Variant report

Variant	rs885337
Chromosome Location	chr7:47971575-47971576
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	chr7:47970714..47972227-chr7:47974264..47976545,2	K562	blood:

Extended variants
information (count: 71 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs1056663	0.96[CEU][hapmap];0.84[JPT][hapmap];0.84[EUR][1000 genomes]
rs12702401	0.91[CEU][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1879833	0.93[CEU][hapmap];0.86[JPT][hapmap];0.85[EUR][1000 genomes]
rs1879834	0.92[CEU][hapmap];0.85[JPT][hapmap];0.85[EUR][1000 genomes]
rs2037483	0.84[EUR][1000 genomes]
rs2037485	0.84[EUR][1000 genomes]
rs2242477	0.88[CEU][hapmap];0.85[JPT][hapmap];0.81[EUR][1000 genomes]
rs2242478	0.88[CEU][hapmap];0.85[JPT][hapmap];0.80[EUR][1000 genomes]
rs2242479	0.88[CEU][hapmap];0.86[JPT][hapmap];0.81[EUR][1000 genomes]
rs2686816	0.88[CEU][hapmap];0.90[CHB][hapmap];0.89[JPT][hapmap];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2686817	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2686820	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2686821	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2686823	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2686825	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2686827	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2686830	0.92[CEU][hapmap];0.85[JPT][hapmap];0.85[EUR][1000 genomes]
rs2686831	0.92[CEU][hapmap];0.85[JPT][hapmap];0.85[EUR][1000 genomes]
rs2686832	0.92[CEU][hapmap];0.81[CHB][hapmap];0.86[JPT][hapmap];0.85[EUR][1000 genomes]
rs2686833	0.85[EUR][1000 genomes]
rs2686834	0.84[EUR][1000 genomes]
rs2686835	0.92[CEU][hapmap];0.85[JPT][hapmap];0.84[EUR][1000 genomes]
rs2686836	0.93[CEU][hapmap];0.86[JPT][hapmap];0.84[EUR][1000 genomes]
rs2686838	0.92[CEU][hapmap];0.85[JPT][hapmap];0.84[EUR][1000 genomes]
rs2686839	0.84[EUR][1000 genomes]
rs2686841	0.82[EUR][1000 genomes]
rs2708853	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2708858	0.81[EUR][1000 genomes]
rs2708859	0.81[EUR][1000 genomes]
rs2708861	0.88[CEU][hapmap];0.85[JPT][hapmap];0.81[EUR][1000 genomes]
rs2708862	0.92[CEU][hapmap];0.81[CHB][hapmap];0.86[JPT][hapmap];0.83[EUR][1000 genomes]
rs2708873	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2708875	0.85[CEU][hapmap]
rs2708877	0.84[EUR][1000 genomes]
rs2708878	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2708880	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2708881	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2708882	0.84[EUR][1000 genomes]
rs2708894	0.92[CEU][hapmap];0.85[JPT][hapmap];0.85[EUR][1000 genomes]
rs2708895	0.92[CEU][hapmap];0.84[JPT][hapmap];0.85[EUR][1000 genomes]
rs2708896	0.88[CEU][hapmap]
rs2708897	0.86[EUR][1000 genomes]
rs2708898	0.85[EUR][1000 genomes]
rs2708901	0.80[CEU][hapmap]
rs2708902	0.82[EUR][1000 genomes]
rs2708903	0.92[CEU][hapmap];0.85[JPT][hapmap];0.84[EUR][1000 genomes]
rs2708905	0.88[CEU][hapmap];0.85[JPT][hapmap]
rs2708910	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2708911	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2708913	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3176478	0.86[JPT][hapmap]
rs3176564	0.92[CEU][hapmap];0.94[JPT][hapmap];0.84[EUR][1000 genomes]
rs34016848	0.85[EUR][1000 genomes]
rs35536957	0.82[EUR][1000 genomes]
rs35719200	0.81[ASN][1000 genomes]
rs4720624	0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs57995674	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs60107343	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67565252	0.82[ASN][1000 genomes]
rs6955251	0.81[JPT][hapmap]
rs939904	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs939905	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs953572	0.88[CEU][hapmap];0.83[EUR][1000 genomes]
rs9648569	0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026223	chr7:47560728-48243287	Genic enhancers Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv869585	chr7:47765428-48151324	Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv830991	chr7:47854530-48025996	Weak transcription Active TSS Genic enhancers Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv532120	chr7:47882757-48195869	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv470221	chr7:47917495-48354363	Strong transcription Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv464442	chr7:47917495-48354820	Genic enhancers Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv606893	chr7:47917495-48354820	Flanking Active TSS Strong transcription Genic enhancers Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs885337	UPP1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:47934000-48001800	Weak transcription	Psoas Muscle	Psoas
2	chr7:47965000-47972200	Weak transcription	Fetal Stomach	stomach
3	chr7:47965800-47980400	Weak transcription	Aorta	Aorta
4	chr7:47966600-47974000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:47967000-47977400	Weak transcription	Right Ventricle	heart
6	chr7:47967600-47993400	Weak transcription	Brain Anterior Caudate	brain
7	chr7:47969200-47972000	Weak transcription	Left Ventricle	heart
8	chr7:47969200-47973800	Weak transcription	Lung	lung
9	chr7:47970600-47972600	Enhancers	Fetal Muscle Trunk	muscle
10	chr7:47970600-47972600	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr7:47970600-47972800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:47970600-47972800	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr7:47970600-47972800	Enhancers	Fetal Muscle Leg	muscle
14	chr7:47970600-47972800	Enhancers	HSMMtube	muscle
15	chr7:47970600-47973200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr7:47970800-47972200	Enhancers	HSMM	muscle
17	chr7:47970800-47972400	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr7:47970800-47972600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr7:47970800-47972600	Enhancers	Adipose Nuclei	Adipose
20	chr7:47970800-47972800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr7:47971000-47971600	Enhancers	Muscle Satellite Cultured Cells	--
22	chr7:47971000-47972000	Weak transcription	Fetal Thymus	thymus
23	chr7:47971000-47972200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr7:47971000-47972200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr7:47971200-47971600	Flanking Active TSS	Osteobl	bone
26	chr7:47971400-47972600	Enhancers	Right Atrium	heart

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