Variant report

Variant	rs72666177
Chromosome Location	chr14:32854147-32854148
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10141597	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17098967	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3784179	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72666176	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72666179	0.90[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs72666181	0.90[ASN][1000 genomes]

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32849000-32867400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:32850800-32854200	Enhancers	NHEK	skin
3	chr14:32850800-32854400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr14:32851000-32854200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr14:32852800-32854400	Enhancers	Brain Anterior Caudate	brain
6	chr14:32853000-32854600	Enhancers	Brain Substantia Nigra	brain
7	chr14:32853400-32854400	Enhancers	Stomach Mucosa	stomach
8	chr14:32853600-32854200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr14:32854000-32854400	Enhancers	Fetal Brain Female	brain

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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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