Variant report

Variant	rs34371023
Chromosome Location	chr11:8872594-8872595
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10734638	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11042099	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1811367	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2060157	0.89[EUR][1000 genomes]
rs2568029	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2568035	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2568056	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2568078	0.95[EUR][1000 genomes]
rs2653558	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2653566	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2653609	0.84[EUR][1000 genomes]
rs2653618	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2742483	0.86[EUR][1000 genomes]
rs2742502	0.93[EUR][1000 genomes]
rs2742549	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2742553	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34023999	0.84[AMR][1000 genomes]
rs34033747	0.86[AMR][1000 genomes]
rs34152382	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34275210	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34418236	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34581555	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs34769330	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35503692	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35563381	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35580466	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35909878	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs36094920	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs36100955	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36180552	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4910068	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7110170	0.80[EUR][1000 genomes]
rs7117900	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7127197	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7950491	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758256	chr11:8784813-9009573	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	esv2759803	chr11:8784813-9009573	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv435923	chr11:8839325-9000602	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv832062	chr11:8849295-9009472	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	nsv975830	chr11:8867561-8873550	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs34371023	C11orf17	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8862200-8881200	Weak transcription	Hela-S3	cervix
2	chr11:8862400-8874600	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr11:8862400-8880000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr11:8862400-8880000	Weak transcription	Spleen	Spleen
5	chr11:8862400-8885000	Weak transcription	NHLF	lung
6	chr11:8862400-8888400	Weak transcription	Right Atrium	heart
7	chr11:8862600-8876600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr11:8862600-8885200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr11:8863200-8890400	Weak transcription	Fetal Muscle Trunk	muscle
10	chr11:8864000-8888000	Weak transcription	Fetal Intestine Small	intestine
11	chr11:8865400-8873600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:8865800-8886000	Weak transcription	Fetal Stomach	stomach
13	chr11:8866000-8874200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr11:8867400-8873400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr11:8868200-8876200	Weak transcription	Ovary	ovary
16	chr11:8868800-8877000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr11:8871000-8873400	Weak transcription	Placenta	Placenta
18	chr11:8871000-8877000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr11:8872000-8873200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:8872200-8872600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr11:8872400-8873000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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