Variant report

Variant	rs1045599
Chromosome Location	chr17:15879910-15879911
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:15861172..15863617-chr17:15879746..15882543,3	K562	blood:
2	chr17:15874041..15877357-chr17:15878347..15881339,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM7-2	chr17:15879883-15880406	NONHSAT145880

Variant related genes	Relation type
ENSG00000170425	Chromatin interaction

Extended variants
information (count: 97 )
Associated
traits (count: 20 )

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

rs_ID	r²[population]
rs1075901	0.81[CEU][hapmap];0.87[CHD][hapmap];0.82[MEX][hapmap];0.89[TSI][hapmap];0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11078320	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11078327	0.88[EUR][1000 genomes]
rs11078331	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11652025	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11654	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11655456	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11656046	0.89[EUR][1000 genomes]
rs11657160	0.85[CEU][hapmap];0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11869450	0.89[CEU][hapmap];0.92[CHB][hapmap];0.87[CHD][hapmap];0.95[GIH][hapmap];0.81[JPT][hapmap];0.87[MEX][hapmap];0.93[TSI][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11869563	0.89[CEU][hapmap];0.92[CHB][hapmap];0.97[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12945463	0.85[EUR][1000 genomes]
rs178838	0.84[CEU][hapmap]
rs178839	0.85[CEU][hapmap]
rs1860643	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1860644	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1860645	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2015353	1.00[MEX][hapmap];0.91[TSI][hapmap]
rs2078050	0.85[CEU][hapmap];0.84[CHD][hapmap];0.83[MEX][hapmap];0.86[TSI][hapmap];0.86[EUR][1000 genomes]
rs2109632	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2157990	0.81[CEU][hapmap];0.80[CHD][hapmap];0.82[MEX][hapmap];0.86[TSI][hapmap];0.89[EUR][1000 genomes]
rs2157991	0.85[CEU][hapmap];0.84[CHD][hapmap];0.83[MEX][hapmap];0.91[TSI][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2159643	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2285582	0.88[EUR][1000 genomes]
rs2285583	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2286795	1.00[CEU][hapmap];0.92[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2286796	1.00[CEU][hapmap];0.92[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2302415	0.89[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];0.87[MEX][hapmap];0.93[TSI][hapmap]
rs2324082	0.82[CEU][hapmap]
rs2324141	0.85[CEU][hapmap];0.81[CHD][hapmap];0.83[MEX][hapmap];0.91[TSI][hapmap]
rs2324142	0.85[CEU][hapmap];0.81[CHD][hapmap];0.87[MEX][hapmap];0.89[TSI][hapmap]
rs2535614	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2779207	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2779208	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2779210	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2779211	0.80[EUR][1000 genomes]
rs2779212	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];0.94[JPT][hapmap];0.97[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35168566	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3760297	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3785628	0.85[CEU][hapmap];0.84[CHD][hapmap];0.87[MEX][hapmap];0.89[TSI][hapmap];0.88[EUR][1000 genomes]
rs3785629	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3785632	0.81[CEU][hapmap]
rs4435297	0.81[CEU][hapmap];0.84[CHD][hapmap];0.83[MEX][hapmap];0.88[TSI][hapmap];0.86[EUR][1000 genomes]
rs4792707	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4792708	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4792709	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4792712	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4792713	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4792715	0.89[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];0.87[MEX][hapmap];0.93[TSI][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4792716	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4792717	0.85[CEU][hapmap];0.89[EUR][1000 genomes]
rs4792718	0.89[CEU][hapmap];0.85[CHB][hapmap];0.90[CHD][hapmap];0.94[JPT][hapmap];0.83[MEX][hapmap];0.93[TSI][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6416868	0.88[CEU][hapmap];0.92[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6502479	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6502480	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6502482	0.85[CEU][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6502488	0.85[CEU][hapmap];0.87[CHD][hapmap];0.87[MEX][hapmap];0.89[TSI][hapmap];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7209094	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7210655	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7214695	0.85[CEU][hapmap]
rs7216949	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7223346	0.85[CEU][hapmap];0.84[CHD][hapmap];0.83[MEX][hapmap];0.91[TSI][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs8064702	0.87[EUR][1000 genomes]
rs8065190	0.89[EUR][1000 genomes]
rs8066902	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8070859	0.89[CEU][hapmap];0.92[CHB][hapmap];0.97[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8075345	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8076669	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs8079969	0.85[CEU][hapmap];0.81[CHD][hapmap];0.83[MEX][hapmap];0.91[TSI][hapmap]
rs8080221	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8081406	0.88[EUR][1000 genomes]
rs8081667	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9652827	0.89[EUR][1000 genomes]
rs9709250	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9891938	1.00[ASW][hapmap];0.88[CEU][hapmap];0.83[CHB][hapmap];0.96[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];0.92[MKK][hapmap];0.93[TSI][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9896441	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9897542	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9899995	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9916868	0.89[EUR][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	nsv1062951	chr17:15561070-15890644	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1066023	chr17:15607267-16053512	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	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
5	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
6	nsv1061222	chr17:15672934-15999778	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
7	nsv907706	chr17:15731923-16056442	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
8	nsv1067555	chr17:15804228-16001117	Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	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
10	nsv907707	chr17:15846535-15950751	Strong transcription Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
11	nsv907709	chr17:15851196-15937487	Weak transcription Genic enhancers Strong transcription Active TSS 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	28 gene(s)	inside rSNPs	diseases
12	nsv907708	chr17:15851196-15950751	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats 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	30 gene(s)	inside rSNPs	diseases
13	nsv1057493	chr17:15852125-15930718	Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
14	nsv543215	chr17:15852125-15930718	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
15	nsv907710	chr17:15854257-15950751	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	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
17	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
18	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

mRNA abundance (count:20)

