Variant report

Variant	rs11607986
Chromosome Location	chr11:34878809-34878810
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:34870702..34872577-chr11:34878120..34880872,2	K562	blood:
2	chr11:34868671..34870522-chr11:34876282..34878999,2	MCF-7	breast:
3	chr11:34870702..34874791-chr11:34878120..34882301,4	K562	blood:
4	chr11:34875503..34877981-chr11:34878649..34881731,3	K562	blood:
5	chr11:34878119..34880348-chr11:34884856..34886591,2	K562	blood:

Extended variants
information (count: 86 )
Associated
traits (count: 9 )

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs10488802	0.96[CEU][hapmap];0.82[AMR][1000 genomes]
rs10836316	0.86[EUR][1000 genomes]
rs10836317	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11032891	0.81[EUR][1000 genomes]
rs11032894	0.82[EUR][1000 genomes]
rs11032895	0.82[EUR][1000 genomes]
rs11032898	0.86[EUR][1000 genomes]
rs11032899	0.86[EUR][1000 genomes]
rs11032903	0.86[EUR][1000 genomes]
rs1117050	0.96[CEU][hapmap];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11601737	0.81[AMR][1000 genomes]
rs11602364	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11602584	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11605600	0.96[CEU][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11605972	0.81[AMR][1000 genomes]
rs11605993	0.94[CEU][hapmap];0.81[AMR][1000 genomes]
rs11606871	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11608116	0.81[AMR][1000 genomes]
rs12278318	0.86[EUR][1000 genomes]
rs12280958	0.86[EUR][1000 genomes]
rs12294339	0.81[EUR][1000 genomes]
rs1409718	0.82[AMR][1000 genomes]
rs1509659	0.82[EUR][1000 genomes]
rs1509660	0.82[EUR][1000 genomes]
rs1509661	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17347979	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17348697	0.96[CEU][hapmap];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17348711	0.96[CEU][hapmap];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17349298	0.96[CEU][hapmap];0.82[AMR][1000 genomes]
rs17432226	0.96[CEU][hapmap];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17433496	0.91[CEU][hapmap];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17434808	0.96[CEU][hapmap];0.82[AMR][1000 genomes]
rs17434946	0.96[CEU][hapmap];0.82[AMR][1000 genomes]
rs17711539	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17783998	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17784324	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1828299	0.86[EUR][1000 genomes]
rs2217479	0.95[CEU][hapmap];0.82[AMR][1000 genomes]
rs2421744	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3852515	0.85[CEU][hapmap];0.82[AMR][1000 genomes]
rs3852516	0.82[AMR][1000 genomes]
rs3852517	0.88[CEU][hapmap];0.81[AMR][1000 genomes]
rs4534556	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs55672020	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs55796371	0.86[EUR][1000 genomes]
rs55868872	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs55911702	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs55929026	0.82[AMR][1000 genomes]
rs55957800	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61734605	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6484738	0.81[EUR][1000 genomes]
rs7106831	0.88[EUR][1000 genomes]
rs7110461	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7111695	0.85[EUR][1000 genomes]
rs7115749	0.81[EUR][1000 genomes]
rs7122048	0.86[EUR][1000 genomes]
rs7123029	0.86[EUR][1000 genomes]
rs7129517	0.86[EUR][1000 genomes]
rs7129533	0.86[EUR][1000 genomes]
rs7130678	0.86[EUR][1000 genomes]
rs7130774	0.86[EUR][1000 genomes]
rs7131229	0.86[EUR][1000 genomes]
rs7131272	0.86[EUR][1000 genomes]
rs72912924	0.82[AMR][1000 genomes]
rs72912934	0.82[AMR][1000 genomes]
rs72922479	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72922482	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72924508	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72924541	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72924562	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72926580	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72928507	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72930433	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72930443	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72930458	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72930462	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72930468	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72930480	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7479823	0.96[CEU][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7937316	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7947848	0.86[EUR][1000 genomes]
rs7948977	0.82[AMR][1000 genomes]
rs7950996	0.96[CEU][hapmap];0.82[AMR][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	nsv832118	chr11:34743123-34903951	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv832119	chr11:34815528-35009370	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
3	esv275183	chr11:34877761-34881376	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

mRNA abundance (count:9)

SNP	Gene	Cis/trans	Tissue	Source
rs11607986	APIP	cis	lung	GTEx
rs11607986	APIP	cis	Esophagus Muscularis	GTEx
rs11607986	APIP	cis	Artery Tibial	GTEx
rs11607986	APIP	cis	Nerve Tibial	GTEx
rs11607986	APIP	cis	Adipose Subcutaneous	GTEx
rs11607986	APIP	cis	Artery Aorta	GTEx
rs11607986	APIP	cis	Heart Left Ventricle	GTEx
rs11607986	APIP	cis	Thyroid	GTEx
rs11607986	APIP	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34859000-34909400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr11:34872200-34886600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:34876600-34896000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:34876800-34880400	Weak transcription	Esophagus	oesophagus
5	chr11:34877000-34880800	Weak transcription	HepG2	liver
6	chr11:34877400-34881000	Weak transcription	Left Ventricle	heart
7	chr11:34877400-34886400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr11:34877600-34880000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr11:34877600-34881600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr11:34877600-34906400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr11:34878000-34880800	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr11:34878200-34881000	Weak transcription	Fetal Muscle Leg	muscle
13	chr11:34878200-34881600	Weak transcription	Psoas Muscle	Psoas
14	chr11:34878200-34891400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:34878800-34879400	Enhancers	Stomach Mucosa	stomach

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