:79142227-79142245 chr1:79142233-79142242 chr1:79142228-79142244 chr1:79142222-79142243
49	CTCF	chr1:79142101-79142369	GM12878	blood:	n/a	chr1:79142229-79142242 chr1:79142227-79142245 chr1:79142233-79142242 chr1:79142228-79142244 chr1:79142222-79142243
50	CTCF	chr1:79142035-79142388	A549	lung:	n/a	chr1:79142229-79142242 chr1:79142227-79142245 chr1:79142233-79142242 chr1:79142228-79142244 chr1:79142222-79142243

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79118191-79118241	SK-N-SH_RA	brain:	n/a
2	chr1:79114976-79115026	NT2-D1	testis:	n/a
3	chr1:79114976-79115026	GM12892	blood:	n/a
4	chr1:79114976-79115026	U87	brain:	n/a
5	chr1:79111320-79111370	HUVEC	blood vessel:	n/a
6	chr1:79118191-79118241	HEK293	kidney:	embryo
7	chr1:79118191-79118241	PrEC	prostate:	n/a
8	chr1:79118191-79118241	SK-N-SH	brain:	n/a
9	chr1:79114976-79115026	LNCaP	prostate:	n/a
10	chr1:79111320-79111370	A549	lung:	n/a
11	chr1:79118191-79118241	HMEC	breast:	n/a
12	chr1:79111320-79111370	AG09309	skin:	n/a
13	chr1:79111320-79111370	SK-N-MC	brain:	n/a
14	chr1:79118191-79118241	SK-N-MC	brain:	n/a
15	chr1:79118191-79118241	MCF10A-Er-Src	breast:	n/a
16	chr1:79111320-79111370	K562	blood:	n/a
17	chr1:79118191-79118241	CMK	blood:	n/a
18	chr1:79114976-79115026	HL-60	blood:	n/a
19	chr1:79114976-79115026	GM19239	blood:	n/a
20	chr1:79114976-79115026	A549	lung:	n/a
21	chr1:79111320-79111370	SAEC	small airway:	n/a
22	chr1:79118191-79118241	HCF	heart:	n/a
23	chr1:79114976-79115026	BE2_C	brain:	n/a
24	chr1:79118191-79118241	AG04450	lung:	fetal
25	chr1:79114976-79115026	BJ	skin:	n/a
26	chr1:79114976-79115026	ovcar-3	ovarian:	n/a
27	chr1:79118191-79118241	HCT-116	colon:	n/a
28	chr1:79111320-79111370	AG04449	skin:	fetal
29	chr1:79111320-79111370	GM12878	blood:	n/a
30	chr1:79111320-79111370	SK-N-SH	brain:	n/a
31	chr1:79118191-79118241	NB4	blood:	n/a
32	chr1:79118191-79118241	AG04449	skin:	fetal
33	chr1:79114976-79115026	H1-hESC	embryonic stem cell:	embryo
34	chr1:79118191-79118241	Jurkat	blood:	n/a
35	chr1:79118191-79118241	ovcar-3	ovarian:	n/a
36	chr1:79114976-79115026	MCF-7	breast:	n/a
37	chr1:79111320-79111370	AoSMC	blood vessel:	n/a
38	chr1:79114976-79115026	NH-A	brain:	n/a
39	chr1:79114976-79115026	GM12878	blood:	n/a
40	chr1:79111320-79111370	HIPEpiC	eye:	n/a
41	chr1:79118191-79118241	PFSK-1	brain:	n/a
42	chr1:79118191-79118241	NT2-D1	testis:	n/a
43	chr1:79118191-79118241	HIPEpiC	eye:	n/a
44	chr1:79114976-79115026	HMEC	breast:	n/a
45	chr1:79111320-79111370	Hepatocyte	liver:	n/a
46	chr1:79114976-79115026	HCT-116	colon:	n/a
47	chr1:79111320-79111370	NHBE	bronchial:	n/a
48	chr1:79118191-79118241	AoSMC	blood vessel:	n/a
49	chr1:79114976-79115026	GM12891	blood:	n/a
50	chr1:79111320-79111370	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:79082897..79084158-chr1:79141759..79142926,5	MCF-7	breast:
2	chr1:79154179..79155005-chr1:79663219..79663974,2	MCF-7	breast:
3	chr1:79082938..79083884-chr1:79141774..79143085,5	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFI44-6	chr1:79095405-79095600	NONHSAT004078
2	lnc-IFI44-4	chr1:79131957-79132380	NONHSAT004081
3	lnc-IFI44-5	chr1:79107120-79107170	NONHSAT004079
4	lnc-IFI44-5	chr1:79106706-79106806	NONHSAT004079
5	lnc-ELTD1-6	chr1:79127046-79129763	ENSG00000249107
6	lnc-IFI44-3	chr1:79128301-79128563	NONHSAT004080
7	lnc-IFI44-6	chr1:79097126-79097332	NONHSAT004078
8	lnc-IFI44-5	chr1:79102377-79102888	NONHSAT004079
9	lnc-IFI44-3	chr1:79129450-79129763	NONHSAT004080

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	IFI44	hsa-miR-26b-5p	chr1:79126602-79126624
2	IFI44	hsa-miR-26b-5p	chr1:79129630-79129650

Variant related genes	Relation type
IFI44	TF binding region
ENSG00000238015	TF binding region
IFI44L	TF binding region
ENSG00000221683	TF binding region
IFI44	CpG island
ENSG00000238015	CpG island
IFI44L	CpG island
ENSG00000221683	CpG island
HMGA2	miRNA target sites

