Variant report

Variant	rs12613921
Chromosome Location	chr2:21668283-21668284
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:23339522..23342253-chr2:21666341..21668692,2	K562	blood:

Variant related genes	Relation type
ENSG00000197324	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10490609	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10490610	0.89[ASN][1000 genomes]
rs11895666	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12611495	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12611610	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12613395	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12614377	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12615116	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12615149	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12616024	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12616733	1.00[AMR][1000 genomes]
rs12619415	0.89[ASN][1000 genomes]
rs12621032	1.00[AMR][1000 genomes]
rs12622330	1.00[AMR][1000 genomes]
rs12623465	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12623812	0.82[ASN][1000 genomes]
rs12624085	1.00[AMR][1000 genomes]
rs1544858	1.00[CHB][hapmap]
rs17042271	0.92[CHB][hapmap];1.00[AMR][1000 genomes]
rs17042275	0.92[CHB][hapmap]
rs17042324	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17042327	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17042331	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17042333	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17042337	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17042346	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17042350	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17042355	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17042358	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17042361	0.89[ASN][1000 genomes]
rs17042368	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17042369	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17042388	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17042399	0.89[ASN][1000 genomes]
rs17042402	0.89[ASN][1000 genomes]
rs17042404	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs55692465	1.00[ASN][1000 genomes]
rs58352420	1.00[AMR][1000 genomes]
rs59092457	1.00[AMR][1000 genomes]
rs60005484	0.89[ASN][1000 genomes]
rs60036630	1.00[ASN][1000 genomes]
rs61007556	0.89[ASN][1000 genomes]
rs6714370	0.84[CHB][hapmap]
rs73919240	1.00[AMR][1000 genomes]
rs73919244	1.00[AMR][1000 genomes]
rs73919245	1.00[AMR][1000 genomes]
rs73919246	1.00[AMR][1000 genomes]
rs73919247	1.00[AMR][1000 genomes]
rs73919248	1.00[AMR][1000 genomes]
rs73919249	1.00[AMR][1000 genomes]
rs73919263	1.00[ASN][1000 genomes]
rs73919265	1.00[ASN][1000 genomes]
rs73919285	1.00[ASN][1000 genomes]
rs73919288	1.00[ASN][1000 genomes]
rs73919289	1.00[ASN][1000 genomes]
rs73919290	1.00[ASN][1000 genomes]
rs73919295	0.89[ASN][1000 genomes]
rs73919296	0.89[ASN][1000 genomes]
rs73919299	0.89[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	nsv1011486	chr2:21475803-22364002	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv535602	chr2:21475803-22364002	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21646800-21690600	Weak transcription	Aorta	Aorta
2	chr2:21664800-21675200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:21667000-21668600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr2:21667000-21671600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:21667400-21669200	Weak transcription	Ovary	ovary
6	chr2:21667400-21671800	Weak transcription	Rectal Smooth Muscle	rectum

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