Variant report

Variant	rs6941969
Chromosome Location	chr6:82485646-82485647
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1000276	1.00[CEU][hapmap];0.85[CHB][hapmap];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12524158	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1931623	0.94[CHB][hapmap]
rs194611	0.87[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs194615	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs194616	0.81[ASN][1000 genomes]
rs1981090	0.83[CHB][hapmap]
rs6924759	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6928409	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6929407	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71558975	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9344221	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9353027	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9359505	0.89[CHB][hapmap]
rs9361861	0.94[CHB][hapmap]

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82474200-82485800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:82480400-82485800	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr6:82483000-82487400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr6:82483000-82487400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:82483000-82497400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:82483800-82485800	Weak transcription	Hela-S3	cervix
7	chr6:82484400-82488400	Enhancers	HepG2	liver
8	chr6:82485400-82486600	Enhancers	Placenta	Placenta
9	chr6:82485600-82486600	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr6:82485600-82486600	Enhancers	Liver	Liver
11	chr6:82485600-82486800	Enhancers	Monocytes-CD14+_RO01746	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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