Variant report

Variant	rs7129970
Chromosome Location	chr11:93572256-93572257
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:93561270..93566142-chr11:93569079..93572564,4	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10765635	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10831105	0.80[AFR][1000 genomes]
rs11020532	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11020533	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1150326	0.85[ASN][1000 genomes]
rs1298531	0.93[ASN][1000 genomes]
rs16919444	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34057693	0.83[ASN][1000 genomes]
rs3763808	0.92[ASN][1000 genomes]
rs55734929	0.92[ASN][1000 genomes]
rs58063272	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs584084	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs58976781	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59726694	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs601792	0.93[ASN][1000 genomes]
rs61498836	0.88[ASN][1000 genomes]
rs61904957	0.92[ASN][1000 genomes]
rs61906576	0.94[ASN][1000 genomes]
rs61906579	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs625359	0.94[EUR][1000 genomes]
rs625685	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs626216	0.92[ASN][1000 genomes]
rs636482	0.93[ASN][1000 genomes]
rs654896	0.93[ASN][1000 genomes]
rs664257	0.81[ASN][1000 genomes]
rs66483735	0.81[ASN][1000 genomes]
rs66487029	0.89[ASN][1000 genomes]
rs66760087	0.92[ASN][1000 genomes]
rs66797025	0.81[ASN][1000 genomes]
rs66887806	0.94[ASN][1000 genomes]
rs669565	0.85[ASN][1000 genomes]
rs66963387	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs670391	0.80[ASN][1000 genomes]
rs67594435	0.89[ASN][1000 genomes]
rs67681709	0.81[ASN][1000 genomes]
rs677019	0.93[ASN][1000 genomes]
rs67734074	0.86[ASN][1000 genomes]
rs679241	0.93[ASN][1000 genomes]
rs7103466	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7114611	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7115115	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7119738	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7125525	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7125919	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7126745	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72976543	0.81[ASN][1000 genomes]
rs72976568	0.81[ASN][1000 genomes]
rs7924366	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7949505	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898181	chr11:93072843-93662459	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
2	nsv898182	chr11:93381845-93637462	Strong transcription Genic enhancers Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	108 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93565000-93575200	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr11:93565400-93575400	Weak transcription	Duodenum Mucosa	Duodenum
3	chr11:93566200-93577000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr11:93567800-93575600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr11:93570400-93579200	Enhancers	Stomach Mucosa	stomach
6	chr11:93571400-93574400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr11:93572200-93572400	Active TSS	HepG2	liver
8	chr11:93572200-93572600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr11:93572200-93572800	Enhancers	Fetal Intestine Small	intestine
10	chr11:93572200-93573200	Enhancers	Placenta	Placenta

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