Variant report

Variant	rs262940
Chromosome Location	chr6:37184396-37184397
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1150787	0.89[ASN][1000 genomes]
rs1150790	0.91[ASN][1000 genomes]
rs1224328	0.89[ASN][1000 genomes]
rs1224329	0.91[ASN][1000 genomes]
rs1224384	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2622900	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs262939	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs262942	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs398739	0.82[ASN][1000 genomes]
rs418343	0.82[ASN][1000 genomes]
rs437956	0.83[AMR][1000 genomes]
rs438802	0.85[EUR][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:37176200-37189800	Weak transcription	Thymus	Thymus
2	chr6:37179000-37185600	Weak transcription	Dnd41	blood
3	chr6:37180200-37185400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr6:37183000-37185400	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr6:37184200-37184400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

Quick Search:

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

what's new

Quick links