Variant report

Variant	rs178820
Chromosome Location	chr17:16090785-16090786
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:16089835..16092985-chr17:16117505..16120902,3	K562	blood:
2	chr17:16089561..16091475-chr17:16117842..16119372,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000108474	Chromatin interaction
ENSG00000141027	Chromatin interaction

Extended variants
information (count: 144 )
Associated
traits (count: 18 )

rSNPs within LD-proxies of this variant (count:126)

rs_ID	r²[population]
rs1029809	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs1065822	1.00[CEU][hapmap]
rs1075901	0.81[CEU][hapmap]
rs1079533	1.00[ASW][hapmap];1.00[CEU][hapmap];0.80[LWK][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs10852833	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11078332	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1125156	1.00[CEU][hapmap];1.00[YRI][hapmap];0.88[AMR][1000 genomes]
rs1126148	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1160109	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11650427	0.85[CEU][hapmap];1.00[CHB][hapmap];0.82[GIH][hapmap];0.83[TSI][hapmap]
rs11650678	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11651290	1.00[ASW][hapmap];1.00[CEU][hapmap];0.80[LWK][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs11651578	0.84[YRI][hapmap]
rs11655773	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11656811	0.83[LWK][hapmap];0.92[YRI][hapmap]
rs11657160	0.85[CEU][hapmap]
rs11869450	0.82[CEU][hapmap]
rs11871961	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11872032	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs12150017	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12449895	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12936233	0.81[CEU][hapmap];1.00[CHB][hapmap];0.85[GIH][hapmap];0.83[TSI][hapmap]
rs12937088	0.81[ASN][1000 genomes]
rs12938397	0.90[MEX][hapmap]
rs12939418	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12945855	0.81[CEU][hapmap];1.00[CHB][hapmap];0.83[TSI][hapmap]
rs12947205	0.82[AMR][1000 genomes]
rs178657	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs178658	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs178659	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs178662	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs178789	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.97[MKK][hapmap];0.98[TSI][hapmap];0.92[YRI][hapmap];0.93[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs178790	0.83[AMR][1000 genomes]
rs178791	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes]
rs178792	0.88[AMR][1000 genomes]
rs178793	0.87[AMR][1000 genomes]
rs178794	0.92[AMR][1000 genomes]
rs178795	0.87[AMR][1000 genomes]
rs178796	0.88[AMR][1000 genomes]
rs178797	1.00[ASW][hapmap];0.96[CEU][hapmap];0.85[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.94[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs178798	1.00[CEU][hapmap];0.85[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs178799	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs178800	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs178801	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs178802	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs178804	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs178805	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs178806	0.84[EUR][1000 genomes]
rs178808	0.85[EUR][1000 genomes]
rs178809	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs178810	0.81[EUR][1000 genomes]
rs178814	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs178815	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs178816	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs178817	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs178821	0.82[EUR][1000 genomes]
rs178822	0.85[CEU][hapmap];0.83[EUR][1000 genomes]
rs178824	0.83[EUR][1000 genomes]
rs178826	0.82[EUR][1000 genomes]
rs178827	0.82[EUR][1000 genomes]
rs178828	0.83[EUR][1000 genomes]
rs178829	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs178830	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs178831	0.80[EUR][1000 genomes]
rs178833	0.83[EUR][1000 genomes]
rs178834	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs178835	0.82[EUR][1000 genomes]
rs178836	0.82[EUR][1000 genomes]
rs178837	0.91[ASW][hapmap];0.92[CEU][hapmap];0.83[GIH][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs178838	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs178839	0.85[CEU][hapmap];0.83[EUR][1000 genomes]
