Variant report

Variant	rs860895
Chromosome Location	chr1:175820514-175820515
allele	C/T
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]
rs12023065	0.82[ASN][1000 genomes]
rs1340998	0.85[EUR][1000 genomes]
rs1575824	0.81[EUR][1000 genomes]
rs1575825	0.82[ASN][1000 genomes]
rs1750293	0.93[EUR][1000 genomes]
rs1925947	0.81[EUR][1000 genomes]
rs2090977	0.85[EUR][1000 genomes]
rs2209558	0.85[EUR][1000 genomes]
rs2222419	0.83[EUR][1000 genomes]
rs34010246	0.82[ASN][1000 genomes]
rs485526	0.95[EUR][1000 genomes]
rs515007	0.85[EUR][1000 genomes]
rs566433	0.94[EUR][1000 genomes]
rs6656072	0.84[EUR][1000 genomes]
rs7537684	0.82[ASN][1000 genomes]
rs942958	0.82[ASN][1000 genomes]
rs990707	0.85[EUR][1000 genomes]

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	esv33328	chr1:175446583-175910001	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv872560	chr1:175648631-175869554	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:175815800-175830400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:175817600-175821000	Weak transcription	Brain Germinal Matrix	brain
3	chr1:175817600-175825400	Weak transcription	Fetal Brain Male	brain
4	chr1:175817800-175822200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr1:175817800-175823400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr1:175817800-175825600	Weak transcription	Brain Angular Gyrus	brain
7	chr1:175818000-175823000	Weak transcription	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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