Variant report

Variant	rs10922338
Chromosome Location	chr1:197926219-197926220
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10922332	0.82[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs10922335	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10922337	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12029707	1.00[CEU][hapmap];0.90[CHB][hapmap];0.82[JPT][hapmap];0.93[EUR][1000 genomes]
rs17644383	0.83[EUR][1000 genomes]
rs2047539	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2088651	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs413713	0.80[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs4915135	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4915136	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6667492	1.00[CEU][hapmap];0.90[CHB][hapmap];0.91[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6671069	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6692087	0.92[YRI][hapmap]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:197923800-197927200	Weak transcription	Pancreas	Pancrea
2	chr1:197924200-197927600	Weak transcription	K562	blood
3	chr1:197925600-197927600	Weak transcription	Fetal Intestine Large	intestine

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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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