Variant report

Variant	rs476474
Chromosome Location	chr12:10165469-10165470
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs1447875	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2200744	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2634166	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61913542	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61913543	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs637790	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6488243	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7302084	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898755	chr12:10069302-10186284	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1043125	chr12:10121288-10177037	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1042106	chr12:10121288-10177636	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1040610	chr12:10121288-10179374	Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv898756	chr12:10142538-10174314	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10163200-10170200	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr12:10163800-10165600	Weak transcription	HUVEC	blood vessel
3	chr12:10165200-10165600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr12:10165200-10165600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr12:10165200-10165600	Bivalent/Poised TSS	Brain Anterior Caudate	brain
6	chr12:10165200-10165600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
7	chr12:10165200-10165600	Enhancers	Gastric	stomach
8	chr12:10165200-10165800	Active TSS	Brain Cingulate Gyrus	brain
9	chr12:10165200-10165800	Active TSS	Brain Inferior Temporal Lobe	brain
10	chr12:10165200-10165800	Active TSS	Brain Substantia Nigra	brain
11	chr12:10165200-10166000	Active TSS	Brain Angular Gyrus	brain
12	chr12:10165200-10169000	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr12:10165400-10165600	Enhancers	H1 Cell Line	embryonic stem cell
14	chr12:10165400-10165600	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr12:10165400-10165600	Enhancers	Esophagus	oesophagus
16	chr12:10165400-10165800	Active TSS	Brain Hippocampus Middle	brain
17	chr12:10165400-10167600	Strong transcription	Primary neutrophils fromperipheralblood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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