Variant report

Variant	rs34591697
Chromosome Location	chr11:17086927-17086928
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	chr11:17085165..17088143-chr11:17093678..17095207,2	MCF-7	breast:

Extended variants
information (count: 37 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10832728	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10832733	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10832734	0.85[AMR][1000 genomes]
rs10832735	0.82[AMR][1000 genomes]
rs10832736	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10832739	0.81[EUR][1000 genomes]
rs11024143	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11024148	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11024158	0.81[EUR][1000 genomes]
rs11024159	0.81[EUR][1000 genomes]
rs11024163	0.81[EUR][1000 genomes]
rs11821773	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12286505	0.80[EUR][1000 genomes]
rs17472886	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2052188	0.81[EUR][1000 genomes]
rs35933265	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6486352	0.80[EUR][1000 genomes]
rs7104247	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7106705	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7107283	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7107745	0.80[EUR][1000 genomes]
rs7118006	0.80[EUR][1000 genomes]
rs7123301	0.80[EUR][1000 genomes]
rs7125607	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7396382	0.81[EUR][1000 genomes]
rs7927240	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7930058	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7932916	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7938820	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7939614	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7939750	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7946010	0.80[EUR][1000 genomes]
rs7946165	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9919540	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9919600	0.83[AMR][1000 genomes];0.83[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	nsv467711	chr11:17027555-17320797	Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv553568	chr11:17027555-17320797	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs34591697	OR7E14P	cis	Nerve Tibial	GTEx
rs34591697	NUCB2	Cis_1M	lymphoblastoid	RTeQTL
rs34591697	OR7E14P	cis	Esophagus Mucosa	GTEx

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17069400-17096200	Weak transcription	Pancreas	Pancrea
2	chr11:17070600-17088400	Weak transcription	Fetal Intestine Small	intestine
3	chr11:17079400-17094600	Weak transcription	Primary B cells from cord blood	blood
4	chr11:17083800-17093800	Weak transcription	A549	lung
5	chr11:17084400-17095000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr11:17084800-17095200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr11:17085400-17088600	Weak transcription	Brain Substantia Nigra	brain
8	chr11:17085400-17089000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr11:17085400-17089000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr11:17085400-17097200	Weak transcription	Right Ventricle	heart
11	chr11:17085400-17098200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr11:17086000-17094600	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr11:17086600-17088400	Weak transcription	Fetal Stomach	stomach
14	chr11:17086800-17094200	Weak transcription	Duodenum Mucosa	Duodenum

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