Variant report

Variant	rs12510174
Chromosome Location	chr4:74322255-74322256
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10001225	0.87[ASN][1000 genomes]
rs10002756	0.95[CEU][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10020432	0.95[CEU][hapmap];0.83[JPT][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10022167	0.91[CEU][hapmap]
rs10031441	0.95[CEU][hapmap];0.83[JPT][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12504308	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12506899	0.95[CEU][hapmap];0.83[JPT][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12649712	0.92[CEU][hapmap]
rs13138734	0.92[CEU][hapmap]
rs13150293	0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1358592	0.83[JPT][hapmap]
rs1475934	0.92[CEU][hapmap]
rs16849341	0.91[CEU][hapmap]
rs16849384	0.95[CEU][hapmap];0.88[EUR][1000 genomes]
rs16849508	0.84[JPT][hapmap]
rs2051512	0.91[CEU][hapmap]
rs2070849	0.96[CEU][hapmap]
rs2276937	0.96[CEU][hapmap]
rs2298839	0.95[CEU][hapmap];0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs3756066	0.91[CEU][hapmap]
rs3775485	0.92[CEU][hapmap]
rs3775486	0.92[CEU][hapmap]
rs3796676	1.00[CEU][hapmap]
rs3822100	0.84[JPT][hapmap]
rs4018	0.95[CEU][hapmap]
rs4024	0.95[CEU][hapmap]
rs4403016	0.96[CEU][hapmap]
rs4446279	0.83[JPT][hapmap]
rs4513532	0.92[CEU][hapmap]
rs4575963	0.91[CEU][hapmap]
rs4640638	0.84[JPT][hapmap]
rs4694613	0.92[CEU][hapmap]
rs6446931	0.92[CEU][hapmap]
rs6446937	0.83[JPT][hapmap]
rs6446938	0.83[JPT][hapmap]
rs6820167	0.86[CEU][hapmap]
rs6834059	0.84[JPT][hapmap]
rs6850155	0.87[CEU][hapmap]
rs6852772	0.83[JPT][hapmap]
rs6853164	0.86[CEU][hapmap]
rs714825	0.91[CEU][hapmap]
rs737241	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7660680	0.95[CEU][hapmap];0.84[JPT][hapmap];0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7668327	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7688274	0.91[CEU][hapmap]
rs9996318	0.91[CEU][hapmap]

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	esv3430875	chr4:74243646-74420354	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74319600-74324400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr4:74322000-74322400	Genic enhancers	HepG2	liver
3	chr4:74322000-74322800	Enhancers	Fetal Intestine Large	intestine
4	chr4:74322000-74322800	Enhancers	Fetal Intestine Small	intestine

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