Variant report

Variant	rs35884660
Chromosome Location	chr16:31522008-31522009
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:31482449..31485901-chr16:31517810..31523430,5	MCF-7	breast:
2	chr16:31516310..31522725-chr16:31722480..31728998,9	MCF-7	breast:
3	chr16:31468357..31473774-chr16:31516772..31522690,14	K562	blood:
4	chr16:31463366..31472153-chr16:31517209..31524290,14	MCF-7	breast:
5	chr16:31468899..31473390-chr16:31518411..31522821,12	MCF-7	breast:
6	chr16:31468972..31472729-chr16:31517678..31523478,11	K562	blood:

Variant related genes	Relation type
ENSG00000197302	Chromatin interaction
ENSG00000140691	Chromatin interaction
ENSG00000260267	Chromatin interaction
ENSG00000140682	Chromatin interaction
ENSG00000261731	Chromatin interaction
ENSG00000261474	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10596	0.80[AFR][1000 genomes];0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11150624	0.80[ASN][1000 genomes]
rs11150628	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11646054	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs11646911	0.82[ASN][1000 genomes]
rs12596058	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12920273	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4243237	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4313820	0.81[ASN][1000 genomes]
rs4423435	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4482295	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4544258	0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4597343	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4627374	0.91[ASN][1000 genomes]
rs4889661	0.81[ASN][1000 genomes]
rs4889664	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4889666	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6565253	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7192364	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7201796	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7205058	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7206531	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8048218	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8050563	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8050712	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8054784	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8057029	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs8060914	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3392534	chr16:31303038-31573066	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	104 gene(s)	inside rSNPs	diseases
2	nsv833194	chr16:31358179-31528545	Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	97 gene(s)	inside rSNPs	diseases
3	nsv905747	chr16:31394179-31888684	Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	123 gene(s)	inside rSNPs	diseases
4	nsv905748	chr16:31427678-31559220	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	94 gene(s)	inside rSNPs	diseases
5	nsv905749	chr16:31427678-31565597	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	96 gene(s)	inside rSNPs	diseases
6	nsv905750	chr16:31427678-31587662	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	98 gene(s)	inside rSNPs	diseases
7	nsv905752	chr16:31436932-31565597	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	95 gene(s)	inside rSNPs	diseases
8	nsv905753	chr16:31436932-31587662	Enhancers Active TSS Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	97 gene(s)	inside rSNPs	diseases
9	nsv905754	chr16:31451699-31565597	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	93 gene(s)	inside rSNPs	diseases
10	nsv1060240	chr16:31495873-31581450	Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
11	esv1823209	chr16:31521276-31580272	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31520600-31523000	Enhancers	Primary T killer memory cells from peripheral blood	blood
2	chr16:31520600-31523600	Weak transcription	Esophagus	oesophagus
3	chr16:31520800-31522200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr16:31520800-31523600	Weak transcription	HSMM	muscle
5	chr16:31520800-31524000	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr16:31520800-31524200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr16:31520800-31524200	Weak transcription	HMEC	breast
8	chr16:31520800-31524600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr16:31521000-31524000	Weak transcription	Osteobl	bone
10	chr16:31521000-31524200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr16:31521000-31524200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr16:31521200-31522200	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr16:31521200-31524200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr16:31521200-31524200	Weak transcription	Fetal Muscle Leg	muscle
15	chr16:31521400-31522200	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr16:31521400-31523600	Weak transcription	HSMMtube	muscle
17	chr16:31521400-31524000	Weak transcription	Primary B cells from peripheral blood	blood
18	chr16:31521400-31524200	Weak transcription	NHEK	skin
19	chr16:31521400-31524400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr16:31521400-31525400	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr16:31521600-31522200	Enhancers	K562	blood
22	chr16:31521600-31522800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr16:31521600-31523800	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr16:31522000-31522200	Enhancers	Sigmoid Colon	Sigmoid Colon

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links