Variant report

Variant	rs2103445
Chromosome Location	chr8:91443772-91443773
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs1028252	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1028253	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10481088	0.80[ASN][1000 genomes]
rs2091901	0.80[AMR][1000 genomes]
rs2103442	0.81[AMR][1000 genomes]
rs34309716	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs34359428	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35349778	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4301407	0.80[ASN][1000 genomes]
rs4734968	0.80[AMR][1000 genomes]
rs7010132	0.80[ASN][1000 genomes]
rs7845025	0.82[ASN][1000 genomes]
rs9297851	0.80[ASN][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2103445	RUNX1T1	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91441000-91445800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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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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