Variant report

Variant	rs73411269
Chromosome Location	chr18:30345171-30345172
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1523578	1.00[EUR][1000 genomes]
rs1523583	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1893242	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1893243	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1916650	0.96[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2421642	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2421643	0.92[EUR][1000 genomes]
rs41446249	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61737324	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6506987	1.00[ASN][1000 genomes]
rs73411297	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:30341400-30345400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr18:30341800-30347200	Enhancers	Primary B cells from cord blood	blood
3	chr18:30342200-30347400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr18:30343000-30346200	Enhancers	HepG2	liver
5	chr18:30343800-30348200	Weak transcription	Fetal Brain Male	brain
6	chr18:30344000-30347400	Weak transcription	Primary B cells from peripheral blood	blood
7	chr18:30344200-30348800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr18:30345000-30345200	Enhancers	Fetal Kidney	kidney

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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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