Variant report

Variant	rs4932693
Chromosome Location	chr17:57110327-57110328
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:56735243..56738118-chr17:57106929..57111052,4	MCF-7	breast:
2	chr17:57109264..57111051-chr20:52551167..52554043,2	MCF-7	breast:
3	chr17:57107380..57108951-chr17:57108997..57111149,2	K562	blood:
4	chr17:57095356..57201201-chr17:57905452..57953516,1644	MCF-7	breast:
5	chr17:57110155..57112090-chr17:57931438..57934360,2	MCF-7	breast:
6	chr17:57102868..57113101-chr17:57913364..57925976,42	MCF-7	breast:
7	chr17:57108964..57110507-chr8:126441843..126444197,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000173334	Chromatin interaction
ENSG00000062716	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000201524	Chromatin interaction
ENSG00000202077	Chromatin interaction

Extended variants
information (count: 103 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs10853008	0.81[CEU][hapmap]
rs11079365	0.82[EUR][1000 genomes]
rs11079368	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11654986	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[GIH][hapmap];0.96[LWK][hapmap];0.96[MEX][hapmap];0.95[MKK][hapmap];0.90[TSI][hapmap];1.00[YRI][hapmap]
rs11656413	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];0.95[MEX][hapmap];0.90[MKK][hapmap];0.98[TSI][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11658694	0.80[EUR][1000 genomes]
rs11868348	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12051897	0.82[GIH][hapmap]
rs12232477	0.81[EUR][1000 genomes]
rs12452313	0.88[CEU][hapmap];0.83[CHB][hapmap]
rs12603238	1.00[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.97[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12936058	0.96[CEU][hapmap];0.90[CHB][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12938821	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12940681	0.82[EUR][1000 genomes]
rs12944948	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.96[MEX][hapmap];0.88[TSI][hapmap];0.83[EUR][1000 genomes]
rs12947785	0.96[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.96[MEX][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12948039	0.84[ASN][1000 genomes]
rs12948746	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12952832	0.80[EUR][1000 genomes]
rs1472288	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.96[MEX][hapmap];0.88[TSI][hapmap]
rs1588322	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.96[MEX][hapmap];0.88[TSI][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1871751	0.80[EUR][1000 genomes]
rs1967415	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2055779	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.92[MEX][hapmap];0.90[TSI][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2158966	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2333410	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];0.96[MEX][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34523895	0.81[ASN][1000 genomes]
rs3826353	0.92[ASW][hapmap];1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.91[JPT][hapmap];0.92[MEX][hapmap];0.85[MKK][hapmap];0.98[TSI][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4076229	1.00[CEU][hapmap];0.91[CHB][hapmap];0.82[EUR][1000 genomes]
rs4132925	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.96[MEX][hapmap];0.88[TSI][hapmap];0.82[EUR][1000 genomes]
rs4372750	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.95[MEX][hapmap];0.90[TSI][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4398153	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.96[MEX][hapmap];0.88[TSI][hapmap];0.81[EUR][1000 genomes]
rs4500802	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4597376	0.81[EUR][1000 genomes]
rs4598970	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4636974	1.00[CEU][hapmap];0.91[CHB][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs56297715	0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56360354	0.80[EUR][1000 genomes]
rs57869245	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58092632	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6416932	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];0.81[LWK][hapmap];0.96[MEX][hapmap];0.91[MKK][hapmap];0.98[TSI][hapmap];0.81[YRI][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6416933	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6503882	0.91[CHB][hapmap];0.82[CHD][hapmap]
rs6503883	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.96[MEX][hapmap];0.88[TSI][hapmap];0.82[EUR][1000 genomes]
rs6503887	1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6503889	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6503890	0.96[CEU][hapmap];0.95[CHB][hapmap];0.85[CHD][hapmap];0.81[GIH][hapmap];0.91[JPT][hapmap];0.96[MEX][hapmap];0.90[TSI][hapmap];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6503893	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.95[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6503894	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7207693	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.87[MEX][hapmap];0.90[TSI][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7208505	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.95[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.80[EUR][1000 genomes]
rs7209253	0.80[EUR][1000 genomes]
rs7213269	0.86[YRI][hapmap]
rs7214098	1.00[ASW][hapmap];0.88[CEU][hapmap];1.00[GIH][hapmap];0.96[LWK][hapmap];0.96[MEX][hapmap];0.95[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.80[EUR][1000 genomes]
rs7214335	0.91[CEU][hapmap];0.86[YRI][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7214892	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7215808	1.00[CEU][hapmap];0.85[CHB][hapmap];0.80[EUR][1000 genomes]
rs7216680	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7217845	0.86[YRI][hapmap]
rs7218105	1.00[CEU][hapmap];0.90[CHB][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7223955	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.96[MEX][hapmap];0.88[TSI][hapmap];0.82[EUR][1000 genomes]
rs72628394	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7502947	0.83[MEX][hapmap]
rs7503190	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.95[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8067264	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8069033	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8071280	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[CHD][hapmap];0.83[GIH][hapmap];0.96[MEX][hapmap];0.90[TSI][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs8072182	0.86[YRI][hapmap]
rs8072712	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8076121	1.00[CEU][hapmap];0.91[CHB][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8079774	0.80[EUR][1000 genomes]
rs8081297	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8081967	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.91[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.95[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8082544	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.91[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.95[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8182277	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9303403	0.86[YRI][hapmap]
rs9892062	0.91[CEU][hapmap];0.90[CHB][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9892425	0.86[YRI][hapmap]
rs9892795	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9893351	0.81[ASN][1000 genomes]
rs9894274	1.00[CEU][hapmap];0.91[CHB][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9898916	0.91[CEU][hapmap];0.84[CHB][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9901181	1.00[CEU][hapmap];0.91[CHB][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9902994	1.00[CEU][hapmap];0.95[CHB][hapmap];0.82[EUR][1000 genomes]
rs9907499	0.82[EUR][1000 genomes]
rs9911578	0.84[EUR][1000 genomes]
rs9911583	0.86[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv908643	chr17:56803028-57249010	Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
2	nsv908644	chr17:56803028-57371432	Strong transcription Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	238 gene(s)	inside rSNPs	diseases
3	esv3335958	chr17:56849544-57385398	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
4	nsv908645	chr17:56857281-57208752	Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	150 gene(s)	inside rSNPs	diseases
5	nsv1065063	chr17:56954121-57346694	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS 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 miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
6	nsv1064384	chr17:57049519-57346694	Active TSS ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	219 gene(s)	inside rSNPs	diseases
7	nsv908646	chr17:57061238-57255810	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	206 gene(s)	inside rSNPs	diseases
8	nsv833499	chr17:57070693-57288410	Enhancers Weak transcription Active TSS Flanking Active TSS 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 miRNA	208 gene(s)	inside rSNPs	diseases
9	nsv1066388	chr17:57082013-57339981	Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	209 gene(s)	inside rSNPs	diseases
10	esv2758462	chr17:57082579-57425634	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	213 gene(s)	inside rSNPs	diseases
11	esv2758699	chr17:57082579-57425634	Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	213 gene(s)	inside rSNPs	diseases
12	nsv9574	chr17:57109423-57118739	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	17 gene(s)	inside rSNPs	diseases
13	nsv962452	chr17:57109521-57125839	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	19 gene(s)	inside rSNPs	diseases
14	nsv828068	chr17:57109775-57118266	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	17 gene(s)	inside rSNPs	diseases
15	nsv514855	chr17:57110074-57117978	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
16	esv2421884	chr17:57110327-57118121	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs4932693	TRIM37	cis	Adipose Subcutaneous	GTEx
rs4932693	RAD51C	cis	lymphoblastoid	seeQTL
rs4932693	RAD51C	Cis_1M	lymphoblastoid	RTeQTL
rs4932693	TRIM37	cis	Whole Blood	GTEx
rs4932693	TRIM37	cis	Muscle Skeletal	GTEx

