Variant report

Variant	rs10261881
Chromosome Location	chr7:106781650-106781651
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:106780093..106782800-chr7:107098466..107101440,2	K562	blood:
2	chr7:106781336..106783880-chr7:106809504..106811989,2	K562	blood:
3	chr7:106772470..106774021-chr7:106779836..106782677,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000105856	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs1004570	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10232542	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10241141	0.91[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10241155	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10248105	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10249866	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10253172	0.81[ASN][1000 genomes]
rs10253291	0.81[ASN][1000 genomes]
rs10271426	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10272371	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10281856	0.95[YRI][hapmap]
rs11509187	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11760966	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11762123	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11764389	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11767623	0.81[ASN][1000 genomes]
rs11767753	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11772066	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12055946	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12154324	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12705405	0.81[ASN][1000 genomes]
rs17153823	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17153861	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17340358	0.85[EUR][1000 genomes]
rs17340479	0.85[EUR][1000 genomes]
rs17340577	0.88[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs17341680	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17425839	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1860803	1.00[YRI][hapmap]
rs1860804	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1860805	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1981696	0.81[ASN][1000 genomes]
rs2041525	0.84[EUR][1000 genomes]
rs2041526	0.84[EUR][1000 genomes]
rs2191917	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2237653	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2250121	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2536490	1.00[JPT][hapmap]
rs257371	0.81[ASN][1000 genomes]
rs257372	0.81[ASN][1000 genomes]
rs257373	0.81[ASN][1000 genomes]
rs257375	0.81[ASN][1000 genomes]
rs257377	0.81[ASN][1000 genomes]
rs257378	0.81[ASN][1000 genomes]
rs257379	0.81[ASN][1000 genomes]
rs257381	0.81[ASN][1000 genomes]
rs257382	0.81[ASN][1000 genomes]
rs257385	0.81[ASN][1000 genomes]
rs257386	0.81[ASN][1000 genomes]
rs257387	0.81[ASN][1000 genomes]
rs28610544	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28873708	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3729876	0.81[ASN][1000 genomes]
rs3729877	0.81[ASN][1000 genomes]
rs3752645	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3779500	0.81[ASN][1000 genomes]
rs4460293	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56704102	0.85[EUR][1000 genomes]
rs58386564	0.84[EUR][1000 genomes]
rs58979869	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6466160	0.81[ASN][1000 genomes]
rs6946931	0.81[ASN][1000 genomes]
rs6947857	0.81[ASN][1000 genomes]
rs6960708	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6971393	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6977868	0.81[ASN][1000 genomes]
rs6978486	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs717099	1.00[YRI][hapmap]
rs7778076	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7780728	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7780784	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7780830	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7786296	0.86[ASN][1000 genomes]
rs7786692	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8180787	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9641372	0.80[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831087	chr7:106673465-106872460	Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:106760200-106782000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr7:106760400-106808400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:106763000-106807800	Weak transcription	Stomach Smooth Muscle	stomach
4	chr7:106767400-106797600	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr7:106767800-106782400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr7:106773200-106786800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:106778400-106807800	Weak transcription	Brain Germinal Matrix	brain
8	chr7:106778800-106782800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr7:106779800-106790800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr7:106780000-106782400	Weak transcription	Fetal Stomach	stomach
11	chr7:106780000-106787000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:106780000-106807800	Weak transcription	Fetal Heart	heart
13	chr7:106780200-106782400	Weak transcription	Adipose Nuclei	Adipose
14	chr7:106780200-106787800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:106780200-106792000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr7:106780200-106792200	Weak transcription	Fetal Brain Female	brain
17	chr7:106781200-106782600	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr7:106781400-106783800	Strong transcription	K562	blood

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