rs1972503	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1989856	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2041460	1.00[ASW][hapmap];0.96[CEU][hapmap];0.95[MEX][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap]
rs2051736	0.86[AMR][1000 genomes]
rs2078050	0.85[CEU][hapmap]
rs21180	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2157990	0.82[CEU][hapmap]
rs2157991	0.85[CEU][hapmap]
rs2157992	1.00[CEU][hapmap];0.82[MEX][hapmap];0.93[TSI][hapmap]
rs2301652	0.81[CEU][hapmap];0.84[TSI][hapmap]
rs2302415	0.82[CEU][hapmap]
rs2324141	0.85[CEU][hapmap]
rs2324142	0.85[CEU][hapmap]
rs34243080	0.84[AMR][1000 genomes]
rs34351630	0.82[AMR][1000 genomes]
rs35160872	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35799415	0.87[AMR][1000 genomes]
rs36001065	0.82[AMR][1000 genomes]
rs3760298	0.96[CEU][hapmap];0.86[MEX][hapmap];0.93[TSI][hapmap]
rs3785625	0.84[YRI][hapmap]
rs3785628	0.85[CEU][hapmap]
rs3785631	1.00[CEU][hapmap];0.86[MEX][hapmap];0.93[TSI][hapmap]
rs3785633	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs3815039	1.00[ASW][hapmap];1.00[CEU][hapmap];0.80[LWK][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs3826360	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs4435297	0.81[CEU][hapmap]
rs4791661	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4791662	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4792715	0.82[CEU][hapmap]
rs4792717	0.85[CEU][hapmap]
rs4792718	0.82[CEU][hapmap]
rs4792721	0.83[TSI][hapmap]
rs545738	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6416868	0.85[CEU][hapmap]
rs6502482	0.85[CEU][hapmap]
rs6502488	0.85[CEU][hapmap]
rs7207889	0.83[EUR][1000 genomes]
rs7214695	0.85[CEU][hapmap]
rs7216834	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7223346	0.85[CEU][hapmap]
rs72833498	0.88[AMR][1000 genomes]
rs758853	1.00[ASW][hapmap];0.96[CEU][hapmap];0.95[MEX][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap]
rs8076864	1.00[ASW][hapmap];1.00[CEU][hapmap];0.80[LWK][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs8079969	0.85[CEU][hapmap]
rs8080706	0.81[AMR][1000 genomes]
rs9890012	1.00[CEU][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap]
rs9891379	1.00[CEU][hapmap];0.80[GIH][hapmap];0.82[MEX][hapmap];0.95[TSI][hapmap]
rs9891646	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9891938	0.82[CEU][hapmap]
rs9899002	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs9902141	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9903464	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9907313	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9908031	1.00[CEU][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap]
rs9909697	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934185	chr17:15552960-16551197	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	190 gene(s)	inside rSNPs	diseases
2	esv3330182	chr17:15652014-16569534	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
3	esv3446844	chr17:15654843-16572246	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
4	nsv1063459	chr17:15804228-16543593	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Strong transcription 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 miRNA target site	164 gene(s)	inside rSNPs	diseases
5	nsv1062220	chr17:15869557-16093156	Genic enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
6	nsv1064878	chr17:15869557-16097241	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
7	nsv1055173	chr17:15875935-16097241	Flanking Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
8	nsv833377	chr17:15912013-16104515	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
9	nsv522169	chr17:15923709-16147821	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
10	nsv907711	chr17:15978663-16092902	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv907712	chr17:15981874-16103426	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	nsv907713	chr17:15981874-16127206	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
13	nsv907714	chr17:15990013-16110384	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
14	nsv907715	chr17:16019978-16206540	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	44 gene(s)	inside rSNPs	diseases
15	nsv907716	chr17:16068422-16116835	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
16	nsv907717	chr17:16076898-16239832	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	44 gene(s)	inside rSNPs	diseases
17	nsv907718	chr17:16080849-16143709	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
18	nsv960423	chr17:16089865-16112673	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:18)

