Variant report

Variant	rs584377
Chromosome Location	chr17:37460128-37460129
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	chr17:37459079..37461538-chr17:37464843..37466379,2	MCF-7	breast:

Extended variants
information (count: 178 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:163)

rs_ID	r²[population]
rs10221223	0.81[ASN][1000 genomes]
rs10432030	0.83[ASN][1000 genomes]
rs10432031	0.82[ASN][1000 genomes]
rs10445306	0.87[CHB][hapmap]
rs10491128	0.82[CHB][hapmap]
rs10491129	0.82[CHB][hapmap];0.87[ASN][1000 genomes]
rs11078893	0.82[CHB][hapmap]
rs11078894	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11078895	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11078896	0.85[ASN][1000 genomes]
rs11078897	0.82[CHB][hapmap];0.85[ASN][1000 genomes]
rs11078898	0.82[CHB][hapmap]
rs11078901	0.82[CHB][hapmap]
rs11078902	0.82[CHB][hapmap]
rs11655972	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11657899	0.82[CHB][hapmap]
rs11871813	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12150047	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs12449852	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12452509	0.82[CHB][hapmap]
rs12452880	0.82[CHB][hapmap]
rs12600751	0.82[CHB][hapmap]
rs12938099	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs12950186	1.00[CEU][hapmap];0.93[CHB][hapmap];0.83[JPT][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13341996	0.82[CHB][hapmap]
rs1966915	0.85[ASN][1000 genomes]
rs1966916	0.85[ASN][1000 genomes]
rs1971663	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2024073	0.87[ASN][1000 genomes]
rs2061338	0.82[CHB][hapmap];0.85[ASN][1000 genomes]
rs2061342	0.84[ASN][1000 genomes]
rs2100651	0.83[ASN][1000 genomes]
rs2168785	0.85[ASN][1000 genomes]
rs2302073	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2338755	0.82[CHB][hapmap];0.85[ASN][1000 genomes]
rs2338795	0.85[ASN][1000 genomes]
rs2338799	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2338800	0.82[CHB][hapmap];0.81[ASN][1000 genomes]
rs2338801	0.80[ASN][1000 genomes]
rs28482878	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2879258	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2879259	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28799952	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs33933929	0.84[ASN][1000 genomes]
rs34473775	0.81[ASN][1000 genomes]
rs3744348	0.82[CHB][hapmap];0.85[ASN][1000 genomes]
rs3744349	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];0.90[YRI][hapmap];0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3964723	0.82[CHB][hapmap];0.83[JPT][hapmap];0.85[ASN][1000 genomes]
rs4287601	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4325601	0.84[ASN][1000 genomes]
rs4511574	0.82[CHB][hapmap]
rs4516267	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4794808	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4795355	0.82[CHB][hapmap];0.82[ASN][1000 genomes]
rs4795356	0.82[CHB][hapmap]
rs4795357	0.82[CHB][hapmap]
rs4795358	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4795367	0.81[ASN][1000 genomes]
rs55689507	0.85[ASN][1000 genomes]
rs57933226	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs582088	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs582176	0.91[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs583980	0.83[ASN][1000 genomes]
rs585961	0.82[CHB][hapmap];0.87[ASN][1000 genomes]
rs587343	0.87[ASN][1000 genomes]
rs587880	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs588193	0.82[CHB][hapmap];0.85[ASN][1000 genomes]
rs590051	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs593480	0.92[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs594794	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs597069	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs600010	0.82[CHB][hapmap];0.85[ASN][1000 genomes]
rs602282	0.84[ASN][1000 genomes]
rs602688	0.82[CHB][hapmap];0.87[ASN][1000 genomes]
rs612209	0.90[ASN][1000 genomes]
rs61368704	0.88[AFR][1000 genomes];0.80[ASN][1000 genomes]
rs620686	0.82[CHB][hapmap];0.87[ASN][1000 genomes]
rs632202	0.82[CHB][hapmap];0.87[ASN][1000 genomes]
rs632606	0.84[ASN][1000 genomes]
rs634365	0.84[ASN][1000 genomes]
rs638201	0.87[ASN][1000 genomes]
rs644173	0.82[CHB][hapmap];0.85[ASN][1000 genomes]
rs649180	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs650106	0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs6503500	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6503502	0.81[ASN][1000 genomes]
rs6503503	0.82[CHB][hapmap]
rs6503504	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6503507	0.82[CHB][hapmap]
rs6503513	0.85[CEU][hapmap];0.82[CHB][hapmap]
rs651827	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs665413	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs667193	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs667239	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs676882	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs677888	0.89[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs679995	0.87[ASN][1000 genomes]
