Variant report

Variant	rs35594487
Chromosome Location	chr2:208913180-208913181
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 108 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:104)

rs_ID	r²[population]
rs10193505	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10193523	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10198217	0.80[EUR][1000 genomes]
rs10497891	0.81[EUR][1000 genomes]
rs10497892	0.82[EUR][1000 genomes]
rs10497894	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10804164	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10932218	0.81[EUR][1000 genomes]
rs10932220	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10932221	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10932223	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10932225	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10932226	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10932227	0.89[ASN][1000 genomes]
rs10932228	0.89[ASN][1000 genomes]
rs11676872	0.82[EUR][1000 genomes]
rs11679374	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11687255	0.85[ASN][1000 genomes]
rs11688041	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11688936	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11694308	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11891423	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12465154	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12469400	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12612391	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13002375	0.81[EUR][1000 genomes]
rs13002973	0.81[ASN][1000 genomes]
rs13005382	0.80[ASN][1000 genomes]
rs13006024	0.80[EUR][1000 genomes]
rs13387203	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13420900	0.83[EUR][1000 genomes]
rs13421034	0.83[EUR][1000 genomes]
rs1466185	0.83[EUR][1000 genomes]
rs1545503	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16840362	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16840390	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16840392	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17598650	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17641035	0.88[ASN][1000 genomes]
rs1965865	0.82[EUR][1000 genomes]
rs2084870	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2084871	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2100348	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2100349	0.80[EUR][1000 genomes]
rs2362783	0.82[EUR][1000 genomes]
rs2362786	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2362788	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2362789	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2885599	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2885600	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34025579	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34335027	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34354040	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35726860	0.80[EUR][1000 genomes]
rs35783183	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35968595	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3795911	0.80[EUR][1000 genomes]
rs3795912	0.80[EUR][1000 genomes]
rs4673377	0.82[EUR][1000 genomes]
rs4675722	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4675723	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4675724	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4675725	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4675726	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56007263	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56340702	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56812613	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs60679550	0.82[EUR][1000 genomes]
rs6435403	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6435404	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6712527	0.82[EUR][1000 genomes]
rs6718363	0.80[EUR][1000 genomes]
rs6718487	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6723557	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6733857	0.80[EUR][1000 genomes]
rs67351199	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6741366	0.82[EUR][1000 genomes]
rs67417299	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6757323	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6757327	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7424035	0.81[ASN][1000 genomes]
rs7559294	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7559399	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7560222	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7570588	0.82[EUR][1000 genomes]
rs7573629	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7582996	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7583013	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7585863	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7592525	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7599531	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7604044	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7608939	0.83[ASN][1000 genomes]
rs7609428	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs764299	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs896636	0.82[EUR][1000 genomes]
rs921554	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs921555	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs930746	0.81[EUR][1000 genomes]
rs966317	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9789442	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9789446	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9789586	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9789678	0.80[EUR][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	nsv1010531	chr2:208610639-209176782	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv536130	chr2:208610639-209176782	Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv875743	chr2:208688648-208940023	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv534496	chr2:208814372-209302791	Strong transcription Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:208907000-208913800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr2:208912600-208915000	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr2:208912800-208913200	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr2:208912800-208913200	Weak transcription	Small Intestine	intestine
5	chr2:208912800-208913600	Weak transcription	Stomach Mucosa	stomach
6	chr2:208912800-208913800	Weak transcription	HMEC	breast
7	chr2:208912800-208914000	Weak transcription	Duodenum Mucosa	Duodenum
8	chr2:208912800-208929400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links