Variant report

Variant	rs61828230
Chromosome Location	chr1:211865716-211865717
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10494938	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10494940	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17651870	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2083903	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35573429	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs41275370	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41314254	0.83[ASN][1000 genomes]
rs61828229	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61828232	0.84[EUR][1000 genomes]
rs61849678	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61849681	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61849682	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61849684	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61849685	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6697046	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6704128	0.99[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754845	chr1:211846605-211878605	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr1:211859600-211868000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:211859600-211872000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:211862000-211868400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr1:211862200-211868000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr1:211862200-211868200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr1:211865200-211868000	Weak transcription	K562	blood
7	chr1:211865200-211868200	Weak transcription	HepG2	liver
8	chr1:211865400-211867600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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Input of quick search could be:

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

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