rs683948	0.87[ASN][1000 genomes]
rs7208252	0.92[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7208487	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7212621	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7215983	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7218484	0.80[ASN][1000 genomes]
rs7218670	0.81[ASN][1000 genomes]
rs7220650	0.82[CHB][hapmap];0.81[ASN][1000 genomes]
rs7221117	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7221875	0.82[CHB][hapmap]
rs7222252	0.81[CHB][hapmap]
rs7223331	0.81[ASN][1000 genomes]
rs7223438	0.82[CHB][hapmap]
rs7501488	0.82[CHB][hapmap]
rs7503081	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs752314	0.82[CHB][hapmap];0.85[ASN][1000 genomes]
rs755500	0.82[CHB][hapmap];0.85[ASN][1000 genomes]
rs801417	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs801418	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs801419	0.87[ASN][1000 genomes]
rs801420	0.87[ASN][1000 genomes]
rs801426	0.82[CHB][hapmap];0.87[ASN][1000 genomes]
rs801427	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs801429	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs801430	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs8066704	0.82[CHB][hapmap];0.81[ASN][1000 genomes]
rs8067302	0.81[ASN][1000 genomes]
rs8067948	0.81[ASN][1000 genomes]
rs8070695	0.82[CHB][hapmap];0.81[ASN][1000 genomes]
rs8071300	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8073511	0.90[ASN][1000 genomes]
rs8073907	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8074855	0.81[ASN][1000 genomes]
rs8076462	0.82[CHB][hapmap]
rs8076494	0.82[CHB][hapmap]
rs8076546	0.82[CHB][hapmap]
rs8078599	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8079355	0.84[ASN][1000 genomes]
rs8079560	0.81[ASN][1000 genomes]
rs8079590	0.82[CHB][hapmap];0.85[ASN][1000 genomes]
rs8079662	0.85[ASN][1000 genomes]
rs8081033	0.80[ASN][1000 genomes]
rs8081220	0.87[ASN][1000 genomes]
rs8081338	0.85[ASN][1000 genomes]
rs9646419	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs9747342	0.87[ASN][1000 genomes]
rs9890198	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9891892	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9892055	0.82[CHB][hapmap]
rs9893735	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9894586	0.82[CHB][hapmap];0.81[ASN][1000 genomes]
rs9894864	0.80[ASN][1000 genomes]
rs9899069	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9903363	0.81[ASN][1000 genomes]
rs9904334	0.82[CHB][hapmap];0.87[ASN][1000 genomes]
rs9905617	0.81[ASN][1000 genomes]
rs9906612	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9908131	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9908760	0.81[ASN][1000 genomes]
rs9909064	0.81[ASN][1000 genomes]
rs9909304	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9912212	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9912310	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9913320	0.85[ASN][1000 genomes]
rs9944411	0.82[CHB][hapmap];0.81[ASN][1000 genomes]
rs9944459	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1057470	chr17:37135183-37549816	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
2	nsv543339	chr17:37135183-37549816	Strong transcription Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
3	nsv932024	chr17:37192290-37850932	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	92 gene(s)	inside rSNPs	diseases
4	nsv833441	chr17:37320807-37476796	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
5	nsv1061084	chr17:37333956-37501598	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
6	nsv1060126	chr17:37333956-37659189	Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
7	nsv1057655	chr17:37333956-37732451	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
8	nsv1066033	chr17:37333956-37795617	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	78 gene(s)	inside rSNPs	diseases
9	nsv543340	chr17:37333956-37795617	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	78 gene(s)	inside rSNPs	diseases
10	nsv908204	chr17:37349655-37682657	Genic enhancers Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
11	nsv1057057	chr17:37395082-37627025	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
12	nsv1055612	chr17:37409865-37563236	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
13	nsv510709	chr17:37438419-37508395	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
14	nsv1061951	chr17:37442228-37770903	Bivalent Enhancer Strong transcription Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
15	nsv543341	chr17:37442228-37770903	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs584377	CRKRS	Cis_1M	lymphoblastoid	RTeQTL
rs584377	PGAP3	cis	Thyroid	GTEx

