Variant report

Variant	rs2212434
Chromosome Location	chr11:76281593-76281594
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11236791	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11236797	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61893460	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7110818	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7126418	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7936312	0.84[EUR][1000 genomes]
rs7936323	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76273200-76285200	Weak transcription	NHDF-Ad	bronchial
2	chr11:76275200-76285800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr11:76278200-76288000	Weak transcription	HSMM	muscle
4	chr11:76278600-76283200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:76278800-76283400	Weak transcription	Placenta	Placenta
6	chr11:76279600-76284800	Weak transcription	Osteobl	bone

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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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