Variant report

Variant	rs4468641
Chromosome Location	chr16:31096876-31096877
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:31096333..31099820-chr16:31152202..31155374,3	MCF-7	breast:
2	chr16:30993142..30995962-chr16:31096037..31098055,3	K562	blood:
3	chr16:31096486..31099181-chr16:31109176..31111486,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000178226	Chromatin interaction

Extended variants
information (count: 152 )
Associated
traits (count: 20 )

rSNPs within LD-proxies of this variant (count:139)

rs_ID	r²[population]
rs1046276	0.88[GIH][hapmap];1.00[JPT][hapmap]
rs1060506	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.95[ASN][1000 genomes]
rs10782001	0.89[JPT][hapmap]
rs10782002	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs10871454	1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs11076	0.88[JPT][hapmap]
rs1108431	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11150599	0.88[JPT][hapmap]
rs11150600	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs11150601	0.83[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap]
rs11150604	1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11640534	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs11640767	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11640957	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11640961	0.89[JPT][hapmap]
rs11642003	0.82[ASN][1000 genomes]
rs11642192	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11647284	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11647442	0.95[ASN][1000 genomes]
rs11649653	1.00[JPT][hapmap]
rs11862744	0.92[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.91[MKK][hapmap];0.88[TSI][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11864806	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11864839	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11865038	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.82[YRI][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11865499	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.95[ASN][1000 genomes]
rs12102776	0.82[CHB][hapmap];0.92[CHD][hapmap]
rs12445568	0.83[CEU][hapmap];0.88[GIH][hapmap];0.86[MEX][hapmap];0.81[TSI][hapmap]
rs12445650	0.92[CEU][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12448321	0.89[ASN][1000 genomes]
rs12597511	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs12716981	0.95[ASN][1000 genomes]
rs12716982	0.95[ASN][1000 genomes]
rs12924903	0.88[GIH][hapmap];1.00[JPT][hapmap]
rs12928852	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs12930545	0.88[GIH][hapmap]
rs12931046	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs12934418	0.89[ASN][1000 genomes]
rs13708	0.83[CEU][hapmap];0.89[JPT][hapmap]
rs14235	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1458201	0.89[JPT][hapmap]
rs1458202	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs1549293	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs17839567	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17839568	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1870293	0.83[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap]
rs1978485	0.95[ASN][1000 genomes]
rs1978487	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2032915	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2054213	0.83[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap]
rs2288004	0.89[ASN][1000 genomes]
rs2303222	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2303223	1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2305880	0.83[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap]
rs2305884	0.83[CEU][hapmap];0.85[GIH][hapmap];0.89[JPT][hapmap]
rs2359612	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2855475	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs28725459	0.91[ASN][1000 genomes]
rs28814987	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2884738	0.95[ASN][1000 genomes]
rs34649473	0.85[ASN][1000 genomes]
rs35351013	0.93[ASN][1000 genomes]
rs35468353	0.92[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.91[MKK][hapmap];0.88[TSI][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35675346	1.00[JPT][hapmap]
rs35713203	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35961830	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3751855	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3813020	0.88[GIH][hapmap]
rs4527034	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs4889525	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs4889526	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4889530	0.87[ASN][1000 genomes]
rs4889599	0.83[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap]
rs4889603	0.89[JPT][hapmap]
rs4889604	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs4889606	0.89[JPT][hapmap]
rs4889609	0.92[CEU][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.81[MKK][hapmap];0.86[TSI][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4889619	0.84[ASN][1000 genomes]
rs4889620	0.95[ASN][1000 genomes]
rs4889623	0.82[CHB][hapmap]
rs55766044	0.95[ASN][1000 genomes]
rs55979739	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56284083	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56314408	0.95[ASN][1000 genomes]
rs56813533	0.93[ASN][1000 genomes]
rs57434408	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57576577	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs58726213	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59061704	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs59735493	0.95[ASN][1000 genomes]
rs60996860	0.91[ASN][1000 genomes]
rs61162043	1.00[ASN][1000 genomes]
rs61320757	0.95[ASN][1000 genomes]
rs6565217	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.94[MKK][hapmap];0.95[TSI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6950	0.83[CEU][hapmap];0.89[JPT][hapmap]
rs7184567	0.92[CEU][hapmap]
rs7187995	0.93[ASN][1000 genomes]
rs7190802	0.82[CHB][hapmap]
rs7196161	1.00[ASN][1000 genomes]
rs7196726	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7197717	0.81[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7199949	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7200879	1.00[JPT][hapmap]
rs7203999	0.83[CEU][hapmap];0.82[CHD][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap];0.91[MEX][hapmap];0.86[TSI][hapmap]
rs7204459	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs7206511	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs7294	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.90[TSI][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs729482	0.83[CEU][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap]
rs732172	0.92[CEU][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs732173	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73530203	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs749670	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs749671	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs749767	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs7500176	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs750952	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.90[TSI][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8046707	0.89[JPT][hapmap]
rs8047803	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8050588	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs8050894	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs8056842	0.92[CEU][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8060857	0.88[GIH][hapmap];0.89[JPT][hapmap]
rs8061047	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8062719	0.83[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap]
rs881929	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs889548	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs889555	1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs897986	0.83[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap]
rs9673641	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9923231	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9925964	0.95[ASN][1000 genomes]
rs9926533	0.82[CHD][hapmap];0.89[JPT][hapmap]
rs9929899	0.86[ASN][1000 genomes]
rs9933843	0.88[JPT][hapmap]
rs9934438	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9936329	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs9938550	0.83[CEU][hapmap];0.88[GIH][hapmap]
rs9939417	1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs9939558	0.89[ASN][1000 genomes]
rs9972727	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
3	nsv905729	chr16:30642867-31247924	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
4	nsv431451	chr16:30682399-31340999	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
5	nsv905734	chr16:30877544-31191482	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
6	nsv905735	chr16:30890538-31247924	Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	264 gene(s)	inside rSNPs	diseases
7	nsv457483	chr16:30903679-31191482	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
8	nsv571820	chr16:30903679-31191482	Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
9	esv1797877	chr16:30948643-31188432	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
10	nsv833193	chr16:30960796-31133604	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
11	nsv905740	chr16:31066249-31232437	Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
12	nsv905741	chr16:31066249-31247924	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
13	esv993244	chr16:31091981-31101565	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:20)