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37408000-37463000	Weak transcription	Small Intestine	intestine
2	chr17:37409800-37464000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr17:37417600-37460800	Weak transcription	Fetal Brain Male	brain
4	chr17:37425000-37473000	Weak transcription	Pancreas	Pancrea
5	chr17:37426600-37460800	Weak transcription	Colonic Mucosa	Colon
6	chr17:37426800-37468600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr17:37430800-37462600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr17:37431200-37462600	Weak transcription	Colon Smooth Muscle	Colon
9	chr17:37431400-37473400	Weak transcription	Esophagus	oesophagus
10	chr17:37435600-37469400	Weak transcription	Gastric	stomach
11	chr17:37436000-37496200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr17:37436800-37497800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr17:37437800-37462400	Weak transcription	Brain Anterior Caudate	brain
14	chr17:37438400-37461800	Weak transcription	A549	lung
15	chr17:37438800-37463000	Weak transcription	NHDF-Ad	bronchial
16	chr17:37439000-37462800	Weak transcription	NH-A	brain
17	chr17:37439200-37462600	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr17:37439200-37462800	Weak transcription	Fetal Heart	heart
19	chr17:37444000-37478400	Weak transcription	Psoas Muscle	Psoas
20	chr17:37444600-37462600	Strong transcription	Fetal Intestine Small	intestine
21	chr17:37448400-37461800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr17:37449200-37461000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr17:37450800-37460200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr17:37451400-37460200	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr17:37452600-37461200	Strong transcription	Fetal Thymus	thymus
26	chr17:37453400-37461200	Strong transcription	Primary T cells from cord blood	blood
27	chr17:37453400-37463200	Weak transcription	NHLF	lung
28	chr17:37453400-37507800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr17:37453600-37461200	Strong transcription	Fetal Stomach	stomach
30	chr17:37453600-37461200	Strong transcription	Thymus	Thymus
31	chr17:37454000-37511600	Weak transcription	Hela-S3	cervix
32	chr17:37454600-37473600	Weak transcription	Brain Substantia Nigra	brain
33	chr17:37454800-37464400	Weak transcription	Aorta	Aorta
34	chr17:37454800-37471800	Weak transcription	Left Ventricle	heart
35	chr17:37454800-37473800	Weak transcription	Spleen	Spleen
36	chr17:37454800-37474400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr17:37455000-37463000	Weak transcription	Brain Angular Gyrus	brain
38	chr17:37455000-37463200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr17:37455000-37463200	Weak transcription	Rectal Smooth Muscle	rectum
40	chr17:37455000-37464600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr17:37455200-37462400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr17:37455200-37463200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr17:37455200-37499800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr17:37455400-37462400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr17:37455400-37477400	Weak transcription	Ovary	ovary
46	chr17:37455400-37485200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr17:37455400-37495600	Weak transcription	Right Ventricle	heart
48	chr17:37455600-37462200	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr17:37455600-37462200	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr17:37455600-37462200	Weak transcription	Adipose Nuclei	Adipose

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