Variant report

Variant	rs13422674
Chromosome Location	chr2:21790466-21790467
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:21789116..21791651-chr2:21801369..21803273,2	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10200683	0.85[ASN][1000 genomes]
rs10209178	0.91[AMR][1000 genomes]
rs10211154	0.91[AMR][1000 genomes]
rs10211567	0.91[AMR][1000 genomes]
rs11126823	1.00[AMR][1000 genomes]
rs11126835	0.91[AMR][1000 genomes]
rs11126863	0.91[AMR][1000 genomes]
rs13000075	0.91[AMR][1000 genomes]
rs13397909	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13427297	0.81[AMR][1000 genomes]
rs1477471	0.91[AMR][1000 genomes]
rs1477472	0.91[AMR][1000 genomes]
rs17042253	0.85[JPT][hapmap]
rs17042257	0.85[JPT][hapmap]
rs1968279	0.91[AMR][1000 genomes]
rs1991128	0.85[ASN][1000 genomes]
rs2042523	1.00[AMR][1000 genomes]
rs2194558	0.85[ASN][1000 genomes]
rs2194559	0.85[ASN][1000 genomes]
rs2194567	0.91[AMR][1000 genomes]
rs2194571	0.85[ASN][1000 genomes]
rs2288150	1.00[AMR][1000 genomes]
rs2288151	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28361438	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4473414	0.91[AMR][1000 genomes]
rs4665367	0.91[AMR][1000 genomes]
rs4665368	0.91[AMR][1000 genomes]
rs4665369	1.00[AMR][1000 genomes]
rs56149559	0.81[AMR][1000 genomes]
rs57208668	0.91[AMR][1000 genomes]
rs6547383	0.91[AMR][1000 genomes]
rs6547384	0.91[AMR][1000 genomes]
rs6547423	0.91[AMR][1000 genomes]
rs6547698	0.85[ASN][1000 genomes]
rs6729222	0.85[ASN][1000 genomes]
rs6738468	0.91[AMR][1000 genomes]
rs6743443	0.91[AMR][1000 genomes]
rs6744152	0.91[AMR][1000 genomes]
rs6745563	1.00[JPT][hapmap]
rs6747084	0.91[AMR][1000 genomes]
rs6747935	0.91[AMR][1000 genomes]
rs72892296	0.81[AMR][1000 genomes]
rs72894021	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs72894032	0.85[ASN][1000 genomes]
rs72894034	0.85[ASN][1000 genomes]
rs7575945	1.00[AMR][1000 genomes]
rs970125	0.91[AMR][1000 genomes]
rs970126	0.91[AMR][1000 genomes]
rs979038	0.91[AMR][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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21790000-21791400	Enhancers	Ovary	ovary
2	chr2:21790400-21790600	Enhancers	Aorta	Aorta

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