Extended variants
information (count: 2402 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2402 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs987495	chr1:79095581-79095582	Weak transcription Strong transcription Transcr. at gene 5' and 3'	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369929636	chr1:79095594-79095595	Weak transcription Strong transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
3	rs200596419	chr1:79095595-79095596	Weak transcription Strong transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
4	rs377658566	chr1:79095599-79095600	Weak transcription Strong transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
5	rs369207233	chr1:79095601-79095602	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs372774950	chr1:79095605-79095606	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs574438852	chr1:79095644-79095645	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs185745103	chr1:79095682-79095683	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs561124765	chr1:79095731-79095732	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs377104309	chr1:79095747-79095748	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs141846023	chr1:79095758-79095759	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs565241386	chr1:79095772-79095773	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs532498188	chr1:79095775-79095776	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs115110596	chr1:79095785-79095786	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs181017204	chr1:79095793-79095794	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs185619943	chr1:79095818-79095819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs199953378	chr1:79095834-79095835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557080542	chr1:79095843-79095844	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577392405	chr1:79095845-79095846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566640617	chr1:79095850-79095851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188564126	chr1:79095860-79095861	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552451063	chr1:79095861-79095862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs72506845	chr1:79095991-79095992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200621084	chr1:79095992-79095993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs33930882	chr1:79095993-79095994	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570662894	chr1:79096033-79096034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146273099	chr1:79096054-79096055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs76598202	chr1:79096078-79096079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574401133	chr1:79096081-79096082	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181327469	chr1:79096090-79096091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs114034106	chr1:79096109-79096110	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185928469	chr1:79096171-79096172	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553092549	chr1:79096200-79096201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573054441	chr1:79096210-79096211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191586464	chr1:79096289-79096290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78277846	chr1:79096379-79096380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541850824	chr1:79096514-79096515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs3820092	chr1:79096536-79096537	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs184029415	chr1:79096566-79096567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs80079339	chr1:79096616-79096617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575859767	chr1:79096651-79096652	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548671015	chr1:79096763-79096764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566144793	chr1:79096769-79096770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560567708	chr1:79096802-79096803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527440385	chr1:79096906-79096907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187377812	chr1:79096937-79096938	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570671528	chr1:79096975-79096976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190959964	chr1:79097043-79097044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550082880	chr1:79097047-79097048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376827861	chr1:79097080-79097081	Weak transcription Strong 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
Breast cancer	21990379	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:884 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79086800-79108800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr1:79087200-79097400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr1:79088600-79110600	Weak transcription	Fetal Thymus	thymus
4	chr1:79089000-79095800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr1:79089400-79098800	Weak transcription	Fetal Muscle Leg	muscle
6	chr1:79089400-79107200	Weak transcription	Ovary	ovary
7	chr1:79089600-79098800	Weak transcription	Aorta	Aorta
8	chr1:79089800-79115000	Weak transcription	Small Intestine	intestine
9	chr1:79090800-79110000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr1:79090800-79110000	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr1:79093400-79095800	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
12	chr1:79093600-79097800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:79094000-79097600	Weak transcription	Left Ventricle	heart
14	chr1:79094200-79096600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:79094400-79110600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr1:79094600-79110000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
17	chr1:79094600-79110200	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr1:79094600-79115200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:79095000-79107200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr1:79095800-79097600	Strong transcription	GM12878-XiMat	blood
21	chr1:79097600-79099600	ZNF genes & repeats	GM12878-XiMat	blood
22	chr1:79097800-79103000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:79098600-79099400	Weak transcription	Left Ventricle	heart
24	chr1:79098800-79099200	ZNF genes & repeats	Esophagus	oesophagus
25	chr1:79098800-79099400	ZNF genes & repeats	Aorta	Aorta
26	chr1:79098800-79099400	ZNF genes & repeats	Fetal Muscle Leg	muscle
27	chr1:79099000-79099200	Enhancers	Lung	lung
28	chr1:79099200-79112800	Weak transcription	Lung	lung
29	chr1:79099400-79107200	Weak transcription	Aorta	Aorta
30	chr1:79099400-79107200	Weak transcription	Fetal Muscle Leg	muscle
31	chr1:79099600-79101000	Weak transcription	GM12878-XiMat	blood
32	chr1:79101000-79101200	ZNF genes & repeats	GM12878-XiMat	blood
33	chr1:79101200-79101400	Enhancers	Primary T cells from cord blood	blood
34	chr1:79101200-79103400	Strong transcription	GM12878-XiMat	blood
35	chr1:79101400-79109800	Weak transcription	Primary T cells from cord blood	blood
36	chr1:79101400-79115400	Weak transcription	Left Ventricle	heart
37	chr1:79102200-79114800	Weak transcription	Adipose Nuclei	Adipose
38	chr1:79102600-79109200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr1:79103000-79111600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:79103000-79112800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr1:79103400-79106800	Genic enhancers	GM12878-XiMat	blood
42	chr1:79103400-79113000	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr1:79104800-79105600	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr1:79105000-79115400	Weak transcription	Psoas Muscle	Psoas
45	chr1:79105400-79107200	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr1:79105600-79107400	Weak transcription	Liver	Liver
47	chr1:79105600-79107400	Weak transcription	Brain Hippocampus Middle	brain
48	chr1:79105600-79115400	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr1:79106200-79106400	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr1:79106400-79110600	Weak transcription	Primary monocytes fromperipheralblood	blood

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