Variant report

Variant	rs4537315
Chromosome Location	chr8:126469308-126469309
allele	A/G
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]
rs10216709	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10808545	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17730649	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4518686	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6984241	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7007811	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:126464800-126470800	Weak transcription	Lung	lung
2	chr8:126464800-126478000	Weak transcription	Gastric	stomach
3	chr8:126465200-126471800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:126465200-126477800	Weak transcription	Fetal Heart	heart
5	chr8:126465600-126470400	Weak transcription	Pancreas	Pancrea
6	chr8:126468200-126470200	Weak transcription	Hela-S3	cervix

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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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