Variant report

Variant	rs1845691
Chromosome Location	chr4:81291929-81291930
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10009812	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs10020144	0.88[ASN][1000 genomes]
rs10033567	1.00[JPT][hapmap]
rs10213482	0.82[ASN][1000 genomes]
rs10434062	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12648594	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3816574	0.84[ASN][1000 genomes]
rs6853244	0.81[ASN][1000 genomes]
rs731658	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7655270	0.81[ASN][1000 genomes]
rs7680580	0.84[ASN][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:81291000-81310200	Weak transcription	Osteobl	bone
2	chr4:81291800-81292000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr4:81291800-81292400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:81291800-81292600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:81291800-81292600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr4:81291800-81292600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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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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