Variant report

Variant	rs11211134
Chromosome Location	chr1:45993118-45993119
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:45984791..45989119-chr1:45989451..45994043,12	MCF-7	breast:
2	chr1:45980210..45995142-chr1:46046095..46057139,89	K562	blood:
3	chr1:45974558..45995867-chr1:46046173..46057010,94	K562	blood:

Variant related genes	Relation type
ENSG00000132780	Chromatin interaction
ENSG00000117450	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 14 )

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10157597	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1044717	0.92[EUR][1000 genomes]
rs10736426	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10789466	0.90[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs1088099	0.91[EUR][1000 genomes]
rs11211132	0.94[EUR][1000 genomes]
rs12038608	0.88[EUR][1000 genomes]
rs12048936	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12082256	0.85[EUR][1000 genomes]
rs12145526	0.92[EUR][1000 genomes]
rs12729974	0.92[EUR][1000 genomes]
rs12749658	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1337902	0.91[EUR][1000 genomes]
rs1494813	0.91[EUR][1000 genomes]
rs1974271	0.93[EUR][1000 genomes]
rs2077808	0.94[EUR][1000 genomes]
rs2152077	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2356555	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2356560	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2356561	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2991966	0.92[EUR][1000 genomes]
rs2993257	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2993259	0.93[EUR][1000 genomes]
rs34315657	0.88[AFR][1000 genomes];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3748643	0.91[EUR][1000 genomes]
rs4233498	0.94[EUR][1000 genomes]
rs4660306	0.94[EUR][1000 genomes]
rs4660309	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4660860	0.91[EUR][1000 genomes]
rs4660862	0.91[EUR][1000 genomes]
rs4660864	0.91[EUR][1000 genomes]
rs4660867	0.93[EUR][1000 genomes]
rs4660868	0.94[EUR][1000 genomes]
rs4660871	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4660872	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6429567	0.91[EUR][1000 genomes]
rs6429569	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6667191	0.92[EUR][1000 genomes]
rs6688424	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6688516	0.92[EUR][1000 genomes]
rs7516006	0.92[EUR][1000 genomes]
rs7522705	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7534467	0.94[EUR][1000 genomes]
rs7536557	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7539253	0.87[EUR][1000 genomes]
rs7543076	0.91[EUR][1000 genomes]
rs7546268	0.91[EUR][1000 genomes]
rs7549093	0.94[EUR][1000 genomes]
rs781066	0.91[EUR][1000 genomes]
rs882803	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs937290	0.91[EUR][1000 genomes]
rs945179	0.93[EUR][1000 genomes]
rs9725380	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9803979	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498036	chr1:45428030-46050934	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	esv1795802	chr1:45819489-46009818	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
3	esv1831217	chr1:45819489-46009818	Strong transcription Enhancers Genic enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
4	nsv530016	chr1:45868543-46069020	Flanking Active TSS Genic enhancers Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
5	nsv829726	chr1:45897581-46103186	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
6	nsv529631	chr1:45905936-46335246	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS 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	207 gene(s)	inside rSNPs	diseases
7	nsv932680	chr1:45935520-46686477	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases
8	nsv868828	chr1:45953923-46686477	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases

mRNA abundance (count:14)

SNP	Gene	Cis/trans	Tissue	Source
rs11211134	CCDC163P	cis	lung	GTEx
rs11211134	CCDC163P	cis	Artery Tibial	GTEx
rs11211134	CCDC163P	cis	Nerve Tibial	GTEx
rs11211134	CCDC163P	cis	Adipose Subcutaneous	GTEx
rs11211134	CCDC163P	cis	Whole Blood	GTEx
rs11211134	CCDC163P	cis	Thyroid	GTEx
rs11211134	CCDC163P	cis	Esophagus Mucosa	GTEx
rs11211134	CCDC163P	cis	Muscle Skeletal	GTEx
rs11211134	CCDC163P	cis	Skin Sun Exposed Lower leg	GTEx
rs11211134	CCDC163P	cis	Heart Left Ventricle	GTEx
rs11211134	CCDC163P	cis	Esophagus Muscularis	GTEx
rs11211134	CCDC163P	cis	Artery Aorta	GTEx
rs11211134	CCDC163P	cis	Stomach	GTEx
rs11211134	LOC126661	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45988400-45993400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr1:45988400-45997200	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr1:45988600-45993400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr1:45989000-45993200	Weak transcription	Placenta	Placenta
5	chr1:45989200-46000600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr1:45991000-45993400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr1:45991000-45993400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr1:45991000-45993400	Weak transcription	K562	blood
9	chr1:45991200-45993400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr1:45991200-45993400	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr1:45992600-45993600	Weak transcription	A549	lung
12	chr1:45992800-45993200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr1:45992800-45993200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr1:45992800-45993400	Weak transcription	Stomach Mucosa	stomach
15	chr1:45992800-45998600	Weak transcription	HepG2	liver
16	chr1:45992800-46002400	Weak transcription	Fetal Intestine Small	intestine

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