Variant report

Variant	rs4852900
Chromosome Location	chr2:73082563-73082564
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10204141	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10496187	0.94[CEU][hapmap];0.93[YRI][hapmap];0.88[EUR][1000 genomes]
rs11126378	0.96[YRI][hapmap]
rs11126382	0.88[EUR][1000 genomes]
rs11126386	0.95[EUR][1000 genomes]
rs11693376	1.00[JPT][hapmap]
rs11886503	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12614041	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12615163	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs12615875	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12619068	0.93[CEU][hapmap];0.96[YRI][hapmap];0.95[EUR][1000 genomes]
rs12619565	0.94[CEU][hapmap];0.96[YRI][hapmap];0.88[EUR][1000 genomes]
rs12994646	0.84[ASN][1000 genomes]
rs13008515	1.00[JPT][hapmap]
rs1508060	0.84[ASN][1000 genomes]
rs1532970	1.00[JPT][hapmap]
rs1562361	0.96[YRI][hapmap]
rs17008369	0.93[YRI][hapmap]
rs17008371	0.96[YRI][hapmap]
rs1876488	0.94[CEU][hapmap];0.93[YRI][hapmap];0.95[EUR][1000 genomes]
rs1876489	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs1876490	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs2063168	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2068410	0.94[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap];0.87[EUR][1000 genomes]
rs2135982	0.82[ASN][1000 genomes]
rs4597553	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.87[EUR][1000 genomes]
rs4852896	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4852897	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55749009	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55802296	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs56181835	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56711961	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57264301	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs58890506	0.84[EUR][1000 genomes]
rs59615613	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs60584321	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61619102	0.84[EUR][1000 genomes]
rs6713143	0.96[YRI][hapmap]
rs6716335	0.94[CEU][hapmap];0.93[YRI][hapmap];0.83[EUR][1000 genomes]
rs6761253	0.94[CEU][hapmap];0.93[YRI][hapmap];0.83[EUR][1000 genomes]
rs67919884	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs67927720	0.95[EUR][1000 genomes]
rs7567893	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7577528	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7586339	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7586886	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7593084	0.87[CEU][hapmap];0.96[YRI][hapmap];0.87[EUR][1000 genomes]
rs7600718	1.00[JPT][hapmap]
rs7604402	0.92[CEU][hapmap];0.83[YRI][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7607226	0.94[CEU][hapmap];0.93[YRI][hapmap];0.87[EUR][1000 genomes]
rs970577	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834259	chr2:72941118-73114106	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	esv3457893	chr2:73081432-73082593	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
3	esv3457894	chr2:73081432-73082593	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73079000-73083800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr2:73079000-73088200	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr2:73082200-73088200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:73082400-73082600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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