Variant report

Variant	rs61817697
Chromosome Location	chr1:151890958-151890959
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:151885641..151887671-chr1:151889557..151892276,2	K562	blood:
2	chr1:151890687..151893442-chr1:151973018..151975930,2	MCF-7	breast:
3	chr1:151887271..151889135-chr1:151889620..151891203,2	MCF-7	breast:
4	chr1:151890104..151891897-chr1:151945321..151946956,2	K562	blood:
5	chr1:151880051..151885155-chr1:151889040..151897172,18	K562	blood:

Variant related genes	Relation type
ENSG00000159445	Chromatin interaction

Extended variants
information (count: 78 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10494270	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11204906	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11204919	0.83[ASN][1000 genomes]
rs11204920	0.83[ASN][1000 genomes]
rs11582739	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12083193	0.81[AMR][1000 genomes]
rs12095483	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12566232	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16833668	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16833669	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16833670	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16833728	0.83[ASN][1000 genomes]
rs16833743	0.81[AMR][1000 genomes]
rs1844543	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2337685	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2337686	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2338206	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28415528	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2932580	0.83[ASN][1000 genomes]
rs3791153	0.81[AMR][1000 genomes]
rs56000812	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56028913	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs56078223	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56170235	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56313205	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs57674198	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57785325	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs58087484	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61814883	0.85[AMR][1000 genomes]
rs61817695	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61817719	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61817720	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61817722	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61817723	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61817724	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs61817725	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6587632	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6587633	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6587634	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6587635	0.83[ASN][1000 genomes]
rs6587636	0.83[ASN][1000 genomes]
rs6587637	0.83[ASN][1000 genomes]
rs6587638	0.83[ASN][1000 genomes]
rs6657658	0.82[ASN][1000 genomes]
rs6659662	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6662602	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6662728	0.83[ASN][1000 genomes]
rs6663064	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6672064	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6675930	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6678672	0.82[AMR][1000 genomes]
rs6682605	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6684114	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6684312	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6686874	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6690449	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6693388	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6693396	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6693901	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6695324	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6701374	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6703448	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6703465	0.83[ASN][1000 genomes]
rs72694840	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7535002	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7538652	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7541099	0.83[ASN][1000 genomes]
rs7554832	0.83[ASN][1000 genomes]
rs7554859	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs902313	0.83[ASN][1000 genomes]
rs971887	0.83[ASN][1000 genomes]
rs9943221	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9943251	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];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	nsv1007097	chr1:151832796-152227977	Strong transcription Genic enhancers Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
2	nsv1012327	chr1:151835544-152200890	Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
3	nsv535159	chr1:151835544-152200890	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
4	nsv547852	chr1:151843044-151955230	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
5	nsv872441	chr1:151850072-152034430	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	191 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs61817697	THEM4	cis	multi-tissue	Pritchard
rs61817697	THEM4	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151883200-151892200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr1:151885800-151891200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:151888400-151891600	Weak transcription	GM12878-XiMat	blood
4	chr1:151889400-151892200	Weak transcription	K562	blood
5	chr1:151889600-151892600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr1:151890400-151891600	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr1:151890600-151891400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr1:151890800-151891800	Weak transcription	Primary monocytes fromperipheralblood	blood

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