Variant report

Variant	rs10916632
Chromosome Location	chr1:224708176-224708177
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10753474	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10916628	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10916629	0.94[EUR][1000 genomes]
rs10916630	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10916631	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12093242	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12140117	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12140906	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12141016	0.85[AMR][1000 genomes]
rs12141708	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12142949	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12566578	0.88[EUR][1000 genomes]
rs1891244	0.88[EUR][1000 genomes]
rs2648743	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3738367	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4653589	0.87[EUR][1000 genomes]
rs59319739	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61825792	0.88[EUR][1000 genomes]
rs6426133	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6665956	0.90[EUR][1000 genomes]
rs6688146	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6695773	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6699035	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs712065	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs712066	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7541723	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7541917	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7545252	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7550648	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs791504	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv8868	chr1:224383023-224752531	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv1014717	chr1:224551939-224885543	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv535311	chr1:224551939-224885543	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224694200-224717600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:224694200-224727600	Weak transcription	Brain Anterior Caudate	brain
3	chr1:224696400-224716600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr1:224701800-224709200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:224701800-224716600	Weak transcription	Ovary	ovary
6	chr1:224702000-224709200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr1:224702000-224716600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr1:224702200-224716600	Weak transcription	Dnd41	blood
9	chr1:224703400-224711200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr1:224705200-224713600	Weak transcription	Fetal Brain Male	brain
11	chr1:224706400-224711400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr1:224706600-224709400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr1:224706600-224711600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:224707000-224708600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr1:224707600-224708200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr1:224707600-224708400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr1:224707600-224708600	Enhancers	NHDF-Ad	bronchial
18	chr1:224707800-224708200	Enhancers	HSMMtube	muscle
19	chr1:224708000-224708400	Enhancers	HSMM	muscle
20	chr1:224708000-224708600	Enhancers	GM12878-XiMat	blood

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