Variant report

Variant	rs6905903
Chromosome Location	chr6:14054510-14054511
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs10949221	0.88[CEU][hapmap];1.00[YRI][hapmap];0.90[EUR][1000 genomes]
rs4712224	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9358027	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:14052400-14057200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:14053600-14054600	Enhancers	NHDF-Ad	bronchial
3	chr6:14053800-14054600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:14053800-14054600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr6:14054000-14054600	Enhancers	NHEK	skin
6	chr6:14054200-14054600	Enhancers	Osteobl	bone
7	chr6:14054400-14054600	Enhancers	NH-A	brain
8	chr6:14054400-14059800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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