Variant report

Variant	rs2073545
Chromosome Location	chr7:39460668-39460669
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10231896	1.00[AMR][1000 genomes]
rs10237217	1.00[AMR][1000 genomes]
rs10241938	1.00[AMR][1000 genomes]
rs10246249	1.00[AMR][1000 genomes]
rs10249232	1.00[AMR][1000 genomes]
rs10252450	1.00[AMR][1000 genomes]
rs10266285	1.00[AMR][1000 genomes]
rs10275109	1.00[AMR][1000 genomes]
rs12111665	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs12112344	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs12533673	1.00[CHB][hapmap];0.82[CHD][hapmap];0.86[JPT][hapmap]
rs17171576	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs17171578	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.91[ASN][1000 genomes]
rs17713095	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs17713107	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs17713143	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs17769981	0.81[ASN][1000 genomes]
rs17769987	0.81[ASN][1000 genomes]
rs2052017	1.00[CHB][hapmap];0.82[CHD][hapmap];0.86[JPT][hapmap]
rs2052018	1.00[CHB][hapmap];0.82[CHD][hapmap];0.86[JPT][hapmap]
rs2052019	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs2073539	1.00[CHB][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs2237384	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.91[ASN][1000 genomes]
rs2237386	0.91[ASN][1000 genomes]
rs2237387	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs2237388	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs2237392	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2237394	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2237397	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2237398	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2237399	1.00[ASN][1000 genomes]
rs2282915	1.00[CHB][hapmap];0.82[CHD][hapmap];0.86[JPT][hapmap]
rs2299134	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs28513923	1.00[AMR][1000 genomes]
rs28755939	1.00[AMR][1000 genomes]
rs3800850	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs3819416	0.89[ASN][1000 genomes]
rs73388309	0.91[ASN][1000 genomes]
rs73388311	0.91[ASN][1000 genomes]
rs7810746	1.00[AMR][1000 genomes]
rs980392	1.00[ASN][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	nsv1021180	chr7:39424988-39642261	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1026951	chr7:39429036-39642261	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv966782	chr7:39454992-39581886	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1018430	chr7:39455497-39643569	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39455000-39462000	Weak transcription	Fetal Muscle Leg	muscle
2	chr7:39460600-39460800	Enhancers	Brain Germinal Matrix	brain
3	chr7:39460600-39461200	Enhancers	Fetal Brain Male	brain
4	chr7:39460600-39461600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr7:39460600-39462400	Enhancers	HSMMtube	muscle

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