Variant report

Variant	rs5744533
Chromosome Location	chr5:74806104-74806105
allele	C/T
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	ZNF263	chr5:74805797-74808068	HEK293-T-REx	kidney:	n/a	chr5:74807566-74807575 chr5:74807116-74807137 chr5:74807154-74807175
2	MAX	chr5:74805816-74808456	NB4	blood:	n/a	n/a
3	RFX5	chr5:74806082-74806223	K562	blood:	n/a	n/a
4	TBL1XR1	chr5:74805994-74806409	GM12878	blood:	n/a	n/a
5	POLR2A	chr5:74805908-74806130	MCF10A-Er-Src	breast:	n/a	n/a
6	TBP	chr5:74805929-74806644	Hela-S3	cervix:	n/a	n/a
7	USF1	chr5:74805756-74806110	K562	blood:	n/a	n/a
8	MAZ	chr5:74805364-74806376	GM12878	blood:	n/a	n/a
9	RFX5	chr5:74805811-74806713	Hela-S3	cervix:	n/a	chr5:74805942-74805957
10	CHD1	chr5:74805200-74808587	GM12878	blood:	n/a	chr5:74806845-74806855
11	MAX	chr5:74805812-74806115	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr5:74805819-74806104	K562	blood:	n/a	chr5:74805908-74805919
13	MYC	chr5:74805548-74807020	NB4	blood:	n/a	n/a
14	USF2	chr5:74805820-74806529	Hela-S3	cervix:	n/a	n/a
15	MXI1	chr5:74805703-74808471	GM12878	blood:	n/a	n/a
16	TBP	chr5:74805510-74806208	GM12878	blood:	n/a	n/a
17	USF2	chr5:74805773-74806104	GM12878	blood:	n/a	n/a
18	MYC	chr5:74805763-74806133	K562	blood:	n/a	n/a
19	MYC	chr5:74805921-74806443	MCF10A-Er-Src	breast:	n/a	n/a
20	CHD1	chr5:74806090-74806207	H1-hESC	embryonic stem cell:	n/a	n/a
21	MAX	chr5:74805546-74806109	GM12878	blood:	n/a	n/a
22	MXI1	chr5:74805813-74806925	Hela-S3	cervix:	n/a	n/a
23	E2F4	chr5:74805810-74806129	MCF10A-Er-Src	breast:	n/a	n/a
24	BHLHE40	chr5:74805827-74808119	K562	blood:	n/a	n/a
25	CEBPB	chr5:74805510-74806822	Hela-S3	cervix:	n/a	chr5:74805908-74805919
26	BHLHE40	chr5:74805785-74806457	GM12878	blood:	n/a	n/a
27	EP300	chr5:74805901-74806278	GM12878	blood:	n/a	n/a
28	HCFC1	chr5:74805817-74808663	Hela-S3	cervix:	n/a	n/a
29	RCOR1	chr5:74805740-74806112	K562	blood:	n/a	n/a
30	UBTF	chr5:74805863-74808381	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:74806025..74808781-chr5:74906137..74908952,2	MCF-7	breast:
2	chr5:74804574..74807080-chr5:74963425..74964973,2	K562	blood:
3	chr5:74630713..74633733-chr5:74805590..74808087,5	MCF-7	breast:

Variant related genes	Relation type
POLK	TF binding region
ENSG00000113161	Chromatin interaction
ENSG00000247372	Chromatin interaction
ENSG00000189045	Chromatin interaction