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:57055800-57116200	Weak transcription	Gastric	stomach
2	chr17:57055800-57153600	Weak transcription	Aorta	Aorta
3	chr17:57056400-57120800	Weak transcription	Right Ventricle	heart
4	chr17:57058000-57116600	Weak transcription	Brain Germinal Matrix	brain
5	chr17:57058800-57116400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr17:57060600-57116400	Weak transcription	Esophagus	oesophagus
7	chr17:57063000-57116200	Weak transcription	Spleen	Spleen
8	chr17:57063200-57116400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr17:57064800-57116200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr17:57066000-57151400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr17:57066200-57110600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr17:57070400-57113200	Weak transcription	NHEK	skin
13	chr17:57071000-57110800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr17:57073200-57143800	Weak transcription	Fetal Brain Male	brain
15	chr17:57074600-57120600	Weak transcription	Colon Smooth Muscle	Colon
16	chr17:57079200-57113200	Weak transcription	Fetal Kidney	kidney
17	chr17:57079200-57116200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr17:57079200-57116200	Weak transcription	Ovary	ovary
19	chr17:57079800-57167000	Weak transcription	Small Intestine	intestine
20	chr17:57082400-57120000	Weak transcription	Brain Angular Gyrus	brain
21	chr17:57085600-57116200	Weak transcription	Brain Cingulate Gyrus	brain
22	chr17:57085600-57134600	Weak transcription	Pancreas	Pancrea
23	chr17:57086400-57120800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr17:57087800-57116200	Weak transcription	Brain Substantia Nigra	brain
25	chr17:57088000-57112600	Weak transcription	HSMMtube	muscle
26	chr17:57089600-57113000	Weak transcription	HUVEC	blood vessel
27	chr17:57089600-57115600	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr17:57089800-57116200	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr17:57089800-57116200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr17:57089800-57116200	Weak transcription	Lung	lung
31	chr17:57090800-57117600	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr17:57093400-57110800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr17:57094600-57110800	Weak transcription	Fetal Intestine Small	intestine
34	chr17:57094800-57113400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr17:57094800-57113400	Weak transcription	Fetal Muscle Trunk	muscle
36	chr17:57102200-57120800	Weak transcription	Colonic Mucosa	Colon
37	chr17:57103200-57120600	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr17:57103600-57111400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr17:57104000-57111400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr17:57104200-57159600	Weak transcription	Psoas Muscle	Psoas
41	chr17:57104400-57114200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr17:57104600-57110800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr17:57104600-57112400	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr17:57105200-57113600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr17:57105200-57113800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr17:57105200-57139600	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr17:57105400-57113400	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr17:57105400-57117400	Weak transcription	Rectal Smooth Muscle	rectum
49	chr17:57105600-57113200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr17:57105600-57113200	Weak transcription	Brain Anterior Caudate	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links