Variant report

Variant	rs707813
Chromosome Location	chr6:11624338-11624339
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs4574630	0.82[ASN][1000 genomes]
rs490280	0.82[EUR][1000 genomes]
rs491225	0.82[EUR][1000 genomes]
rs515885	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs546173	0.82[EUR][1000 genomes]
rs571984	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9394184	0.80[EUR][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11610200-11631400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr6:11618800-11625200	Weak transcription	HSMM	muscle
3	chr6:11618800-11627200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr6:11622000-11625200	Weak transcription	HSMMtube	muscle
5	chr6:11623600-11625600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:11623600-11625600	Weak transcription	Fetal Muscle Leg	muscle
7	chr6:11623600-11632600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured 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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