Variant report

Variant	rs11618507
Chromosome Location	chr13:30172751-30172752
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 2 )

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

rs_ID	r²[population]
rs11619313	0.94[EUR][1000 genomes]
rs2482096	1.00[CHB][hapmap]
rs4319605	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4769018	0.95[EUR][1000 genomes]
rs56021221	0.98[EUR][1000 genomes]
rs61947194	0.86[EUR][1000 genomes]
rs882953	1.00[CHB][hapmap]

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11618507	SLC7A1	cis	cerebellum	SCAN
rs11618507	MTMR6	cis	cerebellum	SCAN

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:30170400-30173200	Bivalent Enhancer	Fetal Muscle Leg	muscle
2	chr13:30172600-30173000	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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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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