Variant report

Variant	rs73017236
Chromosome Location	chr6:164156031-164156032
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:164149744..164152325-chr6:164152772..164156227,3	K562	blood:
2	chr6:164137255..164140112-chr6:164154106..164157033,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs12209978	0.87[ASN][1000 genomes]
rs12214405	0.87[ASN][1000 genomes]
rs12663209	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12664781	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12665755	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12665812	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1407656	0.87[ASN][1000 genomes]
rs55660929	0.86[ASN][1000 genomes]
rs55896086	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56262560	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56292260	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58218631	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58940838	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61555711	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs66767192	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67071357	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68041511	0.97[ASN][1000 genomes]
rs6938954	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73013417	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73017240	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73017247	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73017275	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73017284	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73019106	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73019121	0.83[EUR][1000 genomes]
rs73029220	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73029224	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73029225	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73029241	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73029267	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73029269	0.89[EUR][1000 genomes]
rs750810	0.97[ASN][1000 genomes]
rs7752027	0.97[ASN][1000 genomes]
rs7775940	0.87[ASN][1000 genomes]
rs9458881	0.87[ASN][1000 genomes]
rs9458883	0.87[ASN][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	nsv1018860	chr6:163939347-164532579	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538526	chr6:163939347-164532579	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	esv2758092	chr6:163992064-164161903	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	esv2759490	chr6:163992064-164161903	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv1025171	chr6:164113981-164170027	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr6:164146400-164158000	Weak transcription	Spleen	Spleen
2	chr6:164152200-164161000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:164152200-164162600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:164152600-164161600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:164154600-164159400	Weak transcription	Left Ventricle	heart
6	chr6:164154800-164156800	Weak transcription	Fetal Muscle Leg	muscle
7	chr6:164154800-164159200	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr6:164154800-164159200	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr6:164154800-164160800	Weak transcription	Fetal Heart	heart
10	chr6:164154800-164161000	Weak transcription	Right Atrium	heart
11	chr6:164154800-164161200	Weak transcription	Lung	lung
12	chr6:164155800-164156400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:164156000-164156200	Enhancers	Primary B cells from peripheral blood	blood
14	chr6:164156000-164156400	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr6:164156000-164156400	Enhancers	GM12878-XiMat	blood
16	chr6:164156000-164156800	Enhancers	K562	blood
17	chr6:164156000-164157200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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