Variant report

Variant	rs10108945
Chromosome Location	chr8:91523522-91523523
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10089332	0.82[ASN][1000 genomes]
rs10091178	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10093767	0.92[ASN][1000 genomes]
rs10095288	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10098239	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs10098532	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10103375	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs10105230	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10106046	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs10106178	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10109473	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs10112962	0.92[ASN][1000 genomes]
rs10454349	0.96[ASN][1000 genomes]
rs10808602	0.92[ASN][1000 genomes]
rs12114208	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12114338	0.92[ASN][1000 genomes]
rs12114484	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs13438978	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs16904659	0.92[ASN][1000 genomes]
rs28370967	0.87[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs28418603	0.87[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs28458242	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs28571853	0.86[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs28625286	0.80[AMR][1000 genomes]
rs28628063	0.80[AMR][1000 genomes]
rs28635136	0.87[AFR][1000 genomes]
rs28642916	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs28646030	0.82[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs28654995	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs28861773	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs28880105	0.92[ASN][1000 genomes]
rs28884543	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4518620	0.92[ASN][1000 genomes]
rs4531005	0.80[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs58288406	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs59158124	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs73697715	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73697720	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs73697729	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs7813183	0.92[ASN][1000 genomes]
rs7825039	0.90[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs7834137	0.92[ASN][1000 genomes]
rs9642911	0.92[ASN][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91522000-91532400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:91522400-91524800	Enhancers	Placenta Amnion	Placenta Amnion
3	chr8:91523000-91524000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr8:91523200-91523800	Enhancers	HMEC	breast
5	chr8:91523400-91523800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:91523400-91524000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:91523400-91524000	Enhancers	K562	blood

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