SNP	Gene	Cis/trans	Tissue	Source
rs178820	ADORA2B	cis	Nerve Tibial	GTEx
rs178820	LOC125150	cis	normal skin	skin_eQTL
rs178820	TTC19	cis	lymphoblastoid	seeQTL
rs178820	CENPV	cis	lymphoblastoid	seeQTL
rs178820	CENPV	cis	Artery Tibial	GTEx
rs178820	LOC125150	cis	lesional skin	skin_eQTL
rs178820	ADORA2B	cis	Adipose Subcutaneous	GTEx
rs178820	NCOR1	Cis_1M	lymphoblastoid	RTeQTL
rs178820	ADORA2B	cis	Muscle Skeletal	GTEx
rs178820	CENPV	cis	parietal	SCAN
rs178820	TTC19	Cis_1M	lymphoblastoid	RTeQTL
rs178820	NCOR1	cis	parietal	SCAN
rs178820	ADORA2B	cis	Esophagus Muscularis	GTEx
rs178820	ZSWIM7	cis	Muscle Skeletal	GTEx
rs178820	ZSWIM7	Cis_1M	lymphoblastoid	RTeQTL
rs178820	ADORA2B	cis	Thyroid	GTEx
rs178820	LOC125150	cis	uninvolved skin	skin_eQTL
rs178820	ADORA2B	cis	Artery Tibial	GTEx

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16035800-16103400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr17:16039200-16096800	Weak transcription	K562	blood
3	chr17:16042000-16094200	Weak transcription	Psoas Muscle	Psoas
4	chr17:16049200-16093200	Weak transcription	Aorta	Aorta
5	chr17:16049200-16103400	Weak transcription	Spleen	Spleen
6	chr17:16049200-16108600	Weak transcription	Esophagus	oesophagus
7	chr17:16052200-16100400	Weak transcription	Ovary	ovary
8	chr17:16055200-16102600	Weak transcription	Brain Angular Gyrus	brain
9	chr17:16055400-16094000	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr17:16055400-16104000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr17:16055800-16102000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr17:16059400-16094200	Weak transcription	Rectal Smooth Muscle	rectum
13	chr17:16059400-16102400	Weak transcription	Small Intestine	intestine
14	chr17:16059400-16102400	Weak transcription	NHLF	lung
15	chr17:16059400-16102800	Weak transcription	Pancreas	Pancrea
16	chr17:16059800-16093200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr17:16062200-16093200	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr17:16064000-16101000	Weak transcription	Lung	lung
19	chr17:16064600-16106000	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr17:16067400-16094000	Weak transcription	Brain Anterior Caudate	brain
21	chr17:16069000-16093800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr17:16075400-16092800	Weak transcription	NHEK	skin
23	chr17:16075400-16093400	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr17:16075400-16094000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr17:16075400-16096800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr17:16075600-16093400	Weak transcription	Brain Substantia Nigra	brain
27	chr17:16082000-16094000	Weak transcription	Fetal Heart	heart
28	chr17:16083200-16091200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr17:16083600-16097000	Weak transcription	Brain Hippocampus Middle	brain
30	chr17:16084000-16094200	Weak transcription	Gastric	stomach
31	chr17:16084200-16092000	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr17:16084800-16098000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr17:16086000-16098000	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr17:16086400-16090800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
35	chr17:16086600-16101600	Strong transcription	Primary monocytes fromperipheralblood	blood
36	chr17:16086600-16102400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr17:16086800-16091200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr17:16086800-16102200	Weak transcription	Stomach Mucosa	stomach
39	chr17:16087000-16090800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr17:16087000-16091400	Strong transcription	Primary hematopoietic stem cells	blood
41	chr17:16087200-16090800	Strong transcription	Primary B cells from cord blood	blood
42	chr17:16087200-16091000	Strong transcription	Primary B cells from peripheral blood	blood
43	chr17:16087200-16091400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
44	chr17:16087200-16097600	Strong transcription	Primary T helper cells fromperipheralblood	blood
45	chr17:16087200-16098000	Strong transcription	Fetal Intestine Large	intestine
46	chr17:16087200-16108200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr17:16087400-16091000	Strong transcription	HUES48 Cell Line	embryonic stem cell
48	chr17:16087400-16097400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr17:16087600-16090800	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr17:16087800-16091600	Strong transcription	Fetal Thymus	thymus

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