Variant report

Variant	rs62337921
Chromosome Location	chr4:174757021-174757022
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10014581	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4544692	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4695745	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55747243	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs55775817	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62337914	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62337922	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62337923	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:174756800-174757600	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr4:174756800-174757600	Enhancers	Fetal Heart	heart
3	chr4:174756800-174757800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:174756800-174757800	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr4:174756800-174757800	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr4:174756800-174757800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr4:174757000-174757200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr4:174757000-174757600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr4:174757000-174757600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr4:174757000-174757600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr4:174757000-174757800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr4:174757000-174757800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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