Variant report

Variant	rs170510
Chromosome Location	chr6:44244602-44244603
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:44244057..44246531-chr6:44270330..44272647,2	MCF-7	breast:
2	chr6:44235774..44239606-chr6:44242951..44245858,3	MCF-7	breast:
3	chr6:44242284..44246953-chr6:44248645..44251734,5	K562	blood:
4	chr6:44243596..44246439-chr6:44318248..44320876,2	K562	blood:

Variant related genes	Relation type
ENSG00000178233	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1123523	0.85[ASN][1000 genomes]
rs12205227	0.86[ASN][1000 genomes]
rs12215176	0.86[ASN][1000 genomes]
rs12664825	0.87[ASN][1000 genomes]
rs12943	0.88[ASN][1000 genomes]
rs2297335	0.87[ASN][1000 genomes]
rs2297336	0.87[ASN][1000 genomes]
rs324138	0.88[ASN][1000 genomes]
rs324139	0.88[ASN][1000 genomes]
rs324140	0.87[ASN][1000 genomes]
rs324142	0.87[ASN][1000 genomes]
rs324144	0.87[ASN][1000 genomes]
rs324145	0.87[ASN][1000 genomes]
rs324146	0.87[ASN][1000 genomes]
rs324147	0.87[ASN][1000 genomes]
rs325017	0.88[ASN][1000 genomes]
rs325018	0.88[ASN][1000 genomes]
rs325019	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs34865422	0.81[ASN][1000 genomes]
rs3734710	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4714773	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4714774	0.88[ASN][1000 genomes]
rs516582	0.88[ASN][1000 genomes]
rs524533	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs529948	0.94[ASN][1000 genomes]
rs545970	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs551145	0.94[ASN][1000 genomes]
rs557373	0.87[ASN][1000 genomes]
rs570469	0.88[ASN][1000 genomes]
rs571770	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs614715	0.87[ASN][1000 genomes]
rs694349	0.88[ASN][1000 genomes]
rs844315	0.91[ASN][1000 genomes]
rs9369469	0.88[ASN][1000 genomes]
rs9381305	0.88[ASN][1000 genomes]
rs9381306	0.88[ASN][1000 genomes]
rs9381307	0.87[ASN][1000 genomes]
rs9381308	0.87[ASN][1000 genomes]
rs9394999	0.81[ASN][1000 genomes]
rs9395000	0.86[ASN][1000 genomes]
rs9395001	0.85[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	nsv931987	chr6:43624625-44350167	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	201 gene(s)	inside rSNPs	diseases
2	nsv603003	chr6:44191920-44253765	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
3	nsv462936	chr6:44191920-44282316	Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
4	nsv603004	chr6:44191920-44282316	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
5	nsv885853	chr6:44197181-44274797	Weak transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
6	nsv524398	chr6:44200953-44253765	Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
7	nsv885854	chr6:44211867-44274797	Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
8	nsv462937	chr6:44211867-44279111	Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
9	nsv603005	chr6:44211867-44279111	Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
10	nsv885857	chr6:44223010-44250165	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	28 gene(s)	inside rSNPs	diseases
11	esv3422155	chr6:44242599-44245147	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44239600-44247600	Enhancers	Fetal Brain Male	brain
2	chr6:44240800-44245000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:44241200-44252200	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr6:44242400-44245200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr6:44243200-44244800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr6:44243600-44246600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:44243800-44245600	Strong transcription	Fetal Brain Female	brain
8	chr6:44244000-44244800	Bivalent Enhancer	Fetal Stomach	stomach
9	chr6:44244000-44247000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
10	chr6:44244200-44244800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:44244200-44245000	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
12	chr6:44244200-44245000	Genic enhancers	Brain Germinal Matrix	brain
13	chr6:44244200-44245000	Bivalent Enhancer	Fetal Muscle Leg	muscle
14	chr6:44244200-44247800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:44244200-44250600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr6:44244400-44244800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr6:44244400-44251000	Weak transcription	Gastric	stomach
18	chr6:44244400-44257400	Weak transcription	Pancreas	Pancrea
19	chr6:44244400-44264800	Weak transcription	Right Atrium	heart
20	chr6:44244600-44244800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:44244600-44245200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin

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