SNP	Gene	Cis/trans	Tissue	Source
rs1045599	CENPV	cis	parietal	SCAN
rs1045599	ADORA2B	cis	Heart Left Ventricle	GTEx
rs1045599	ZSWIM7	Cis_1M	lymphoblastoid	RTeQTL
rs1045599	Hs.379903	cis	multi-tissue	Pritchard
rs1045599	ADORA2B	cis	Artery Tibial	GTEx
rs1045599	ADORA2B	cis	Esophagus Muscularis	GTEx
rs1045599	CENPV	cis	Artery Tibial	GTEx
rs1045599	ADORA2B	cis	lung	GTEx
rs1045599	ADORA2B	cis	Adipose Subcutaneous	GTEx
rs1045599	LOC125150	cis	lesional skin	skin_eQTL
rs1045599	TTC19	cis	lymphoblastoid	seeQTL
rs1045599	TTC19	Cis_1M	lymphoblastoid	RTeQTL
rs1045599	PRPSAP2	cis	parietal	SCAN
rs1045599	ADORA2B	cis	Muscle Skeletal	GTEx
rs1045599	LOC125150	cis	uninvolved skin	skin_eQTL
rs1045599	ADORA2B	cis	Nerve Tibial	GTEx
rs1045599	ZSWIM7	cis	Muscle Skeletal	GTEx
rs1045599	ADORA2B	cis	Thyroid	GTEx
rs1045599	LOC125150	cis	normal skin	skin_eQTL
rs1045599	NCOR1	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15868800-15880000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr17:15870200-15880200	Weak transcription	Primary B cells from peripheral blood	blood
3	chr17:15870200-15883600	Weak transcription	Fetal Heart	heart
4	chr17:15870400-15880000	Weak transcription	Brain Germinal Matrix	brain
5	chr17:15870400-15881200	Weak transcription	Fetal Kidney	kidney
6	chr17:15870400-15883600	Weak transcription	Brain Angular Gyrus	brain
7	chr17:15870400-15883800	Weak transcription	Gastric	stomach
8	chr17:15870400-15902400	Weak transcription	Small Intestine	intestine
9	chr17:15870600-15880000	Weak transcription	Brain Substantia Nigra	brain
10	chr17:15870600-15880000	Weak transcription	Rectal Smooth Muscle	rectum
11	chr17:15870600-15883600	Weak transcription	Pancreas	Pancrea
12	chr17:15870600-15883800	Weak transcription	Fetal Brain Male	brain
13	chr17:15870800-15880000	Weak transcription	Primary B cells from cord blood	blood
14	chr17:15870800-15902400	Weak transcription	Esophagus	oesophagus
15	chr17:15871600-15880200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr17:15871800-15880000	Weak transcription	Primary hematopoietic stem cells	blood
17	chr17:15871800-15880200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr17:15872000-15883400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr17:15873200-15902200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr17:15873800-15881200	Weak transcription	HepG2	liver
21	chr17:15874600-15880000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr17:15874600-15883600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr17:15874800-15880000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr17:15874800-15902400	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr17:15875000-15880000	Weak transcription	Psoas Muscle	Psoas
26	chr17:15875000-15880600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr17:15875200-15884200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr17:15875400-15880000	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr17:15876000-15880000	Weak transcription	HSMMtube	muscle
30	chr17:15876200-15880000	Weak transcription	Colon Smooth Muscle	Colon
31	chr17:15876400-15880400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr17:15876600-15885400	Weak transcription	Hela-S3	cervix
33	chr17:15876800-15880000	Weak transcription	Ovary	ovary
34	chr17:15876800-15882200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr17:15876800-15882200	Strong transcription	HMEC	breast
36	chr17:15876800-15882200	Strong transcription	NHEK	skin
37	chr17:15877000-15881600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr17:15877200-15880000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr17:15877200-15880600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr17:15877200-15882200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr17:15877200-15882200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr17:15877400-15882200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr17:15877400-15882200	Strong transcription	Primary T cells from cord blood	blood
44	chr17:15877600-15882200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr17:15877600-15882200	Strong transcription	Skeletal Muscle Female	skeletal muscle
46	chr17:15877600-15882200	Strong transcription	HSMM	muscle
47	chr17:15877600-15883600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr17:15877600-15888800	Weak transcription	NHDF-Ad	bronchial
49	chr17:15877800-15880400	Strong transcription	Duodenum Smooth Muscle	Duodenum
50	chr17:15877800-15881200	Weak transcription	K562	blood

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