Variant report

Variant	rs16853361
Chromosome Location	chr2:168119691-168119692
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs12616657	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs1479590	1.00[EUR][1000 genomes]
rs16853297	1.00[EUR][1000 genomes]
rs16853326	1.00[EUR][1000 genomes]
rs16853333	1.00[EUR][1000 genomes]
rs59064569	0.87[AMR][1000 genomes]
rs6735236	0.87[AMR][1000 genomes]
rs6753496	0.87[AMR][1000 genomes]
rs7600115	0.80[AFR][1000 genomes]
rs7600329	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv583591	chr2:168037489-168132892	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
2	nsv875377	chr2:168084857-168203116	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
3	nsv979347	chr2:168092753-168141678	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases
4	nsv875378	chr2:168107491-168297961	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
5	esv3364733	chr2:168109919-168302141	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:168104000-168122200	Weak transcription	Left Ventricle	heart
2	chr2:168115800-168120200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr2:168116000-168120200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr2:168116000-168120600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr2:168116000-168120800	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr2:168116000-168121200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr2:168116000-168121600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr2:168119200-168119800	Enhancers	HUES48 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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