Variant report

Variant	rs821431
Chromosome Location	chr1:153271524-153271525
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1094362	0.85[EUR][1000 genomes]
rs1433678	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1433679	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1655310	0.87[MEX][hapmap];0.91[TSI][hapmap];0.82[EUR][1000 genomes]
rs1836118	0.81[EUR][1000 genomes]
rs2570443	0.84[CHB][hapmap];0.88[CHD][hapmap];0.91[GIH][hapmap];0.93[JPT][hapmap];0.83[MEX][hapmap];0.87[ASN][1000 genomes]
rs2771110	1.00[CHB][hapmap];0.86[JPT][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2771112	0.84[CHB][hapmap];0.88[CHD][hapmap];0.91[GIH][hapmap];0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs2771115	0.83[EUR][1000 genomes]
rs2771116	0.83[EUR][1000 genomes]
rs2771118	0.92[MEX][hapmap];0.88[TSI][hapmap];0.81[EUR][1000 genomes]
rs2771120	0.81[EUR][1000 genomes]
rs821408	0.81[EUR][1000 genomes]
rs821411	0.84[EUR][1000 genomes]
rs821418	0.83[MEX][hapmap]
rs821424	0.83[MEX][hapmap]
rs821427	0.84[CHB][hapmap];0.88[CHD][hapmap];0.93[GIH][hapmap];0.93[JPT][hapmap];0.92[MEX][hapmap];0.91[TSI][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs843971	0.91[GIH][hapmap]

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	nsv1001834	chr1:152648853-153279143	Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
2	nsv1010488	chr1:152901263-153670972	Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
3	nsv535171	chr1:152901263-153670972	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
4	nsv533877	chr1:152923645-153468131	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
5	nsv999024	chr1:153255005-153325685	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs821431	LCE3B	cis	parietal	SCAN
rs821431	ILF2	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153266800-153284400	Weak transcription	Esophagus	oesophagus
2	chr1:153268000-153278200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:153269600-153272400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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