Variant report

Variant	rs34766974
Chromosome Location	chr5:42575381-42575382
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs34521671	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34580109	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35525634	0.95[EUR][1000 genomes]
rs56144821	0.95[EUR][1000 genomes]
rs66531739	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68070657	1.00[ASN][1000 genomes]
rs6868132	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6883523	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];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	nsv933208	chr5:41879946-42876624	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	112 gene(s)	inside rSNPs	diseases
2	nsv492147	chr5:41902086-42896162	Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	113 gene(s)	inside rSNPs	diseases
3	nsv1020464	chr5:42488628-42699394	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1018751	chr5:42491883-42697923	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:42566000-42576200	Weak transcription	Spleen	Spleen
2	chr5:42568000-42579400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr5:42568000-42581400	Weak transcription	Fetal Muscle Trunk	muscle
4	chr5:42568000-42582200	Weak transcription	Fetal Intestine Small	intestine
5	chr5:42568400-42581800	Weak transcription	Fetal Stomach	stomach
6	chr5:42568400-42582800	Weak transcription	Ovary	ovary
7	chr5:42571800-42579400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr5:42571800-42581200	Weak transcription	Adipose Nuclei	Adipose
9	chr5:42571800-42583400	Weak transcription	Stomach Smooth Muscle	stomach
10	chr5:42572000-42578600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr5:42572200-42587800	Weak transcription	Left Ventricle	heart
12	chr5:42572400-42582800	Weak transcription	Right Ventricle	heart
13	chr5:42572800-42579400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr5:42572800-42583000	Weak transcription	Fetal Muscle Leg	muscle
15	chr5:42573000-42579400	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr5:42573000-42581800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr5:42573000-42582000	Weak transcription	Fetal Lung	lung
18	chr5:42573400-42579000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr5:42573600-42586600	Weak transcription	Psoas Muscle	Psoas
20	chr5:42574600-42579400	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr5:42575200-42575400	Enhancers	Aorta	Aorta
22	chr5:42575200-42575800	Enhancers	Liver	Liver

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