Variant report

Variant	rs13313041
Chromosome Location	chr1:166242363-166242364
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs12063590	0.83[CHD][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs12064378	0.83[CHD][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes]
rs12085753	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1368021	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16856819	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1823620	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1864792	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1991725	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2163630	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2568108	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2568109	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2568110	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2798411	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2798417	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2871591	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58934650	1.00[EUR][1000 genomes]
rs6665803	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916491	chr1:166000783-166948513	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	esv3332610	chr1:166111288-166282689	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:166240400-166242400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr1:166240800-166242800	Weak transcription	Psoas Muscle	Psoas
3	chr1:166241400-166242600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr1:166241400-166242600	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr1:166241400-166243400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr1:166241600-166242600	Enhancers	H1 Cell Line	embryonic stem cell
7	chr1:166242000-166242400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr1:166242000-166243600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr1:166242200-166242600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:166242200-166242600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:166242200-166243200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr1:166242200-166243400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr1:166242200-166243400	Enhancers	HUES6 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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