Variant report

Variant	rs72681629
Chromosome Location	chr1:77893313-77893314
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10873937	0.84[ASN][1000 genomes]
rs12131772	0.84[ASN][1000 genomes]
rs1498404	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1532507	0.84[ASN][1000 genomes]
rs1532511	0.86[ASN][1000 genomes]
rs34277277	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3844166	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72681614	0.88[AMR][1000 genomes]
rs7512893	0.84[ASN][1000 genomes]
rs7546409	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs9633480	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005183	chr1:77728990-77949309	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv535010	chr1:77728990-77949309	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv932557	chr1:77730247-77958687	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1003714	chr1:77756861-77949309	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv470719	chr1:77774413-78269207	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
6	nsv546591	chr1:77774413-78269207	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
7	esv1848735	chr1:77885282-77918347	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv871605	chr1:77889505-77918347	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77872200-77893400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr1:77872200-77913800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr1:77888000-77893600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr1:77888000-77897000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:77888200-77893400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr1:77888400-77893600	Weak transcription	Brain Angular Gyrus	brain
7	chr1:77889800-77893600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr1:77890200-77893400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr1:77890200-77893400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr1:77890400-77893600	Weak transcription	Brain Hippocampus Middle	brain
11	chr1:77890400-77893600	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr1:77892000-77894000	ZNF genes & repeats	Primary T cells from cord blood	blood
13	chr1:77892200-77893400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr1:77892400-77893400	Weak transcription	Brain Substantia Nigra	brain
15	chr1:77892600-77893400	Weak transcription	HSMM	muscle
16	chr1:77892600-77893400	Weak transcription	NHDF-Ad	bronchial
17	chr1:77893000-77895200	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr1:77893000-77895800	Strong transcription	Muscle Satellite Cultured Cells	--
19	chr1:77893200-77893400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:77893200-77894200	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood

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