Variant report

Variant	rs6682147
Chromosome Location	chr1:171793615-171793616
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 104 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs10158220	0.92[ASN][1000 genomes]
rs10158235	0.92[ASN][1000 genomes]
rs10158943	0.92[ASN][1000 genomes]
rs10159080	0.92[ASN][1000 genomes]
rs10489253	0.92[ASN][1000 genomes]
rs10753190	0.87[ASN][1000 genomes]
rs10753195	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10753196	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10753197	0.89[ASN][1000 genomes]
rs10753198	0.89[ASN][1000 genomes]
rs1079820	0.92[ASN][1000 genomes]
rs10798657	0.92[ASN][1000 genomes]
rs10798658	0.90[ASN][1000 genomes]
rs10798661	0.92[ASN][1000 genomes]
rs10798679	0.92[ASN][1000 genomes]
rs10913651	0.85[ASN][1000 genomes]
rs10913730	0.81[ASN][1000 genomes]
rs10913743	0.92[ASN][1000 genomes]
rs10913799	0.89[ASN][1000 genomes]
rs10913803	0.88[ASN][1000 genomes]
rs11579138	0.92[ASN][1000 genomes]
rs11580187	0.92[ASN][1000 genomes]
rs11585645	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11588649	0.92[ASN][1000 genomes]
rs11589200	0.92[ASN][1000 genomes]
rs11589823	0.87[ASN][1000 genomes]
rs11590059	0.90[ASN][1000 genomes]
rs11590829	0.92[ASN][1000 genomes]
rs12022693	0.92[ASN][1000 genomes]
rs12022753	0.92[ASN][1000 genomes]
rs12031686	0.87[ASN][1000 genomes]
rs12057976	0.82[ASN][1000 genomes]
rs12063769	0.92[ASN][1000 genomes]
rs12562644	0.89[ASN][1000 genomes]
rs12723938	0.92[ASN][1000 genomes]
rs1555101	0.87[ASN][1000 genomes]
rs1555102	0.87[ASN][1000 genomes]
rs17597528	0.92[ASN][1000 genomes]
rs17597542	0.92[ASN][1000 genomes]
rs2206541	0.90[ASN][1000 genomes]
rs2206542	0.92[ASN][1000 genomes]
rs2232804	0.87[ASN][1000 genomes]
rs2232809	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2232811	0.87[ASN][1000 genomes]
rs2294719	0.87[ASN][1000 genomes]
rs2294720	0.87[ASN][1000 genomes]
rs2294721	0.87[ASN][1000 genomes]
rs2294722	0.87[ASN][1000 genomes]
rs2421912	0.89[ASN][1000 genomes]
rs2421913	0.92[ASN][1000 genomes]
rs4292987	0.87[ASN][1000 genomes]
rs6425416	0.89[ASN][1000 genomes]
rs6425417	0.89[ASN][1000 genomes]
rs6425422	0.89[ASN][1000 genomes]
rs6425428	0.92[ASN][1000 genomes]
rs6425435	0.92[ASN][1000 genomes]
rs6425436	0.92[ASN][1000 genomes]
rs6425437	0.92[ASN][1000 genomes]
rs6425440	0.92[ASN][1000 genomes]
rs6425441	0.92[ASN][1000 genomes]
rs6657803	0.92[ASN][1000 genomes]
rs6658116	0.92[ASN][1000 genomes]
rs6658730	0.92[ASN][1000 genomes]
rs6658980	0.90[ASN][1000 genomes]
rs6659621	0.92[ASN][1000 genomes]
rs6665727	0.92[ASN][1000 genomes]
rs6668165	0.92[ASN][1000 genomes]
rs6674810	0.92[ASN][1000 genomes]
rs6675011	0.92[ASN][1000 genomes]
rs6678230	0.89[ASN][1000 genomes]
rs6685030	0.86[ASN][1000 genomes]
rs6689108	0.92[ASN][1000 genomes]
rs6689213	0.92[ASN][1000 genomes]
rs6690544	0.92[ASN][1000 genomes]
rs6695736	0.89[ASN][1000 genomes]
rs6698366	0.89[ASN][1000 genomes]
rs6698467	0.89[ASN][1000 genomes]
rs6698892	0.89[ASN][1000 genomes]
rs6700184	0.92[ASN][1000 genomes]
rs6700384	0.92[ASN][1000 genomes]
rs732304	0.87[ASN][1000 genomes]
rs732305	0.87[ASN][1000 genomes]
rs7517546	0.92[ASN][1000 genomes]
rs7517555	0.92[ASN][1000 genomes]
rs7520688	0.92[ASN][1000 genomes]
rs752514	0.87[ASN][1000 genomes]
rs7525313	0.92[ASN][1000 genomes]
rs7537173	0.87[ASN][1000 genomes]
rs7537770	0.92[ASN][1000 genomes]
rs7537931	0.86[ASN][1000 genomes]
rs7537935	0.86[ASN][1000 genomes]
rs7539505	0.92[ASN][1000 genomes]
rs7541128	0.87[ASN][1000 genomes]
rs7545100	0.88[ASN][1000 genomes]
rs7549347	0.92[ASN][1000 genomes]
rs7550603	0.92[ASN][1000 genomes]
rs7552369	0.87[ASN][1000 genomes]
rs7556602	0.92[ASN][1000 genomes]
rs764179	0.92[ASN][1000 genomes]
rs764180	0.92[ASN][1000 genomes]
rs909959	0.89[ASN][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	esv3512995	chr1:171329123-171994470	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	esv3512997	chr1:171329123-171994470	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	nsv872545	chr1:171735198-171805448	Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 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	chr1:171770200-171794600	Weak transcription	Primary T cells from cord blood	blood
2	chr1:171773000-171796000	Weak transcription	Pancreas	Pancrea
3	chr1:171787600-171795800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:171787600-171796000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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