Variant report

Variant	rs61915687
Chromosome Location	chr12:26256670-26256671
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs17365537	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2137547	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2343072	0.88[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs55694223	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61915685	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7300076	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:26251000-26265800	Weak transcription	HSMM	muscle
2	chr12:26254600-26257400	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr12:26254600-26259400	Weak transcription	Psoas Muscle	Psoas
4	chr12:26255600-26264400	Weak transcription	Fetal Intestine Small	intestine
5	chr12:26255800-26257400	Weak transcription	Fetal Intestine Large	intestine
6	chr12:26256200-26259000	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr12:26256200-26259200	Weak transcription	Fetal Muscle Leg	muscle

Quick Search:

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

what's new

Quick links