Variant report

Variant	rs10193451
Chromosome Location	chr2:151956318-151956319
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10174574	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10176186	0.84[AMR][1000 genomes]
rs10183699	0.81[ASN][1000 genomes]
rs10187168	0.86[AMR][1000 genomes]
rs10188675	0.86[AMR][1000 genomes]
rs10221581	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10930435	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1115140	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11883593	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11883594	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11889216	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11890910	0.85[AMR][1000 genomes]
rs12992820	0.84[AMR][1000 genomes]
rs1351930	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1485097	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1485099	0.84[AMR][1000 genomes]
rs1485112	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1485113	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1485117	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1843271	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2086914	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35956016	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3940993	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4606923	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4664951	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4664952	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4664953	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6433191	0.81[ASN][1000 genomes]
rs6433192	0.81[ASN][1000 genomes]
rs6707611	0.81[ASN][1000 genomes]
rs6725316	0.81[ASN][1000 genomes]
rs6735499	0.81[ASN][1000 genomes]
rs7584360	0.81[ASN][1000 genomes]
rs936766	0.84[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525350	chr2:151711700-152044794	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv523849	chr2:151718133-152143524	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	esv3693426	chr2:151725792-152295862	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv1002140	chr2:151833257-152054910	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:151942400-151958800	Weak transcription	Fetal Brain Female	brain
2	chr2:151953600-151958800	Weak transcription	Fetal Brain Male	brain
3	chr2:151954200-151958800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr2:151954200-151959400	Weak transcription	Fetal Stomach	stomach
5	chr2:151954400-151958600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr2:151954400-151958800	Weak transcription	Brain Germinal Matrix	brain
7	chr2:151955800-151959200	Weak transcription	Fetal Lung	lung

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