SNP	Gene	Cis/trans	Tissue	Source
rs4468641	MYST1	cis	lymphoblastoid	seeQTL
rs4468641	HSD3B7	cis	Esophagus Mucosa	GTEx
rs4468641	KAT8	cis	Skin Sun Exposed Lower leg	GTEx
rs4468641	VKORC1	cis	cerebellum	SCAN
rs4468641	ZNF785	cis	lymphoblastoid	seeQTL
rs4468641	RP11-196G11.2	cis	Muscle Skeletal	GTEx
rs4468641	TAOK2	cis	parietal	SCAN
rs4468641	MYST1	cis	parietal	SCAN
rs4468641	HSD3B7	cis	Muscle Skeletal	GTEx
rs4468641	STX1B	cis	Thyroid	GTEx
rs4468641	ZNF747	cis	parietal	SCAN
rs4468641	YPEL3	cis	parietal	SCAN
rs4468641	RP11-196G11.2	cis	lung	GTEx
rs4468641	STX4	Cis_1M	lymphoblastoid	RTeQTL
rs4468641	NCRNA00095	cis	cerebellum	SCAN
rs4468641	MYST1	cis	cerebellum	SCAN
rs4468641	ZNF48	cis	cerebellum	SCAN
rs4468641	RABEP2	cis	cerebellum	SCAN
rs4468641	RP11-196G11.2	cis	Esophagus Muscularis	GTEx
rs4468641	MYST1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31086400-31104400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr16:31086600-31104200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr16:31086600-31105200	Weak transcription	Right Atrium	heart
4	chr16:31087200-31097000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr16:31087200-31102000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr16:31087200-31103800	Strong transcription	NHLF	lung
7	chr16:31087200-31104200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr16:31087400-31099200	Strong transcription	HepG2	liver
9	chr16:31087400-31101800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr16:31087400-31102800	Strong transcription	Thymus	Thymus
11	chr16:31087400-31103000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr16:31087400-31104400	Strong transcription	Primary T cells from cord blood	blood
13	chr16:31087400-31104400	Strong transcription	Fetal Intestine Small	intestine
14	chr16:31087600-31097000	Strong transcription	Sigmoid Colon	Sigmoid Colon
15	chr16:31087600-31098400	Strong transcription	Fetal Thymus	thymus
16	chr16:31087600-31100200	Weak transcription	Hela-S3	cervix
17	chr16:31087600-31103000	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chr16:31087600-31103000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr16:31087800-31101800	Strong transcription	Liver	Liver
20	chr16:31087800-31101800	Strong transcription	Placenta Amnion	Placenta Amnion
21	chr16:31087800-31102200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr16:31087800-31102800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr16:31087800-31103000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr16:31087800-31104000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr16:31088000-31099400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr16:31090000-31105200	Weak transcription	Fetal Kidney	kidney
27	chr16:31090400-31104200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr16:31090600-31099000	Strong transcription	Esophagus	oesophagus
29	chr16:31090800-31101200	Weak transcription	HMEC	breast
30	chr16:31090800-31101800	Weak transcription	A549	lung
31	chr16:31090800-31102000	Weak transcription	HUVEC	blood vessel
32	chr16:31090800-31102200	Weak transcription	Primary B cells from cord blood	blood
33	chr16:31091000-31104000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr16:31091200-31097000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr16:31091200-31099200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr16:31091400-31099000	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr16:31091400-31102800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
38	chr16:31091800-31100800	Strong transcription	Fetal Intestine Large	intestine
39	chr16:31092000-31104600	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr16:31092600-31097800	Weak transcription	Rectal Smooth Muscle	rectum
41	chr16:31092600-31101800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr16:31092600-31101800	Weak transcription	NHDF-Ad	bronchial
43	chr16:31092800-31100400	Weak transcription	Aorta	Aorta
44	chr16:31092800-31101800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr16:31093000-31101800	Weak transcription	Primary hematopoietic stem cells	blood
46	chr16:31093000-31104600	Weak transcription	Small Intestine	intestine
47	chr16:31093400-31101800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr16:31093400-31103800	Weak transcription	Fetal Brain Male	brain
49	chr16:31093600-31099000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr16:31093600-31102800	Strong transcription	Lung	lung

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