Extended variants
information (count: 89 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs10038723	0.83[AFR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10043621	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10044053	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10060260	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10067641	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10075139	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10434644	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10462517	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10474433	0.87[CHD][hapmap];0.81[JPT][hapmap]
rs10474436	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1051795	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10942739	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11957913	0.84[ASN][1000 genomes]
rs12234032	0.80[AFR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13354407	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1427924	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17739580	0.94[CEU][hapmap];0.85[CHB][hapmap];0.90[JPT][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1863934	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1863935	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1995267	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2287711	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs253392	0.81[CHB][hapmap];0.83[JPT][hapmap]
rs253393	0.95[CHB][hapmap];0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs253407	0.95[CHB][hapmap];0.93[CHD][hapmap];0.80[GIH][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs253409	0.95[CHB][hapmap];0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs28609217	0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2878519	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2878520	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3213801	0.94[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34340	0.82[ASN][1000 genomes]
rs3761742	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.92[CHD][hapmap];0.98[GIH][hapmap];0.94[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3761743	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[TSI][hapmap];0.89[ASN][1000 genomes]
rs3846665	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3846666	0.89[ASN][1000 genomes]
rs3931914	0.95[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap]
rs4045166	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[TSI][hapmap];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4385188	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4440336	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4703670	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4703674	0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4704214	0.80[AFR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4704224	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4704228	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57149337	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57312935	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs5744555	1.00[CEU][hapmap];0.95[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs5744575	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs5744595	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs5744598	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs5744601	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs5744621	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs5744663	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs5744703	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs59506842	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61430233	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6453134	0.90[ASN][1000 genomes]
rs67969809	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6861279	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.94[TSI][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6863398	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6872314	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6874781	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6886841	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6891949	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs698912	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.94[TSI][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73120833	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7356637	0.85[CEU][hapmap];0.95[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.84[TSI][hapmap];0.84[ASN][1000 genomes]
rs7445415	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs767676	0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7700468	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[TSI][hapmap];0.89[ASN][1000 genomes]
rs7701925	1.00[CEU][hapmap];0.85[CHB][hapmap];0.90[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.87[TSI][hapmap]
rs7706857	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7709282	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[TSI][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7717505	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7723531	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7737959	0.89[ASN][1000 genomes]
rs924452	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9293656	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9332464	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9885386	0.80[AFR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882193	chr5:74656175-74917862	ZNF genes & repeats Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv882194	chr5:74656175-74946455	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv882195	chr5:74678937-74896798	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv882196	chr5:74678937-74917862	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv882197	chr5:74692776-74946455	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	nsv882198	chr5:74736065-74896798	Strong transcription Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv882199	chr5:74757758-74946455	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
8	nsv1027368	chr5:74759999-75663712	Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
9	nsv882200	chr5:74781439-74830808	ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
10	nsv882201	chr5:74787310-74890618	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs5744533	GCNT4	cis	cerebellum	SCAN
rs5744533	HMGCR	cis	cerebellum	SCAN

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74778600-74806400	Weak transcription	Gastric	stomach
2	chr5:74785800-74806400	Weak transcription	Spleen	Spleen
3	chr5:74794800-74806200	Weak transcription	Lung	lung
4	chr5:74795000-74806400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:74803000-74806600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr5:74804000-74809000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr5:74804200-74806600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr5:74804600-74808600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr5:74804600-74809800	Active TSS	NHLF	lung
10	chr5:74804800-74806400	Weak transcription	Small Intestine	intestine
11	chr5:74804800-74809600	Active TSS	K562	blood
12	chr5:74805000-74808600	Active TSS	Fetal Stomach	stomach
13	chr5:74805000-74810200	Active TSS	GM12878-XiMat	blood
14	chr5:74805200-74806200	Flanking Active TSS	Brain Anterior Caudate	brain
15	chr5:74805200-74806200	Enhancers	Placenta Amnion	Placenta Amnion
16	chr5:74805200-74806200	Flanking Active TSS	Thymus	Thymus
17	chr5:74805200-74806200	Flanking Active TSS	Dnd41	blood
18	chr5:74805200-74806400	Flanking Active TSS	Primary hematopoietic stem cells	blood
19	chr5:74805200-74806400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr5:74805200-74806400	Flanking Active TSS	HUVEC	blood vessel
21	chr5:74805200-74806600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr5:74805200-74806800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
23	chr5:74805200-74806800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr5:74805200-74806800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr5:74805200-74808200	Active TSS	Cortex derived primary cultured neurospheres	brain
26	chr5:74805200-74808400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr5:74805200-74808400	Active TSS	Brain Cingulate Gyrus	brain
28	chr5:74805200-74808600	Active TSS	HSMMtube	muscle
29	chr5:74805200-74809000	Active TSS	ES-I3 Cell Line	embryonic stem cell
30	chr5:74805200-74809000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr5:74805200-74809000	Active TSS	NHDF-Ad	bronchial
32	chr5:74805200-74809400	Active TSS	Right Atrium	heart
33	chr5:74805400-74806200	Flanking Active TSS	Primary T cells from cord blood	blood
34	chr5:74805400-74806200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr5:74805400-74806200	Flanking Active TSS	Liver	Liver
36	chr5:74805400-74806200	Flanking Active TSS	Brain Hippocampus Middle	brain
37	chr5:74805400-74806200	Flanking Active TSS	Duodenum Mucosa	Duodenum
38	chr5:74805400-74806200	Flanking Active TSS	Fetal Brain Male	brain
39	chr5:74805400-74806400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
40	chr5:74805400-74806400	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
41	chr5:74805400-74806600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
42	chr5:74805400-74806600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
43	chr5:74805400-74806800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
44	chr5:74805400-74806800	Flanking Active TSS	Adipose Nuclei	Adipose
45	chr5:74805400-74808200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr5:74805400-74808400	Active TSS	Skeletal Muscle Male	skeletal muscle
47	chr5:74805400-74808600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr5:74805400-74808600	Active TSS	Fetal Intestine Large	intestine
49	chr5:74805400-74808600	Active TSS	Right Ventricle	heart
50	chr5:74805400-74808600	Active TSS	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links