Variant report

Variant	rs73091731
Chromosome Location	chr12:44451824-44451825
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:44446827..44449468-chr12:44449634..44452541,2	K562	blood:
2	chr12:44450654..44453609-chr12:44454497..44456502,2	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11182381	0.86[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs56040109	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs56070984	0.81[EUR][1000 genomes]
rs56189744	0.83[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs58729113	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs59110659	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs73085780	0.81[EUR][1000 genomes]
rs73085785	0.81[EUR][1000 genomes]
rs73087608	0.81[EUR][1000 genomes]
rs73087620	0.81[EUR][1000 genomes]
rs73087623	0.81[EUR][1000 genomes]
rs73087628	0.81[EUR][1000 genomes]
rs73087631	0.81[EUR][1000 genomes]
rs73087638	0.80[EUR][1000 genomes]
rs73087643	0.81[EUR][1000 genomes]
rs73087652	0.80[EUR][1000 genomes]
rs73087657	0.80[EUR][1000 genomes]
rs73087667	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs73087672	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs73087674	0.81[EUR][1000 genomes]
rs73087678	0.80[EUR][1000 genomes]
rs73087690	0.80[EUR][1000 genomes]
rs73087697	0.83[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs73087699	0.83[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs73089709	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs73089717	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs73089719	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs73089736	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs73089738	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs73089749	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs73089758	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs73091734	1.00[EUR][1000 genomes]
rs74084623	0.83[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs74087905	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs74087909	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7979716	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832390	chr12:44318071-44512114	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1041188	chr12:44331098-44528712	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv832391	chr12:44394137-44552555	ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44439200-44464400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:44447000-44459800	Weak transcription	Gastric	stomach
3	chr12:44448200-44452000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr12:44451000-44453200	Enhancers	Fetal Brain Male	brain

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