Variant report

Variant	rs12207114
Chromosome Location	chr6:15801889-15801890
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]
rs12192181	0.84[CEU][hapmap]
rs12193135	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12216459	0.81[JPT][hapmap];0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4712257	0.84[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4715998	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6935121	0.84[CEU][hapmap]
rs6940942	0.80[JPT][hapmap];0.87[ASN][1000 genomes]
rs742387	0.84[CEU][hapmap]
rs9464832	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9476906	0.84[CEU][hapmap]
rs9476934	0.84[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15800400-15816200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:15801200-15802200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr6:15801600-15802800	Weak transcription	Fetal Kidney	kidney
4	chr6:15801800-15803400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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