Variant report

Variant	rs9532298
Chromosome Location	chr13:39467523-39467524
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:39460498..39462808-chr13:39464798..39467531,2	K562	blood:

Extended variants
information (count: 117 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:115)

rs_ID	r²[population]
rs11618742	1.00[ASN][1000 genomes]
rs12864816	1.00[ASN][1000 genomes]
rs12869426	1.00[ASN][1000 genomes]
rs12869876	1.00[ASN][1000 genomes]
rs12869917	1.00[ASN][1000 genomes]
rs12875224	1.00[ASN][1000 genomes]
rs1333506	1.00[ASN][1000 genomes]
rs1333508	1.00[ASN][1000 genomes]
rs1333510	0.83[AMR][1000 genomes]
rs1894106	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1894107	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1945496	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1945509	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1945510	0.94[EUR][1000 genomes]
rs34127262	1.00[ASN][1000 genomes]
rs34943621	1.00[ASN][1000 genomes]
rs35252750	1.00[ASN][1000 genomes]
rs35429023	1.00[ASN][1000 genomes]
rs35459396	1.00[ASN][1000 genomes]
rs35657252	1.00[ASN][1000 genomes]
rs35944548	1.00[ASN][1000 genomes]
rs35986835	1.00[ASN][1000 genomes]
rs36088006	1.00[ASN][1000 genomes]
rs4287442	1.00[ASN][1000 genomes]
rs4334155	1.00[ASN][1000 genomes]
rs4369521	1.00[ASN][1000 genomes]
rs4397983	1.00[ASN][1000 genomes]
rs4426230	1.00[ASN][1000 genomes]
rs4426231	1.00[ASN][1000 genomes]
rs4533148	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4643179	1.00[ASN][1000 genomes]
rs4943606	1.00[ASN][1000 genomes]
rs4943607	1.00[ASN][1000 genomes]
rs4943608	1.00[ASN][1000 genomes]
rs4943609	1.00[ASN][1000 genomes]
rs4943610	1.00[ASN][1000 genomes]
rs4943611	1.00[ASN][1000 genomes]
rs4943612	1.00[ASN][1000 genomes]
rs4943614	0.94[EUR][1000 genomes]
rs4943615	1.00[ASN][1000 genomes]
rs61945515	1.00[ASN][1000 genomes]
rs61945516	1.00[ASN][1000 genomes]
rs61945763	1.00[ASN][1000 genomes]
rs61947983	1.00[ASN][1000 genomes]
rs61948017	1.00[ASN][1000 genomes]
rs61948018	1.00[ASN][1000 genomes]
rs66889481	1.00[ASN][1000 genomes]
rs71198492	1.00[ASN][1000 genomes]
rs71423186	1.00[ASN][1000 genomes]
rs71423187	1.00[ASN][1000 genomes]
rs71439788	1.00[ASN][1000 genomes]
rs71439789	1.00[ASN][1000 genomes]
rs73169477	1.00[ASN][1000 genomes]
rs7328953	1.00[ASN][1000 genomes]
rs7331927	1.00[ASN][1000 genomes]
rs7332206	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7982313	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9532285	1.00[ASN][1000 genomes]
rs9532287	1.00[ASN][1000 genomes]
rs9532288	1.00[ASN][1000 genomes]
rs9532294	1.00[ASN][1000 genomes]
rs9532295	0.90[EUR][1000 genomes]
rs9532297	1.00[ASN][1000 genomes]
rs9532310	1.00[ASN][1000 genomes]
rs9548466	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs9548467	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs9548468	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs9548471	1.00[ASN][1000 genomes]
rs9548473	1.00[ASN][1000 genomes]
rs9548474	1.00[ASN][1000 genomes]
rs9548475	1.00[ASN][1000 genomes]
rs9548476	1.00[ASN][1000 genomes]
rs9548478	1.00[ASN][1000 genomes]
rs9548479	1.00[ASN][1000 genomes]
rs9548480	1.00[ASN][1000 genomes]
rs9548488	1.00[ASN][1000 genomes]
rs9548489	1.00[ASN][1000 genomes]
rs9548490	1.00[ASN][1000 genomes]
rs9548492	1.00[ASN][1000 genomes]
rs9548493	1.00[ASN][1000 genomes]
rs9548494	1.00[ASN][1000 genomes]
rs9548495	1.00[ASN][1000 genomes]
rs9548496	1.00[ASN][1000 genomes]
rs9548497	1.00[ASN][1000 genomes]
rs9548498	1.00[ASN][1000 genomes]
rs9548499	1.00[ASN][1000 genomes]
rs9548500	1.00[ASN][1000 genomes]
rs9548501	1.00[ASN][1000 genomes]
rs9548502	1.00[ASN][1000 genomes]
rs9548503	1.00[ASN][1000 genomes]
rs9548504	1.00[ASN][1000 genomes]
rs9548505	1.00[ASN][1000 genomes]
rs9548507	1.00[ASN][1000 genomes]
rs9548515	1.00[ASN][1000 genomes]
rs9548516	0.92[EUR][1000 genomes]
rs9548521	1.00[CHB][hapmap];0.84[MEX][hapmap];1.00[ASN][1000 genomes]
rs9548523	1.00[ASN][1000 genomes]
rs9548524	1.00[ASN][1000 genomes]
rs9548525	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9548531	1.00[ASN][1000 genomes]
rs9548532	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9548535	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9548546	1.00[CHB][hapmap]
rs9548550	1.00[CHB][hapmap]
rs9548552	1.00[ASN][1000 genomes]
rs9548554	1.00[ASN][1000 genomes]
rs9548555	1.00[ASN][1000 genomes]
rs9548556	1.00[ASN][1000 genomes]
rs9548557	1.00[ASN][1000 genomes]
rs9548560	1.00[ASN][1000 genomes]
rs9548562	1.00[ASN][1000 genomes]
rs9548563	1.00[ASN][1000 genomes]
rs9548569	1.00[ASN][1000 genomes]
rs9548573	1.00[ASN][1000 genomes]
rs9548576	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754118	chr13:39347702-40222644	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv1008	chr13:39458830-39468613	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9532298	MAB21L1	cis	parietal	SCAN

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:39432600-39468600	Weak transcription	Psoas Muscle	Psoas
2	chr13:39451400-39468200	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr13:39458400-39469200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr13:39462800-39471800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr13:39463000-39476200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr13:39466400-39470000	Weak transcription	Fetal Kidney	kidney

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