Variant report

Variant	rs7137784
Chromosome Location	chr12:103854762-103854763
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10507166	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10735387	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10778257	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10861013	0.85[EUR][1000 genomes]
rs10861015	0.85[EUR][1000 genomes]
rs10861016	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10861022	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10861025	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11111579	0.83[EUR][1000 genomes]
rs11111582	0.83[EUR][1000 genomes]
rs1320345	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2374078	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2888733	0.85[EUR][1000 genomes]
rs4597156	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7136280	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7298211	0.86[EUR][1000 genomes]
rs7305169	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7961410	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:103851400-103855400	Weak transcription	GM12878-XiMat	blood
2	chr12:103851800-103856600	Weak transcription	Primary B cells from peripheral blood	blood
3	chr12:103852200-103865400	Weak transcription	Primary T cells from cord blood	blood

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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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